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547-44-4 | Sulfacarbamide
CAS No: 547-44-4 Catalog No: AG003KRO MDL No:MFCD00025437
Product Description
Catalog Number:
AG003KRO
Chemical Name:
Sulfacarbamide
CAS Number:
547-44-4
Molecular Formula:
C7H9N3O3S
Molecular Weight:
215.2297
MDL Number:
MFCD00025437
IUPAC Name:
(4-aminophenyl)sulfonylurea
InChI:
InChI=1S/C7H9N3O3S/c8-5-1-3-6(4-2-5)14(12,13)10-7(9)11/h1-4H,8H2,(H3,9,10,11)
InChI Key:
WVAKABMNNSMCDK-UHFFFAOYSA-N
SMILES:
NC(=O)NS(=O)(=O)c1ccc(cc1)N
EC Number:
208-922-7
UNII:
W6CD25Z4QR
Properties
Complexity:
301
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
215.036g/mol
Formal Charge:
0
Heavy Atom Count:
14
Hydrogen Bond Acceptor Count:
4
Hydrogen Bond Donor Count:
3
Isotope Atom Count:
0
Molecular Weight:
215.227g/mol
Monoisotopic Mass:
215.036g/mol
Rotatable Bond Count:
2
Topological Polar Surface Area:
124A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-1.5
Literature
| Title | Journal |
|---|---|
| Translating clinical findings into knowledge in drug safety evaluation--drug induced liver injury prediction system (DILIps). | PLoS computational biology 20111201 |
| Heparanase levels are elevated in the urine and plasma of type 2 diabetes patients and associate with blood glucose levels. | PloS one 20110101 |
| [Treatment of the diabetic foot in general surgery]. | Klinichna khirurhiia 20010801 |
| Inhibition of recombinant Pneumocystis carinii dihydropteroate synthetase by sulfa drugs. | Antimicrobial agents and chemotherapy 19950801 |
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