CAS 256424-63-2

(S,E)-2-(4-(2,4-Dichlorophenyl)-1,3-dithiolan-2-ylidene)-2-(1H-imidazol-1-yl)acetonitrile

CAS: 256424-63-2

Fórmula: C₁₄H₉Cl₂N₃S₂

Cor e Forma: Solid

Peso molecular: 354.2774

Ref: IN-DA00BHGR

(S)-Luliconazole-E-Isomer

CAS: 256424-63-2

Fórmula: C₁₄H₉Cl₂N₃S₂

Cor e Forma: Brown Yellow Solid

Peso molecular: 354.27

Ref: 4Z-L-363

Luliconazole, (+)-

CAS: 256424-63-2

Luliconazole, (+)- is a bioactive chemical.

Fórmula: C₁₄H₉Cl₂N₃S₂

Cor e Forma: Solid

Peso molecular: 354.28

Ref: TM-T32943

(S)-Luliconazole

Produto Controlado

CAS: 256424-63-2

Applications (S)-Luliconazole is the (S)--enantiomer of Luliconazole, an azole antifungal drug. Luliconazole was found to interfere with ergosterol biosynthesis in cell-free extracts of Candida albican, while no interference due to (S)-Luliconazole was found.
References Uhida, K., et al.: J. Infect. Chemother., 10, 216 (2004); Niwano, ., et al.: Antimicro. Agents Chemother., 42, 967 (1998); Niwanno, Y., et al.: Med. Mycol., 37, 351 (1999)

Fórmula: C₁₄H₉Cl₂N₃S₂

Cor e Forma: Neat

Peso molecular: 354.28

Ref: TR-L473775

(S)-Luliconazole-E-Isomer

CAS: 256424-63-2

Fórmula: C₁₄H₉Cl₂N₃S₂

Peso molecular: 354.27

Ref: ST-EA-CP-L43004

(S)-Luliconazole

CAS: 256424-63-2

(S)-Luliconazole is an antifungal agent that is synthesized from an imidazole compound. This compound is biphenyl in structure and is often derived through chiral synthesis techniques to isolate the (S)-enantiomer, which is the active form that enhances pharmacological effects. Its mode of action involves inhibiting the enzyme lanosterol 14α-demethylase, an essential component in fungal cell membrane synthesis. This inhibition disrupts the production of ergosterol, a critical sterol in fungal membranes, ultimately leading to increased membrane permeability and cell death.

Fórmula: C₁₄H₉Cl₂N₃S₂

Pureza: Min. 95%

Peso molecular: 354.3 g/mol

Ref: 3D-GKA42463