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Journal articles on the topic '1 Corinthians 6:9-10'

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Published: 4 June 2021

Last updated: 6 February 2022

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1

Pranoto, David Susilo. "PELAYANAN PENYEBARAN INJIL BERDASARKAN 2 KORINTUS 6:1-10." Manna Rafflesia 3, no. 1 (October 31, 2016): 1–20. http://dx.doi.org/10.38091/man_raf.v3i1.63.

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This 2nd Corinthian letter, written by the Apostle Paul, was addressed to the Corinthians. This letter is intended for the purpose, so that in conveying the gospel has the correct method so that the gospel can be accepted. The duty of believers is to convey the gospel / good news to everyone who does not know Christ. In writing this article we will explore how the Apostle Paul's perspective on the ministry of spreading the gospel based on 2 Corinthians 6: 1-10. Therefore through this writing, we will again remind and refresh believers about the importance of the ministry of spreading the gospel.

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2

Drake Williams, H. H. "“IMITATE ME”: INTERPRETING IMITATION IN 1 CORINTHIANS IN RELATION TO IGNATIUS OF ANTIOCH." Perichoresis 11, no. 1 (June 1, 2013): 77–95. http://dx.doi.org/10.2478/perc-2013-0004.

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ABSTRACTSeveral times within 1 Corinthians Paul encourages the Corinthians to imitate him. These are found at critical junctures in the epistle in 1 Corinthians 4:16 and 11:1. The meaning of these sections is in question from the perspective of Corinthian scholars. Several believe that Paul is appealing to apostolic power and authority to coerce the Corinthians to obey him, whereas others find him responding to social situations. This is different from the way that imitation and discipleship are presented within the writings of Ignatius of Antioch. Pauline ideas, specifically those from 1 Corinthians, are known to have influenced Ignatius of Antioch’s writing, and thus Ignatius’ ideas about imitation are likely to reflect the meaning that Paul intended. Ignatius specifically speaks about imitation and discipleship in several places: Ign. Eph. 1, 2, 4; 3:1-3, Ign. Magn. 4:1; 5:1-2; 9:1-6, Ign. Rom. 3:1-2; 6, 3, 1. When these passages are considered, imitation involves suffering and possibly martyrdom. Imitation is also connected to the cross of Christ and is not a means to enforce superiority. Ignatius’ view of imitation would contradict the opinions of some scholars who see Paul’s injunction for imitation as a claim for power. It also supplies more information to the idea than those who claim that it is simply a counter example to the social situation.

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3

Tamba, Tiffany. "Recalling to Warning:Sosial-Scientific Criticism (SSC) of 1 Corinthians 10:1-13." Jurnal Teologi Cultivation 4, no. 2 (January 22, 2021): 36–55. http://dx.doi.org/10.46965/jtc.v4i2.348.

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AbstractThe meeting of certain cultures and religions with outside cultures and religions results in complex cultural contacts that even overlap. Add more, the high heterogeneity which will affect the process of acculturation, assimilation, inculturation and even enculturation which may increase diversity immunity, but on the contrary triggers sosial irregularities experienced by the Corinthian Christians in 1 Cor. 10: 1-13. The purpose of this study is to see the sosial dynamics of 1 Cor. 10: 1-13 and find the theological message in it by using the interpretation of Sosial-Scientific Criticism (SSC). The use of this method is successful in tracing the sosial aspects that accompany Paul's warnings, advice and message to the diverse Corinthian Christian church. As a result, Paul did a recalling to warning (vv. 1-5) regarding the parallel experiences between his ancestors and them to become learning (vv. 6-10) to then turn to turn (vv. 11-13) towards optimal and total balance. starting with religious regularity, namely loyalty to Allah.

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4

Elliott, John H. "No Kingdom of God for Softies? or, What Was Paul Really Saying? 1 Corinthians 6:9–10 in Context." Biblical Theology Bulletin: Journal of Bible and Culture 34, no. 1 (February 2004): 17–40. http://dx.doi.org/10.1177/014610790403400103.

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5

Starling, David. "The ἄπιστοι of 2 Cor 6:14." Novum Testamentum 55, no. 1 (2013): 45–60. http://dx.doi.org/10.1163/15685365-12341406.

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Abstract Amongst defenders of the Pauline authorship of 2 Cor 6:14-7:1, an impasse exists between those who read the ἄπιστοι of v. 14 as a reference to the Gentile pagans of the city and those who read it as a reference to the “false apostles” of chs. 10-13. In this article I suggest a possible resolution of that impasse, based on a re-examination of the content and function of holiness concepts within 2 Corinthians. The ἄπιστοι in view are indeed the Gentile pagans of Corinth, but the principal issue over which Paul is urging the Corinthians to separate from them is the pagan σοφία σαρκική that has distorted their assessments of Paul and his opponents.

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6

Engberg-Pedersen, Troels. "Paul's Temporal Thinking: 2 Cor 2.14–7.4 as Paraenetic Autobiography." New Testament Studies 67, no. 2 (March 4, 2021): 157–80. http://dx.doi.org/10.1017/s0028688520000326.

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A precise temporal (and sometimes topographical) scheme is found behind Second Corinthians at three levels: (i) 1–7 (past: Ephesus → Macedonia), 8–9 (present: Macedonia), 10–13 (future: Macedonia → Corinth); (ii) 2.12–7.16 (Troas (2.12–13) → the Hellespont (2.14–7.4) → Macedonia (7.5–16)); (iii) 2.14–7.4. For (i)-(ii), see 1 Thess 1–3 and 2.17–3.10. For (iii), I detail this temporal structure: (a) 3.1–18 → 4.1–6; (b) 4.7–5.10 → 5.11–13; (c) 5.14–6.10 → 6.11–7.4, viz. (a) Paul's initial call and (b) his life in the present and future → his general missionary practice, including to ‘you’, and (c) his now directly addressing ‘you’ with strong paraenesis.

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7

Harris, M. "15th January: Second Sunday after Epiphany: 1 Samuel 3:1-10, (11-20); Psalm 139:1-6, 13-18; 1 Corinthians 6:12-20; John 1:43-51." Expository Times 123, no. 3 (November 14, 2011): 128–30. http://dx.doi.org/10.1177/0014524611421734b.

