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Campesterol 1x1ml chloroform 100ug/ml is a chemical solution containing campesterol, a plant-derived steroid, dissolved in chloroform at a concentration of 100 micrograms per milliliter. Campesterol is a phytosterol, which is a type of plant sterol that plays a role in plant growth and development. It is structurally similar to cholesterol and has been studied for its potential health benefits, such as reducing cholesterol absorption in the human body. The chloroform serves as a solvent, which is a substance that dissolves other substances to form a solution. This specific concentration of campesterol in chloroform is used for various applications in research and industry, such as in the analysis of plant sterols or as a component in the synthesis of other compounds.

632-32-6

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632-32-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 632-32-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,3 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 632-32:
(5*6)+(4*3)+(3*2)+(2*3)+(1*2)=56
56 % 10 = 6
So 632-32-6 is a valid CAS Registry Number.
InChI:InChI=1/C28H48O/c1-18(2)19(3)7-8-20(4)24-11-12-25-23-10-9-21-17-22(29)13-15-27(21,5)26(23)14-16-28(24,25)6/h18-22,24,26,29H,7-17H2,1-6H3/t19-,20+,21-,22-,24+,26-,27-,28+/m0/s1

632-32-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 17-(5,6-dimethylheptan-2-yl)-10,13-dimethyl-2,3,4,5,6,7,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

1.2 Other means of identification

Product number -
Other names Ergost-8(14)-en-3-ol, (3β,5α)-

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 -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:632-32-6 SDS

632-32-6Relevant academic research and scientific papers

?8(14)-Ergostenol Glycoside Derivatives Inhibit the Expression of Inflammatory Mediators and Matrix Metalloproteinase

Kim, Hakwon,Kim, Jeonguk,Ko, Myoungsil,Lee, Eunjoohwang,Lee, Taehoon,Moon, Hyejin,Park, Yujin,Yoon, Dowon

, (2021)

Arthritis is a chronic inflammatory disease accompanied by pathological reactions such as swelling, redness, fever, and pain in various joint areas. The drugs currently available to treat arthritis are associated with diverse side-effects. Therefore, ther

NOVEL ERGOSTENOL GLYCOSIDE DERIVATIVE

-

Paragraph 0073-0075, (2019/11/19)

The present invention provides ergostenol glycoside derivatives, method for preventing, treating, or alleviating dermatitis using the same. The present invention also provides a method for preparing the ergostenol and glycoside derivatives thereof. The er

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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