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6339-79-3 | 4-Thiazolidinone, 5-[(4-hydroxyphenyl)methylene]-2-thioxo-
CAS No: 6339-79-3 Catalog No: AG00F3J1 MDL No:
Product Description
Catalog Number:
AG00F3J1
Chemical Name:
4-Thiazolidinone, 5-[(4-hydroxyphenyl)methylene]-2-thioxo-
CAS Number:
6339-79-3
IUPAC Name:
(5Z)-5-[(4-hydroxyphenyl)methylidene]-2-sulfanylidene-1,3-thiazolidin-4-one
InChI:
InChI=1S/C10H7NO2S2/c12-7-3-1-6(2-4-7)5-8-9(13)11-10(14)15-8/h1-5,12H,(H,11,13,14)/b8-5-
InChI Key:
RAYIDZVPIAJJPF-YVMONPNESA-N
NSC Number:
43399
Properties
Complexity:
319
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
Exact Mass:
236.992g/mol
Formal Charge:
0
Heavy Atom Count:
15
Hydrogen Bond Acceptor Count:
4
Hydrogen Bond Donor Count:
2
Isotope Atom Count:
0
Molecular Weight:
237.291g/mol
Monoisotopic Mass:
236.992g/mol
Rotatable Bond Count:
1
Topological Polar Surface Area:
107A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.4
Literature
| Title | Journal |
|---|---|
| Privileged scaffolds or promiscuous binders: a comparative study on rhodanines and related heterocycles in medicinal chemistry. | Journal of medicinal chemistry 20120126 |
| Evaluation of dihydropyrimidin-(2H)-one analogues and rhodanine derivatives as tyrosinase inhibitors. | Bioorganic & medicinal chemistry letters 20110415 |
| In vitro evaluation of 5-arylidene-2-thioxo-4-thiazolidinones active as aldose reductase inhibitors. | Bioorganic & medicinal chemistry letters 20110101 |
| Selective small molecule inhibitors of the potential breast cancer marker, human arylamine N-acetyltransferase 1, and its murine homologue, mouse arylamine N-acetyltransferase 2. | Bioorganic & medicinal chemistry 20090115 |
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