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Journal articles on the topic 'Limonoid mexicanolide'

Author: Grafiati
Published: 4 June 2021
Last updated: 15 February 2022

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1

Inoue, Takanobu, Shoko Ohmori, Takashi Kikuchi, Takeshi Yamada, and Reiko Tanaka. "Carapanosins D—F from the Seeds of Andiroba (Carapa guianensis, Meliaceae) and Their Effects on LPS-Activated NO Production." Molecules 23, no. 7 (2018): 1778. http://dx.doi.org/10.3390/molecules23071778.

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A novel nor-phragmalin-type limonoid, named carapanosin D (1), and two novel mexicanolide-type limonoids, carapanosins E (2) and F (3), were isolated from the seed oil of andiroba (Carapa guianensis Aublet), a traditional medicine in Brazil and Latin American countries. Their structures were unambiguously determined on the basis of spectroscopic analyses using one-dimensional (1D) and two-dimensional (2D) NMR techniques and High resolution Fast Atom Bombardment Mass Spectrometry (HRFABMS). Compounds 1–3 were evaluated for their effects on the production of nitric oxide (NO) in Lipopolysacchari
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2

Li, Hui, Yi Li, Xiao-Bing Wang, et al. "Mexicanolide limonoids with in vitro neuroprotective activities from seeds of Khaya senegalensis." RSC Advances 5, no. 51 (2015): 40465–74. http://dx.doi.org/10.1039/c5ra05006e.

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Fourteen new mexicanolide-type limonoids khasenegasins A–N (1–14) were isolated from the seeds of Khaya senegalensis, and bioactivity scan indicated that these mexicanolide-type limonoids displayed neuroprotective activities.
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3

Sun, Dong-Mei, Fa-Liang An, Shan-Shan Wei, et al. "Cipadessains A–K, eleven limonoids from the fruits ofCipadessa cinerascens." RSC Advances 8, no. 19 (2018): 10437–45. http://dx.doi.org/10.1039/c8ra00728d.

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4

Leite, Ana C., João B. Fernandes, M. Fátima das G. F. da Silva, and Paulo C. Vieira. "Limonoids From Cipadessa Fruticosa." Zeitschrift für Naturforschung B 60, no. 3 (2005): 351–55. http://dx.doi.org/10.1515/znb-2005-0321.

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The fruits of Cipadessa fruticosa Bl. afforded two new limonoids: methyl 8α,30α-epoxide-3β - (2’-methylbutyryloxy)-1-oxomeliacate (cipadesin A) and methyl 21,23-dihydro-23-hydroxy-21-oxo- 3β -tigloyloxy-1-oxomeliac-8(30)-enate (febrifugin A), along with the known limonoids cipadesin, khayasin T, febrifugin, ruageanin A and mexicanolide. Their structures were elucidated on the basis of spectroscopic methods
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5

Asmara, Anjar Purba. "A PRELIMINARY STUDY OF INVESTIGATING OF COMPOUND GROUP CONTAINED IN ETHANOLIC EXTRACT OF MAHAGONY (Swietenia mahagoni L. Jacq.) SEEDS RELATED TO Α-GLUCOSIDASE INHIBITION". Jurnal Natural 18, № 2 (2018): 49–56. http://dx.doi.org/10.24815/jn.v18i2.9236.

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A preliminary study to determine the group of compound contained in the ethanolic extract of mahagony (Swietenia mahagoni L. Jacq.) seeds and its inhibitory activity to a-glucosidase enzyme has been done. The information from this study will be used in the further investigation about the specific constituents related to the bioactivity. The seed was grounded and then extracted with ethanol by maceration technique. The crude extract was separated with liquid-liquid extraction by using n-hexane, ethyl acetate, and methanol as the solvents. The best eluent for isolation, chloroform:ethanol (1:1),
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6

Wu, Jun, Si Zhang, Qiang Xiao, et al. "Xyloccensin M and N, Two New B, D-seco Limonoids from Xylocarpus granatum." Zeitschrift für Naturforschung B 58, no. 12 (2003): 1216–19. http://dx.doi.org/10.1515/znb-2003-1210.

