Sulfadimidin

Sulfadimidin

Nama sistematis (IUPAC)
4-amino-N-(4,6-dimetilpirimidin-2-il) benzena-1-sulfonamida
Data klinis
AHFS/Drugs.com	International Drug Names
Kat. kehamilan	?
Status hukum	?
Pengenal
Nomor CAS	57-68-1 Y
Kode ATC	J01EB03 QJ01EQ03 QP51AG01 QP51AG51
PubChem	CID 5327
DrugBank	DB01582
ChemSpider	5136 Y
UNII	48U51W007F Y
KEGG	D02436 Y
ChEBI	CHEBI:102265 Y
ChEMBL	CHEMBL446 Y
NIAID ChemDB	AIDSNO:027749
Data kimia
Rumus	C12H14N4O2S
SMILES	eMolecules & PubChem
InChI InChI=1S/C12H14N4O2S/c1-8-7-9(2)15-12(14-8)16-19(17,18)11-5-3-10(13)4-6-11/h3-7H,13H2,1-2H3,(H,14,15,16) Y Key:ASWVTGNCAZCNNR-UHFFFAOYSA-N Y
Data fisik
Titik lebur	176 °C (349 °F)

Sulfadimidin atau sulfametazin adalah salah satu antibiotik sulfonamida.

Ada singkatan yang tidak terstandarisasi^a untuknya seperti "sulfadimidin" (disingkat SDI^[1][2] dan lebih umum tetapi kurang dapat diandalkan^b SDD^[3][4]) dan sebagai "sulfametazin" (disingkat SMT^[5][6] dan lebih umum tetapi kurang dapat diandalkan^c SMZ^[7][8]).

1. ^ Romváry A, Simon F (1992). "Sulfonamide residues in eggs". Acta Veterinaria Hungarica. 40 (1–2): 99–106. PMID 1476095. 
2. ^ Reddy KS, Jain SK, Uppal RP (1988). "Pharmacokinetic studies of sulphonamides in poultry". Indian Journal of Animal Sciences. 
3. ^ Kamakura K, Hasegawa M, Koiguchi S, Miyata M, Okamoto K, Narita M, et al. (1993). "[Studies on the identification of sulfadimidine in pork by high performance liquid chromatography with photodiode array detector and gas chromatograph-mass spectrometry]". Eisei Shikenjo Hokoku. Bulletin of National Institute of Hygienic Sciences (111): 61–5. PMID 7920569. 
4. ^ Garg SK, Ghosh SS, Mathur VS (January 1986). "Comparative pharmacokinetic study of four different sulfonamides in combination with trimethoprim in human volunteers". International Journal of Clinical Pharmacology, Therapy, and Toxicology. 24 (1): 23–5. PMID 3485584. 
5. ^ Peña MS, Salinas F, Mahedero MC, Aaron JJ (February 1994). "Solvent effect on the determination of sulfamethazine by room-temperature photochemically induced fluorescence". Talanta. 41 (2): 233–6. doi:10.1016/0039-9140(94)80113-4. PMID 18965913. 
6. ^ Kaniou S, Pitarakis K, Barlagianni I, Poulios I (July 2005). "Photocatalytic oxidation of sulfamethazine". Chemosphere. 60 (3): 372–80. Bibcode:2005Chmsp..60..372K. doi:10.1016/j.chemosphere.2004.11.069. PMID 15924956. 
7. ^ Calvo R, Sarabia S, Carlos R, Du Souich P (Mar 1987). "Sulfamethazine absorption and disposition: effect of surgical procedures for gastroduodenal ulcers". Biopharmaceutics & Drug Disposition. 8 (2): 115–24. doi:10.1002/bdd.2510080203. PMID 3593892. 
8. ^ De Liguoro M, Fioretto B, Poltronieri C, Gallina G (June 2009). "The toxicity of sulfamethazine to Daphnia magna and its additivity to other veterinary sulfonamides and trimethoprim". Chemosphere. 75 (11): 1519–24. Bibcode:2009Chmsp..75.1519D. doi:10.1016/j.chemosphere.2009.02.002. PMID 19269673.