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533887-50-2 | 2(3H)-Thiazolone, 4-mercapto-
CAS No: 533887-50-2 Catalog No: AG00DY7D MDL No:
Product Description
Catalog Number:
AG00DY7D
Chemical Name:
2(3H)-Thiazolone, 4-mercapto-
CAS Number:
533887-50-2
IUPAC Name:
4-sulfanyl-3H-1,3-thiazol-2-one
InChI:
InChI=1S/C3H3NOS2/c5-3-4-2(6)1-7-3/h1,6H,(H,4,5)
InChI Key:
TZTORYWYZQQJTH-UHFFFAOYSA-N
Properties
Complexity:
131
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
132.966g/mol
Formal Charge:
0
Heavy Atom Count:
7
Hydrogen Bond Acceptor Count:
3
Hydrogen Bond Donor Count:
2
Isotope Atom Count:
0
Molecular Weight:
133.183g/mol
Monoisotopic Mass:
132.966g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
55.4A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.6
Literature
| Title | Journal |
|---|---|
| Discovery of new inhibitors of Schistosoma mansoni PNP by pharmacophore-based virtual screening. | Journal of chemical information and modeling 20100927 |
| Synthesis, antimicrobial and cytotoxic activities of some 5-arylidene-4-thioxo-thiazolidine-2-ones. | European journal of medicinal chemistry 20090501 |
| Synthesis of novel thiazolone-based compounds containing pyrazoline moiety and evaluation of their anticancer activity. | European journal of medicinal chemistry 20090401 |
| HD-PTP is a catalytically inactive tyrosine phosphatase due to a conserved divergence in its phosphatase domain. | PloS one 20090101 |
| Small-molecule inhibitors of islet amyloid polypeptide fibril formation. | Angewandte Chemie (International ed. in English) 20080101 |
| Synthesis and evaluation of aryl thioxothiazolidinone inhibitors of ADAMTS-5 (Aggrecanase-2). | Bioorganic & medicinal chemistry letters 20070301 |
| Cellular inhibition of protein tyrosine phosphatase 1B by uncharged thioxothiazolidinone derivatives. | Chembiochem : a European journal of chemical biology 20070122 |
| [New substituted 4-thioxothiazolidin-2-one derivatives: synthesis and structural study]. | Annales pharmaceutiques francaises 20021101 |
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