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8

Lee, Minkyu. "The homosexuality in Ancient Greece and Rome, and the Meaning of μαλακοί and ᾀρσϵνοκοῑται in 1 Corinthians 6:9." Korean New Testament Studies 25, no. 4 (December 31, 2018): 1013–46. http://dx.doi.org/10.31982/knts.2018.12.25.4.1015.

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9

Smit, Joop. ""WHAT IS APOLLOS? WHAT IS PAUL?" IN SEARCH FOR THE COHERENCE OF FIRST CORINTHIANS 1:10-4:21." Novum Testamentum 44, no. 3 (2002): 231–51. http://dx.doi.org/10.1163/156853602320249464.

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The coherence of 1 Cor. 1:10-4:21 is studied in three steps. With regard to the textual syntax it is shown that this passage consists of an introduction (1:10-17), followed by four separate sections elaborating first the theme of wisdom (1:18-2:5; 2:6-3:4) and next the division among the Corinthians (3:5-4:5; 4:6-21). At the semantic level it is argued that adherents of Apollos are Paul's main target and that in 1:18-19 he alludes to them. Further it is clarified that in rejecting σoϕiα λoγoυ he does not attack rhetoric as such, but human reasoning which they greatly admire. Finally a pragmatic analysis demonstrates that, following classical status theory, Paul defends himself in four steps against the depreciatory opinion adherents of Apollos harbor against him.

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10

Hustler, Jonathan. "27th January: 3rd Sunday after Epiphany: Nehemiah 8.1–3, 5–6, 8–10; Psalm 19; 1 Corinthians 12.12–31a; Luke 4.14–21." Expository Times 130, no. 3 (November 7, 2018): 130–32. http://dx.doi.org/10.1177/0014524618798299c.

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11

Parker, David M. "Tithing: Instruction or Instructive?" Journal of Pentecostal Theology 21, no. 2 (2012): 201–20. http://dx.doi.org/10.1163/17455251-02102003.

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After surveying the disparate Old Testament material on tithing, this paper isolated 1 Corinthians 9 as the loudest echo of that practice. It then modelled 1Corinthians 9 and 10 as illustrative rather than regulative in its approach to the former testament. Utilizing the ‘lesser-to-greater’ (qal wāḥômer) argument inherent in 1 Corinthians 9, it developed an implied benchmark of tithing in 1 Corinthians 9 and 1 Tim. 5.17 to argue such as the base upon which NT giving is predicated. Noting the socio-economic disparity of Corinth, in comparison with the ideal distribution by which the Hebrew Scriptures regulated tithes, the paper then invoked the gift of giving from Rom. 12.8 to suggest proportional giving rather than the strict regulation of the Mosaic legislation. Finally, returning to the literary setting of 1 Corinthians 9, any conclusion, at least from the Pauline corpus, was shown to be contextually suggestive, not invariably regulative.

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12

AMADOR, J. D. H. "Revisiting 2 Corinthians: Rhetoric and the Case for Unity." New Testament Studies 46, no. 1 (January 2000): 92–111. http://dx.doi.org/10.1017/s0028688500000060.

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The current work argues for the compositional unity of 2 Corinthians. First, it addresses the chronological and argumentative relationship of chapters 10–13 to chapters 1–9. It next rejects the presence of so-called ‘interpolations’ and ‘sources’ in chapters 1–9. Finally, it considers the integrity of chapters 8 and 9. The uniqueness of this effort lies in its emphasis upon rhetorical reasons and warrants against the widely accepted partition hypothesis of Pauline historical- and source-critical scholarship. It does so by demonstrating the complex integrity of the argumentative development and trajectories in 2 Corinthians. It concludes with a new, suggestive approach to the correspondence as a complex, but nevertheless coherent, act of persuasion.

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13

Schmeller, Thomas. "No Bridge over Troubled Water? The Gap between 2 Corinthians 1–9 and 10–13 Revisited." Journal for the Study of the New Testament 36, no. 1 (July 25, 2013): 73–84. http://dx.doi.org/10.1177/0142064x13495136.

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14

Wright, D. F. "Translating APSENOKOITAI (1 Cor. 6:9; 1 Tim. 1:10)." Vigiliae Christianae 41, no. 4 (December 1987): 396. http://dx.doi.org/10.2307/1583743.

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15

Wright, D. F. "Translating APΣENOKOITAI (1 Cor. 6:9; 1 Tim. 1:10)." Vigiliae Christianae 41, no. 4 (1987): 396–98. http://dx.doi.org/10.1163/157007287x00247.

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16

Winter, Sean F. "‘He Will Rescue Us Again’: Affliction and Hope in 2 Corinthians 1:8–11." Religions 11, no. 5 (May 1, 2020): 222. http://dx.doi.org/10.3390/rel11050222.

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Dark times can generate crippling despair all too easily. Resources for resistance to despair and for the discovery and articulation of hope are not always readily apparent. This essay considers Paul’s account of his own immersion in such a situation: An ‘affliction’ that left him ‘unbearably crushed’, ‘despairing of life itself’ (2 Cor 1:9), and under a ‘sentence of death’ (2 Cor 1:10). Making a speculative proposal about the nature of Paul’s experience, the essay goes on to argue that Paul identified two fundamental resources for hope. The first is a conviction about an eschatological act that undoes the sentence of death and effects the possibility of rescue or deliverance. The second is a form of human solidarity that generates potential reorientation to the reality of ‘rescue’. While the essay explores these ideas within the terms and framework of Paul’s rhetoric in 2 Corinthians, it will do so with one clear eye on the potential resources that Pauline theology offers those who live in inexplicably dark times today, not least by considering the potential resources for political optimism.

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17

Hałas, Stanisław. "Chciwość pieniędzy korzeniem wszelkiego zła według 1 Tm 6, 9–10." Ruch Biblijny i Liturgiczny 40, no. 4 (August 31, 1987): 297. http://dx.doi.org/10.21906/rbl.2076.

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18

May, David M. "Timothy A. Brookins and Bruce W. Longenecker, I Corinthians 1–9: A Handbook on the Greek Text Timothy A. Brookins and Bruce W. Longenecker, I Corinthians 10–16: A Handbook on the Greek Text." Review & Expositor 117, no. 2 (May 2020): 301–2. http://dx.doi.org/10.1177/0034637320923300.

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19

Višnjevac, Aleksandar, Biserka Kojić-Prodić, Marijana Vinković, and Kata Mlinarić-Majerski. "Dispiro[adamantane-2,2′-1′,3′,6′,9′,11′,14′-hexathiacyclohexadecane-10′,2′′-adamantane]." Acta Crystallographica Section C Crystal Structure Communications 59, no. 6 (May 20, 2003): o314—o316. http://dx.doi.org/10.1107/s0108270103008369.

