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T3146BMS-202PD1-PDL1 inhibitor 2；PD-1/PD-L1 inhibitor 2
PD1-PDL1 inhibitor 2 is an inhibitor of the PD-1 (Programmed death- 1) /PD-Ll (Programmed death-ligand 1) protein/protein interaction, extracted from patent WO/2015034820 A1.
价 格：￥电议型 号：T3146产 地：中国大陆
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T3144BML-284Wnt agonist 1
Wnt agonist 1 (BML-284) is a potent, selective and , cell-permeable Wnt signaling activator.
价 格：￥电议型 号：T3144产 地：中国大陆
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T3046BMY 7378 dihydrochlorideBMY7378 HCl
BMY-7378, α1D-adrenergic receptor antagonist, is a weak partial agonist/antagonist of 5-HT1A receptor.
价 格：￥电议型 号：T3046产 地：中国大陆
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T2699BMS 777607BMS777607；BMS-777607；BMS 817378
BMS-777607 is a Met-related inhibitor for c-Met/Axl/Ron/Tyro3 (IC50: 3.9/1.1/1.8/4.3 nM). BMS-777607 has been investigated for the basic science of Malignant Solid Tumour.
价 格：￥电议型 号：T2699产 地：中国大陆
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T26869BMS-986122BMS986122；BMS 986122
BMS 986122 is a positive allosteric modulator of μ-opioid receptors that increases β-arrestin recruitment stimulated by endomorphin 1 in U2OS-OPRM1 human osteosarcoma cells expressing μ-opioid receptors (EC50 = 3 μM).
价 格：￥电议型 号：T26869产 地：中国大陆
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T26859BMS-8BMS8；BMS 8
BMS-8 is a novel inhibitor of the PD-1/PD-L1 interaction (IC50: 7.2 μM) by binding directly to PD-L1 and inducing the formation of PD-L1 homodimers.
价 格：￥电议型 号：T26859产 地：中国大陆
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T2679BMS-265246BMS265246；BMS 265246
BMS-265246 is a potent and selective CDK1/2 inhibitor.
价 格：￥电议型 号：T2679产 地：中国大陆
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T2658BMS-777607
BMS-777607 is a Met-related inhibitor for c-Met, Axl, Ron and Tyro3.
价 格：￥电议型 号：T2658产 地：中国大陆
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T2586Cabozantinib卡博替尼；XL184；BMS-907351
Cabozantinib (XL184) is a potent pan-tyrosine kinases inhibitor that inhibits VEGFR2, c-Met, Kit, Axl, and Flt3 (IC50s: 0.035, 1.3, 4.6, 7 and 11.3 nM).
价 格：￥电议型 号：T2586产 地：中国大陆
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T2576Brivanib (alaninate)丙氨酸布立尼布；BMS-582664；Brivanib Alaninate
Brivanib Alaninate is the alaninate salt of a vascular endothelial growth factor receptor 2 (VEGFR2) inhibitor with potential antineoplastic activity. Brivanib strongly binds to and inhibits VEGFR2, a tyrosine kinase receptor expressed almost exclusively
价 格：￥电议型 号：T2576产 地：中国大陆
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T2509TozasertibMK-0457；VX 680
MK-0457 is a pan-Aurora kinase inhibitor (Kis: 0.6/18/4.6 nM for Aurora A/Aurora B/Aurora C). It shows selectivity against more than 190 different kinases.
价 格：￥电议型 号：T2509产 地：中国大陆
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T2508BinimetinibMEK162；ARRY-162；ARRY-438162
Binimetinib (MEK162, ARRY-162, ARRY-438162) is an orally available inhibitor of MEK1/2 (IC50: 12 nM) in a cell-free assay.
价 格：￥电议型 号：T2508产 地：中国大陆
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T2490OsimertinibMereletinib；AZD-9291；奥希替尼
Osimertinib is a small molecule tyrosine kinase receptor inhibitor and antineoplastic agent that is used in the therapy of selected forms of advanced non-small cell lung cancer (NSCLC).
价 格：￥电议型 号：T2490产 地：中国大陆
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T2419BMS-794833BMS794833
BMS-794833 is a potent ATP competitive inhibitor of Met/VEGFR2; a prodrug of BMS-817378.
价 格：￥电议型 号：T2419产 地：中国大陆
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T2399BortezomibMG 341；DPBA；Brotezamide；NSC 681239；Radiciol；LDP 341；硼替佐米
Bortezomib (PS-341) is a potent 20S proteasome inhibitor (Ki: 0.6 nM, in a cell-free assay).
价 格：￥电议型 号：T2399产 地：中国大陆
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T2389Dapagliflozin达格列净；BMS-512148
Dapagliflozin is a selective sodium-glucose co-transporter subtype 2 (SGLT2) inhibitor with antihyperglycemic activity.
价 格：￥电议型 号：T2389产 地：中国大陆
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T23860CAY10444BML-241；CAY 10444；BML241；BML 241；CAY-10444
CAY10444 is an S1P3 specific antagonist.
价 格：￥电议型 号：T23860产 地：中国大陆
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T23840BUR11-{1-苯基-1H-吡唑并[3,4-D]嘧啶-4-基}哌啶；BMP upregulator 1；BUR-1；BUR 1；BMP upregulator-1
BUR1 is a Saccharomyces cerevisiae cyclin-dependent kinase (CDK) and is homologous to mammalian Cdk9, which functions in transcriptional elongation.
价 格：￥电议型 号：T23840产 地：中国大陆
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T2349BMS-754807BMS 754807；BMS754807
Dual IGF-1R/InsR Inhibitor BMS-754807 is an oral small molecule inhibitor of insulin-like growth factor 1 receptor (IGF-1R) and insulin receptor (InsR) tyrosine kinases with potential antineoplastic activity.
价 格：￥电议型 号：T2349产 地：中国大陆
