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Product introduction
Obtusifoliol is a specific CYP51 inhibitor, Obtusifoliol shows the affinity with K d values of 1.2 µM and 1.4 µM for Trypanosoma brucei (TB) and human CYP51 , respectively In Vitro Obtusifoliol (0.1-100 µM; 48 hours) inhibit MCF-7 and MDA-MB231 breast cancer cells proliferation via arresting cell cycle progression and induction of apoptosis. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Cell Viability AssayCell Line: MCF-7; MDA-MB231 breast cancer cells Concentration: 0.1, 1, 10, 40, 80, and 100 µM Incubation Time: 48 hours Result: Inhibited MCF-7 and MDA-MB231 breast cancer cells proliferation. Form:Solid IC50& Target:CYP51 Trypanosoma
Chinese name
Obtusifoliol
English name
Obtusifoliol
Chinese alias
钝叶醇
English alias
4.alpha.,14.alpha.-Dimethyl-5.alpha.-ergosta-8,24(28)-dien-3.beta.-ol | Ergosta-8,24(28)-dien-3-ol, 4,14-dimethyl-, (3beta,4alpha,5alpha)- | (+)-OBTUSIFOLIOL | SCHEMBL2511101 | EECD77B7-C927-4E6E-B634-DEDFB042A6B9 | 4a,14a-dimethyl-5a-ergosta-8,24(28)-die
CAS number
16910-32-0
molecular formula
C30H50O
molecular weight
426.72 g/mol
Exact mass
≥99%
PSA
20.200 Ų
Logp
9
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Research chemical CAS 16910-32-0 HPLC ≥98% 5mg

Yuanye Research chemical CAS 16910-32-0 HPLC ≥98% 5mg, complete specifications; suitable for production, research, laboratory testing and inspection; digital one-stop procurement platform for scientific materials.

item number:B22262-5mg
Product model:5mg
level: HPLC ≥98% 5mg
Lead Time:30days
sold 151 Items
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