Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6686 |
Sulconazole mononitrate
Exelderm,Sulconazole Nitrate,RS 44872,硝酸硫康唑 |
Antibacterial; Antibiotic; Antifungal | Microbiology/Virology |
Sulconazole mononitrate (Exelderm) 是一种咪唑类广谱杀菌剂。它可研究皮肤真菌病,花斑糠疹病,皮肤念珠菌病。 | |||
T4991 |
Ertapenem sodium
厄他培南钠,MK-826,L-749345,尔他培南钠 |
Antibacterial; Antibiotic | Microbiology/Virology |
Ertapenem sodium (MK-826) 是碳青霉烯,是一种 β-内酰胺抗生素,具有广谱抗菌活性。 | |||
T23830 |
BU-2313 A
BU 2313 A |
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BU-2313 A is a new antibiotic complex. It also active against anaerobes. | |||
T74657 |
Balhimycin
|
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Balhimycin为一种源自Amycolatopsis sp.发酵产物的糖肽类抗生素,其展现出针对葡萄球菌和厌氧菌的显著抗菌效果。 | |||
T40662 |
Isepamicin
Sch 21420 |
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Isepamicin (Sch 21420) is a potent aminoglycoside antibacterial compound with enhanced efficacy against strains harboring type I 6'-acetyltransferase. Its antibacterial spectrum encompasses Enterobacteriaceae and staphylococci, while exhibiting resistance against anaerobes, Neisseriaceae, and streptococci. Moreover, Isepamicin displays a robust concentration-dependent bactericidal effect, a prolonged post-antibiotic effect lasting several hours, and is capable of inducing adaptive resistance. | |||
T38458 |
Faropenem
|
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Faropenem, a highly efficacious and orally bioavailable beta-lactam antibiotic, exhibits an extensive range of in vitro antimicrobial activity against diverse gram-positive and -negative aerobes and anaerobes. Notably, Faropenem possesses inherent resistance to hydrolysis by virtually all beta-lactamases, including extended-spectrum beta-lactamases and AmpC beta-lactamases. Moreover, Faropenem has been developed as an oral prodrug, namely faropenem medoxomil, for the investigation of respiratory... | |||
T71490 |
Gepotidacin hydrochloride
|
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Gepotidacin hydrochloride, also known as GSK-2140944 hydrochloride, is a potent Type II DNA topoisomerase inhibitor. Gepotidacin hydrochloride is a novel antibacterial drug candidate. Gepotidacin hydrochloride Demonstrates Absence of Fluoroquinolone-Like Arthropathy in Juvenile Rats. Gepotidacin hydrochloride is efficacious in a nonhuman primate model of pneumonic plague. When tested against Gram-negative (n = 333) and Gram-positive (n = 225) anaerobes by agar dilution, Gepotidacin hydrochloride... | |||
T70358 |
Gepotidacin mesylate dihydrate
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Gepotidacin mesylate dihydrate, also known as GSK-2140944 mesylate dihydrate, is a potent Type II DNA topoisomerase inhibitor. Gepotidacin mesylate dihydrate is a novel antibacterial drug candidate. Gepotidacin mesylate dihydrate Demonstrates Absence of Fluoroquinolone-Like Arthropathy in Juvenile Rats. Gepotidacin mesylate dihydrate is efficacious in a nonhuman primate model of pneumonic plague. When tested against Gram-negative (n = 333) and Gram-positive (n = 225) anaerobes by agar dilution, ... |