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Longispinogenin

NMR下載 COA and HPLC MSDS下載
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號：
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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中文別名	Longispinogenin
英文別名	Longispinogenin;
CAS號	465-94-1
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
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	Longispinogenin(CAS:465-94-1):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	Longispinogenin is a triterpenetriol fatty acid ester isolated from Trichocereus chilensis.
Application1
Application2
Application3

警示圖
危險性	Warning
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[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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