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BHPI, also known as 2-methoxyestradiol, is a naturally occurring compound derived from the plant Butyrospermum parkii. It functions as an antagonist of estrogen receptor α (ERα), which plays a crucial role in the development and progression of various hormone-dependent cancers. BHPI has demonstrated the ability to block the proliferation of drug-resistant cancer cells, making it a promising candidate for cancer treatment.

56632-39-4

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56632-39-4 Usage

Uses

Used in Anticancer Applications:
BHPI is used as an antagonist of estrogen receptor α (ERα) for blocking the proliferation of drug-resistant breast, endometrial, and ovarian cancer cell lines. It effectively inhibits 17β-estradiol-induced cell growth at concentrations ranging from 10 to 1,000 nM, both in vitro and in vivo. In mice bearing MCF-7 xenografts, BHPI drives tumor regression at a daily dose of 15 mg/kg. Additionally, it specifically suppresses ERα-dependent gene expression and protein synthesis by activating the unfolded protein response in cells.
Used in Pharmaceutical Industry:
BHPI is used as a potential therapeutic agent for the treatment of hormone-dependent cancers, such as breast, endometrial, and ovarian cancers. Its ability to inhibit the proliferation of drug-resistant cancer cells and its effectiveness in vivo make it a valuable compound for the development of novel cancer treatments and drug formulations.

Check Digit Verification of cas no

The CAS Registry Mumber 56632-39-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,6,3 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 56632-39:
(7*5)+(6*6)+(5*6)+(4*3)+(3*2)+(2*3)+(1*9)=134
134 % 10 = 4
So 56632-39-4 is a valid CAS Registry Number.

56632-39-4SDS

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 3,3-bis(4-hydroxyphenyl)-7-methyl-1H-indol-2-one

1.2 Other means of identification

Product number -
Other names HMS2153B10

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:56632-39-4 SDS

56632-39-4Downstream Products

56632-39-4Relevant academic research and scientific papers

Syntheses and antiproliferative evaluation of oxyphenisatin derivatives

Uddin, Muhammed K.,Reignier, Serge G.,Coulter, Tom,Montalbetti, Christian,Granaes, Charlotta,Butcher, Steven,Krog-Jensen, Christian,Felding, Jakob

, p. 2854 - 2857 (2008/02/13)

Syntheses and structure-antiproliferative relationship for oxyphenisatin analogues are described. The cell proliferation data showed that the presence of substituents (especially F, Cl, Me, CF3, and OMe) in the 6- and 7-position of oxyphenisati

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