설파디미딘

술파메타진
임상자료
AHFS/Drugs.com	국제 마약 이름
ATC 코드	J01EB03(WHO) QJ01EQ03(WHO) QP51AG01(WHO);
식별자
	IUPAC 이름 4-아미노-N-(4,6-디메틸피리미딘-2-yl); 벤젠-1-벤조나미드;
CAS 번호	57-68-1 ;
펍켐 CID	5327;
드러그뱅크	DB01582 ;
켐스파이더	5136 ;
유니	48U51W007f;
케그	D02436 ;
체비	CHEBI:102265 ;
켐벨	켐블446 ;
NIAID 화학DB	027749;
CompTox 대시보드 (EPA)	DTXSID6021290 ;
ECHA InfoCard	100.000.315
화학 및 물리적 데이터
공식	C12H14N4O2S
어금질량	278.33 g·mits−1
3D 모델(JSmol)	인터랙티브 이미지;
녹는점	176°C(349°F)
	스마일즈 O=S(=O)(Nc1nc(n1)C)c2cc(N)cc2;
	인치 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) ; 키:ASWVTGNCAZCNR-UHFFFAOYSA-N ;
	(iii)

Sulfadimidine 또는 Sulfamethazine은 Sulfonamide 항균제다.null

이를 "술파디미딘"(약칭 SDI^[1]^[2] 및 더 일반적이지만 덜 신뢰할^b 수 있는 SDD^[3]^[4]) 및 "술파메타진"(약칭 SMT^[5]^[6] 및 더 일반적이지만 덜 신뢰할^c 수 있는 SMZ^[7]^[8])으로 표준화되지^a 않은 약어가 있다.다른 이름으로는 설파디메라진, 설파디메진, 설파디메틸피리미딘 등이 있다.null

참조

^ Romváry A, Simon F (1992). "Sulfonamide residues in eggs". Acta Veterinaria Hungarica. 40 (1–2): 99–106. PMID 1476095.
^ Reddy KS, Jain SK, Uppal RP (1988). "Pharmacokinetic studies of sulphonamides in poultry". Indian Journal of Animal Sciences.
^ 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.
^ 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.
^ 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.
^ Kaniou S, Pitarakis K, Barlagianni I, Poulios I (July 2005). "Photocatalytic oxidation of sulfamethazine". Chemosphere. 60 (3): 372–80. doi:10.1016/j.chemosphere.2004.11.069. PMID 15924956.
^ 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.
^ 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. doi:10.1016/j.chemosphere.2009.02.002. PMID 19269673.

추가 읽기

ChemDB. "Sulfamethazine", ChemDB, 국립 알레르기 및 전염병 연구소(NIAID), 국립 보건 연구소(National Institute of Health, NIH)
화학의 설파디미딘IDplus 데이터베이스
펍켐"술파메타진 - 물질 요약", 펍켐, 국립생명공학정보센터(NCBI), 국립도서관(NLM), 국립보건원(NIH)

이 체계적인 항생제 관련 기사는 단조롭다.위키피디아를 확장하여 도울 수 있다.

[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. 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. doi:10.1016/j.chemosphere.2009.02.002. PMID 19269673.

[1]

[2]

b

[3]

[4]

[5]

[6]

c

[7]

[8]

a

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