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SMB00113

Sigma-Aldrich

6-Geranyl-7-hydroxycoumarin

≥95% (LC/MS-ELSD)

Synonyme(s) :

6-(3,7-Dimethyl-2,6-octadienyl)-7-hydroxycoumarin, Ostruthin, Ostruthine

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About This Item

Formule empirique (notation de Hill):
C19H22O3
Numéro CAS:
148-83-4
Poids moléculaire :
298.38
Numéro MDL:
MFCD07771988
Code UNSPSC :
12352205
ID de substance PubChem :
329824791
Nomenclature NACRES :
NA.25

Pureté

≥95% (LC/MS-ELSD)

Forme

solid

Application(s)

metabolomics
vitamins, nutraceuticals, and natural products

Température de stockage

−20°C

Chaîne SMILES 

C\C(C)=C\CC\C(C)=C\Cc1cc2C=CC(=O)Oc2cc1O

InChI

1S/C19H22O3/c1-13(2)5-4-6-14(3)7-8-15-11-16-9-10-19(21)22-18(16)12-17(15)20/h5,7,9-12,20H,4,6,8H2,1-3H3/b14-7+

Clé InChI

INBMTJJPUABOQJ-VGOFMYFVSA-N

Description générale

Natural product derived from plant source.

Pictogrammes

Environment
GHS09

Mention d'avertissement

Warning

Mentions de danger

H410

Conseils de prudence

P273 - P501

Classification des risques

Aquatic Acute 1 - Aquatic Chronic 1

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

Feng Li et al.
Planta medica, 78(8), 796-799 (2012-04-21)
During a search for potent anticancer agents from natural products based on an anti-austerity strategy, we found that a CHCl3 extract of Rhizoma et Radix Notopterygii (Qianghuo), a Chinese crude drug, exhibited strong cytotoxicity against PANC-1 human pancreatic cancer cells
Andreas Schinkovitz et al.
Planta medica, 69(4), 369-371 (2003-04-24)
Following a bioassay-guided fractionation, ostruthin (6-geranyl-7-hydroxycoumarin) was isolated from the roots of Peucedanum ostruthium Koch (Apiaceae) as a compound with pronounced in vitro activity against several species of rapidly growing Mycobacteria, namely Mycobacterium abscesus, M. aurum, M. fortuitum, M. phlei
Helge Joa et al.
Journal of natural products, 74(6), 1513-1516 (2011-06-02)
Inhibition of vascular smooth muscle cell (VSMC) proliferation is of substantial interest in combating cardiovascular disease. A dichloromethane extract from the rhizomes of Peucedanum ostruthium, a traditionally used Austrian medicinal plant with anti-inflammatory properties, was examined for a putative antiproliferative
J Qi et al.
Bioscience, biotechnology, and biochemistry, 63(8), 1501-1502 (1999-09-29)
A search for neuritogenic compounds in Chinese herbs resulted in the isolation of two known substances, ostruthin and (-)-bornyl ferulate, from Notopterygium incisum (and/or N. forbesii). Both compounds induced comparable neurite-like structures in 20% of rat PC12 cells at 2
Y Cai et al.
Carcinogenesis, 18(8), 1521-1527 (1997-08-01)
Several naturally occurring coumarins previously found to be potent inhibitors of mouse hepatic ethoxyresorufin-O-deethylase (EROD) and/or pentoxyresorufin-O-dealkylase (PROD) were examined for their effects on formation of benzo[a]pyrene (B[a]P) and 7,12-dimethylbenz[a]anthracene (DMBA) DNA adducts in mouse epidermis, as well as, their

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