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カタログ番号 | 製品名 | 別名 | ターゲット |
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T21881 | Fluconazole hydrate | ||
Fluconazole (hydrate) is a triazole antifungal agent used for the oral treatment and prevention of both superficial and systemic fungal infections, including but not limited to balanitis, various Candida infections, Cryp... | |||
T61960 | Fluconazole mesylate | ||
Fluconazole (mesylate) is a triazole antifungal drug. Fluconazole (mesylate) can used in the treatment and prevention of superficial and systemic fungal infections | |||
T27617 | Inz-1 | P450 | |
Inz-1 is an effective and fungal-selective inhibitor of mitochondrial cytochrome bc1 with IC50s of 8.092 and 45.320 μM for yeast and human. Inz-1 reverses Fluconazole or other triazole antifungals’ resistance in the path... | |||
T5328 | Fosfluconazole | Antifungal | |
Fosfluconazole is water-soluble phosphate prodrug of fluconazole. Fluconazole is an antifungal drug. | |||
T11991 | Mefentrifluconazole | P450 , Antifungal | |
Mefentrifluconazole is a potent, selective and orally active fungal CYP51 (Kd= 0.5 nM) inhibitor, but shows less inhibitory activity on human aromatase (IC50=0.92 μM). Mefentrifluconazole is a novel azole derivative and ... | |||
T2213 | Terconazole | Gyno-Terazol,Terazol 3,Terazol 7,Triaconazole,R42470 | Antifection , Antifungal |
Terconazole (Terazol 7) is a synthetic triazole derivative structurally related to fluconazole, antifungal Terconazole seems to disrupt cell wall synthesis by inhibiting biosynthesis of ergosterol or other sterols, damag... | |||
T8826 | 3-AMINO-1,2,4-TRIAZINE | Others | |
3-AMINO-1,2,4-TRIAZINE is an aromatic bioactive compound. It has been used to synthesize a variety of drugs, including the antifungal drug fluconazole, the anti-inflammatory drug ibuprofen and the anticancer drug paclita... | |||
T38240 | 2,6-Dichlorodiphenylamine | Antibacterial | |
2,6-Dichlorodiphenylamine is an analogue of Diclofenac Sodium and has anti-Candida albicans activity. Diclofenac Sodium is a potent and nonselective anti-inflammatory agent, acts as a COX inhibitor, with IC50s of 4 and 1... | |||
T35297 | ZD 0870 | D 0870,D0870,ZD0870 | |
ZD 0870, used to treat infections caused by fluconazole-resistant candida albicans. | |||
T63478 | Antifungal agent 12 | ||
Antifungal agent 12 is a new fluconazole-like compound that exhibits good antifungal effects. | |||
T79709 | PK-10 | ||
PK-10, when combined with Fluconazole, exhibits potent synergistic antifungal activity against multiple Fluconazole-resistant Candida albicans strains. This compound impedes hyphae formation, stimulates reactive oxygen s... | |||
T63157 | Antifungal agent 16 | ||
Antifungal agent 16 has antimicrobial activity comparable to that of ciprofloxacin and has higher antifungal activity than fluconazole. | |||
T63802 | Antifungal agent 35 | ||
Antifungal agent 35 is an effective antifungal agent that potentiates the antifungal activity of fluconazole against C. albicans. | |||
T79413 | Antifungal agent 73 | ||
Antifungal agent 73 (compound A32) effectively combats azole-resistant candidiasis by disrupting the fungal cell wall and membrane. It demonstrates potent in vivo activity against pathogenic fungi, including fluconazole-... | |||
T61188 | Chitin synthase inhibitor 2 | ||
Chitin synthase inhibitor 2 (compound 2b) is a highly potent inhibitor of chitin synthase, with an IC50 value of 0.09 mM and a K i value of 0.12 mM. This compound exhibits antimicrobial activities in vitro and demonstrat... | |||
T79384 | Antifungal agent 72 | ||
Antifungal agent 72 (Compound B8) demonstrates potent activity by inhibiting the efflux pump function and downregulating resistance-associated genes via disruption of the Pdr1-KIX interaction (K i : 11.7 μM). It exhibits... | |||
T62167 | BI-10 | ||
BI-10 is an antifungal compound that, in combination with fluconazole, inhibits mycelial growth, accumulates ROS, reduces mitochondrial membrane potential (MMP) and alters membrane permeability. | |||
T64235 | Antifungal agent 25 | ||
Antifungal agent 25 is an effective, broad-spectrum, metabolically stable antifungal agent in vivo. antifungal agent 25 exhibits antifungal effects against both Candida albicans and fluconazole-resistant Candida albicans... | |||
T75178 | Antifungal agent 55 | ||
Antifungal agent 55 (Compound A07) effectively inhibits Fluconazole-resistant strains of Candida albicans, demonstrating greater efficacy than Miconazole. It exhibits minimum inhibitory concentrations (MIC) values rangin... | |||
T70029 | Ibrexafungerp citrate | ||
Ibrexafungerp citrate is a triterpenoid antifungal. Similarly to echinocandins, it inhibits the synthesis of 1,3-β-d-glucan. However, it binds to a different site on the enzyme than echinocandins, resulting in limited cr... | |||
T75179 | Antifungal agent 56 | ||
Antifungal agent 56 (compound A09) is a potent antifungal agent, demonstrating superior efficacy against Fluconazole-resistant strains and outperforming Miconazole. It effectively inhibits Candida albicans strains, with ... | |||
T75180 | Antifungal agent 57 | ||
Antifungal Agent 57 (Compound A19) demonstrates potent efficacy against Fluconazole-resistant strains, outperforming Miconazole. It effectively inhibits Candida albicans strains, exhibiting minimum inhibitory concentrati... | |||
T75181 | Antifungal agent 58 | ||
Antifungal agent 58 (compound A21) exhibits high potency against Fluconazole-resistant strains and outperforms Miconazole in effectiveness. It inhibits Candida albicans strains with minimum inhibitory concentration (MIC)... | |||
T68562 | FTR-1335 | ||
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 inhibi... | |||
T35902 | Milbemycin A4 oxime | ||
Milbemycin A4 oxime is a derivative of milbemycin A4 and a component of milbemycin oxime , compounds that both have insecticidal and nematocidal activity. Milbemycin A4 oxime (0.05 mg/kg) reduces the number of microfilar... | |||
T79467 | Antifungal agent 60 | ||
Antifungal agent 60 (compound 16), a broad-spectrum ergosterol biosynthesis inhibitor, demonstrates potent activity against seven human pathogenic fungal species, including two fluconazole-resistant C. albicans isolates ... | |||
T75177 | Antifungal agent 54 | ||
Antifungal agent 54 (compound A05) serves as a potent inhibitor against Fluconazole-resistant strains, outperforming Miconazole in efficacy. It exhibits considerable activity against Candida albicans, with minimum inhibi... | |||
T62098 | Antifungal agent 28 | ||
Antifungal agent 28 (compound 18) is a selective and potent antifungal agent that disrupts mature Candida biofilms and inhibits pathogenic strains of Candida albicans and non-Candida albicans, including fluconazole-resis... |
カタログ番号 | 製品名 | 別名 | ターゲット |
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T1388 | Fluconazole | UK-49858 | Antibiotic , Antifection , Antifungal |
Fluconazole (UK-49858) is a triazole antifungal agent that is used to treat oropharyngeal candidiasis and cryptococcal meningitis in AIDS. |