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20

Becker, H., L. Hansen, BW Skelton, and AH White. "(E)-1-(9-Anthryl)-2-(10-methyl-9-anthryl)ethene: Molecular Structure and Spectroscopic Properties." Australian Journal of Chemistry 38, no. 5 (1985): 809. http://dx.doi.org/10.1071/ch9850809.

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(E)-1-(9-Anthryl)-2-(10-methyl-9-anthryl) ethelle has been synthesized from 10-methyl-9-anthraldehyde and (9-anthrylmethyl) triphenylphosphonium bromide, and its crystal structure has been determined by X-ray diffraction. Its molecular geometry was found to be such as to have the planes of the two anthracene moieties form an angle of 70.8°, the plane of the ethene bond bring twisted out of the planes of the anthracenes by an angle of about 55°. The intermolecular arrangement of parallel adjacent molecules in the crystal lattice is characterized by shifts about the short and long axes of the anthracenes. The excimer-like crystal fluorescence is attributed to the interplanar distance of 3.5 Ǻ between anthracene π- systems in parallel adjacent molecules. Crystals are triclinic, Pī , a 12.95(1), b 9.316(6), c 9.098(9) Ǻ, α 86.17(7), β 72.26(7), γ 74.61(6)°,Z 2; R was 0.054 for 1059 independent 'observed' reflections.

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21

Rádl, Stanislav. "Preparation of 1-Hydroxyxanthen-9(9H)-ones and 1-Hydroxyacridin-9(10H)-ones via Corresponding 3,4-Dihydro-1,9(2H)-diones." Collection of Czechoslovak Chemical Communications 60, no. 12 (1995): 2127–36. http://dx.doi.org/10.1135/cccc19952127.

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Target 10-cyclopropyl-7-fluoro-1-hydroxy-6-(4-methyl-1-piperazinyl)acridin-9(10H)-one (IVc) and 7-fluoro-1-hydroxy-6-(4-methyl-1-piperazinyl)-9H-xanthen-9-one (IVd) were obtained from corresponding difluoro derivatives IVa and IVb, respectively. These intermediates were synthesized via respective 3,4-dihydro-1,9(2H)-diones Va and Vb. Acridine derivative (10-cyclopropyl-6,7-difluoro-3,4-dihydro-1H-acridine-1,9(2H,10H)-dione, Va) was synthesized from 1-cyclopropyl-6,7-difluoroisatoic anhydride (XI) and xanthene derivative (6,7-difluoro-3,4-dihydro-1H-xanthen-1,9(2H)-dione, Vb) from cyclohexenone derivative VIb. Several unsuccessful attempts to prepare hydroxyacridone IVc and/or some useful intermediates of its synthesis are also described.

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22

Cui, Hao, Xin-Ting Yan, Wenya Chen, and Tao Yang. "The crystal structure of 2,4,6-tris[4-(1H-imidazol-1-yl)phenyl]-1,3,5-triazine — dimethylformamide (1/1), C33H28N10O." Zeitschrift für Kristallographie - New Crystal Structures 234, no. 6 (November 26, 2019): 1275–78. http://dx.doi.org/10.1515/ncrs-2019-0401.

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AbstractC33H28N10O, triclinic, P1̄ (no. 2), a = 14.7148(9) Å, b = 15.5185(10) Å, c = 16.1128(9) Å, α = 113.219(6)°, β = 96.735(5)°, γ = 115.259(6)°, V = 2872.0(3) Å3, Z = 4, Rgt(F) = 0.0426, wRref(F2) = 0.1108, T = 150(2) K.

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23

Bentley, D. R., P. Deloukas, A. Dunham, L. French, S. G. Gregory, S. J. Humphray, A. J. Mungall, et al. "The physical maps for sequencing human chromosomes 1, 6, 9, 10, 13, 20 and X." Nature 409, no. 6822 (February 2001): 942–43. http://dx.doi.org/10.1038/35057165.

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24

Wilk, Janusz. "The Economy of Salvation According to 2 Tm 1 : 9–10." Ruch Biblijny i Liturgiczny 66, no. 1 (March 31, 2013): 33. http://dx.doi.org/10.21906/rbl.58.

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Artykuł podejmuje analizę hymniczno-liturgicznego dwuwiersza, który porusza trzy aspekty tematyczne: odkupienie człowieka przez Boga (w. 9a); odwieczne postanowienie zbawienia człowieka przez Jezusa Chrystusa (w. 9b) oraz skutki odkupienia – nowe, nieprzemijające życie (w. 10). 2 Tm 1, 9–10 eksponuje zbawienie jako łaskę Boga wobec człowieka, który w żaden sposób nie mógł sam zainicjować lub zrealizować tego dzieła. Człowiek jednakże mógł i wciąż może przyjąć lub odrzucić jego skutki. Studium 2 Tm 1, 9–10 wskazuje również na semantyczną i tematyczną integralność tego dwuwiersza z całą perykopą 2 Tm 1, 6–14. Nie tylko nie przerywa on głównej myśli całej wypowiedzi (wierność i wytrwałość w służbie Ewangelii), ale stanowi jej szczegółowe wyjaśnienie, wskazując, czym jest Ewangelia, dla której warto przyjąć cierpienie wiążące się z niedalekim męczeństwem lub też z codzienną, systematyczną i uciążliwą pracą związaną z przepowiadaniem Dobrej Nowiny o zbawieniu człowieka dokonanym przez Boga w osobie Jezusa Chrystusa.

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25

Aritonang, Buha. "Bentuk Numeralia 1--10 dalam Bahasa-Bahasa Daerah di Kabupaten Kepulauan Yafen." Gramatika: Jurnal Ilmiah Kebahasaan dan Kesastraan 5, no. 1 (June 1, 2017): 12–26. http://dx.doi.org/10.31813/gramatika/5.1.2017.88.12--26.

