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T6229Daclatasvir达卡他韦；达拉他韦；BMS-790052；EBP 883；Daklinza
Daclatasvir (BMS-790052) is a highly selective inhibitor of HCV NS5A with EC50 of 9-50 pM, for a broad range of HCV replicon genotypes and the JFH-1 genotype 2a infectious virus in cell culture. Phase 3.
价 格：￥电议型 号：T6229产 地：中国大陆
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T6203Saxagliptin沙克列汀；沙格列汀；BMS-477118；Onglyza
Saxagliptin is a selective and reversible DPP4 inhibitor with IC50 of 26 nM.
价 格：￥电议型 号：T6203产 地：中国大陆
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T6121TepotinibMSC2156119；EMD-1214063；特泊替尼
Tepotinib is an inhibitor of MET tyrosine kinase with potential antineoplastic activity.
价 格：￥电议型 号：T6121产 地：中国大陆
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T6049SNS-032SNS 032；BMS-387032；SNS032
SNS-032 is a selective inhibitor of CDK2 (IC50: 48 nM ) and is 10- and 20-fold selective over CDK1/CDK4. It is also sensitive to CDK7/9 (IC50: 62 nM/4 nM), and no effect on CDK6.
价 格：￥电议型 号：T6049产 地：中国大陆
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T5697BMS-1166BMS1166
BMS-1166 is a potent PD-1/PD-L1 interaction inhibitor.
价 格：￥电议型 号：T5697产 地：中国大陆
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T5532BMS-687453
BMS-687453 is a potent and selective PPAR alpha agonist, with an EC(50) of 10 nM for human PPARalpha and approximately 410-fold selectivity vs human PPARgamma in PPAR-GAL4 transactivation assays.
价 格：￥电议型 号：T5532产 地：中国大陆
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T5407BranebrutinibBMS986195
BMS986195 is a potent, covalent inhibitor of Bruton´s tyrosine kinase (BTK), >5,000-fold selective over all kinases outside of the Tec family (IC50 <1 nM for BTK).
价 格：￥电议型 号：T5407产 地：中国大陆
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T5398BMS 599626 2HCl (873837-23-1(HCl))AC480 dihydrochloride
BMS-599626 (AC480) is a selective inhibitor of HER1 and HER2 (IC50s: 20 nM and 30 nM), ~8-fold less potent to HER4, >100-fold to Lck, VEGFR2, c-Kit, MET, etc.
价 格：￥电议型 号：T5398产 地：中国大陆
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T5164Cabozantinib hydrochlorideCabozantinib hydrochloride (849217-68-1(free base))；BMS-907351；XL184；盐酸卡博替
Cabozantinib (XL184) is a potent pan-tyrosine kinases inhibitor that inhibits VEGFR2, c-Met, Kit, Axl, and Flt4 (IC50s: 0.035, 1.3, 4.6, 7 and 6 nM).
价 格：￥电议型 号：T5164产 地：中国大陆
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T5138BMS-986142BMS986142；BMS 986142
BMS-986142 is a potent and highly selective reversible BTK inhibitor (IC50: 0.5 nM).
价 格：￥电议型 号：T5138产 地：中国大陆
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T4696BMS202 hydrochloride (1675203-84-5(free base))PD-1/PD-L1 inhibitor 2 hydrochloride
PD-1/PD-L1 inhibitor 2 is a small-molecule PD-1/PD-L1 interaction inhibitor (IC50: 18 nM). Biophysical studies demonstrate that BMS202 binds directly to PD-L1. Binding of BMS202 promotes PD-L1 dimerisation and blocks the PD-L1/ PD1 interaction.
价 格：￥电议型 号：T4696产 地：中国大陆
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T4665TemsavirBMS626529
BMS-626529 is a novel attachment inhibitor that targets HIV-1 gp120 and prevents its binding to CD4+ T cells.
价 格：￥电议型 号：T4665产 地：中国大陆
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T4654(±)-Ibipinabant(±)-SLV319；SLV319；(±)-BMS6462
SLV319 has been used in trials studying the treatment of Obesity and Obesity and Type 2 Diabetes.
价 格：￥电议型 号：T4654产 地：中国大陆
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T4600BMS-3BMS3；BMS 3
BMS-3 is a potent LIMK inhibitor with IC50s of 5 nM and 6 nM for LIMK1 and LIMK2, respectively.
价 格：￥电议型 号：T4600产 地：中国大陆
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T4598BMS-5LIMKi 3；BMS5；BMS 5
BMS-5 is a potent LIMK inhibitor with IC50s of 7 nM and 8 nM for LIMK1 and LIMK2, respectively.
价 格：￥电议型 号：T4598产 地：中国大陆
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T4584BMS-813160BMS 813160
BMS-813160 is the first dual CCR2/CCR5 antagonist to enter Clinical development for cardiovascular.
价 格：￥电议型 号：T4584产 地：中国大陆
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T4534BMS-309403BMS309403；BMS 309403
BMS-309403 is an effective, selective and cell-permeable inhibitor of fatty acid binding protein 4 (FABP4) with a Ki of less than 2 nM.
价 格：￥电议型 号：T4534产 地：中国大陆
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T4532LinrodostatBMS-986205
BMS-986205 is a selective indoleamine 2, 3-dioxygenase 1 (IDO1) inhibitor.
价 格：￥电议型 号：T4532产 地：中国大陆
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T4474Asunaprevir阿那匹韦；BMS-650032
Asunaprevir is an effective hepatitis C virus (HCV) NS3 protease inhibitor.
价 格：￥电议型 号：T4474产 地：中国大陆
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T4132BPTUBMS-646786
Allosteric antagonist of P2Y1 (EC50 = 0.06-0.3 μM). Non-nucleotide ligand. Binds receptor outside of the helical bundle. Blocks inhibition of spontaneous contraction of rat and mouse colon induced by electrical field stimulation, nicotine and P2Y agonists
价 格：￥电议型 号：T4132产 地：中国大陆
