BAVACHIN

BAVACHIN Basic information
Product Name:BAVACHIN
Synonyms:BAVACHIN;(S)-2,3-Dihydro-7-hydroxy-2-(4-hydroxyphenyl)-6-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one;(2S)-2,3-Dihydro-7-hydroxy-2-(4-hydroxyphenyl)-6-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one;7-hydroxy-2-(4-hydroxyphenyl)-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one;4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-(4-hydroxyphenyl)-6-(3-methyl-2-butenyl)-, (2S)-;Bavachin from Psoralea coryfolia, >=97% (HPLC);(2S)-7-hydroxy-2-(4-hydroxyphenyl)-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one;(S)-7-Hydroxy-2-(4-hydroxyphenyl)-6-(3-methylbut-2-en-1-yl)chroman-4-one
CAS:19879-32-4
MF:C20H20O4
MW:324.37
EINECS:
Product Categories:
Mol File:19879-32-4.mol
BAVACHIN Structure
BAVACHIN Chemical Properties
Boiling point 558.3±50.0 °C(Predicted)
density 1.244
storage temp. Inert atmosphere,Store in freezer, under -20°C
solubility ≤20mg/ml in ethanol;30mg/ml in DMSO;50mg/ml in dimethyl formamide
form crystalline solid
pka8.27±0.40(Predicted)
color White
CAS DataBase Reference19879-32-4
Safety Information
MSDS Information
BAVACHIN Usage And Synthesis
DescriptionBavachin is a flavonoid first isolated from seeds of P. corylifolia. It is a phytoestrogen that activates the estrogen receptors ERα and ERβ (EC50s = 320 and 680 nM, respectively). Through this action, bavachin stimulates osteoblast proliferation and differentiation and prevents bone loss following ovariectomy in rats. Bavachin less potently inhibits acyl-coenzyme A:cholesterol acyltransferase (IC50 = 86 μM).
UsesBavachin has therapeutic potential for type 2 diabetes by activating insulin signaling pathways. Also, it has anabolic and potent anticatabolic biological effects on chondrocytes. Strong inhibitor of human UDP-glucuronosyltransferase (UGT1A1)
targetNF-kB | p65 | IkB | VEGFR | IL Receptor | AP-1 | AMPK | PPAR | GLUT | Akt | IKK | Estrogen receptor α | Estrogen receptor β
references[1] choi j h, rho m c, lee s w, et al. bavachin and isobavachalcone, acyl-coenzyme a: cholesterol acyltransferase inhibitors from psoralea corylifolia[j]. archives of pharmacal research, 2008, 31(11): 1419-1423.
[2] park j, kim d h, ahn h n, et al. activation of estrogen receptor by bavachin from psoralea corylifolia[j]. biomolecules & therapeutics, 2012, 20(2): 183-188.
[3] lee h, li h, noh m, et al. bavachin from psoralea corylifolia improves insulin-dependent glucose uptake through insulin signaling and ampk activation in 3t3-l1 adipocytes[j]. international journal of molecular sciences, 2016, 17(4): 527.
BAVACHIN Preparation Products And Raw materials
kalopanax saponin H Bavachalcone Isopsoralenoside Curcumol Mangostin Psoralenoside Bilobalide α-Hederin tuberostemonine 8-SHOGAOL 3''-PRENYLDAIDZEIN BAVACHININ A Acetytastragaloside MAGNOFLORINE IODIDE, (+)-(RG) 8-Methyl Chrysophanol Hederagenin 28-O-beta-D-glucopyranosyl ester 8-Methoxypsoralen 3-O-alpha-L-Arabinopyranosylhederagenin 28-O-alpha-L-rhamnopyranosyl-(1->4)-beta-D-glucopyranosyl-(1->6)-beta-D-glucopyranosyl ester

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