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Numeralia itu tidak semudah berhitung satu, dua, tiga, dan seterusnya dan bentuknya pun dalam setiap bahasa berbeda-beda. Tujuan penelitian ini adalah untuk untuk mendeskripsikan bentuk numeralia 1—10 dalam bahasa-bahasa daerah di Kabupaten kepulauan Yafen Penelitian dilakukan di 12 kampung yang berdeda bahasa. Metode penelitian menggunakan metode kualitatif. Hasil analisis menunjukkan bahwa (i) bentuk numeralia 1—10 dibedakan menjadi (a) numeralia dasar seperti numeralia 1—5 dan 10 dalam bahasa Ambai, Saweru, Yawa Onate, Serui Laut, Warari Onate, Busami, Marau, Munggui, Ansus-Papuma, Poom, Wabo, dan Wooi Dumani; 6—7 dalam bahasa Ambai; dan 6—9 dalam bahasa Marau, Munggui, Ansus-Papuma, Poom, Wabo, dan Wooi Dumani dan (b) numeralia gabungan seperti numeralia 8 dan 9 dalam bahasa Ambai dan 6—9 dalam bahasa Saweru, Yawa Onate, Serui Laut, dan Warari Onate; (ii) Sebagian numeralia turunan bahasa-bahasa daerah di Kabupaten kepulauan Yafen dihubungkan penghubung (linker) rei/iji ‘tambah’ seperti numeralia enam dalam bahasa Saweru dan Yawa; (iii) penghubung ko ‘tambah’ sangat penting untuk mewujudkan bentuk numeralia gabungan untuk pembentukan numeralia gabungan angka 6—9; (iv) numeralia gabungan tanpa penghubung untuk menyatakan angka 6—9 dalam Warari Onate; dan (v) numeralia gabungan dapat berbentuk pengurangan seperti bentuk numeralia gabungan untuk menyatakan angka 10 dalam bahasa Ambai.

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Ming-Lun, Chen, and Yu Xiao-Guang. "Spectra and oscillator strengths of 3p 6 3d 9 –3p 5 3d 10 and 3p 6 3d 9 –3p 6 3d 8 4p transitions for cobalt-like Sn 23 + ion." Chinese Physics B 18, no. 1 (January 2009): 157–60. http://dx.doi.org/10.1088/1674-1056/18/1/024.

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Kinev, Evgeny A. "16Cr-19Ni steel swelling at dose rates from 1×10-8 to 1.6×10-6 dpa/s." Nuclear Energy and Technology 6, no. 4 (November 18, 2020): 249–52. http://dx.doi.org/10.3897/nucet.6.60371.

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The article presents the first data on EK-164ID steel swelling after operational irradiation in a fast nuclear reactor in the temperature range of 370–630 °C and maximum damaging doses of 66–77 dpa. The dose accumulation rate along the cladding tubes made of this material was 1×10-8–1.6×10-6 dpa/s. The swelling was determined by the hydrostatic weighing method with an error of no more than 0.5%. The results obtained were analyzed depending on the irradiation parameters and in comparison with the 16Cr-15Ni grade material. The objectives of the study were to estimate the characteristic values of the maximum swelling temperature and dose as well as to calculate the average material swelling rate at the working temperature of irradiation, the incubation period for the onset of swelling, and the stationary swelling rate. It was found that the tube samples, characterized with austenite grain sizes of 9–12 µm before irradiation, have an average swelling rate of 0.035–0.05 %/dpa after reaching the maximum damaging doses of 66–77 dpa (at a rate of (1–1.5)×10-6 dpa/s) and not more than 0.035%/dpa at doses less than 20 dpa (at a rate of 5×10-7 dpa/s). The characteristic maximum swelling temperature of the studied material is in the range of 430–500 °C. The characteristic maximum swelling dose is in the range of 61–72.5 dpa or 70–80% of the maximum accumulated dose. The incubation stationary swelling period for the material is 30 dpa. The stationary swelling rate is 0.1% /dpa. The radiation resistance characteristics of the studied material have an advantage over those for 16Cr-15Ni grade cladding materials under similar irradiation conditions and a similar structural state, which inherits grain sizes of 9–14 μm during the tube processing.

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28

Gong, Yi-Xia, and Yi-Ding Geng. "The crystal structure of 2-[(S)-1-(naphthalen-1-yl)ethyl]-2,3,7,7a- tetrahydro-3a,6-epoxyisoindol-1(6H)-one, C19H20NO2." Zeitschrift für Kristallographie - New Crystal Structures 236, no. 1 (January 26, 2021): 167–68. http://dx.doi.org/10.1515/ncrs-2020-0439.

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29

Gichumbi, Joel M., Bernard Omondi, and Holger B. Friedrich. "Crystal structure of chlorido-(η6-p-cymene)-(N-(2-fluorophenyl)-1-(pyridin-2-yl)methanimine-κ2N,N′)ruthenium(II) – acetone (1/1), C22H23ClN2F7OPRu." Zeitschrift für Kristallographie - New Crystal Structures 235, no. 3 (April 28, 2020): 551–53. http://dx.doi.org/10.1515/ncrs-2019-0793.

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AbstractC22H23ClN2F7OPRu, monoclinic, P21/c (no. 14), a = 7.30480(10) Å, b = 12.9540(3) Å, c = 28.7076(6) Å, β = 96.6990(10)°, V = 2697.95(9) Å3, Z = 4, Rgt(F) = 0.0196, wRref(F2) = 0.0479, T = 100(2) K.

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Poddubikov, Vladimir Valerievich. "Emma Gilberthorpe and Gavin Hilson (eds.): Natural Resource Extraction and Indigenous Livelihoods: Development Challenges in an Era of Globalization. Surrey, Burlington: Ashgate Publishing Limited, 2014. ISBN 978-1-4094-3777-2 (hardback); ISBN 978-1-4094-3778-9 (ebook); ISBN 978-1-4094-7268-1 (epub)." Sibirskie istoricheskie issledovaniya, no. 4 (December 1, 2015): 73–85. http://dx.doi.org/10.17223/2312461x/10/6.

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31

Li, Zhao-Hao. "Crystal structure of tetraaqua-bis[6-(1H-imidazol-1-yl-κN)nicotinato]zinc(II), C18H20N6O8Zn." Zeitschrift für Kristallographie - New Crystal Structures 233, no. 2 (March 28, 2018): 273–74. http://dx.doi.org/10.1515/ncrs-2017-0271.

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AbstractC18H20N6O8Zn, triclinic, P1̅, a = 6.2576(6) Å, b = 6.9645(8) Å, c = 12.1262(15) Å, α = 78.536(10)°, β = 86.677(9)°, γ = 72.340(9)°, Z = 1, V = 493.52(10) Å3, Rgt(F) = 0.0603, wRref (F2) = 0.1290, T = 291(2) K.

