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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
18 Results for "
Voriconazole
" in MedChemExpress (MCE) Product Catalog:
Products (18)
18 Results for "Voriconazole" in MCE Product Catalog:
11
Research Areas:
Voriconazole (UK-109496) is a second-generation, broad-spectrum triazole antifungal agent that inhibits fungal ergosterol biosynthesis. Voriconazole exerts its antifungal activity by inhibition of 14-α-lanosterol demethylation, which is mediated by fungal cytochrome P450 enzymes. Voriconazole can penetrate the blood brain barrier (BBB) .
Cat. No.: HY-W337569
CAS No.: 188416-29-7
Synonyms: (±)-UK-109496
(±)-Voriconazole ((±)-UK-109496) is a relative configuration of Voriconazole (HY-76200). Voriconazole is an antifungal agent .
2
Cat. No.: HY-137989A
Purity: 99.52%
Synonyms: Voriconazole oxynitride hydrochloride
Target:
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Voriconazole N-oxide (Voriconazole oxynitride) (hydrochloride) is the main metabolite of Voriconazole (HY-76200) , a widely used triazole antibiotic (fungal). Voriconazole N-oxide (hydrochloride) provides information on the patient's drug metabolism capacity .
Cat. No.: HY-76200R
CAS No.: 137234-62-9
Synonyms: UK-109496 (Standard)
Category:
Target:
Cat. No.: HY-Y0850U5
CAS No.: 9002-89-5
Synonyms: Polyvinyl alcohol (Mw 27000, 98-99% hydrolyzed, ~600 polymerization); Poly(Ethenol) (Mw 27000, 98-99% hydrolyzed, ~600 polymerization)
Cat. No.: HY-W329384
CAS No.: 108481-13-6
Synonyms: Ethyl camphorsulfonates
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Research Areas:
10-Camphorsulfonic acid ethyl ester (Ethyl camphorsulfonates) is a Voriconazole (HY-76200) impurity.
Cat. No.: HY-137989
CAS No.: 618109-05-0
Synonyms: Voriconazole oxynitride
Voriconazole N-oxide (Voriconazole oxynitride) is a potent antifungal agent. Voriconazole N-oxide has phototoxicity and photocarcinogenicity. Voriconazole N-oxide does not sensitize keratinocytes to ultraviolet B (UVB) .
Cat. No.: HY-76200B
CAS No.: 137234-71-0
Synonyms: UK-109496 camphorsulfonate
Voriconazole (UK-109496) camphorsulfonate is a second-generation, broad-spectrum triazole antifungal agent that inhibits fungal ergosterol biosynthesis. Voriconazole camphorsulfonate exerts its antifungal activity by inhibition of 14-α-lanosterol demethylation, which is mediated by fungal cytochrome P450 enzymes .
Cat. No.: HY-137989S
CAS No.: 1217851-84-7
Synonyms: Voriconazole oxynitride-d3
Cat. No.: HY-139688S
CAS No.: 1126743-89-2
Cat. No.: HY-144242S
Cat. No.: HY-76200A
CAS No.: 137330-52-0
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Voriconazole impurity 1 is an impurity of Voriconazole (HY-76200).
Cat. No.: HY-159585
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Research Areas:
CYP51-IN-20 (compound 5b) is an inhibitor of CYP51 and has antifungal activity. CYP51-IN-20 has a significant inhibitory effect on Candida albicans ATCC 10231, downregulates ERG11 (Cyp51) gene expression, and significantly reduces the yeast-to-hyphae morphological transition. CYP51-IN-20 can synergize with Voriconazole (HY-76200) to occupy the entire CYP51 binding site and exert a synergistic inhibitory effect in the Glechoma moth model .
Cat. No.: HY-76200C
CAS No.: 239807-03-5
Synonyms: (R,R)-UK-109496
Target:
Research Areas:
(R,R)-Voriconazole ((R,R)-UK-109496) is an enantiomer of Voriconazole (HY-76200). Voriconazole (UK-109496) is a second-generation broad-spectrum triazole antifungal compound that inhibits the biosynthesis of fungal ergosterol. Voriconazole exerts its antifungal activity by inhibiting the 14-α-lanosterol demethylation mediated by fungal cytochrome P450 enzymes. Voriconazole exhibits blood-brain barrier permeability .
Cat. No.: HY-W754411
CAS No.: 2747918-02-9
Cat. No.: HY-76200AR
CAS No.: 137330-52-0
Target:
Rel-(2R,3R)-2-(2,4-difluorophenyl)-3-(5-fluoropyrimidin-4-yl)-1-(1H-1,2,4-triazol-1-yl)butan-2-ol (Standard) is the analytical standard of Rel-(2R,3R)-2-(2,4-difluorophenyl)-3-(5-fluoropyrimidin-4-yl)-1-(1H-1,2,4-triazol-1-yl)butan-2-ol. This product is intended for research and analytical applications.
Cat. No.: HY-184165
F2F-202 is a selective HDAC6 inhibitor with an IC50 of 7.1 nM, exhibiting high selectivity toward HDAC1. F2F-202 does not directly bind to or inhibit the Hda1 protease activity of Candida albicans itself, but reduces the mRNA transcription level of the Hda1 gene. When combined with Voriconazole (HY-76200), F2F-202 decreases the yeast-hypha transition rate of azole-resistant Candida albicans and impairs the antioxidant response of azole-resistant Candida albicans. F2F-202 can be used in studies related to azole-resistant Candida albicans infections .
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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