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Two new mexicanolide-type B, D-seco limonoids named xyloccensin M(1) and N (2) were isolated from the stem bark of Xylocarpus granatum. Their structures were elucidated with the help of modern spectroscopic techniques.
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7

Alozieuwa, Blessing U., Shehu U. Abdullahi, Abdulhakeem Rotimi Agboola, et al. "Mexicanolide, a bioactive compound from Cedrela odorata: In silico study of its pharmacokinetics, drug-likeness, potential drug targets, and cytotoxic activities against cancer cell lines." BIOMED natural and applied science 1, no. 2 (2021): 1–10. http://dx.doi.org/10.53858/bnas01020110.

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Mexicanolide is a limonoids type of compound identified from Cedrela odorata, a forest plant with various medicinal properties. Several biological activities have been reported for Mexicanolide. In the present study, we used an in silico approach to evaluate the physicochemical, pharmacokinetics, drug-likeness, drug targets, and cytotoxic activities of mexicanolide from Cedrela odorata. The results revealed that mexicanolide has favorable physicochemical and pharmacokinetic properties of a good drug-like candidate. Notably, the compound has a high GI absorption rate but could not permeate the
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8

Shen, Li-Ru, Mei Dong, Bao-Wei Yin та ін. "Xylomexicanins A and B, New Δ14,15-Mexicanolides from Seeds of the Chinese Mangrove Xylocarpus granatum". Zeitschrift für Naturforschung C 64, № 1-2 (2009): 37–42. http://dx.doi.org/10.1515/znc-2009-1-207.

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Two new mexicanolide-type limonoids, named xylomexicanin A (1) and xylomexicanin B (2), were isolated from seeds of the Chinese mangrove Xylocarpus granatum. Their structures were elucidated on the basis of spectroscopic methods. Compound 1 exhibited antiproliferative activity against human breast carcinoma cells (KT), while 2 did not show inhibitory effects on eleven human tumour cell lines tested.
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9

Coombes, Philip H., Dulcie A. Mulholland, and Milijaona Randrianarivelojosia. "Mexicanolide limonoids from the Madagascan Meliaceae Quivisia papinae." Phytochemistry 66, no. 10 (2005): 1100–1107. http://dx.doi.org/10.1016/j.phytochem.2005.03.002.

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10

Xu, Jin-Biao, Yuan Lin, Shi-Hui Dong, Fei Wang, and Jian-Min Yue. "Trichinenlides A–T, Mexicanolide-Type Limonoids fromTrichilia sinensis." Journal of Natural Products 76, no. 10 (2013): 1872–80. http://dx.doi.org/10.1021/np400408s.

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11

Yang, Wei, Ling-Mei Kong, Shi-Fei Li, et al. "Five new mexicanolide type limonoids from Heynea trijuga." Natural Products and Bioprospecting 2, no. 4 (2012): 145–49. http://dx.doi.org/10.1007/s13659-012-0040-1.

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12

Camero, César Muñoz, Antonio Vassallo, Marinella De Leo, Abeer Temraz, Nunziatina De Tommasi, and Alessandra Braca. "Limonoids from Aphanamixis polystachya Leaves and Their Interaction with Hsp90." Planta Medica 84, no. 12/13 (2018): 964–70. http://dx.doi.org/10.1055/a-0624-9538.

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AbstractA phytochemical study of n-hexane, CHCl3, and CHCl3-MeOH extracts of Aphanamixis polystachya leaves led to the isolation of 10 compounds. Five of them turned out to be new natural compounds, including two mexicanolide-type (1, 2) and three polyoxyphragmalin-type (3–5) limonoids, together with two known andirobin-type limonoids (6, 7) and three phenolic derivatives. The structures of the new compounds were established on the basis of spectroscopic methods to be 8-hydro-14,15-en-cabralin (1), 3-deacetyl-8-hydro-cabralin-14,15-en-3-one (2), 20,22-dihydroxy-21,23-dimethoxytetrahydrofuran k
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13

Liu, Shou-Bai, Wen-Li Mei, Hui-Qin Chen, Zhi-Kai Guo, Hao-Fu Dai, and Zhu-Nian Wang. "Mexicanolide-Type Limonoids from the Roots of Trichilia sinensis." Molecules 21, no. 9 (2016): 1152. http://dx.doi.org/10.3390/molecules21091152.

