54632-04-1|Albicanol|((1S,4aS,8aR)-5,5,8a-trimethyl-2-methylenedecahydronaphthalen-1-yl)methanol|-范德生物科技公司

Albicanol

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names：
((1S,4aS,8aR)-5,5,8a-trimethyl-2-methylenedecahydronaphthalen-1-yl)methanol
CAS号：
54632-04-1
MDL Number：
MF(分子式)： C15H26O MW(分子量)： 222.37
EINECS: Reaxys Number:
Pubchem ID: Brand:BIOFOUNT

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中文别名	Albicanol
英文别名	Albicanol; CCRIS 8459; CCRIS-8459; CCRIS8459
CAS号	54632-04-1
SMILES	CC([C@@H]1CC2)(C)CCC[C@@]1(C)[C@@H](CO)C2=C
Inchi	InChI=1S/C15H26O/c1-11-6-7-13-14(2,3)8-5-9-15(13,4)12(11)10-16/h12-13,16H,1,5-10H2,2-4H3/t12-,13-,15-/m0/s1
InchiKey	ZPTSRWNMMWXEHX-YDHLFZDLSA-N
分子式 Formula	C15H26O
分子量 Molecular Weight	222.37
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	Albicanol(CAS:54632-04-1):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	Albicanol is a biochemical.
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

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[2]Fratoni E, Claudino VD, Yunes RA, Franchi GC Jr, Nowill AE, Filho VC, Monache FD, Malheiros A. Further drimane sesquiterpenes from Drimys brasiliensis stem barks with cytotoxic potential. Naunyn Schmiedebergs Arch Pharmacol. 2016 Jul;389(7):791-7. doi: 10.1007/s00210-016-1241-7. Epub 2016 Apr 19. PubMed PMID: 27095358.

[3] Zhao DD, Zhao QS, Liu L, Chen ZQ, Zeng WM, Lei H, Zhang YL. Compounds from Dryopteris fragrans (L.) Schott with cytotoxic activity. Molecules. 2014 Mar 18;19(3):3345-55. doi: 10.3390/molecules19033345. PubMed PMID: 24647035.

[4] Wu LS, Hu CL, Han T, Zheng CJ, Ma XQ, Rahman K, Qin LP. Cytotoxic metabolites from Perenniporia tephropora, an endophytic fungus from Taxus chinensis var. mairei. Appl Microbiol Biotechnol. 2013 Jan;97(1):305-15. doi: 10.1007/s00253-012-4189-7. Epub 2012 Jun 3. PubMed PMID: 22660771.

[5] Ishii S, Fujii M, Akita H. First syntheses of (-)-tauranin and antibiotic (-)-BE-40644 based on lipase-catalyzed optical resolution of albicanol. Chem Pharm Bull (Tokyo). 2009 Oct;57(10):1103-6. PubMed PMID: 19801866.

6: Henderson JR, Parvez M, Keay BA. A concise Diels-Alder strategy for the asymmetric synthesis of (+)-albicanol, (+)-albicanyl acetate, (+)-dihydrodrimenin, and (-)-dihydroisodrimeninol. Org Lett. 2009 Aug 6;11(15):3178-81. doi: 10.1021/ol901372m. PubMed PMID: 19594165.7: Miyake T, Uda K, Kinoshita M, Fujii M, Akita H. Concise syntheses of coronarin A, coronarin E, austrochaparol and pacovatinin A. Chem Pharm Bull (Tokyo). 2008 Mar;56(3):398-403. PubMed PMID: 18310958.8: Shen ZB, Luo WY, Yan YS, Zhu JF. [Study on terpene of Dryopteris fragrans L]. Zhong Yao Cai. 2006 Apr;29(4):334-5. Chinese. PubMed PMID: 16913486.9: Hua DH, Huang X, Chen Y, Battina SK, Tamura M, Noh SK, Koo SI, Namatame I, Tomoda H, Perchellet EM, Perchellet JP. Total syntheses of (+)-chloropuupehenone and (+)-chloropuupehenol and their analogues and evaluation of their bioactivities. J Org Chem. 2004 Sep 3;69(18):6065-78. PubMed PMID: 15373492.10: Goodwin TE, Brown FD, Counts RW, Dowdy NC, Fraley PL, Hughes RA, Liu DZ, Mashburn CD, Rankin JD, Roberson RS, Wooley KD, Rasmussen EL, Riddle SW, Riddle HS, Schulz S. African elephant sesquiterpenes. II. Identification and synthesis of new derivatives of 2,3-dihydrofarnesol. J Nat Prod. 2002 Sep;65(9):1319-22. PubMed PMID: 12350155.1

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