11 Results for "

CYP51A1

" in MedChemExpress (MCE) Product Catalog:
Products (11)

11 Results for "CYP51A1" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-N7266
CAS No.: 16910-32-0
Obtusifoliol is a specific CYP51 inhibitor, Obtusifoliol shows the affinity with Kd values of 1.2 μM and 1.4 μM for Trypanosoma brucei (TB) and human CYP51, respectively .
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Cat. No.: HY-RS03486
Research Areas:  

Others

CYP51A1 Human Pre-designed siRNA Set A contains three designed siRNAs for CYP51A1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-W714655
CAS No.: 112893-26-2
Target:  

Fungal Cytochrome P450

Research Areas:  

Infection

Becliconazole is a fungal CYP51A1 inhibitor. Becliconazole can be used in research on fungal infections .
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Cat. No.: HY-149617
CAS No.: 3032391-34-4
Research Areas:  

Infection

CYP51/PD-L1-IN-4 (compound 14a-2) is a potent dual-target (CYP51/PD-L1) inhibitor, with IC50 values of 0.17 and 0.021 μM, respectively. CYP51/PD-L1-IN-4 exhibits excellent antifungal and antidrug-resistant fungal activity in vitro. CYP51/PD-L1-IN-4 can be used for fungal infections research .
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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-116568R
CAS No.: 178928-70-6
Synonyms: JAU-6476 (Standard)
Research Areas:  

Infection

Prothioconazole (Standard) is the analytical standard of Prothioconazole. This product is intended for research and analytical applications. Prothioconazole is a triazolinthione fungicide. Prothioconazole is a CYP51 inhibitor .
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Cat. No.: HY-156149
CAS No.: 3032386-49-2
Research Areas:  

Infection

CYP51/PD-L1-IN-1 (compound L11) is a quinazoline compound with antifungal activity. CYP51/PD-L1-IN-1 is a dual inhibitor of CYP51 (IC50: 0.884 μM) and PD-L1 (IC50: 0.083 μM), which can induce early apoptosis of fungal cells in the cell cycle. CYP51/PD-L1-IN-1 also significantly reduced intracellular IL-2, NLRP3, and NF-κBp65 protein levels, induced mitochondrial damage and ROS accumulation, and ultimately led to fungal lysis and death .
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Cat. No.: HY-156150
CAS No.: 3032386-58-3
Research Areas:  

Infection

CYP51/PD-L1-IN-2 (compound L20) is a quinazoline compound with antifungal activity. CYP51/PD-L1-IN-2 is a dual inhibitor of CYP51 (IC50: 0.263 μM) and PD-L1 (IC50: 0.017 μM), which can induce early apoptosis of fungal cells in the cell cycle. CYP51/PD-L1-IN-2 also significantly reduced intracellular IL-2, NLRP3, and NF-κBp65 protein levels, induced mitochondrial damage and ROS accumulation, and ultimately led to fungal lysis and death .
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Cat. No.: HY-156151
CAS No.: 3032386-59-4
Research Areas:  

Infection

CYP51/PD-L1-IN-3 (compound L21) is a quinazoline compound with antifungal activity. CYP51/PD-L1-IN-3 is a dual inhibitor of CYP51 (IC50: 0.205 μM) and PD-L1 (IC50: 0.039 μM), which can induce early apoptosis of fungal cells in the cell cycle. CYP51/PD-L1-IN-3 also significantly reduced intracellular IL-2, NLRP3, and NF-κBp65 protein levels, induced mitochondrial damage and ROS accumulation, and ultimately led to fungal lysis and death .
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Cat. No.: HY-116568S
Synonyms: JAU-6476-d4
Prothioconazole-d4 (JAU-6476-d4) is the deuterium labeled Prothioconazole (HY-116568). Prothioconazole is a triazolinthione fungicide. Prothioconazole is a CYP51 inhibitor .
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Cat. No.: HY-P72049
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: CYP51A1; P450-14DM; Prev. CYP51; CYPL1; LDM; CYPLI; Lanosterol 14-Alpha Demethylase; CP51; Sterol 14-Alpha Demethylase; Cytochrome P450, Family 51, Subfamily A, Polypeptide 1; Cytochrome P450 51A1; Cytochrome P450, 51 (Lanosterol 14-Alpha-Demethylase); Cy
Species:  
Source:  
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