Quilseconazole

目录号: A19305

fungal Cyp51 inhibitor

Quilseconazole

Quilseconazole Chemical Structure

CAS NO. 1340593-70-5

Quilseconazole (VT-1129) is a potent, orally active fungal Cyp51 (lanosterol 14-α-demethylase) inhibitor, binds tightly to cryptococcal CYP51, but weakly inhibits humans CYP450 enzymes.

库存: 现货

规格 价格 数量
1 mg
¥ 2,240.00
5 mg
¥ 6,720.00
10 mg
¥ 11,200.00
Warning 产品仅用于科学研究,不针对患者销售,望谅解.

产品详情

Quilseconazole (VT-1129) is a potent, orally active fungal Cyp51 (lanosterol 14-α-demethylase) inhibitor, binds tightly to cryptococcal CYP51, but weakly inhibits humans CYP450 enzymes.
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
0.1 mM 19.48 mL 97.4 mL 194.79 mL
0.5 mM 3.9 mL 19.48 mL 38.96 mL
1 mM 1.95 mL 9.74 mL 19.48 mL
5 mM 0.39 mL 1.95 mL 3.9 mL

*The above data is based on the productmolecular weight 513.37. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.

目录号 A19305
M. Wt 513.37
Formula C22H14F7N5O2
Purity >99%
Storage

Store lyophilized at -20ºC, keep desiccated.
In lyophilized form, the chemical is stable for 36 months.
In solution, store at -20ºC and use within 3 months to prevent loss of potency. Aliquot to avoid multiple freeze/thaw cycles.

CAS No. 1340593-70-5
Synonyms VT-1129, VT1129, VT 1129
SMILES O[C@@](CN1C=NN=N1)(C(C=CC(F)=C2)=C2F)C(F)(C3=CC=C(C4=CC=C(OC(F)(F)F)C=C4)C=N3)F

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