4-Amino-N-[5-(1-methylethyl)-1,3,4-thiadiazol-2-yl]benzenesulfonamide
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4-Amino-N-[5-(1-methylethyl)-1,3,4-thiadiazol-2-yl]benzenesulfonamide
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CAS No:
80-34-2
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Formula:
C11H14N4O2S2
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Chemical Name:
4-Amino-N-[5-(1-methylethyl)-1,3,4-thiadiazol-2-yl]benzenesulfonamide
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Synonyms:
Benzenesulfonamide,4-amino-N-[5-(1-methylethyl)-1,3,4-thiadiazol-2-yl]-;Sulfanilamide,N1-(5-isopropyl-1,3,4-thiadiazol-2-yl)-;4-Amino-N-[5-(1-methylethyl)-1,3,4-thiadiazol-2-yl]benzenesulfonamide;VK 57;IPTD;N1-(5-Isopropyl-1,3,4-thiadiazol-2-yl)sulfanilamide;PASIT;Sulfaisopropylthiadiazole;2-Sulfanilamido-5-isopropylthiadiazole;Glyprothiazole;RP 2254;Glyprothizol
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CAS No:
Description
Glyprothiazol is a sulfonamide derivative with antihyperglycemic activity. Like sulfonylureas, glyprothiazol is able to lower blood glucose levels by increasing the release of insulin from pancreatic beta cells.
4-Amino-N-[5-(1-methylethyl)-1,3,4-thiadiazol-2-yl]benzenesulfonamide Basic Attributes
298.379
298.38
1804FJN4MO
DTXSID80229994
C65812
Characteristics
135
1.3
1.3753 (rough estimate)
195-197 °C
218.7mg/L(37 ºC)
LD50 oral in rat: 3940mg/kg
Computed Properties
Molecular Weight:298.4
XLogP3:1.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:4
Exact Mass:298.05581805
Monoisotopic Mass:298.05581805
Topological Polar Surface Area:135
Heavy Atom Count:19
Complexity:388
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
- Hot Searches
- cl2o7
- magnesium pyrophosphate formula
- h2sio3 ra sio2
- cocl2
- sulpiride
- h2cro4
4-Amino-N-[5-(1-methylethyl)-1,3,4-thiadiazol-2-yl]benzenesulfonamide
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