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32

Носкова, Светлана Юрьевна, Мария Игоревна Зимина, Ольга Олеговна Бабич, Станислав Алексеевич Сухих, Александр Юрьевич Просеков, and Елена Викторовна Ульрих. "Study of the biocompatibility of lactic acid bacteria and other microorganisms-antagonists isolated from natural sources." Food processing industry, no. 5 (May 28, 2021): 40–42. http://dx.doi.org/10.52653/ppi.2021.5.5.009.

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Изучение биосовместимости молочнокислых бактерий и других микроорганизмов-антагонистов, выделенных из природных источников, является актуальной задачей. В данной работе впервые показано взаимное влияние изолятов молочно-кислых бактерий и других микроорганизмов-антагонистов при совместном культивировании. Установлено, что изолят 1 является биосовместимым с изолятами 6, 13, 19 и 20. Изолят 6 активно растет в присутствии изолятов 7, 8, 9, 10, 11, 13 и 16. Изолят 7 биосовместим с изолятами 6, 8, 9, 10, 11, 12, 13, 16, изолят 8 является биосовместимым с изолятами 6, 7, 9, 10, 11, 13 и 16. Для изолята 9 наблюдается биосовместимость с изолятами 6, 7, 8, 10, 11, 12, 13, 16, для изолята 10 - с изолятами 6, 7, 8, 9, 11, 13, 16. Изолят 11 показывает удовлетворительные ростовые характеристики при совместном культивировании с изолятами 6, 7, 8, 9, 10, 12, 13, 16. Изолят 12 биосовместим с изолятами 7, 8, 9, 10, 11, 13 и 16. Изолят 13 является биосовместимым с изолятами 6, 7, 8, 9, 10, 11, 12, 16. Изолят 16 биосовместим с изолятами 6, 7, 8, 9, 10, 11, 12, 13. Изолят 19 является биосовместимым с изолятами 1, 6, 13 и 20, изолят 20 - с изолятами 1, 6, 13 и 19. Полученные результаты позволяют сделать вывод о том, что изоляты 1, 6, 19 и 20 являются близкородственными, так же как изоляты 7, 8, 9, 10, 11, 12, 13 и 16. The study of the biocompatibility of lactic acid bacteria and other antagonist microorganisms isolated from natural sources is an urgent task. This work shows for the first time the mutual influence of isolates of lactic acid bacteria and other microorganisms-antagonists during co-cultivation. It was found that isolate 1 is biocompatible with isolates 6, 13, 19, and 20. Isolate 6 actively grows in the presence of isolates 7, 8, 9, 10, 11, 13, and 16. Isolate 7 is biocompatible with isolates 6, 8, 9, 10 , 11, 12, 13, 16, isolate 8 is biocompatible with isolates 6, 7, 9, 10, 11, 13 and 16. Isolate 9 is biocompatible with isolates 6, 7, 8, 10, 11, 12, 13, 16, for isolate 10 - with isolates 6, 7, 8, 9, 11, 13, 16. Isolate 11 shows satisfactory growth characteristics when co-cultivated with isolates 6, 7, 8, 9, 10, 12, 13, 16. Isolate 12 is biocompatible with isolates 7, 8, 9, 10, 11, 13 and 16. Isolate 13 is biocompatible with isolates 6, 7, 8, 9, 10, 11, 12, 16. Isolate 16 is biocompatible with isolates 6, 7, 8 , 9, 10, 11, 12, 13. Isolate 19 is biocompatible with isolates 1, 6, 13 and 20, isolate 20 - with isolates 1, 6, 13, and 19. The results obtained suggest that isolates 1, 6, 19 and 20 are closely related as well as isolates 7, 8, 9, 10, 11, 1 2, 13 and 16.

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Loezos, J. M., T. A. Vanderah, and J. P. Cline. "New ternary compounds in the BaO:Fe2O3:TiO2 system: Ba2Fe2Ti4O13 (“2:1:4”), Ba3Fe10TiO20 (“3:5:1”), and Ba4Fe2Ti10O27 (“4:1:10”)." Powder Diffraction 12, no. 4 (December 1997): 259–63. http://dx.doi.org/10.1017/s0885715600009866.

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X-ray powder diffraction data and refined unit cell parameters for three compounds found during experimental determination of the BaO:Fe2O3:TiO2 phase diagram are reported here. All three phases crystallize in space group C2/m (No. 12). Ba2Fe2Ti4O13 (“2:1:4”) is isostructural with K2Ti6O13 and Ba2ZnTi5O13: a=15.1939(9), b=3.8912(3), c=9.1244(5) Å, β=98.456(5)°; Z=2, ρcalc=4.890 g/cc. Ba3Fe10TiO20 (“3:5:1”) is structurally analogous to its aluminum congener Ba3Al10TiO20: a=15.336(1), b=11.7986(9), c=5.1700(4) Å, β=91.220(6)° (I2/m setting); Z=2, ρcalc=4.750 g/cc. Ba4Fe2Ti10O27 (“4:1:10”) is also isostructural with its aluminum analog Ba4Al2Ti10O27: a=19.799(1), b=11.4324(6), c=9.8936(6) Å, β=109.146(4)° (C2/m); Z=4, ρcalc=4.934 g/cc. The 2:1:4 and 3:5:1 compounds adopt open-framework type structures while the 4:1:10 phase exhibits an eight-layer close-packed arrangement.

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Clayton, Robert A., Jane E. Nally, Neil C. Thomson, and John C. McGrath. "Interactions between Endothelin-1-induced Contractions and Bronchodilators in Human Isolated Bronchi." Clinical Science 93, no. 6 (December 1, 1997): 527–33. http://dx.doi.org/10.1042/cs0930527.

