Sulfapyridine

HCID 5336CAS 144-83-2

Basic information

Standard SMILES
Nc1ccc(S(=O)(=O)Nc2ccccn2)cc1
InChIKey
GECHUMIMRBOMGK-UHFFFAOYSA-N
Molecular formula
C11H11N3O2S
Average molar mass
249.29 g/mol
Monoisotopic mass
249.05719778

Names & identifiers

Preferred name
Sulfapyridine
IUPAC
4-amino-N-pyridin-2-ylbenzenesulfonamide
English name
Sulfapyridine
Molecular formula
C11H11N3O2S
Molecular weight
249.29

Names & synonyms

sulfapyridine144-83-2Sulphapyridine2-Sulfapyridine2-SulfanilamidopyridineDagenanPiridazolSulfidinSulfidineStreptosilpyridineCoccoclasePlurazol
Show more names
SulfapyridinTHAP114-AMINO-N-[2-PYRIDYL]BENZENE SULFONAMIDE2-hydroxybenzenecarboxylic acid (salicylic acid)RoninA-499m+b693TrianonAdiplon
PyriamidPyridazolEubasin2-SulfanilylaminopyridineEubasinumRelbapiridinaSeptipulmonThioseptal

Database identifiers

CAS
144-83-2
PubChem CID
5336
DTXSID
DTXSID3026067
ChEMBL
CHEMBL700
ChEBI
CHEBI:132842
UNII
Y5V2N1KE8U
EC Number
205-642-7
Nikkaji
J5.831I

Properties

Computed structural properties

XLogP
0
Topological polar surface area
93.5 Ų
Hydrogen bond donors
2
Hydrogen bond acceptors
5
Rotatable bonds
3
Heavy atoms
17

Physicochemical properties

Melting point
191 · 191-193°C
Boiling point
473.5 · 473.5±51.0 °C(Predicted)
Density
1.322 · 1.3220 (rough estimate)
refractive index
1.674 · 1.6740 (estimate)
storage temp.
Keep in dark place,Sealed in dry,Room Temperature
solubility
DMSO (Slightly), Methanol (Slightly)

Safety & regulation

Safety data

wgk
2
tsca
TSCA listed
rtecs
DA9625000
hs_code
29350010
Toxicity
LD50 orally in mice: 7.5 mg/g (Wien)
risk_code
36/37/38

Chemistry & industry

Applications · 5 items

DescriptionSulfapyridine is a sulfonamide antibiotic with antibacterial and anti-inflammatory activities. It is also a metabolite of sulfasalazine formed through bacterial conversion in the colon. It is active against strains of Y. enterocolitica and Salmonella (MICs = 3.1-25 and 25-100 μg/ml, respectively), as well as S. aureus (MBC = 0.8 μM). It is an inhibitor of recombinant P. carinii dihydropteroate synthetase (DHPS; IC50 = 0.18 μM). Sulfapyridine scavenges peroxyl radicals in an oxygen radical absorbance capacity (ORAC) assay. It inhibits histamine release induced by compound 48/80 from isolated rat peritoneal mast cells in a dose-dependent manner. Sulfapyridine (1 μg/kg) also inhibits compound 48/80-induced systemic allergic reaction in rats. Formulations containing sulfapyridine have previously been used in the treatment of dermatological conditions and ulcerative colitis.

UsesUsed in treatment of dermatitis herpetiformis; antibacterial.

Usesantibacterial, dermatitis herpetiformis therapy

General DescriptionSulfapyridine’s plasma half-life is 9 hours.This compound is a white, crystalline, odorless, and tastelesssubstance. It is stable in air but slowly darkens on exposureto light. It is soluble in water (1:3,500), in alcohol(1:440), and in acetone (1:65) at 25°C. It is freely soluble indilute mineral acids and aqueous solutions of sodium andpotassium hydroxide. The pKa is 8.4. Its outstanding effectin curing pneumonia was first recognized by Whitby; however,because of its relatively high toxicity, it has been supplantedlargely by sulfadiazine and sulfamerazine. Severalcases of kidney damage have resulted from acetylsulfapyridinecrystals deposited in the kidneys. It also causes severenausea in most patients. Because of its toxicity, it is usedonly for dermatitis herpetiformis.Sulfapyridine was the first drug to have an outstandingcurative action on pneumonia. It gave impetus to the studyof the whole class of N1 heterocyclically substituted derivativesof sulfanilamide.

General DescriptionOdorless or almost odorless white or yellowish-white crystalline powder. Very slightly bitter taste. Aqueous solution is neutral.

Suppliers50 total

国药集团化学试剂有限公司86-21-63210123 · [email protected]
北京华美互利生物化工010-56205725 · [email protected]
梯希爱(上海)化成工业发展有限公司021-67121386 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]
广州隽沐生物科技股份有限公司020-36607679; 13502246435 · [email protected]

Additional notes

DefinitionChEBI: A sulfonamide consisting of pyridine with a 4-aminobenzenesulfonamido group at the 2-position.

Related reactions

9 records

Linked notes

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