7 Results for "

cryptococcal meningitis

" in MedChemExpress (MCE) Product Catalog:
Products (7)

7 Results for "cryptococcal meningitis" in MCE Product Catalog:

Cat. No.: HY-147110
CAS No.: 2342606-49-7
Purity:  98.12%
Target:  

Fungal

Research Areas:  

Infection Inflammation/Immunology

APX2039 is a brain-penetrant and orally active Gwt1 protein inhibitor. APX2039 inhibits an early step in fungal glycosylphosphatidylinositol anchor biosynthesis. APX2039 can be used for the research of cryptococcal meningitis and invasive mycosis caused by Talaromyces marneffei .
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Cat. No.: HY-109040
CAS No.: 1340593-70-5
Purity:  98.98%
Synonyms: VT-1129
Target:  

Fungal Cytochrome P450

Research Areas:  

Infection Inflammation/Immunology

Quilseconazole (VT-1129) is an orally active, highly selective fungal cytochrome P450 enzyme Cyp51 inhibitor that can cross the blood-brain barrier. Quilseconazole prevents the synthesis of ergosterol, an important component of the fungal cell membrane, by inhibiting Cyp51. Quilseconazole has minimal effects on human CYP enzymes. Quilseconazole has antifungal activity and can be used in the study of cryptococcal meningitis and other diseases .
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Cat. No.: HY-176483
Target:  

Fungal

Research Areas:  

Infection

Antifungal agent 133 (compound D2) is an orally active antifungal agent with a MIC80 of 0.13 ug/mL against C.neoformans H99. Antifungal agent 133 can be used for study of cryptococcal meningitis .
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Cat. No.: HY-144632
CAS No.: 2640054-39-1
Target:  

Fungal

Research Areas:  

Infection

Antifungal agent 22 (compound D16) is a potential and orally active antifungal agent for CM (cryptococcal meningitis), with an IC50 of 0.5 μg/mL. Antifungal agent 22 can penetrate the blood-brain barrier and kill the C. neoformans H99 cells by destroying the integrity of fungal cell membranes. Antifungal agent 22 shows selective anti-Cryptococcus activity with good metabolic stability and low cytotoxicity .
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Cat. No.: HY-144643
CAS No.: 2502095-64-7
Research Areas:  

Inflammation/Immunology

CYP51/HDAC-IN-1 is a potent, orally active CYP51/HDAC dual inhibitor. CYP51/HDAC-IN-1 inhibits important virulence factors and down-regulated resistance-associated genes. CYP51/HDAC-IN-1 exhibits potent therapeutic effects for both tropical candidiasis and cryptococcal meningitis .
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Cat. No.: HY-109040R
CAS No.: 1340593-70-5
Synonyms: VT-1129 (Standard)
Quilseconazole (Standard) is the analytical standard of Quilseconazole (HY-109040). This product is intended for research and analytical applications. Quilseconazole (VT-1129) is an orally active, highly selective fungal cytochrome P450 enzyme Cyp51 inhibitor that can cross the blood-brain barrier. Quilseconazole prevents the synthesis of ergosterol, an important component of the fungal cell membrane, by inhibiting Cyp51. Quilseconazole has minimal effects on human CYP enzymes. Quilseconazole has antifungal activity and can be used in the study of cryptococcal meningitis and other diseases .
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Cat. No.: HY-179704
Target:  

Drug Derivative Fungal

Research Areas:  

Infection

Antifungal agent 141, a Phenoxazine (HY-34463) derivative, is an antifungal agent. Antifungal agent shows potent antifungal activity in Cryptococcus neoformans and Candida albicans with MIC values of 2 and 4 µg/mL. Antifungal agent 141 can be used for the research of cryptococcal meningitis .
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