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1. The aim of this study was to compare the ability of four different bronchodilators (atrial natriuretic peptide, salbutamol, sodium nitroprusside and isosorbide dinitrate) to reverse and also to protect against contractions evoked by the spasmogens endothelin-1 and methacholine in human isolated bronchial rings. 2. Contractions evoked by either endothelin-1 or methacholine were reversed by atrial natriuretic peptide (10−9−10−6 mol/l), salbutamol (10−9−10−5 mol/l), sodium nitroprusside (10−9−10−5 mol/l) and isosorbide dinitrate (10−7−10−4 mol/l). 3. Sodium nitroprusside produced a significantly (P < 0.05 for data points) greater mean maximal inhibition of endothelin-1-induced tone than methacholine-induced tone; however, the other dilators were equally effective at reversing either endothelin-1- or methacholine-induced contractions. Comparing sodium nitroprusside and salbutamol, sodium nitroprusside was significantly (P < 0.05 for data set) less effective than salbutamol at reversing either endothelin-1- or methacholine-induced contractions. 4. To compare the ability of these bronchodilator substances to protect against spasmogen challenge, cumulative concentration—response curves to either endothelin-1 (10−10−3 × 10−7 mol/l) or methacholine (10−9−3 × 10−4 mol/l) were constructed in the presence and absence of each bronchodilator. Atrial natriuretic peptide, at a concentration of 10−6 mol/l, significantly attenuated contractions evoked by methacholine. In contrast, contractions evoked by endothelin-1 were enhanced by atrial natriuretic peptide at concentrations of 3 × 10−7 and 10−6 mol/l. Preincubation of salbutamol at a concentration of 10−6 mol/l significantly attenuated methacholine-induced contractions, but responses to endothelin-1 were not altered by preincubation of salbutamol at concentrations of 3 × 10−7, 10−6 and 3 × 10−6 mol/l. Sodium nitroprusside (10−6 mol/l) and isosorbide dinitrate (3 × 10−5 mol/l) did not alter responses evoked by subsequent addition of either endothelin-1 or methacholine. At a concentration of 10−4 mol/l, however, isosorbide dinitrate significantly attenuated endothelin-1-evoked contractions. 5. These results show that drugs which reverse agonist-induced tone in isolated bronchial rings may not necessarily protect against subsequent challenge with this agonist. This suggests that the pharmacology of relaxation may be dissimilar to that of protection.

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García-Alvarez, Felícito, Marta Monzón, José María Grasa, Antonio Laclériga, Beatriz Amorena, Ignacio García-Alvarez, Marta Navarro-Zorraquino, and Felícito García-Alvarez Alvarez. "Interleukin-1, interleukin-6, and interleukin-10 responses after antibiotic treatment in experimental chronic Staphylococcus aureus osteomyelitis." Journal of Orthopaedic Science 11, no. 4 (July 2006): 370–74. http://dx.doi.org/10.1007/s00776-006-1026-9.

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Khan, Nayab, Changda Liu, Janaki Patel, Nan Yang, and Xiu-Min Li. "2-Methyl-1, 3, 6-Trihydroxy-9, 10-Anthraquinone Isolated from Rubia Cordifolia L Inhibits IgE Production." Journal of Allergy and Clinical Immunology 135, no. 2 (February 2015): AB68. http://dx.doi.org/10.1016/j.jaci.2014.12.1155.

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37

Miazga, Agnieszka, Krzysztof Felczak, Maria A. Siwecka, Andrzej Lipniacki, Andrzej Piasek, and Tadeusz Kulikowski. "Synthesis and anti-HIV properties of novel 6-phenylselenenyl-5-propyluracils." Acta Biochimica Polonica 54, no. 4 (December 8, 2007): 863–68. http://dx.doi.org/10.18388/abp.2007_3189.

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Novel 6-phenylselenenyl-5-propyluracils were synthesized from 5-propyluracil with the use of regioselective synthesis to give 1-[(2-hydroxyethoxy)-methyl]-6-phenylselenenyl-5-propyluracil (6), 1-ethoxymethyl-6-phenylselenenyl-5-propyluracil (9) and 1-benzyloxymethyl-6-phenylselenenyl-5-propyluracil (10). Interaction of these compounds with recombinant HIV-1 reverse transcriptase (RT) was evaluated using a non-isotopic colorimetric method. Compounds 9 and 10 exerted potent HIV RT inhibition (IC(50) 0.06 and 0.05 microM respectively) while compound 6 showed moderate inhibition (IC(50) = 3.5 microM). Potent anti-HIV-1 activity in MT-2 cells inoculated by a syncythia-inducing HIV-1 (cat #3 strain) laboratory isolate was exerted by compounds 9 and 10 (EC(50) 0.62 microM and 0.025 microM, respectively), while compound 6 showed only moderate activity (IC(50) = 4.1 microM). In addition, compound 10 showed very good in vitro therapeutic index (TI > 2046), indicating that it is a potential anti-HIV/AIDS drug.

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38

Li, Hong-Mei, Zhi-Qiang Wang, and Chen Xu. "Crystal structure of 10-bromo-9-phenylanthracene–anthracene-9,10- dione (2:1), (C20H13Br)(C7H4O), C27H17BrO." Zeitschrift für Kristallographie - New Crystal Structures 228, no. 2 (June 1, 2013): 183–84. http://dx.doi.org/10.1524/ncrs.2013.0083.

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Abstract C27H17BrO, triclinic, P1̅ (no. 2), a = 9.269(4) Å, b = 9.734(5) Å, c = 11.437(5) Å, α = 105.816(5)°, β = 95.281(6)°, γ = 99.909(5)°, V = 967.5 Å3, Z = 2, Rgt(F) = 0.0349, wRref(F2) = 0.0834, T = 296 K.

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39

Rossi, Davide, Clara Deambrogi, Tiziana Lischetti, Michaela Cerri, Marianna Spunton, Silvia Rasi, Silvia Franceschetti, et al. "Hypermethylation of SH2-Containing Phosphatase-1 (SHP-1) and Suppressor of Cytokine Signaling-1 and -3 (SOCS-1 and -3) in Philadelphia Negative Chronic Myeloproliferative Disorders (Ph-CMPD)." Blood 108, no. 11 (November 16, 2006): 118. http://dx.doi.org/10.1182/blood.v108.11.118.118.

