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Journal articles on the topic 'Seco-cycloartane'

Author: Grafiati

Published: 4 June 2021

Last updated: 10 February 2022

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1

Grougnet, Raphaël, Prokopios Magiatis, Sofia Mitaku, et al. "seco-Cycloartane Triterpenes fromGardeniaaubryi." Journal of Natural Products 69, no. 12 (2006): 1711–14. http://dx.doi.org/10.1021/np060273t.

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2

Lai-King Sy and Geoffrey D. Brown. "A seco-cycloartane from Illicium verum." Phytochemistry 48, no. 7 (1998): 1169–71. http://dx.doi.org/10.1016/s0031-9422(98)00150-2.

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3

Nuanyai, Thanesuan, Reungrit Sappapan, Thapong Teerawatananond, Nongnuj Muangsin, and Khanitha Pudhom. "Cytotoxic 3,4-seco-Cycloartane Triterpenes fromGardenia sootepensis." Journal of Natural Products 72, no. 6 (2009): 1161–64. http://dx.doi.org/10.1021/np900156k.

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4

Song, Wei-Wu, Xue-Qin Wang, and Bo Li. "New 3,4-seco-cycloartane triterpenes from Gardenia sootepensis." Journal of Asian Natural Products Research 18, no. 7 (2016): 637–42. http://dx.doi.org/10.1080/10286020.2015.1137287.

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5

Song, Wei-Wu, Xue-Qin Wang, and Bo Li. "Two New 3,4-seco-Cycloartane Triterpenes fromGardenia sootepensis." Helvetica Chimica Acta 99, no. 2 (2016): 165–68. http://dx.doi.org/10.1002/hlca.201500220.

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6

Cabrera, Gabriela M., Mariana Gallo, and Alicia M. Seldes. "A 3,4-seco-cycloartane derivative from Tillandsia usneoides." Phytochemistry 39, no. 3 (1995): 665–66. http://dx.doi.org/10.1016/0031-9422(95)00076-j.

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7

Song, Wei-Wu, Xue-Qin Wang, Hua-Li Jia, Zheng-Kun Zhang, Yong-Jie Ding, and Ya-Hong Chen. "Three new 3,4-seco-cycloartane triterpenes from Gardenia sootepensis." Natural Product Research 32, no. 19 (2017): 2338–42. http://dx.doi.org/10.1080/14786419.2017.1413561.

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8

Nishida, Makiko, Hitoshi Yoshimitsu, Masafumi Okawa, Tuyoshi Ikeda, and Toshihiro Nohara. "Two New 15,16-Seco-cycloartane Glycosides from Cimicifuga Rhizome." CHEMICAL & PHARMACEUTICAL BULLETIN 51, no. 10 (2003): 1215–16. http://dx.doi.org/10.1248/cpb.51.1215.

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9

Yoshimitsu, Hitoshi, Makiko Nishida, and Toshihiro Nohara. "Three New 15,16-Seco-cycloartane Glycosides from Cimicifuga Rhizome." CHEMICAL & PHARMACEUTICAL BULLETIN 55, no. 5 (2007): 789–92. http://dx.doi.org/10.1248/cpb.55.789.

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10

Shi, Qiang-Qiang, Wei-Hua Wang, Jing Lu, Da-Shan Li, Lin Zhou, and Ming-Hua Qiu. "New Cytotoxic Cycloartane Triterpenes from the Aerial Parts of Actaea heracleifolia (syn. Cimicifuga heracleifolia)." Planta Medica 85, no. 02 (2018): 154–59. http://dx.doi.org/10.1055/a-0733-7229.

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AbstractOne new 15,16-seco-cycloartane triterpene (1), three new cycloartane triterpene glycosides (2–4), and five known compounds (5–9) were isolated from the aerial parts of Actaea heracleifolia. The chemical structures of these compounds were determined on the basis of NMR analysis, HRTOF-ESIMS data, and other spectroscopic methods. Selected compounds were evaluated for their cytotoxicity against human tumor cell lines (HL-60, SMMC-7721, A549, MCF-7, and SW480) in vitro. Compounds 3 and 4 showed weak activity against the HL-60, A-549, and MCF-7 cell lines with IC50 values ranging from 21.34

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11

Nuanyai, Thanesuan, Sipichar Chokpaiboon, Tirayut Vilaivan, and Khanitha Pudhom. "Cytotoxic 3,4-seco-Cycloartane Triterpenes from the Exudate ofGardenia tubifera." Journal of Natural Products 73, no. 1 (2010): 51–54. http://dx.doi.org/10.1021/np900658t.

