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129655-21-6

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  • Urea,N,N'-bis[2-[[(1S)-1-(chloromethyl)-1,6-dihydro-5-hydroxy-8-methylbenzo[1,2-b:4,3-b']dipyrrol-3(2H)-yl]carbonyl]-1H-indol-5-yl]-

    Cas No: 129655-21-6

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  • Urea,N,N'-bis[2-[[(1S)-1-(chloromethyl)-1,6-dihydro-5-hydroxy-8-methylbenzo[1,2-b:4,3-b']dipyrrol-3(2H)-yl]carbonyl]-1H-indol-5-yl]-

    Cas No: 129655-21-6

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  • Urea,N,N'-bis[2-[[(1S)-1-(chloromethyl)-1,6-dihydro-5-hydroxy-8-methylbenzo[1,2-b:4,3-b']dipyrrol-3(2H)-yl]carbonyl]-1H-indol-5-yl]- cas 129655-21-6

    Cas No: 129655-21-6

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129655-21-6 Usage

Description

Bizelesin is a member of the cyclopropylpyrroloindole family, which is known for causing genomic DNA lesions by alkylating DNA. It is distinct from Adozelesin, another member of the same family, as Bizelesin induces both single-strand DNA lesions and double-strand DNA cross-links, while Adozelesin induces only single-strand DNA lesions. Bizelesin also affects cell proliferation through different pathways, inducing senescence as opposed to apoptosis induced by Adozelesin.

Uses

Used in Pharmaceutical Industry:
Bizelesin is used as a pharmaceutical agent for its DNA-damaging properties. It is particularly effective in inducing both single-strand lesions and double-strand DNA cross-links, which can be useful in the development of cancer treatments.
Used in Cancer Research:
In cancer research, Bizelesin is used as a tool to study the effects of DNA damage on cell proliferation and the mechanisms behind cell senescence. Its ability to induce double-strand DNA cross-links makes it a valuable compound for understanding the cellular responses to various types of DNA damage.
Used in Drug Development:
Bizelesin's unique DNA-damaging capabilities can be harnessed in the development of new drugs targeting cancer cells. Its potential to induce senescence, rather than apoptosis, may offer alternative treatment strategies for certain types of cancer.
Used in Combination Therapies:
Bizelesin can be explored for its potential synergistic effects when combined with other chemotherapeutic drugs. This could enhance the overall efficacy of cancer treatments, particularly in cases where resistance to conventional chemotherapy has developed.

Check Digit Verification of cas no

The CAS Registry Mumber 129655-21-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,6,5 and 5 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 129655-21:
(8*1)+(7*2)+(6*9)+(5*6)+(4*5)+(3*5)+(2*2)+(1*1)=146
146 % 10 = 6
So 129655-21-6 is a valid CAS Registry Number.
InChI:InChI=1/C43H36Cl2N8O5/c1-19-15-46-39-33(54)11-31-37(35(19)39)23(13-44)17-52(31)41(56)29-9-21-7-25(3-5-27(21)50-29)48-43(58)49-26-4-6-28-22(8-26)10-30(51-28)42(57)53-18-24(14-45)38-32(53)12-34(55)40-36(38)20(2)16-47-40/h3-12,15-16,23-24,46-47,50-51,54-55H,13-14,17-18H2,1-2H3,(H2,48,49,58)/t23-,24?/m1/s1

129655-21-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-bis[2-[(8S)-8-(chloromethyl)-4-hydroxy-1-methyl-7,8-dihydro-3H-pyrrolo[3,2-e]indole-6-carbonyl]-1H-indol-5-yl]urea

1.2 Other means of identification

Product number -
Other names Benzo(1,2-b:4,3-b')dipyrrol-4-ol,6,6'-(carbonylbis(imino-1H-indole-5,2-diylcarbonyl))bis(8-(chloromethyl)-3,6,7,8-tetrahydro-1-methyl-,(S-(R*,R*))

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:129655-21-6 SDS

129655-21-6Downstream Products

129655-21-6Relevant articles and documents

Synthesis and DNA cross-linking by a rigid CPI dimer

Mitchell,Kelly,Wicnienski,Hatzenbuhler,Williams,Petzold,Slightom,Siemieniak

, p. 8994 - 8995 (1991)

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