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Abstract A fraction of Ph- CMPD is characterized by JAK2F617F mutation leading to constitutive JAK-STAT activation. The negative regulators of cytokine signaling SHP-1, SOCS-1 and SOCS-3 have a crucial function in the negative regulation of JAK2 activation/phosphorylation in response to EPO, G-CSF and a subset of cytokines. SHP-1, SOCS-1 and SOCS-3 may be silenced by aberrant DNA methylation in human malignancies. Here we tested chronic phase Ph- CMPD and acute myeloid leukaemia (AML) from Ph- CMPD for aberrant DNA methylation of SHP-1, SOCS-1 and SOCS-3. The study was based on: i) 85 Ph- CMPD, including 35 essential thrombocythemia (ET), 20 polycythemia vera (PV), 15 idiopathic myelofibrosis (IMF), 6 chronic myelomonocytic leukemia (CMML) and 9 Ph- chronic myeloid leukemia (Ph- CML); and on ii) 19 AML from Ph- CMPD, including 4 AML from PV, 10 AML from ET and 5 AML from IMF. Cases were analysed for SHP-1, SOCS-1 and SOCS-3 aberrant methylation by methylation-specific PCR and for JAK2V617F mutation by allele specific PCR. For comparison, 10 samples of normal bone marrow hematopoietic cells were also investigated. Among Ph- CMPD, methylation of SHP-1 occurred in 4/20 (20%) PV and 4/35 (11%) ET, while it was absent in IMF (0/15), CMML (0/6) and Ph- CML (0/9). Methylation of SOCS-1 occurred in 5/20 (25%) PV, 5/35 (14%) ET, 2/15 (13%) IMF and in 1/9 (11%) Ph- CML while it was absent in CMML (0/6). Methylation of SOCS-3 occurred in 11/20 (55%) PV, 13/35 (37%) ET, 4/15 (26%) IMF, 3/6 (50%) CMML and 3/9 (33%) Ph- CML. JAK2V617F mutation was detected in 47/85 (55%) Ph-CMPD, including 17/20 (85%) PV, 18/35 (51%) ET, 12/15 (80%) IMF, 0/6 CMML and 0/9 Ph- CML. SHP-1, SOCS-1 and SOCS-3 methylation was analysed according to JAK2 mutation status in PV, ET and IMF. In this group of patients, SHP-1, SOCS-1 and SOCS-3 methylation occurred in both JAK2 mutated cases (6/47, 13% for SHP-1; 10/47, 21% for SOCS-1 and 18/47, 38% for SOCS-3) and germline cases (2/38, 5% for SHP-1; 2/38, 5% for SOCS-1 and 10/38, 26% for SOCS-3). By combining the results of SHP-1, SOCS-1 and SOCS-3 methylation status, 21/47 (45%) JAK2 mutated cases carried SHP-1 and/or SOCS-1 and/or SOCS-3 methylation as opposed to 12/38 (31%) germline cases. This pattern of SHP-1 and SOCS-1 methylation was conserved also when the analysis was restricted to PV, ET and IMF each as a single group and after stratification for JAK2V617F mutation. Among AML from Ph- CMPD, methylation of SHP-1 occurred in 1/10 (10%) AML from ET, while it was absent in AML from PV and AML from IMF. Methylation of SOCS-1 occurred in 1/4 (25%) AML from PV and 1/10 (10%) AML from ET. One ET patient acquired SHP-1 methylation at transformation to AML. All normal bone marrow samples (n=10) scored negative for SHP-1, SOCS-1 and SOCS-3 methylation. The implications of these results are threefold. First, inactivation by aberrant methylation of SHP-1, SOCS-1 and SOCS-3 is involved in the pathogenesis of Ph- CMPD and is selectively associated with neoplastic hemopiesis. Second, among PV, ET and IMF, methylation of SHP-1, SOCS-1 and SOCS-3 may occur in both JAK2V617F positive and negative cases. Third, the low prevalence of SHP-1 and SOCS-1 methylation in AML from Ph- CMPD suggests that SHP-1 and SOCS-1 silencing is not involved in leukemic transformation.

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Maruyama, K., K. Sawada, J. Koike, H. Sato, and K. Yagi. "Examination of deformation mechanism maps in 2.25Cr—1Mo steel by creep tests at strain rates of 10−11 to 10−6 s−1." Materials Science and Engineering: A 224, no. 1-2 (March 1997): 166–72. http://dx.doi.org/10.1016/s0921-5093(96)10566-9.

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41

Yang, Hai-Yan, Fang He, Yao-Min Zhao, Hui Li, Hong-Fang Wang, and Ying-Hua Li. "Crystal structure of Bis{1-[(benzotriazol-1-yl)methyl]-1-H-1,3-(2-methyl-imidazol)}diiodidocadmium(II), [Cd(C11H11N5)2I2], C22H22N10I2Cd." Zeitschrift für Kristallographie - New Crystal Structures 234, no. 5 (September 25, 2019): 919–21. http://dx.doi.org/10.1515/ncrs-2019-0144.

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AbstractC22H22N10I2Cd, triclinic, P1̄ (no. 2), a = 10.5476(8) Å, b = 11.1759(9) Å, c = 12.7735(10) Å, α = 103.372(7)°, β = 105.811(7)°, γ = 100.270(6)°, V = 1361.85(18) Å3, Z = 2, Rgt(F) = 0.0324, wRref(F2) = 0.0661, T = 291(2) K.

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Schultz, Arthur G., Kan K. Eng, and Rudolph K. Kullnig. "Photochemistry of 1-carbomethoxy-6-methyltricyclo[4.3.1.04,6]Dec-2-en-10-one. preparation of a 1,3-cyclooctadiene." Tetrahedron Letters 27, no. 21 (1986): 2331–34. http://dx.doi.org/10.1016/s0040-4039(00)84521-9.

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43

Liu, Xian-Chang, Pei-Pei Zhang, and Yong Wang. "Crystal structure of 6-amino-8-(4-isopropylphenyl)-2-methyl-2,3,8,8a-tetrahydroisoquinoline-5,7,7(1H)-tricarbonitrile-ethanol (1/1), C24H29N5O." Zeitschrift für Kristallographie - New Crystal Structures 234, no. 2 (March 26, 2019): 199–200. http://dx.doi.org/10.1515/ncrs-2018-0172.

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AbstractC24H29N5O, triclinic, P1̄ (no. 2), a = 10.352(9) Å, b = 10.911(10) Å, c = 12.480(6) Å, α = 97.33(2)°, β = 110.29(2)°, γ = 115.353(15)°, V = 1129.6(15) Å3, Z = 2, Rgt(F) = 0.0614, wRref(F2) = 0.1855, T = 296(2) K.

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44

Poirier, F. "APX50, the first fully automatic absolute pressure balance in the range 10 kPa to 1 MPa." Metrologia 36, no. 6 (December 1999): 531–33. http://dx.doi.org/10.1088/0026-1394/36/6/9.

