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Cat. No. | Product Name | Target | Signaling Pathways |
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T67988 |
Embeconazole
R 120758,CS 758 |
Antifungal | Microbiology/Virology |
Embeconazole (R 120758) 是一种三唑类抗真菌剂。Embeconazole 对念珠菌、曲霉菌、新型隐球菌等临床重要真菌具有较强的体外活性。 | |||
T23955 | Dactylfungin B | ||
Dactylfungins B is a novel antifungal antibiotic produced by Dactylaria Parvispora. The antibiotics were active against Candida pseudotropicalis and other fungi, with a MIC value of fewer than 10 micrograms/ml. | |||
T23954 |
Dactylfungin A
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Dactylfungins A is a novel antifungal antibiotic produced by Dactylaria Parvispora. The antibiotics were active against Candida pseudotropicalis and other fungi, with a MIC value of fewer than 10 micrograms/ml. | |||
T75176 | Antifungal agent 53 | ||
Antifungal agent 53 (A03) 是一种有效的白色念珠菌 CYP51抑制剂,具有抗真菌活性。Antifungal agent 53 阻止真菌生物膜的形成。Antifungal agent 53 也显示出良好的安全性。 | |||
T68562 |
FTR-1335
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FTR1335 is a CaNMT inhibitor (IC50 = 0.49 nM) with good fungal selectivity. CaNMT inhibitors are fungicidal and show antifungal activity against Candida (especially fluconazole-resistant strains). They function by inhibiting N-myristoyltransferase (NMT), which catalyzes the transfer of a C14 fatty acif from myristoyl-CoA to the N-terminal of glycine in many fungal proteins. Without this process, fungi can die. This process also occurs in humans, and as such selectivity is an important characteri... | |||
T79413 | Antifungal agent 73 | ||
Antifungalagent 73 (compound A32)是一款用于治疗唑类耐药Candida感染的抗真菌药物。该化合物通过破坏真菌的细胞壁和细胞膜来发挥作用,并且针对病原真菌和氟康唑(Fluconazole)耐药菌株显示出有效的体内抗真菌活性。 | |||
T21881 |
Fluconazole hydrate
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Fluconazole 水合物是抗真菌化合物,用于治疗和预防浅表和全身性的真菌感染。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T1388 |
Fluconazole
氟康唑,UK-49858 |
Antibiotic; Antifection; Antifungal | Microbiology/Virology |
Fluconazole (UK-49858) 是一种对多种真菌具有活性的三唑类抗真菌剂,抑制 C. albicans 和 Candida kefyr 的 IC99为 0.20 μg/mL 至 0.39 μg/mL。 |