17
3
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T8134 |
Cefathiamidine
|
Antibacterial; Antibiotic | Microbiology/Virology |
Cefathiamidine 是一种头孢菌素抗菌剂,可研究由易感细菌引起的感染,还可用于呼吸道、肝脏、五官感觉、尿路感染以及心内膜炎和败血症的研究。 | |||
T12004 |
Meropenem trihydrate
美罗培南三水合物,SM 7338 trihydrate |
Antibacterial; Antibiotic | Microbiology/Virology |
Meropenem trihydrate (SM 7338 trihydrate) 是一种碳青霉烯抗生素,具有广谱抗菌活性。它对敏感和耐药的杜克氏杆菌 (MIC 值为 0.015-0.12 mg/mL), 淋病奈瑟氏球菌 (MIC 值为 0.02-0.06 mg/mL)和流感嗜血杆菌 (MIC 值为 0.03-0.12 mg/mL) 具有活性。 | |||
T20720 |
Norethisterone enanthate
NSC 9564,Norethindrone enanthate,LG-202,LG202,NSC9564,LG 202,炔诺酮庚酸酯,NSC-9564 |
Estrogen/progestogen Receptor | Endocrinology/Hormones |
Norethisterone enanthate (NSC-9564) 是一种口服有效的长效的孕激素。 | |||
T31806 |
Flovagatran
TGN 255 |
Thrombin | Proteases/Proteasome |
Flovagatran (TGN 255) 是一种具有口服活性和有效性的凝血酶和肠外直接因子 II 抑制剂。Flovagatran 可用于研究静脉血栓栓塞。 | |||
T22314 |
Doripenem
|
Antibacterial; Antibiotic | Microbiology/Virology |
Doripenem 是对革兰氏阳性菌、阴性菌和厌氧菌有效的β-内酰胺广谱抗生素。 | |||
T9284 |
Dexketoprofen trometamol
|
COX | Immunology/Inflammation; Neuroscience |
Dexketoprofen trometamol 是一种改良的非选择性 COX 抑制剂,起效迅速,可作为口服和非肠道制剂使用。 | |||
T40475 |
Ceftobiprole medocaril
BAL5788,头孢比普酯 |
Antibacterial | Microbiology/Virology |
Ceftobiprole medocaril (BAL5788) 是 Ceftobiprole 的前药。Ceftobiprole 是一种广谱的头孢菌素,对耐甲氧西林金黄色葡萄球菌具有活性。 | |||
T60254 |
Calcium glycerophosphate
|
Phosphorylase | Metabolism |
Calcium glycerophosphate(CaGP)是肠道碱性磷酸酶 F3 的抑制剂 (intestinal alkaline phosphatase F3)。Calcium glycerophosphate 可作为全肠外营养溶液中钙和磷的来源。 | |||
T9422 |
Fosciclopirox
CPX-POM |
Gamma-secretase | Neuroscience; Proteases/Proteasome; Stem Cells |
Fosciclopirox (CPX-POM) 利用靶向γ-分泌酶,抑制尿路上皮癌的生长。静脉给药后,它选择性地将活性代谢物 Ciclopirox 递送至整个尿路。Ciclopirox 在许多实体和血液恶性肿瘤中显示出抗癌活性。 | |||
T28552 |
Ro 09-1428
Ro-09-1428 |
||
Ro 09-1428, a parenteral cephalosporin, has high antipseudomonal activity. | |||
T31528 |
Disodium sebacate
Sebacic Acid Disodium Salt,Decanedioic Acid Disodium Salt,Disodium Decanedioate |
||
Disodium sebacate is a 10-carbon-atom dicarboxylic acid, proposed as substrate for parenteral nutrition. It has low toxicity. | |||
T22433 |
Sulopenem
CP-70429,硫培南 |
Others | Others |
Sulopenem, an orally active, potent inhibitor of beta-lactamase, is a parenteral penem antibiotic with broad-spectrum activities against Gram-negative and Gram-positive bacteria. | |||
T20107 |
Ertapenem
Invanz,MK0826,MK-0826,MK 0826 |
||
Ertapenem is a parenteral carbapenem. It has a broad spectrum of antimicrobial activity. It is highly resistant to inactivation by a wide variety of beta-lactamases. | |||
T75298 | Cefotiam dihydrochloride hydrate | ||
Cefotiam (SCE-963) dihydrochloride hydrate,一种肠外头孢菌素类抗生素,对革兰氏阳性菌和革兰氏阴性菌展示出广谱活性。 | |||
T38872 | Antibacterial agent 47 | ||
Antibacterial Agent 47 demonstrates potent antibacterial activity as an adjunct therapy to parenteral antibiotic Ceftazidime. By effectively reducing the minimum inhibitory concentration (MIC) of Ceftazidime, Antibacterial Agent 47 acts as a highly promising antimicrobial agent, thereby enhancing the overall efficacy of the treatment. | |||
T75297 | Cefotiam | ||
Cefotiam (SCE-963)为肠外使用的头孢菌素类广谱抗生素,对革兰氏阳性菌和革兰氏阴性菌均有效。 | |||
T72141 |
Ceftobiprole medocaril sodium
头孢比普酯钠盐,BAL5788 sodium |
||
Ceftobiprole medocaril (BAL5788) sodium 是 Ceftobiprole 的胃肠外前药。Ceftobiprole 是一种非肠道吡咯烷酮头孢菌素。Ceftobiprole 是一种广谱头孢菌素,对甲氧西林 (MRSA) 和耐万古霉素葡萄球菌 (VRSA) 和耐青霉素链球菌具有高水平的体外活性。Ceftobiprole 也抑制革兰氏阳性和革兰氏阴性病原体。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T0224 |
Meropenem
美罗培南,SM 7338 |
Others; Antibacterial; Antibiotic | Microbiology/Virology; Others |
Meropenem (SM 7338) 是一种具有广谱抗菌活性的碳青霉烯抗生素,对敏感和耐药的淋病奈瑟氏球菌,流感嗜血杆菌和杜克氏杆菌的 MIC 值分别为 0.02-0.06 mg/mL,0.03-0.12 mg/mL 和 0.015-0.12 mg/mL。 | |||
T0012 |
Cinchonine
LA40221,(8R,9S)-Cinchonine,奎宁树,辛可宁 |
Apoptosis; P-gp; Parasite | Apoptosis; Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience |
Cinchonine (LA40221) 是金鸡纳树皮中的一种天然产物。它可激活内质网应激诱导的人肝癌细胞凋亡。它是一种酰胺类局部麻醉剂。 | |||
T25240 |
Chloramphenicol succinate
Paraxin succinate,Kemicetine succinate,CPSA |
||
Chloramphenicol succinate is an inactive precursor of chloramphenicol. It is used for parenteral administration of chloramphenicol. |