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45

Chantrapromma, Suchada, Boonlerd Nilwanna, Thawanrat Kobkeatthawin, Patcharaporn Jansrisewangwong, and Hoong-Kun Fun. "(E)-1-(2,4-Dinitrophenyl)-2-[1-(3-fluorophenyl)ethylidene]hydrazine." Acta Crystallographica Section E Structure Reports Online 68, no. 6 (May 5, 2012): o1644—o1645. http://dx.doi.org/10.1107/s160053681201937x.

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The molecule of the title hydrazone derivative, C14H11FN4O4, is nearly planar, with a dihedral angle between the benzene rings of 3.71 (7)°. The central ethylidenehydrazine N—N=C—C plane makes dihedral angles of 5.32 (10) and 9.02 (10)° with the 2,4-dinitro- and 3-fluoro-substituted benzene rings, respectively. An intramolecular N—H...O bond generates an S(6) ring motif. In the crystal, molecules are linked by weak C—H...O interactions into a sheet parallel to (10-1). The molecules are further stacked along the a axis by π–π interactions with centroid–centroid distances of 3.6314 (9) and 3.7567 (10) Å. A C...F short contact [2.842 (3) Å] is observed. The 3-fluorophenyl group is disordered over two orientations with a site-occupancy ratio of 0.636 (3):0.364 (3).

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46

de Caen, D., D. L. Kreher, S. P. Radziszowski, and W. H. Mills. "On the covering of t-sets with (t + 1)-sets:C(9, 5, 4) and C(10, 6, 5)." Discrete Mathematics 92, no. 1-3 (November 1991): 65–77. http://dx.doi.org/10.1016/0012-365x(91)90267-6.

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47

de Martino, Maurizio, Francesco Chiarelli, Maria Elisabetta Rossi, Chiara Azzari, Luisa Galli, and Alberto Vierucci. "Interleukin-6 synthesis and IgE overproduction in children with perinatal human immunodeficiency virus-type 1 infection." Annals of Allergy, Asthma & Immunology 82, no. 2 (February 1999): 212–16. http://dx.doi.org/10.1016/s1081-1206(10)62599-9.

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48

Gianini, Aline S., Maria Rita Marques, Nádia Cristina P. Carvalho, and Neli K. Honda. "Activities of 2,4-Dihydroxy-6-n-pentylbenzoic Acid Derivatives." Zeitschrift für Naturforschung C 63, no. 1-2 (February 1, 2008): 29–34. http://dx.doi.org/10.1515/znc-2008-1-206.

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Esters of 2-hydroxy-4-methoxy-6-n-pentylbenzoic acid (2−8) (methyl, ethyl, butyl, pentyl, isopropyl, sec-butyl and benzyl), olivetol (9), methyl, ethyl, butyl perlatolates (10−12), 2,4- dihydroxy-6-n-pentylbenzoic acid (15), and methyl and ethyl esters of (15) were prepared through structural modifications of perlatolic acid (1) with the aim to detect new antifungal and antibacterial substances and also to evaluate the toxicity by the brine shrimp lethality assay against Artemia salina. The antifungal assays were carried out against the fungus Cladosporium sphaerospermum through the bioautography method, and methyl 2,4-dihydroxy- 6-n-pentylbenzoate (13) showed the highest antifungal activity (2.5 μg). Olivetol (9) and 2,4- dihydroxy-6-n-pentylbenzoic acid (15) are also potent inhibitors of the growth of the fungus (5.0 μg). Except for methyl (10), the ethyl (11) and butyl (12) perlatolates were less active than perlatolic acid (1). The activities presented by methyl (2) and ethyl (3) 2-hydroxy-4- methoxy-6-n-pentylbenzoates and methyl (13) and ethyl (14) 2,4-dihydroxy-6-n-pentylbenzoates suggest that compounds with a free hydroxy group in the aromatic ring (C-4) have a more pronounced effect against C. sphaerospermum. Antibacterial activities were tested by the disc diffusion method using pathogenic strains of S. aureus and E. coli. The compounds were weakly active with inhibition zones between 9−15 mm. The 2-hydroxy-4-methoxy-6-npentylbenzoic esters 2−8 and alkyl perlatolates 10−12 were selective against E. coli. Perlatolic acid (1) and methyl 2-hydroxy-4-methoxy-6-n-pentylbenzoate (2) were the most active with LD50 values of 24.1 μM and 27.2 μM, respectively. The other compounds were not toxic to Artemia salina larvae.

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Poirel, Laurent, Gunturu Revathi, Sandrine Bernabeu, and Patrice Nordmann. "Detection of NDM-1-ProducingKlebsiella pneumoniaein Kenya." Antimicrobial Agents and Chemotherapy 55, no. 2 (November 29, 2010): 934–36. http://dx.doi.org/10.1128/aac.01247-10.

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ABSTRACTSeven carbapenem-resistant NDM-1-positiveKlebsiella pneumoniaeisolates were recovered from patients hospitalized between 2007 and 2009 in different wards at a referral and tertiary care center in Nairobi. Most of the isolates were obtained from urine. All isolates carried theblaNDM-1carbapenemase gene previously reported from India, Pakistan, and the United Kingdom. These isolates were clonally related and expressed many other resistance determinants, including β-lactamases CTX-M-15, OXA-1, OXA-9, CMY-6, and aminoglycoside resistance methylase RmtC. This work corresponds to the first report of NDM-1 producers in Africa.

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Afsah, E. M., M. Hammouda, H. Zoorob, M. M. Khalifa, and M. T. Zimaity. "Mannich Reaction with 1 ,3 - Indandione Phenylhydrazones." Zeitschrift für Naturforschung B 45, no. 1 (January 1, 1990): 80–82. http://dx.doi.org/10.1515/znb-1990-0115.

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Abstract Mannich reaction of 1,3-indandione-1-phenylhydrazone (1) or 1,3-diphenylhydrazone (5) withmorpholine or piperazine gave the Mannich base-phenylhydrazone 2 and 3 or the diphenylhydrazone6 and 7, respectively. Whereas, such reaction with 1 or 5 using primary amines affordedthe indeno[2,1-ƒ]-1,2,4-triazepin-6(2H)-one (4) or its 6-phenylhydrazone (8), respectively.Treatment of 5 with ammonium acetate and formalin afforded 9. The indeno[1,2-ƒ]-1,2,4,5-tetrazepin-10(2H)-one (11) was obtained from the 1,2-diphenylhydrazone 10 and formaldehyde.

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