18607-76-6|Sarcostin|(3S,8S,9R,10R,12R,13R,14R,17R)-17-((S)-1-hydroxyethyl)-10,13-dimethyl-2,3,4,7,9,10,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,8,12,14,17-pentaol|-范德生物科技公司

Sarcostin

NMR下载 COA and HPLC MSDS下载
names：
(3S,8S,9R,10R,12R,13R,14R,17R)-17-((S)-1-hydroxyethyl)-10,13-dimethyl-2,3,4,7,9,10,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,8,12,14,17-pentaol
CAS号：
18607-76-6
MDL Number：
MF(分子式)： C21H34O6 MW(分子量)： 382.49
EINECS: Reaxys Number:
Pubchem ID: Brand:BIOFOUNT

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中文别名	(3S,8S,9R,10R,12R,13R,14R,17R)-17-((S)-1-hydroxyethyl)-10,13-dimethyl-2,3,4,7,9,10,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,8,12,14,17-pentaol
英文别名	Sarcostin;
CAS号	18607-76-6
SMILES	C[C@H](O)[C@@]1(O)CC[C@]2(O)[C@]3(O)CC=C4C[C@@H](O)CC[C@]4(C)[C@@]3([H])C[C@@H](O)[C@]12C
Inchi	InChI=1S/C21H34O6/c1-12(22)19(25)8-9-21(27)18(19,3)16(24)11-15-17(2)6-5-14(23)10-13(17)4-7-20(15,21)26/h4,12,14-16,22-27H,5-11H2,1-3H3/t12-,14-,15+,16+,17-,18+,19-,20-,21+/m0/s1
InchiKey	WIOBOUWMWWLZKG-WDGBXWAPSA-N
分子式 Formula	C21H34O6
分子量 Molecular Weight	382.49
闪点 FP
熔点 Melting point
沸点 Boiling point
Polarizability极化度
密度 Density
蒸汽压 Vapor Pressure
溶解度Solubility
性状	Solid powder
储藏条件 Storage conditions	Dry, dark and store at 0-4℃ for short term (days to weeks) or -20℃ for long term (Store correctly 2-3years).

产品说明	Sarcostin(CAS:18607-76-6):仅限应用于工业或者科学研究过程中非医疗目的，不应用于人类或动物的临床诊断以及治过程疗，该产品非药用，非食用。
Introduction	Sarcostin is a pregnane ester glycoside isolated from the aerial parts of Stapelia variegata.
Application1
Application2
Application3

警示图
危险性	Warning
危险性警示
安全声明
安全防护
备注

[1]el Sayed KA, Halim AF, Zaghloul AM, McChesney JD, Stone MP, Voehler M, Hayashi K. Pregnane glycosides from Stapelia variegata. Phytochemistry. 1995 May;39(2):395-403. PubMed PMID: 7495533.

[2]MITSUHASHI H, SHIMIZU Y. Structural relationship between deacylcynanchogenin and sarcostin. Chem Pharm Bull (Tokyo). 1962 May;10:433-4. PubMed PMID: 14474713.

[3] Ma B, Fang T, Ma K, Ni J, Wu H, Ding WP, Jiang C. Novel saponins hainaneosides A and B isolated from Marsdenia hainanensis. J Nat Prod. 1997 Feb;60(2):134-8. PubMed PMID: 9051912.

[4] Lee DU, Shin US, Huh K. Structure-activity relationships of gagaminine and its derivatives on the inhibition of hepatic aldehyde oxidase activity and lipid peroxidation. Arch Pharm Res. 1998 Jun;21(3):273-7. PubMed PMID: 9875443.

[5] Aquino R, Pizza C. New polyoxypregnane ester derivatives from Leptadenia hastata. J Nat Prod. 1995 May;58(5):672-9. PubMed PMID: 7623046.

6: Aquino R, Peluso G, De Tommasi N, De Simone F, Pizza C. New polyoxypregnane ester derivatives from Leptadenia hastata. J Nat Prod. 1996 Jun;59(6):555-64. PubMed PMID: 8786361.7: Warashina T, Noro T. Steroidal glycosides from Cynanchum caudatum. Phytochemistry. 1995 May;39(1):199-204. PubMed PMID: 7786487.8: Deepak D, Srivastava S, Khare A. Pregnane glycosides from Hemidesmus indicus. Phytochemistry. 1997 Jan;44(1):145-51. PubMed PMID: 8983217.9: Li JZ, Liu HY, Lin YJ, Hao XJ, Ni W, Chen CX. Six new C21 steroidal glycosides from Asclepias curassavica L. Steroids. 2008 Jul;73(6):594-600. doi: 10.1016/j.steroids.2008.01.015. Epub 2008 Jan 20. PubMed PMID: 18328519.10: Cioffi G, Sanogo R, Vassallo A, Dal Piaz F, Autore G, Marzocco S, De Tommasi N. Pregnane glycosides from Leptadenia pyrotechnica. J Nat Prod. 2006 Apr;69(4):625-35. PubMed PMID: 16643040.1

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