51020-36-1|Fezelol|2H-1-Benzopyran-2-one, 7-((1,4,4a,5,6,7,8,8a-octahydro-6-hydroxy-2,5,5,8a-tetramethyl-1-naphthalenyl)methoxy)-, (1R-(1alpha,4abeta,6alpha,8aalpha))-|-范德生物科技公司

Fezelol

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names：
2H-1-Benzopyran-2-one, 7-((1,4,4a,5,6,7,8,8a-octahydro-6-hydroxy-2,5,5,8a-tetramethyl-1-naphthalenyl)methoxy)-, (1R-(1alpha,4abeta,6alpha,8aalpha))-
CAS号：
51020-36-1
MDL Number：
MF(分子式)： C24H30O4 MW(分子量)： 382.5
EINECS: Reaxys Number:
Pubchem ID: Brand:BIOFOUNT

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中文别名	Fezelol
英文别名	Fezelol; Feselol; Moschatol
CAS号	51020-36-1
SMILES	O=C1C=CC2=CC=C(OC[C@H]3C(C)=CC[C@@]4([H])C(C)(C)[C@@H](O)CC[C@]34C)C=C2O1
Inchi	InChI=1S/C24H30O4/c1-15-5-9-20-23(2,3)21(25)11-12-24(20,4)18(15)14-27-17-8-6-16-7-10-22(26)28-19(16)13-17/h5-8,10,13,18,20-21,25H,9,11-12,14H2,1-4H3/t18-,20-,21-,24+/m0/s1
InchiKey	MCTDXPDDZLFJHR-SODVOOIJSA-N
分子式 Formula	C24H30O4
分子量 Molecular Weight	382.5
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	Fezelol(CAS:51020-36-1):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	Fezelol is a sesquiterpene coumarin isolated from the fruits of Ferula badrakema.
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]Mollazadeh S, Matin MM, Bahrami AR, Iranshahi M, Behnam-Rassouli M, Rassouli FB, Neshati V. Feselol enhances the cytotoxicity and DNA damage induced by cisplatin in 5637 cells. Z Naturforsch C. 2011 Nov-Dec;66(11-12):555-6[1]PubMed PMID: 22351980.

[2]Mollazadeh S, Matin MM, Iranshahi M, Bahrami AR, Neshati V, Behnam-Rassouli F. The enhancement of vincristine cytotoxicity by combination with feselol. J Asian Nat Prod Res. 2010 Jul;12(7):569-75. doi: 10.1080/10286020.2010.485565. PubMed PMID: 20628935.

[3] Iranshahi M, Barthomeuf C, Bayet-Robert M, Chollet P, Davoodi D, Piacente S, Rezaee R, Sahebkar A. Drimane-Type Sesquiterpene Coumarins from Ferula gummosa Fruits Enhance Doxorubicin Uptake in Doxorubicin-Resistant Human Breast Cancer Cell Line. J Tradit Complement Med. 2014 Apr;4(2):118-25. doi: 10.4103/2225-4110.126181. PubMed PMID: 24860735; PubMed Central PMCID: PMC4003701.

[4] Oughlissi-Dehak K, Lawton P, Michalet S, Bayet C, Darbour N, Hadj-Mahammed M, Badjah-Hadj-Ahmed YA, Dijoux-Franca MG, Guilet D. Sesquiterpenes from aerial parts of Ferula vesceritensis. Phytochemistry. 2008 Jun;69(9):1933-8. doi: 10.1016/j.phytochem.2008.03.010. Epub 2008 May 14. PubMed PMID: 18485426.

[5] Amin A, Tuenter E, Cos P, Maes L, Exarchou V, Apers S, Pieters L. Antiprotozoal and Antiglycation Activities of Sesquiterpene Coumarins from Ferula narthex Exudate. Molecules. 2016 Sep 26;21(10). pii: E1287. PubMed PMID: 27681714; PubMed Central PMCID: PMC6274357.

6: Iranshahi M, Masullo M, Asili A, Hamedzadeh A, Jahanbin B, Festa M, Capasso A, Piacente S. Sesquiterpene coumarins from Ferula gumosa. J Nat Prod. 2010 Nov 29;73(11):1958-62. doi: 10.1021/np100487j. Epub 2010 Oct 20. PubMed PMID: 20961138.7: Li G, Li X, Cao L, Zhang L, Shen L, Zhu J, Wang J, Si J. Sesquiterpene coumarins from seeds of Ferula sinkiangensis. Fitoterapia. 2015 Jun;10

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