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14

Ma, Ya-Qian, Kun Jiang, Yi Deng, Lan Guo, Yi-Qun Wan, and Chang-Heng Tan. "Mexicanolide-type limonoids from the seeds of Swietenia macrophylla." Journal of Asian Natural Products Research 20, no. 4 (2017): 299–305. http://dx.doi.org/10.1080/10286020.2017.1335715.

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15

Wu, Jun, Minyi Li, Si Zhang, Qiang Xiao та Qingxin Li. "Two New Limonoids With A 3-O-β-Tigloyl Group From The Seeds Of The Chinese Mangrove Xylocarpus Granatum". Zeitschrift für Naturforschung B 62, № 6 (2007): 859–62. http://dx.doi.org/10.1515/znb-2007-0616.

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A new mexicanolide and a new phragmalin, named 30α-hydroxyl xylogranatin A and xylogranatin E2, respectively, have been isolated from the seeds of a Chinese mangrove Xylocarpus granatum. Their structures were identified on the basis of spectroscopic data. Each of them has a 3-O-β -tigloyl group. The first complete assignments of 1H and 13C NMR data for these limonoids were achieved by means of 2D NMR techniques, including 1H-1H COSY, HSQC, HMBC and NOESY spectra
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16

Matos, Andreia P., Ana C. Leite, Luciane G. Batista-Pereira, Paulo C. Vieira, João B. Fernandes, and Maria Fátima das G. F. da Silva. "Effects of Limonoids from Cipadessa fruticosa on Fall Armyworm." Zeitschrift für Naturforschung C 64, no. 5-6 (2009): 441–46. http://dx.doi.org/10.1515/znc-2009-5-623.

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Six mexicanolide limonoids isolated from the dichloromethane extract of the fruits of Cipadessa fruticosa Blume (Meliaceae) were evaluated against Spodoptera frugiperda (J. E. Smith). Gedunin was used as a positive control. When incorporated into an artificial diet of neonates at 50.0 mg kg-1, febrifugin A showed 73.3% mortality. All the compounds showed moderate insecticidal activity, except for ruageanin A, when compared with the control. Febrifugin also showed growth inhibition and antifeedant activities (at 100.0 mg kg-1). The correlation between the insecticidal activity of the isolated c
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17

Chen, A.-Hong, Qing Wen, Yan-Lei Ma, et al. "Bioactive mexicanolide-type limonoids from the fruits of Trichilia connaroides." Phytochemistry Letters 20 (June 2017): 17–21. http://dx.doi.org/10.1016/j.phytol.2017.03.008.

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18

Zhang, Qiang, Ying-Tong Di, Hong-Ping He, et al. "Phragmalin- and Mexicanolide-Type Limonoids from the Leaves ofTrichilia connaroides." Journal of Natural Products 74, no. 2 (2011): 152–57. http://dx.doi.org/10.1021/np100428u.

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19

Cao, Dong-Hua, Shang-Gao Liao, Peng Sun, et al. "Mexicanolide-type limonoids from the twigs and leaves of Cipadessa baccifera." Phytochemistry 177 (September 2020): 112449. http://dx.doi.org/10.1016/j.phytochem.2020.112449.

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20

Sarigaputi, Chanin, Thanesuan Nuanyai, Thapong Teerawatananond, Somchai Pengpreecha, Nongnuj Muangsin, and Khanitha Pudhom. "Xylorumphiins A−D, Mexicanolide Limonoids from the Seed Kernels ofXylocarpus rumphii." Journal of Natural Products 73, no. 8 (2010): 1456–59. http://dx.doi.org/10.1021/np100423w.

