購物車 
-
Bivittoside A
- names：
Bivittoside A
- CAS號：
77394-03-7
MDL Number： - MF(分子式)： C41H67O13 MW(分子量)： 767.97
- EINECS: Reaxys Number:
- Pubchem ID: Brand:BIOFOUNT
| 貨品編碼 | 規格 | 純度 | 價格 (￥) | 現價(￥) | 特價(￥) | 庫存描述 | 數量 | 總計 (￥) |
|---|
| 中文別名 | (3S,5R,8R,10S,12S,13R,17S)-3-(((2S,3R,4S,5R)-4,5-dihydroxy-3-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-2-yl)oxy)-12-hydroxy-17-((S)-2-hydroxy-6-methylheptan-2-yl)-4,4,10,14-tetramethyl-1,2,3,4,5,6,7,8,10,12,14,15,16,17-tetradecahydro-14l5-14,13-(epoxymethano)cyclopenta[a]phenanthren-19-one |
| 英文別名 | Bivittoside A; |
| CAS號 | 77394-03-7 |
| Inchi | InChI=1S/C41H67O13/c1-20(2)10-9-15-39(7,49)26-14-17-41(8)23-11-12-25-37(4,5)28(13-16-38(25,6)22(23)18-27(43)40(26,41)36(48)54-41)52-35-33(30(45)24(42)19-50-35)53-34-32(47)31(46)29(44)21(3)51-34/h18,20-21,23-35,42-47,49H,9-17,19H2,1-8H3/t21-,23-,24-,25+,26-,27+,28+,29-,30+,31+,32-,33-,34+,35+,38-,39+,40+/m1/s1 |
| InchiKey | HUMSPESDMWWCRJ-BCUNVWNOSA-N |
| 分子式 Formula | C41H67O13 |
| 分子量 Molecular Weight | 767.97 |
| 溶解度Solubility | |
| 性狀 | Solid powder |
| 儲藏條件 Storage conditions | Dry, dark and store at 0-4℃ for short term (days to weeks) or -20℃ for long term (Store correctly 2-3years). |
| 產品說明 | Bivittoside A(CAS:77394-03-7):僅限應用于工業或者科學研究過程中非醫療目的，不應用于人類或動物的臨床診斷以及治過程療，該產品非藥用，非食用。 |
| Introduction | Bivittoside A is an antifungal agent. |
| Application1 | |
| Application2 | |
| Application3 |
| [1]Lakshmi V, Srivastava S, Mishra SK, Shukla PK. Antifungal activity of bivittoside-D from Bohadschia vitiensis (Semper). Nat Prod Res. 2012;26(10):913-8. doi: 10.1080/14786419.2010.534096. Epub 2011 Aug 2. PubMed PMID: 21809953. |
| [2]Omran NE, Khedr AM. Structure elucidation, protein profile and the antitumor effect of the biological active substance extracted from sea cucumber Holothuria polii. Toxicol Ind Health. 2015 Jan;31(1):1-8. doi: 10.1177/0748233712466135. Epub 2012 Nov 27. PubMed PMID: 23188650. |
| [3] Yuan WH, Yi YH, Tang HF, Liu BS, Wang ZL, Sun GQ, Zhang W, Li L, Sun P. Antifungal triterpene glycosides from the sea cucumber Bohadschia marmorata. Planta Med. 2009 Feb;75(2):168-73. doi: 10.1055/s-0028-1088348. Epub 2008 Dec 18. PubMed PMID: 19096993. |
| [4] Hill JA, Szabat M, Hoesli CA, Gage BK, Yang YH, Williams DE, Riedel MJ, Luciani DS, Kalynyak TB, Tsai K, Ao Z, Andersen RJ, Warnock GL, Piret JM, Kieffer TJ, Johnson JD. A multi-parameter, high-content, high-throughput screening platform to identify natural compounds that modulate insulin and Pdx1 expression. PLoS One. 2010 Sep 23;5(9):e12958. doi: 10.1371/journal.pone.0012958. PubMed PMID: 20886041; PubMed Central PMCID: PMC2944895. |
| [5] Lakshmi V, Saxena A, Mishra SK, Raghubir R, Srivastava MN, Jain RK, Maikhuri JP, Gupta G. Spermicidal activity of bivittoside D from Bohadschia vitiensis. Arch Med Res. 2008 Oct;39(7):631-8. doi: 10.1016/j.arcmed.2008.06.007. PubMed PMID: 18760190. |
6: Honey-Escandón M, Arreguín-Espinosa R, Solís-Marín FA, Samyn Y. Biological and taxonomic perspective of triterpenoid glycosides of sea cucumbers of the family Holothuriidae (Echinodermata, Holothuroidea). Comp Biochem Physiol B Biochem Mol Biol. 2015 Feb;180:16-39. doi: 10.1016/j.cbpb.2014.09.007. Epub 2014 Sep 28. Review. PubMed PMID: 25263252.7: Wang Z, Gong W, Sun G, Tang H, Liu B, Li L, Yi Y, Zhang W. New holostan-type triterpene glycosides from the sea cucumber Apostichopus japonicus. Nat Prod Commun. 2012 Nov;7(11):1431-4. PubMed PMID: 23285801.8: Yu BS, Jo IH. Interaction of sea cucumber saponins with multilamellar liposomes. Chem Biol Interact. 1984 Dec;52(2):185-202. PubMed PMID: 6509686.9: Sun P, Liu BS, Yi YH, Li L, Gui M, Tang HF, Zhang DZ, Zhang SL. A new cytotoxic lanostane-type triterpene glycoside from the sea cucumber Holothuria impatiens. Chem Biodivers. 2007 Mar;4(3):450-7. PubMed PMID: 17372947.
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