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5462-97-5 | 2-Thioxo-5-(4-methoxybenzylidene)thiazolidine-4-one
CAS No: 5462-97-5 Catalog No: AG00E13E MDL No:
Product Description
Catalog Number:
AG00E13E
Chemical Name:
2-Thioxo-5-(4-methoxybenzylidene)thiazolidine-4-one
CAS Number:
5462-97-5
IUPAC Name:
(5Z)-5-[(4-methoxyphenyl)methylidene]-2-sulfanylidene-1,3-thiazolidin-4-one
InChI:
InChI=1S/C11H9NO2S2/c1-14-8-4-2-7(3-5-8)6-9-10(13)12-11(15)16-9/h2-6H,1H3,(H,12,13,15)/b9-6-
InChI Key:
ORGCJYCWFZQEFX-TWGQIWQCSA-N
NSC Number:
12764
Properties
Complexity:
333
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
Exact Mass:
251.007g/mol
Formal Charge:
0
Heavy Atom Count:
16
Hydrogen Bond Acceptor Count:
4
Hydrogen Bond Donor Count:
1
Isotope Atom Count:
0
Molecular Weight:
251.318g/mol
Monoisotopic Mass:
251.007g/mol
Rotatable Bond Count:
2
Topological Polar Surface Area:
95.7A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.8
Literature
| Title | Journal |
|---|---|
| Privileged scaffolds or promiscuous binders: a comparative study on rhodanines and related heterocycles in medicinal chemistry. | Journal of medicinal chemistry 20120126 |
| In vitro evaluation of 5-arylidene-2-thioxo-4-thiazolidinones active as aldose reductase inhibitors. | Bioorganic & medicinal chemistry letters 20110101 |
| Exploration of inhibitors for diaminopimelate aminotransferase. | Bioorganic & medicinal chemistry 20100315 |
| 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 |
| Rhodanine derivatives as novel inhibitors of PDE4. | Bioorganic & medicinal chemistry letters 20080315 |
| Synthesis and antifungal activity of (Z)-5-arylidenerhodanines. | Bioorganic & medicinal chemistry 20070101 |
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