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Merck
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Documenti

152633

Sigma-Aldrich

Olivetol

95%

Sinonimo/i:

1,3-Dihydroxy-5-pentylbenzene, 3,5-Dihydroxyamylbenzene, 5-Pentylresorcinol

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About This Item

Formula condensata:
CH3(CH2)4C6H3-1,3-(OH)2
Numero CAS:
500-66-3
Peso molecolare:
180.24
Numero CE:
207-908-8
Numero MDL:
MFCD00002293
Codice UNSPSC:
12352100
ID PubChem:
24849242
NACRES:
NA.22

Saggio

95%

Forma fisica

solid

Punto di fusione

46-48 °C (lit.)

Stringa SMILE

CCCCCc1cc(O)cc(O)c1

InChI

1S/C11H16O2/c1-2-3-4-5-9-6-10(12)8-11(13)7-9/h6-8,12-13H,2-5H2,1H3
IRMPFYJSHJGOPE-UHFFFAOYSA-N

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Applicazioni

Olivetol was used as a template molecule in the synthesis of molecularly imprinted polymer (MIP). It was also used as an inhibitor of (S)-mephenytoin 4′-hydroxylase activity of recombinant CYP2C19.

Avvertenze

Danger

Indicazioni di pericolo

H302,H315,H317,H318,H370,H371,H410

Classi di pericolo

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 3 - Eye Dam. 1 - Skin Irrit. 2 - Skin Sens. 1B - STOT SE 1 Oral - STOT SE 2 Oral

Organi bersaglio

Central nervous system,Blood, Respiratory system

Codice della classe di stoccaggio

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

235.4 °F - closed cup

Punto d’infiammabilità (°C)

113 °C - closed cup

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

Certificati d'analisi (COA)

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M G Cascio et al.
British journal of pharmacology, 149(4), 431-440 (2006-09-06)
We have previously reported the development of CB-25 and CB-52, two ligands of CB1 and CB2 cannabinoid receptors. We assessed here their functional activity. The effect of the two compounds on forskolin-induced cAMP formation in intact cells or GTP-gamma-S binding
Yafeng Jin et al.
Se pu = Chinese journal of chromatography, 31(6), 587-595 (2013-09-26)
Molecularly imprinted polymer (MIP) was synthesized by bulk polymerization, using olivetol as template molecule, methyl acrylic acid (MAA) as monomer, ethylene glycol dimethacrylate (EDMA) as crosslinker, toluene and dodecanol as solvents. The resulted MIP was characterized by the equilibrium binding
M Fellermeier et al.
FEBS letters, 427(2), 283-285 (1998-06-02)
A new enzyme, geranylpyrophosphate:olivetolate geranyltransferase (GOT), the first enzyme in the biosynthesis of cannabinoids could be detected in extracts of young leaves of Cannabis sativa. The enzyme accepts geranylpyrophosphate (GPP) and to a lesser degree also nerylpyrophosphate (NPP) as a
Rongrong Jiang et al.
Drug metabolism and pharmacokinetics, 28(4), 332-338 (2013-01-16)
The present study investigated the inhibitory effect of cannabidiol (CBD), a major constituent of marijuana, on the catalytic activity of cytochrome P450 2C19 (CYP2C19). (S)-Mephenytoin 4'-hydroxylase activities of human liver microsomes (HLMs) and recombinant CYP2C19 were inhibited by CBD in
R H McClanahan et al.
Journal of natural products, 47(5), 828-834 (1984-09-01)
A study of the biotransformation of olivetol by Syncephalastrum racemosum ATCC 18192 has led to the isolation of three metabolites, which were identified as 4'-hydroxy-olivetol, 3-(3,5-dihydroxyphenyl)-1-propanol, and 3-(3,5-dihydroxyphenyl)-1-propanoic acid. The structures of the isolated metabolites were deduced by comparison of
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