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21

WU, Yi-Bing, Zhi-Yu NI, Chang-Hong HUO, et al. "Xylomexicanins C and D, New Mexicanolide-Type Limonoids from Xylocarpus granatum." Bioscience, Biotechnology, and Biochemistry 77, no. 4 (2013): 736–40. http://dx.doi.org/10.1271/bbb.120815.

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22

Dey, Dipta, Cristina Quispe, Rajib Hossain, et al. "Ethnomedicinal Use, Phytochemistry, and Pharmacology of Xylocarpus granatum J. Koenig." Evidence-Based Complementary and Alternative Medicine 2021 (August 30, 2021): 1–16. http://dx.doi.org/10.1155/2021/8922196.

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The mangrove plants are the potential sources of foods and remedies for people living in the forests and nearby communities. Xylocarpus granatum J. Koenig is traditionally used to treat various diseases including diarrhea, cholera, dysentery, fever, malaria, and viral infections, among others. To summarize critically the taxonomy, ethnomedicinal, phytochemistry, and pharmacological activities of X. granatum, information was collected from different databases. An up-to-date search (till June 2020) was carried out with the help of various scientific web resources from databases such as PubMed, S
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23

Siva, Bandi, B. Poornima, A. Venkanna, et al. "Methyl angolensate and mexicanolide-type limonoids from the seeds of Cipadessa baccifera." Phytochemistry 98 (February 2014): 174–82. http://dx.doi.org/10.1016/j.phytochem.2013.11.006.

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24

Zhang, Wen-Yan, Lu Qiu, Qin-Pei Lu, Miao-Miao Zhou, Jun Luo, and Yi Li. "Furan fragment isomerized mexicanolide-type Limonoids from the stem barks of Khaya senegalensis." Phytochemistry Letters 24 (April 2018): 110–13. http://dx.doi.org/10.1016/j.phytol.2018.01.020.

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25

Li, Hui, Yi Li, Xiao-Bing Wang, et al. "ChemInform Abstract: Mexicanolide Limonoids with in vitro Neuroprotective Activities from Seeds of Khaya senegalensis." ChemInform 46, no. 38 (2015): no. http://dx.doi.org/10.1002/chin.201538217.

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26

Heng, Li, Mengling Zhao, Rong Xu, et al. "Phragmalin and mexicanolide limonoids with reversal of multidrug resistance from the seeds of Chukrasia tabularis A. Juss." Phytochemistry 182 (February 2021): 112606. http://dx.doi.org/10.1016/j.phytochem.2020.112606.

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27

Yang, Wei, Dong-Mei Fang, Hong-Ping He, Xiao-Jiang Hao, Zhi-Jun Wu, and Guo-Lin Zhang. "Analysis of mexicanolide- and phragmalin-type limonoids from Heynea trijuga using high-performance liquid chromatography/electrospray tandem mass spectrometry." Rapid Communications in Mass Spectrometry 27, no. 11 (2013): 1203–12. http://dx.doi.org/10.1002/rcm.6563.

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28

An, Fa-Liang, Dong-Mei Sun, Rui-Zhi Wang, Ming-Hua Yang, Jun Luo, and Ling-Yi Kong. "Trijugin- and mexicanolide-type limonoids from the fruits of Heynea trijuga that reverse multidrug resistance in MCF-7/DOX cells." Phytochemistry 151 (July 2018): 42–49. http://dx.doi.org/10.1016/j.phytochem.2018.04.004.

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29

An, Fa-Liang, Dong-Mei Sun, Rui-Zhi Wang, Ming-Hua Yang, Jun Luo, and Ling-Yi Kong. "Corrigendum to “Trijugin- and mexicanolide-type limonoids from the fruits of Heynea trijuga that reverse multidrug resistance in MCF-7/DOX cells” [Phytochemistry 151 (2018) 42–49]." Phytochemistry 187 (July 2021): 112777. http://dx.doi.org/10.1016/j.phytochem.2021.112777.

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30

Coombes, Philip H., Dulcie A. Mulholland, and Milijaona Randrianarivelojosia. "Mexicanolide Limonoids from the Madagascan Meliaceae Quivisia papinae." ChemInform 36, no. 44 (2005). http://dx.doi.org/10.1002/chin.200544199.

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