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Tasisulam - 98%, high purity , CAS No.519055-62-0

    Grade & Purity:
  • ≥98%
In stock
Item Number
T347903
Grouped product items
SKU Size
Availability
Price Qty
T347903-10mg
10mg
2
$70.90
T347903-50mg
50mg
1
$282.90
T347903-100mg
100mg
1
$509.90

Tasisulam is an antitumor agent .

Basic Description

Synonyms Q27253184 | Tasisulam (LY573636) | s7326 | SCHEMBL1581371 | Tasisulam [INN] | LY 573636 (sodium) | AKOS027250790 | SB19401 | BCP05154 | UNII-1YC4W9MSLJ | AS-38576 | AS-40659 | Tasisulam(LY573636) | 1YC4W9MSLJ | Tasisulam | CS-0003569 | SCHEMBL333061 | AC-
Specifications & Purity ≥98%
Biochemical and Physiological Mechanisms Tasisulam (LY573636) is a SPLAM (SPLicing inhibitor sulfonAMide) that bridges RNA binding motif protein 39 (RBM39; CAPERα, HCC1) and DCAF15 for interaction, thereby promoting (CUL4-DDB1-DDA1-DCAF15) E3 ubiquitin ligase complex-mediated RBM39 ubiquitinatio
Storage Temp Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description

Introduction:

Tasisulam is an antitumor agent that induced growth arrest and apoptosis of human solid tumours. In human malignant hematopoietic cell lines, tasisulam inhibited cells growth with ED50 values of 5, 7, 12, 13, 21 and 31 μM for BALL1, HL60, RCH, NCEB1, SP49 and Daudi cell lines, respectively. Tasisulam induced growth arrest in a dose-dependent way. Also, tasisulam caused induction of ROS, loss of mitochondrial membrane potential and induction of apoptosis. In HL60 and U937 cells, tasisulam induce granulocytic/monocytic differentiation. In solid tumor cell lines, tasisulam induced apoptosis that was mediated by the mitochondrial-mediated cell death pathways . Tasisulam increased phospho-histone H3 expression and cells with 4N DNA, and led to G2-M accumulation and apoptosis. Tasisulam also inhibited endothelial cell cord formation induced by epidermal growth factor, VEGF and fibroblast growth factor with EC50 values of 34, 47 and 103 nM, respectively.

In mice bearing the Calu-6 non-small cell lung xenograft model, tasisulam exhibited antitumor efficacy in a dose-dependent way and reduced tumor volume by 77%. Tasisulam caused G2-M accumulation and increased nuclear fragmentation. Also, tasisulam induced vascular normalization.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Benzene and substituted derivatives
Subclass Benzoic acids and derivatives
Intermediate Tree Nodes Halobenzoic acids and derivatives
Direct Parent 4-halobenzoic acids and derivatives
Alternative Parents 2-halobenzoic acids and derivatives  Benzoyl derivatives  Dichlorobenzenes  2,5-disubstituted thiophenes  Aryl bromides  Aryl chlorides  Vinylogous halides  Organosulfonic acids and derivatives  Aminosulfonyl compounds  Heteroaromatic compounds  Carboxylic acids and derivatives  Organochlorides  Organonitrogen compounds  Organobromides  Organooxygen compounds  Hydrocarbon derivatives  Organic oxides  
Molecular Framework Aromatic heteromonocyclic compounds
Substituents 2-halobenzoic acid or derivatives - 4-halobenzoic acid or derivatives - Benzoyl - 1,3-dichlorobenzene - Chlorobenzene - Halobenzene - 2,5-disubstituted thiophene - Aryl chloride - Aryl halide - Aryl bromide - Aminosulfonyl compound - Heteroaromatic compound - Vinylogous halide - Thiophene - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Organoheterocyclic compound - Carboxylic acid derivative - Organobromide - Organohalogen compound - Organooxygen compound - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Organosulfur compound - Organic oxide - Organochloride - Organonitrogen compound - Aromatic heteromonocyclic compound
Description This compound belongs to the class of organic compounds known as 4-halobenzoic acids and derivatives. These are benzoic acids or derivatives carrying a halogen atom at the 4-position of the benzene ring.
External Descriptors Not available

Associated Targets(Human)

A-375 (9258 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Hdac6 Histone deacetylase 6 (222 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 504765293
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504765293
IUPAC Name N-(5-bromothiophen-2-yl)sulfonyl-2,4-dichlorobenzamide
INCHI InChI=1S/C11H6BrCl2NO3S2/c12-9-3-4-10(19-9)20(17,18)15-11(16)7-2-1-6(13)5-8(7)14/h1-5H,(H,15,16)
InChIKey WWONFUQGBVOKOF-UHFFFAOYSA-N
Smiles C1=CC(=C(C=C1Cl)Cl)C(=O)NS(=O)(=O)C2=CC=C(S2)Br
Isomeric SMILES C1=CC(=C(C=C1Cl)Cl)C(=O)NS(=O)(=O)C2=CC=C(S2)Br
PubChem CID 10160238
Molecular Weight 415.11

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

4 results found

Lot Number Certificate Type Date Item
H2224284 Certificate of Analysis Jun 12, 2025 T347903
H2224283 Certificate of Analysis Jun 12, 2025 T347903
H2224282 Certificate of Analysis Jun 12, 2025 T347903
C2527022 Certificate of Analysis Jun 17, 2022 T347903

Chemical and Physical Properties

Molecular Weight 415.100 g/mol
XLogP3 4.600
Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 4
Rotatable Bond Count 3
Exact Mass 412.835 Da
Monoisotopic Mass 412.835 Da
Topological Polar Surface Area 99.900 Ų
Heavy Atom Count 20
Formal Charge 0
Complexity 471.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Solution Calculators

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