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The chemical compound "5α(H),17α(H),(20R)-β-acetoxyergost-8(14)-ene" is a steroidal compound derived from ergostane, a type of sterol. It features a unique structure with a double bond between carbons 8 and 14, and a β-acetoxy group at the 20 position. The α-hydrogen atoms at the 5 and 17 positions, along with the 20R configuration, contribute to its specific stereochemistry. 5ALPHA(H),17ALPHA(H),(20R)-BETA-ACETOXYERGOST-8(14)-ENE is of interest in the field of organic chemistry, particularly in the study of natural products and the synthesis of bioactive molecules. It may also have applications in pharmaceuticals and the development of cholesterol-lowering drugs, given its structural similarity to cholesterol and other sterols.

4042-95-9

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4042-95-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4042-95-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,4 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4042-95:
(6*4)+(5*0)+(4*4)+(3*2)+(2*9)+(1*5)=69
69 % 10 = 9
So 4042-95-9 is a valid CAS Registry Number.
InChI:InChI=1/C30H50O2/c1-19(2)20(3)8-9-21(4)26-12-13-27-25-11-10-23-18-24(32-22(5)31)14-16-29(23,6)28(25)15-17-30(26,27)7/h19-21,23-24,26,28H,8-18H2,1-7H3

4042-95-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5ALPHA(H),17ALPHA(H),(20R)-β-ACETOXYERGOST-8(14)-ENE

1.2 Other means of identification

Product number -
Other names acetic acid [10,13-dimethyl-17-(1,4,5-trimethylhexyl)-2,3,4,5,6,7,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
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More Details:4042-95-9 SDS

4042-95-9Relevant academic research and scientific papers

Marine and semi-synthetic hydroxysteroids as new scaffolds for pregnane X receptor modulation

Sepe, Valentina,Di Leva, Francesco Saverio,D'Amore, Claudio,Festa, Carmen,De Marino, Simona,Renga, Barbara,D'Auria, Maria Valeria,Novellino, Ettore,Limongelli, Vittorio,D'Souza, Lisette,Majik, Mahesh,Zampella, Angela,Fiorucci, Stefano

, p. 3091 - 3115 (2014/07/08)

In recent years many sterols with unusual structures and promising biological profiles have been identified from marine sources. Here we report the isolation of a series of 24-alkylated-hydroxysteroids from the soft coral Sinularia kavarattiensis, acting as pregnane X receptor (PXR) modulators. Starting from this scaffold a number of derivatives were prepared and evaluated for their ability to activate the PXR by assessing transactivation and quantifying gene expression. Our study reveals that ergost-5-en-3β-ol (4) induces PXR transactivation in HepG2 cells and stimulates the expression of the PXR target gene CYP3A4. To shed light on the molecular basis of the interaction between these ligands and PXR, we investigated, through docking simulations, the binding mechanism of the most potent compound of the series, 4, to the PXR. Our findings provide useful functional and structural information to guide further investigations and drug design.

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