LXS196 (Synonyms: LXS196; IDE196) |
Catalog No.GC32811 |
LXS196(LXS196)은 1.9nM, 0.4nM 및 3.1의 IC50 값을 갖는 강력하고 선택적인 경구 활성 단백질 키나제 C(PKC) 억제제입니다. 및 GSK3β LXS196은 포도막 흑색종 연구의 가능성이 있습니다.
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Cas No.: 1874276-76-2
Sample solution is provided at 25 µL, 10mM.
LXS196 is a potent, selective and orally active protein kinase C (PKC) inhibitor, with IC50 values of 1.9 nM, 0.4 nM and 3.1 μM for PKCα, PKCθ and GSK3β, respectively. It can be used for the treatment of uveal melanoma[1][2].
Upon oral administration, protein kinase C inhibitor LXS196 binds to and inhibits PKC, which prevents the activation of PKC-mediated signaling pathways. This may lead to the induction of cell cycle arrest and apoptosis in susceptible tumor cells. PKC, a serine/threonine protein kinase overexpressed in certain types of cancer cells, is involved in tumor cell differentiation, proliferation, invasion and survival[1].
LXS196 (compound 9) (15, 30, 75, 150 mg/kg, P.O., mice) shows improved efficacy (regression) in a 92.1 GNAQ uveal melanoma xenograft model in a dose-dependently manner[2].|| Animal Model:|Mice implanted with 92.1 GNAQ mutant uveal melanoma cells[2].|Dosage:|15, 30, 75, 150 mg/kg|Administration:|P.O. (bid) for 35 days|Result:|Dose-dependently suppressed the tumor growth.
[1]. Protein Kinase C Inhibitor LXS196 [2]. US20180179181.
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