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搜索结果：“Tutalthromycin second gen”

“Tutalthromycin second gen”的搜索结果

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EGFR-IN-2

Catalog No. A12628
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EGFR inhibitor

EGFR-IN-2 is a a noncovalent, irreversible, mutant-selective second generation EGFR inhibitor. 了解更多

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Defactinib

Catalog No. A21958
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FAK inhibitor

Defactinib (VS-6063; PF-04554878) is a novel FAK inhibitor with potential antiangiogenic and antineoplastic activities. 了解更多

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HS-10296 hydrochloride

Catalog No. A21661
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EGFR/T790M inhibitor

HS-10296 hydrochloride is an orally available and third-Generation inhibitor of epidermal growth factor receptor (EGFR)-activating mutations and T790M-resistant mutation with limited activity against wild-type EGFR. 了解更多

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AG-13958

Catalog No. A21175
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VEGFR inhibitor

AG-13958 (AG-013958), a potent VEGFR tyrosine kinase inhibitor, is used for treatment of choroidal neovascularization associated with age-related macular degeneration (AMD). 了解更多

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BCR-ABL-IN-1

Catalog No. A12496
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BCR-ABL inhibitor

BCR-ABL-IN-1 is an inhibitor of BCR-ABL tyrosine kinase, with a pIC50 of 6.46, and may be used in the research of chronic myelogenous leukemia. 了解更多

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SYP-5

Catalog No. A13031
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HIF-1 inhibitor

SYP-5 is a novel HIF-1 inhibitor, suppresses tumor cells invasion and angiogenesis. 了解更多

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Genistein

Catalog No. A10425
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EGFR inhibitor

Genistein, a soy isoflavone, is a multiple tyrosine kinases (e.g., EGFR) inhibitor which acts as a chemotherapeutic agent against different types of cancer, mainly by altering apoptosis, the cell cycle, and angiogenesis and inhibiting metastasis. 了解更多

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FLT3-IN-4

Catalog No. A18509
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FLT3 inhibitor

FLT3-IN-4 is a potent and orally effective Fms-like tyrosine receptor kinase 3 (FLT3; IC50=7 nM) inhibitor for treating acute myelogenous leukemia. 了解更多

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R916562

Catalog No. A19374
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Axl/VEGFR2 抑制剂

R916562 is an orally active and selective Axl/VEGF-R2 inhibitor with IC50s of 136 nM and 24 nM, respectively. R916562 has anti-angiogenesis and anti-metastasis. 了解更多

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