Sulfadimidin

Sulfadimidin
Data klinis
AHFS/Drugs.comInternational Drug Names
Kode ATC
Pengenal
  • 4-amino-N-(4,6-dimetilpirimidin-2-il)
    benzena-1-sulfonamida
Nomor CAS
PubChem CID
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
NIAID ChemDB
CompTox Dashboard (EPA)
ECHA InfoCard100.000.315 Sunting di Wikidata
Data sifat kimia dan fisik
RumusC12H14N4O2S
Massa molar278,33 g·mol−1
Model 3D (JSmol)
Titik leleh176 °C (349 °F)
  • O=S(=O)(Nc1nc(cc(n1)C)C)c2ccc(N)cc2
  • 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) checkY
  • Key:ASWVTGNCAZCNNR-UHFFFAOYSA-N checkY
  (verify)

Sulfadimidin atau sulfametazin adalah salah satu antibiotik sulfonamida.

Ada singkatan yang tidak terstandarisasia untuknya seperti "sulfadimidin" (disingkat SDI[1][2] dan lebih umum tetapi kurang dapat diandalkanb SDD[3][4]) dan sebagai "sulfametazin" (disingkat SMT[5][6] dan lebih umum tetapi kurang dapat diandalkanc SMZ[7][8]).

Referensi

  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.

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