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AT-101 is a synthetic small molecule that belongs to the class of BH3 mimetics, which mimic the action of pro-apoptotic Bcl-2 family proteins. It has been shown to inhibit the anti-apoptotic Bcl-2 proteins, and is being investigated for its potential as a cancer treatment. AT-101 has been found to induce apoptosis in cancer cells, inhibit tumor growth, and enhance the efficacy of other chemotherapeutic agents. It has also been studied for its potential to overcome drug resistance in cancer cells. Additionally, AT-101 has shown promising results in preclinical studies for its potential to treat other diseases such as hepatitis C and HIV. Overall, AT-101 has demonstrated potential as a therapeutic agent for various diseases and is currently under investigation in clinical trials.

866541-93-7

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866541-93-7 Usage

Uses

Used in Cancer Treatment:
AT-101 is used as a cancer therapeutic agent for its ability to induce apoptosis in cancer cells, inhibit tumor growth, and enhance the efficacy of other chemotherapeutic agents. It is particularly effective in overcoming drug resistance in cancer cells.
Used in Pharmaceutical Industry:
AT-101 is used as a research compound for the development of novel cancer treatments and drug delivery systems. Its potential to target anti-apoptotic Bcl-2 proteins makes it a valuable tool in the discovery of new therapeutic strategies for various types of cancer.
Used in Hepatitis C and HIV Treatment:
AT-101 is used as a potential therapeutic agent for the treatment of hepatitis C and HIV. Its preclinical studies have shown promising results, indicating its potential to be a valuable addition to the treatment options for these diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 866541-93-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,6,5,4 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 866541-93:
(8*8)+(7*6)+(6*6)+(5*5)+(4*4)+(3*1)+(2*9)+(1*3)=207
207 % 10 = 7
So 866541-93-7 is a valid CAS Registry Number.

866541-93-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name [2,?2'-?Binaphthalene]?-?8,?8'-?dicarboxaldehyde, 1,?1',?6,?6',?7,?7'-?hexahydroxy-?3,?3'-?dimethyl-?5,?5'-?bis(1-?methylethyl)?-?, (2R)?-?, compd. with acetic acid (1:1)

1.2 Other means of identification

Product number -
Other names -

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:866541-93-7 SDS

866541-93-7Relevant academic research and scientific papers

A gossypol derivatives and their use in inhibiting urease activity

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Paragraph 0047; 0048; 0052; 0053, (2017/10/20)

The invention relates to the technical field of fertilizer, and particularly relates to gossypol derivatives and an application thereof in inhibition of urease activity. The gossypol derivatives have the chemical structural general formula described in the specification, wherein R represents a part except amino in amino acid, and the amino acid is amino acid containing primary amino. The gossypol derivatives take gossypol as an aldehyde group providing reagent and are prepared by modifying the aldehyde group of gossypol with the amino of the amino acid. When the gossypol derivatives are applied in preparation of urease inhibitors, the urease inhibition effect is good, and the IC50 value inhibiting soil ammonia volatilization effect is as low as 1.56*10 mol.L. Compared with a gossypol raw material, the gossypol derivatives have better solubility, are more stable and are convenient to use; and a part of gossypol derivatives have the urease inhibition activity significantly enhanced.

PRODUCTION OF GOSSYPOL CO-CRYSTALS

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Page/Page column 39-40, (2008/06/13)

This invention relates to relates to methods for producing gossypol acetic acid co- crystals and (-)-gossypol acetic acid co-crystals. The invention also relates to pharmaceutical compositions comprising gossypol acetic acid co-crystals and (-)-gossypol a

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