Tasisulam(LY573636) chemical structure
Chemical structureResearch use only
CAT. NO. DC7312Featured

Tasisulam(LY573636)

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Product overview

Description & Application

Tasisulam is a small molecule antitumor agent that inhibits mitotic progression and induces vascular normalization. Tasisulam induces apoptosis via the intrinsic pathway[1].

ParameterValue
Chemical NameTasisulam
CAS No.519055-62-0
SynonymsTasisulam;N-(2,4-Dichlorobenzoyl)-5-bromothiophene-2-sulfonamide;LY573636;N-(5-bromothiophen-2-yl)sulfonyl-2,4-dichlorobenzamide;N-(5-Bromothiophen-2-ylsulfonyl)-2,4-dichlorobenzamide;UNII-1YC4W9MSLJ;1YC4W9MSLJ;519055-62-0;DTXSID20199869;FT-0763021;AS-38576;HY-14804;AC-32975;P7M;Tasisulam(LY573636);Tasisulam [INN];J-522818;EX-A1367;Q27253184;SW219181-1;CCG-268827;HMS3653O12;BCP05154;s7326;NCGC00386305-05;LY 573636 (sodium);Benzamide, N-((5-bromo-2-thienyl)sulfonyl)-2,4-dichloro-;BCP9000890;NS00069285;519055-63-1;SB19401;CHEMBL2110587;Z442229142;Tasisulam (sodium);AKOS027250790;N-((5-BROMOTHIOPHEN-2-YL)SULFONYL)-2,4-DICHLOROBENZAMIDE;N-[(5-bromothiophen-2-yl)sulfonyl]-2,4-dichlorobenzamide;TASISULAM [WHO-DD];SCHEMBL1581371;Tasisulam (LY573636);LY-573636;DB11941;CS-0003569;LY 573636;MFCD11973637;EN300-6492968;Tasisulam(LY573636)?;CHEBI:231621;tasisulamum;DB-071449;LY573636 sodium;DTXCID30122360;BRD-K42495768-001-01-7;n-((5-bromo-2-thienyl)sulfonyl)-2,4-dichlorobenzamide
FormulaC11H6NO3S2Cl2Br
M.Wt415.11024
SMILESO=C(NS(=O)(C1=CC=C(Br)S1)=O)C2=CC=C(Cl)C=C2Cl
Purity>98%
Storage2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO

Biological Activity

Tasisulam is a small molecule antitumor agent that inhibits mitotic progression and induces vascular normalization. Tasisulam induces apoptosis via the intrinsic pathway[1].

In Vitro

Tasisulam (200 μM-200 nM; 48 hours) induces an antiproliferative response across a wide range of tumor histologies with EC50s is 10 μM and 25 μM for Calu-6 and A-375 cell lines, respectively[1]. Tasisulam (25, 50 μM; 72 hours) induces a concentration-dependent increase in 4N DNA and G2-M accumulation[1]. Tasisulam (200 μM-200 nM; 48 hours) induces apoptosis in a broad range of in vitro cancer cell models[1]. Cell Proliferation Assay[1] Cell Line: Calu-6 non-small cell lung carcinoma and A-375 melanoma models Concentration: 200 μM-200 nM Incubation Time: 48 hours Result: Induced an antiproliferative response across a wide range of tumor histologies with EC50s are 10 μM and 25 μM, respectively. Cell Cycle Analysis[1] Cell Line: Calu-6 and A-375 cell lines Concentration: 25, 50 μM Incubation Time: 72 hours Result: Induced a concentration-dependent increase in 4N DNA and G2-M accumulation. Apoptosis Analysis[1] Cell Line: Calu-6 non-small cell lung carcinoma and A-375 melanoma models Concentration: 200 μM-200 nM Incubation Time: 48 hours Result: Induced apoptosis in a broad range of in vitro cancer cell models.

In Vivo

No in vivo data are provided in the current product source. Contact us for further information.

References & source

DC Chemicals original product information

Published experimental findings depend on the model and assay conditions. They do not guarantee equivalent performance in every application. For laboratory research use only.

Product documentation

Refer to the certificate supplied with your lot for batch-specific release results.

Handling guide

2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO

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