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12

Satiraphan, Malai, Quoc Dang Thai, Uthai Sotanaphun, Chavalit Sittisombut, Sylvie Michel, and Xavier Cachet. "A new 3,4-seco-cycloartane from the leaves ofHopea odorataRoxb." Natural Product Research 29, no. 19 (2015): 1820–27. http://dx.doi.org/10.1080/14786419.2015.1007975.

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13

Li, Chuntong, Fengmin Xi, Junling Mi, Zhijun Wu, and Wansheng Chen. "Two New 3,4;9,10-seco-Cycloartane Type Triterpenoids fromIllicium difengpiand Their Anti-Inflammatory Activities." Evidence-Based Complementary and Alternative Medicine 2013 (2013): 1–9. http://dx.doi.org/10.1155/2013/942541.

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A pair of new 3,4;9,10-seco-cycloartane type triterpenoid stereoisomerides: 24R,25-dihydroxy-3,4;9,10-seco-4(28)-cycloarten-10,3-olide (1) named Illiciumolide A and 24S,25-dihydroxy-3,4;9,10-seco-4(28)-cycloarten-10,3-olide (2) named Illiciumolide B were isolated from the stem bark ofIllicium difengpi, as well as five known biogenetically related triterpenoids, including sootepin E (3), betulinic acid (4), lupeol (5), (all-Z)-1,5,9,13,17,21-hexamethyl-1,5,9,13,17,21-cyclotertracosahexaene (6), and (all-E)-2,6,10,15,19,23-hexamethyl-2,6,10,14,18,22-tetracosahexaene (7). The structures of two ne

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14

Lavoie, Serge, Charles Gauthier, Jean Legault, Sylvain Mercier, Vakhtang Mshvildadze, and André Pichette. "Lanostane- and cycloartane-type triterpenoids from Abies balsamea oleoresin." Beilstein Journal of Organic Chemistry 9 (July 4, 2013): 1333–39. http://dx.doi.org/10.3762/bjoc.9.150.

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Phytochemical analysis of A. balsamea oleoresin led to the isolation of three new 3,4-seco-lanostane triterpenoids 1–3, one new cycloartane triterpenoid 4 along with fourteen known terpenoids. Structure determinations were based on extensive 1D/2D NMR, IR and MS spectroscopic analyses, and comparison with literature data. The isolated compounds were evaluated in vitro for their cytotoxicity against human cell lines (A549, DLD-1, WS1) and their antibacterial activity against E. coli and S. aureus. Abiesonic acid (6) exhibited weak cytotoxic activity against A549 (IC50 = 22 µM) while compounds 1

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15

Zhang, Li-Sha, Yan-Lan Wang, Qian Liu, et al. "Three new 3,4-seco-cycloartane triterpenoids from the flower of Gardenia jasminoides." Phytochemistry Letters 23 (February 2018): 172–75. http://dx.doi.org/10.1016/j.phytol.2017.11.006.

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16

Silva, Gloria L., Roberto R. Gil, Baoliang Cui, et al. "Novel cytotoxic ring-a seco-cycloartane triterpenes from Gardenia coronaria and G. sootepensis." Tetrahedron 53, no. 2 (1997): 529–38. http://dx.doi.org/10.1016/s0040-4020(96)01003-4.

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17

Song, Wei-Wu, and Xue-Qin Wang. "Three New 3,4-Seco-Cycloartane Triterpenes from Leaves and Twigs of Gardenia sootepensis." Chemistry of Natural Compounds 55, no. 5 (2019): 861–64. http://dx.doi.org/10.1007/s10600-019-02833-1.

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18

Wang, Hongmin, Ruonan Ning, Yu Shen, et al. "Lithocarpic Acids A–N, 3,4-seco-Cycloartane Derivatives from the Cupules of Lithocarpus polystachyus." Journal of Natural Products 77, no. 8 (2014): 1910–20. http://dx.doi.org/10.1021/np500379f.

