TIANFU (Z)-Guggulsterone CAS NO.95975-55-6

Min.Order Quantity:: 1 Kilogram

Purity:: 98% min

Port:: SHANGHAI

Payment Terms:: L/C,D/A,D/P,T/T,MoneyGram

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Product Details

Keywords

(Z)-Guggulsterone
95975-55-6
TIANFU (Z)-Guggulsterone

Quick Details

ProName: TIANFU (Z)-Guggulsterone
CasNo: 95975-55-6
Molecular Formula: C21H28O2
Appearance: Solid
Application: Intermediates
DeliveryTime: as client's demand quantity
PackAge: as requested
Port: SHANGHAI
ProductionCapacity: 10 Metric Ton/Month
Purity: 98% min
Storage: room temperature
Transportation: by sea, by air or by courier
LimitNum: 1 Kilogram

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our company was built in 2009 with an iso certificate.in the past 5 years, we have grown up as a famous fine chemicals supplier in china and we had established stable business relationships with samsung,lg,merck,thermo fisher scientific and so on.

our main business covers the fields below:

1.noble metal catalysts (pt.pd...)

2.organic phosphine ligands (tert-butyl-phosphine.cyclohexyl-phosphine...)

3.oled intermediates (fluorene,carbazole,boric acid...)

4.customs synthesis

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Details

(z)-guggulsterone basic information
product name: (z)-guggulsterone
synonyms: cis-4,17(20)-pregnadiene-3,16-dione;cis guggulsterone;gugulsterone;guggulsterone z;guggulsterone (z form);guggulesterone z;guggulsterone;4,17(20)-(cis)-pregnadien-3,16-dione
cas: 95975-55-6
mf: c21h28o2
mw: 312.45
einecs:
product categories: miscellaneous
mol file: 95975-55-6.mol
(z)-guggulsterone structure
(z)-guggulsterone chemical properties
storage temp. 2-8°c
solubility dmso: 5 mg/ml
form powder
color light yellow
cas database reference 95975-55-6(cas database reference)
safety information
hazard codes xi
risk statements 37
safety statements 36
wgk germany 3

(z)-guggulsterone usage and synthesis
biological activity broad spectrum steroid receptor ligand; binds with high affinity to mineralocorticoid receptors (k i = 39 nm) and lower affinity to progesterone, androgen and glucocorticoid receptors (k i values are 201, 240 and 224 nm respectively). functions primarily as an antagonist of these receptors, with the exception of the progesterone receptor where it displays partial agonist effects. also exerts hypolipidemic activity, likely via antagonism of the receptor for bile acids (farnesoid x receptor; fxr).

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