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Merck
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SMB00100

Sigma-Aldrich

Bavachinin

≥95% (LC/MS-ELSD)

Sinónimos:

4′-Hydroxy-7-methoxy-6-(3-methyl-2-butenyl)flavanone, 7-O-Methylbavachin, Bavachinin A

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About This Item

Fórmula empírica (notación de Hill):
C21H22O4
Número de CAS:
19879-30-2
Peso molecular:
338.40
MDL number:
MFCD06858307
UNSPSC Code:
12352205
PubChem Substance ID:
329824778
NACRES:
NA.25

assay

≥95% (LC/MS-ELSD)

form

solid

application(s)

metabolomics
vitamins, nutraceuticals, and natural products

Storage temp.

−20°C

SMILES string

COc1cc2O[C@@H](CC(=O)c2cc1C\C=C(\C)C)c3ccc(O)cc3

InChI

1S/C21H22O4/c1-13(2)4-5-15-10-17-18(23)11-20(14-6-8-16(22)9-7-14)25-21(17)12-19(15)24-3/h4,6-10,12,20,22H,5,11H2,1-3H3/t20-/m0/s1

Inchi Key

VOCGSQHKPZSIKB-FQEVSTJZSA-N

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General description

Natural product derived from plant source.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Manoj Nepal et al.
European journal of pharmacology, 691(1-3), 28-37 (2012-07-05)
Hypoxia-inducible factor-1 (HIF-1) consists of two subunits, the HIF-1β, which is constitutively expressed, and HIF-1α, which is oxygen-responsive. HIF-1α is over-expressed in response to hypoxia, increasing transcriptional activity linked to tumor progression, angiogenesis, metastasis, and invasion. This study aimed to
Hiroyuki Haraguchi et al.
Phytotherapy research : PTR, 16(6), 539-544 (2002-09-19)
A meroterpene and four flavonoids were isolated from the seeds of Psoralea corylifolia as antioxidative components. Their structures were elucidated by spectral data and identified as bakuchiol (1), bavachinin (2), bavachin (3), isobavachin (4) and isobavachalcone (5). In particular, meroterpene
Lei Liu et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 893-894, 21-28 (2012-03-27)
A fully automated on-line solid-phase extraction (SPE) and high-performance liquid chromatography (HPLC) with diode array detection (DAD) method was developed for determination of bavachinin in mouse plasma. Analytical process was performed on two reversed-phase columns (SPE cartridge and analytical column)
Jianmei Luo et al.
Journal of bioscience and bioengineering, 117(2), 191-196 (2013-09-10)
Biotransformation of bavachinin (1) was investigated using three fungal cell cultures of Aspergillus flavus ATCC 30899, Cunninghamella elegans CICC 40250 and Penicillium raistrickii ATCC 10490, respectively. Two major converted products were identified by LC/MS, (1)H NMR and (13)C NMR and
Ming Hong Lee et al.
Biological & pharmaceutical bulletin, 28(12), 2253-2257 (2005-12-06)
The overproduction of nitric oxide (NO) by inducible nitric oxide synthase (iNOS) switches the function of NO from a physiological neuromodulator to a neurotoxic effector in central nervous system (CNS) after brain injury. From the methanol extracts of Psoralea corylifolia
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