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s-(Benzo[d]thiazol-2-yl)-l-cysteine|CS-0270427|399-82-6

s-(Benzo[d]thiazol-2-yl)-l-cysteine

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Sku TS246CS-0270427_100_MG
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Product Information

Product Name
s-(Benzodthiazol-2-yl)-l-cysteine
Brand Name
ChemScene
Product Number
CS-0270427
CAS
399-82-6
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
119392
IUPAC Name
(2R)-2-amino-3-(1,3-benzothiazol-2-ylsulfanyl)propanoic acid
InChI Key
KRBPTLCTECPKGY-LURJTMIESA-N
SMILES
C1=CC=C2C(=C1)N=C(S2)SCC@@H(C(=O)O)N

References Data Source From Pubchem

S68 | HSDBTPS | Transformation Products Extracted from HSDB Content in PubChem
Publication Date: 2025
DOI: 10.5281/zenodo.3827487

N-Acetyl-l-cysteine and aminooxyacetic acid differentially modulate trichloroethylene reproductive toxicity via metabolism in Wistar rats
Publication Name: Archives of Toxicology
Publication Date: 2021-02-18
DOI: 10.1007/s00204-021-02991-8

Cysteine S-conjugate β-lyases: important roles in the metabolism of naturally occurring sulfur and selenium-containing compounds, xenobiotics and anticancer agents
Publication Name: Amino Acids
Publication Date: 2010-03-22
DOI: 10.1007/s00726-010-0552-0

Cysteine Conjugate β-Lyase Activity of Rat Erythrocytes and Formation of β-Lyase-Derived Globin Monoadducts and Cross-Links after in Vitro Exposure of Erythrocytes to S-(1,2-Dichlorovinyl)-l-cysteine
Publication Name: Chemical Research in Toxicology
Publication Date: 2009-07-02
DOI: 10.1021/tx9001429

Role of Cysteine S-Conjugate β-Lyases in the Bioactivation of Renal Toxicants
Publication Name: Advances in Bioactivation Research
Publication Date: 2008
DOI: 10.1007/978-0-387-77300-1_12