Details
Stereochemistry | ACHIRAL |
Molecular Formula | C12H13ClN4O2S |
Molecular Weight | 312.775 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=NC(NS(=O)(=O)C2=CC=C(N)C=C2)=C(Cl)C(C)=N1
InChI
InChIKey=JQBLWVSZNZIWFC-UHFFFAOYSA-N
InChI=1S/C12H13ClN4O2S/c1-7-11(13)12(16-8(2)15-7)17-20(18,19)10-5-3-9(14)4-6-10/h3-6H,14H2,1-2H3,(H,15,16,17)
Molecular Formula | C12H13ClN4O2S |
Molecular Weight | 312.775 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Sulfaclomide is a sulfonamide derivative structurally similar to p-aminobenzoic acid, patented by VEB Farbenfabrik Wolfen as antibacterial agent useful for the treatment of infectious diseases. Sulfanilamide competes with p-aminobenzoic acid for the bacterial enzyme dihydropteroate synthase, thereby preventing the incorporation of p-aminobenzoic acid into dihydrofolic acid, the immediate precursor of folic acid. This leads to an inhibition of bacterial folic acid synthesis and de novo synthesis of purines and pyrimidines, ultimately resulting in cell growth arrest and cell death.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: Deutsche Gesundheitswesen (1973), 28, (27), 1268-71 https://www.ncbi.nlm.nih.gov/pubmed/1189751
1 g
Route of Administration:
Oral
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:36:57 GMT 2023
by
admin
on
Fri Dec 15 15:36:57 GMT 2023
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Record UNII |
AXA8K5U95M
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Record Status |
Validated (UNII)
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Record Version |
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NCI_THESAURUS |
C29739
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4015-18-3
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2219
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CHEMBL2107588
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C72643
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AXA8K5U95M
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DTXSID20960591
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100000083243
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C005740
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71168
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SUB10691MIG
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Related Record | Type | Details | ||
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ACTIVE MOIETY |