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19

SILVA, G. L., R. R. GIL, B. CUI, et al. "ChemInform Abstract: Novel Cytotoxic Ring-A seco-Cycloartane Triterpenes from Gardenia coronaria and G. sootepensis." ChemInform 28, no. 18 (2010): no. http://dx.doi.org/10.1002/chin.199718226.

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20

Isaev, I. M., D. A. Iskenderov, and M. I. Isaev. "Triterpene glycosides and their genins from Astragalus. LXXXIV. Secomacrogenin B, a new 9,10-seco-cycloartane." Chemistry of Natural Compounds 46, no. 1 (2010): 36–38. http://dx.doi.org/10.1007/s10600-010-9519-3.

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21

Lee, Dongho, Muriel Cuendet, Franklin Axelrod, et al. "Novel 29-nor-3,4-seco-cycloartane triterpene methyl esters from the aerial parts of Antirhea acutata." Tetrahedron 57, no. 33 (2001): 7107–12. http://dx.doi.org/10.1016/s0040-4020(01)00664-0.

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22

Pudhom, Khanitha, Thanesuan Nuanyai, Kiminori Matsubara, and Tirayut Vilaivan. "Antiangiogenic activity of 3,4-seco-cycloartane triterpenes from Thai Gardenia spp. and their semi-synthetic analogs." Bioorganic & Medicinal Chemistry Letters 22, no. 1 (2012): 512–17. http://dx.doi.org/10.1016/j.bmcl.2011.10.128.

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23

Lee, Dongho, Muriel Cuendet, Franklin Axelrod, et al. "ChemInform Abstract: Novel 29-nor-3,4-seco-Cycloartane Triterpene Methyl Esters from the Aerial Parts of Antirhea acutata." ChemInform 32, no. 50 (2010): no. http://dx.doi.org/10.1002/chin.200150177.

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24

Kinghorn, A. Douglas, and Djaja Djendoel Soejarto. "Discovery of terpenoid and phenolic sweeteners from plants." Pure and Applied Chemistry 74, no. 7 (2002): 1169–79. http://dx.doi.org/10.1351/pac200274071169.

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Several plant-derived compounds of the terpenoid and phenolic types have commercial use as sweeteners. In our research program directed toward the discovery of additional sweet compounds of these chemical classes, candidate sweet plants for laboratory investigation may be selected after scrutiny of the available literature, as a result of making inquiries in the field, and/or from a limited amount of organoleptic testing. Sweet-tasting plants are extracted according to a standard protocol, and preliminary safety testing is conducted before crude extracts or pure compounds are tasted. The pract

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25

Nomoto, Yuya, Liva Harinantenaina, Sachiko Sugimoto, Katsuyoshi Matsunami, and Hideaki Otsuka. "3,4-seco-24-homo-28-nor-Cycloartane and drimane-type sesquiterpenes and their lactams from the EtOAc-soluble fraction of a leaf extract of Cinnamosma fragrans and their biological activity." Journal of Natural Medicines 68, no. 3 (2014): 513–20. http://dx.doi.org/10.1007/s11418-014-0828-x.

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26

Yoshimitsu, Hitoshi, Makiko Nishida, and Toshihiro Nohara. "Three New 15,16-Seco-cycloartane Glycosides from Cimicifuga Rhizome." ChemInform 38, no. 45 (2007). http://dx.doi.org/10.1002/chin.200745170.

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27

Nishida, Makiko, Hitoshi Yoshimitsu, Masafumi Okawa, Tuyoshi Ikeda, and Toshihiro Nohara. "Two New 15,16-Seco-cycloartane Glycosides from Cimicifuga Rhizome." ChemInform 35, no. 12 (2004). http://dx.doi.org/10.1002/chin.200412184.

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28

Song, Wei-Wu, Xue-Qin Wang, and Bo Li. "ChemInform Abstract: Two New 3,4-seco-Cycloartane Triterpenes from Gardenia sootepensis." ChemInform 47, no. 28 (2016). http://dx.doi.org/10.1002/chin.201628229.

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