S7507
磺胺甲噁唑
别名:
4-氨基- N -（5-甲基-3-异恶唑基）苯磺酰胺, N 1 -（5-甲基异恶唑-3-基）磺胺
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经验公式（希尔记法）:
C10H11N3O3S
化学文摘社编号:
分子量:
253.28
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
211-963-3
Beilstein/REAXYS Number:
6732984
MDL number:
InChI
1S/C10H11N3O3S/c1-7-6-10(12-16-7)13-17(14,15)9-4-2-8(11)3-5-9/h2-6H,11H2,1H3,(H,12,13)
InChI key
JLKIGFTWXXRPMT-UHFFFAOYSA-N
SMILES string
Cc1cc(NS(=O)(=O)c2ccc(N)cc2)no1
technique(s)
HPLC: suitable
gas chromatography (GC): suitable
application(s)
forensics and toxicology
pharmaceutical (small molecule)
storage temp.
2-8°C
Quality Level
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Application
有关合适仪器技术的更多信息，请参考产品的分析证书。如需进一步支持，请联系技术服务。
磺胺甲恶唑用作分析参考标准品，使用分析 和微生物测定技术，定量牛乳样品中的分析物。
Biochem/physiol Actions
通过抑制二氢叶酸合成酶阻断二氢叶酸合成的磺胺类抗生素。
作用方式：在原核生物中抑制叶酸合成。
抗菌谱：革兰氏阳性菌、革兰氏阴性菌、衣原体
抗性机理：二氢叶酸合成酶或叶酸合成替代路径的改变。
作用方式：在原核生物中抑制叶酸合成。
抗菌谱：革兰氏阳性菌、革兰氏阴性菌、衣原体
抗性机理：二氢叶酸合成酶或叶酸合成替代路径的改变。
General description
磺胺甲恶唑是抑菌抗生素，属于磺胺类。广泛用于治疗肺囊虫病、 球虫病、胃肠炎、腹泻和呼吸系统疾病（如肺炎等）。
signalword
Warning
hcodes
Hazard Classifications
Aquatic Chronic 2 - Repr. 2
存储类别
11 - Combustible Solids
wgk
WGK 2
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Sulfamethoxazole abatement by means of ozonation
Journal of Hazardous Materials, 150(3), 790-794 (2008)
Drugs: Synonyms and Properties (2017)
Use of chemometric techniques to design a microbiological method for sulfonamide detection in milk
Nagel.GO, et al.
Czech Journal of Food Sciences, 31(6), 627-632 (2013)
Karl J Schreiber et al.
BMC plant biology, 12, 226-226 (2012-11-28)
The sulfanilamide family comprises a clinically important group of antimicrobial compounds which also display bioactivity in plants. While there is evidence that sulfanilamides inhibit folate biosynthesis in both bacteria and plants, the complete network of plant responses to these compounds
Ming Xie et al.
Water research, 47(13), 4567-4575 (2013-06-15)
The impact of humic acid fouling on the membrane transport of two pharmaceutically active compounds (PhACs) - namely carbamazepine and sulfamethoxazole - in forward osmosis (FO) was investigated. Deposition of humic acid onto the membrane surface was promoted by the
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