465-94-1|Longispinogenin|(3S,4aR,6aR,6bS,8S,8aS,12aS,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-icosahydropicene-3,8-diol|-范德生物科技公司

Longispinogenin

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names：
(3S,4aR,6aR,6bS,8S,8aS,12aS,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-icosahydropicene-3,8-diol
CAS号：
465-94-1
MDL Number：
MF(分子式)： C30H50O3 MW(分子量)： 458.727
EINECS: Reaxys Number:
Pubchem ID: Brand:BIOFOUNT

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中文别名	Longispinogenin
英文别名	Longispinogenin;
CAS号	465-94-1
SMILES	C[C@]12CC[C@@H](C([C@@H]1CC[C@@]3([C@@H]2CC=C4[C@]3(C[C@@H]([C@@]5([C@H]4CC(CC5)(C)C)CO)O)C)C)(C)C)O
Inchi	InChI=1S/C30H50O3/c1-25(2)14-15-30(18-31)20(16-25)19-8-9-22-27(5)12-11-23(32)26(3,4)21(27)10-13-28(22,6)29(19,7)17-24(30)33/h8,20-24,31-33H,9-18H2,1-7H3/t20-,21-,22+,23-,24-,27-,28+,29+,30+/m0/s1
InchiKey	YHGVYECWZWIVJC-MZGFOBBZSA-N
分子式 Formula	C30H50O3
分子量 Molecular Weight	458.727
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	Longispinogenin(CAS:465-94-1):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	Longispinogenin is a triterpenetriol fatty acid ester isolated from Trichocereus chilensis.
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]Morales G, McLaughlin JL. 3 beta-O-palmityl longispinogenin from Trichocereus chilensis. J Nat Prod. 1989 Mar-Apr;52(2):381-4. PubMed PMID: 2746261.

[2]Liu Y, Xu TH, Zhang MQ, Li X, Xu YJ, Jiang HY, Liu TH, Xu DM. Chemical constituents from the stems of Gymnema sylvestre. Chin J Nat Med. 2014 Apr;12(4):300-4. doi: 10.1016/S1875-5364(14)60059-5. PubMed PMID: 24863357.

[3] Li J, Pan L, Fletcher JN, Lv W, Deng Y, Vincent MA, Slack JP, McCluskey TS, Jia Z, Cushman M, Kinghorn AD. In vitro evaluation of potential bitterness-masking terpenoids from the Canada goldenrod (Solidago canadensis). J Nat Prod. 2014 Jul 25;77(7):1739-43. doi: 10.1021/np5001413. Epub 2014 Jul 7. PubMed PMID: 24999828.

[4] Ye W, Liu X, Zhang Q, Che CT, Zhao S. Antisweet saponins from Gymnema sylvestre. J Nat Prod. 2001 Feb;64(2):232-5. PubMed PMID: 11430009.

[5] Yasukawa K, Akihisa T, Oinuma H, Kasahara Y, Kimura Y, Yamanouchi S, Kumaki K, Tamura T, Takido M. Inhibitory effect of Di- and trihydroxy triterpenes from the flowers of compositae on 12-O-tetradecanoylphorbol-13-acetate-induced inflammation in mice. Biol Pharm Bull. 1996 Oct;19(10):1329-31. PubMed PMID: 8913506.

6: Harinantenaina L, Brodie PJ, Callmander MW, Razafitsalama LJ, Rasamison VE, Rakotobe E, Kingston DG. Two antiproliferative saponins of Tarenna grevei from the Madagascar dry forest [1]. Nat Prod Commun. 2012 Jun;7(6):705-8. PubMed PMID: 22816288; PubMed Central PMCID: PMC3480188.7: Ye WC, Zhang QW, Liu X, Che CT, Zhao SX. Oleanane saponins from Gymnema sylvestre. Phytochemistry. 2000 Apr;53(8):893-9. PubMed PMID: 10820799.8: Yoshikawa K, Mizutani A, Kan Y, Arihara S. Antisweet natural products. XII. Structures of sitakisosides XI-XX from Stephanotis lutchuensis Koidz. var. japonica. Chem Pharm Bull (Tokyo). 1997 Jan;45(1):62-7. PubMed PMID: 9023968.9: Yoshikawa K, Taninaka H, Kan Y, Arihara S. Antisweet natural products. XI. Structures of sitakisosides VI-X from Stephanotis lutchuensis Koidz. var. japonica. Chem Pharm Bull (Tokyo). 1994 Dec;42(12):2455-60. PubMed PMID: 7697761.10: Ukiya M, Akihisa T, Tokuda H, Suzuki H, Mukainaka T, Ichiishi E, Yasukawa K, Kasahara Y, Nishino H. Constituents of Compositae plants III. Anti-tumor promoting effects and cytotoxic activity against human cancer cell lines of triterpene diols and triols from edible chrysanthemum flowers. Cancer Lett. 2002 Mar 8;177(1):7-12. PubMed PMID: 11809525.

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