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Supelco

Bakuchiol

analytical standard

Sinônimo(s):

(S)-Bakuchiol, 4-[(1E,3S)-3-Ethenyl-3,7-dimethyl-1,6-octadien-1-yl]phenol

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About This Item

Fórmula empírica (Notação de Hill):
C18H24O
Número CAS:
10309-37-2
Peso molecular:
256.38
Beilstein:
3611720
Número MDL:
MFCD01707441
Código UNSPSC:
85151701
ID de substância PubChem:
329761022
NACRES:
NA.24

grau

analytical standard

Nível de qualidade

100

Ensaio

≥95.0% (HPLC)

atividade óptica

[α]/D +24.0 to +30.0°, c = 0.1 in chloroform

prazo de validade

limited shelf life, expiry date on the label

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

aplicação(ões)

food and beverages

Formato

neat

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

C\C(C)=C/CC[C@@](C)(C=C)\C=C\c1ccc(O)cc1

InChI

1S/C18H24O/c1-5-18(4,13-6-7-15(2)3)14-12-16-8-10-17(19)11-9-16/h5,7-12,14,19H,1,6,13H2,2-4H3/b14-12+/t18-/m1/s1

chave InChI

LFYJSSARVMHQJB-QIXNEVBVSA-N

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Aplicação

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pictogramas

Environment
GHS09

Palavra indicadora

Warning

Frases de perigo

H410

Declarações de precaução

P273 - P391 - P501

Classificações de perigo

Aquatic Acute 1 - Aquatic Chronic 1

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

363.2 °F - Pensky-Martens closed cup

Ponto de fulgor (°C)

184 °C - Pensky-Martens closed cup

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Certificados de análise (COA)

Lot/Batch Number
BCCG7662
BCCG0499
BCCD6908
BCCB9679
BCBZ9454

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Sun-Hye Lim et al.
Phytomedicine : international journal of phytotherapy and phytopharmacology, 18(5), 425-430 (2011-03-09)
Estrogenic activities of ethanol extract and its active components from Psoralea corylifolia L. were studied using various in vitro assays. The main components from ethanol extract were analyzed to be bakuchiol, psoralen, isobavachalcone, isobavachromene, and bavachinin. In a fractionation procedure
P-J Hsu et al.
Natural product research, 23(8), 781-788 (2009-05-07)
Bioactivity guided fractionation of an EtOAc extract from Psoralidium tenuiflorum (Pursh) Rydb. (family : Fabaceae) yielded the known compound bakuchiol as a racemic mixture. This compound was purified by liquid-liquid partitioning and chromatography followed by NMR and GCMS characterisation. This
Gang Zhao et al.
Biochemical pharmacology, 75(9), 1835-1847 (2008-03-11)
Monoamine transporters play key roles in controlling monoamine levels and modulating monoamine reuptake. The objective of the present study was to identify monoamine transporter inhibitors from herbal sources. We discovered that bakuchiol analogs isolated from Fructus Psoraleae inhibited monoamine transporter
Hong-li Chen et al.
Yao xue xue bao = Acta pharmaceutica Sinica, 45(4), 467-470 (2011-03-02)
The in vitro antitumor activity of bakuchiol was exploited, compared with tamoxifen. The result of biological activities showed that bakuchiol could inhibit human breast cancer and the IC50 values were 2.89 x 10(-5) mol L(-1) and 8.29 x 10(-3) mol
Hongli Chen et al.
Bioorganic & medicinal chemistry, 16(5), 2403-2411 (2007-12-08)
A series of derivatives of bakuchiol were synthesized and tested in vitro for their cytotoxicity, and inhibition of T cell proliferation and B cell proliferation. The data obtained provided preliminary structure-activity relationships of the compounds as immunosuppressive activity.
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