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T2699BMS-777607BMS-777607,BMS777607,BMS 777607
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：美洲
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T4532LinrodostatLinrodostat,BMS-986205,
BMS-986205 is a selective indoleamine 2,3-dioxygenase 1 (IDO1) inhibitor.
价 格：￥电议型 号：T4532产 地：美洲
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T4534BMS-309403BMS-309403,BMS309403,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：美洲
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T4584BMS-813160BMS-813160,BMS813160,BMS 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：美洲
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T4598BMS-5BMS-5,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：美洲
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T4600BMS-3BMS-3,BMS3,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：美洲
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T4654SLV319SLV319,(±)-BMS6462,(±)-Ibipinabant
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：美洲
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T4665BMS626529BMS626529,Temsavir,
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：美洲
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T5138BMS-986142BMS-986142,BMS986142,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：美洲
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T5407BMS986195BMS986195,Branebrutinib,
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：美洲
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T5532BMS-687453BMS-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：美洲
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T6203SaxagliptinSaxagliptin,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：美洲
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T6229DaclatasvirDaclatasvir,EBP 883,BMS-790052
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：美洲
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T6249AvagacestatAvagacestat,BMS-708163,
Avagacestat (BMS-708163) is a potent, selective, orally bioavailable γ-secretase inhibitor of Aβ40 and Aβ42 with IC50 of 0.3 nM and 0.27 nM, demonstrating a 193-fold selectivity against Notch. Phase 2.
价 格：￥电议型 号：T6249产 地：美洲
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T6326BMS-345541BMS-345541,BMS345541,BMS 345541
BMS-345541 is a highly selective inhibitor of the catalytic subunits of IKK-2 and IKK-1 with IC50 of 0.3 μM and 4 μM, respectively.
价 格：￥电议型 号：T6326产 地：美洲
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T6420BMS-707035BMS-707035,BMS707035,BMS 707035
BMS-707035 is a specific HIV-I integrase (IN) inhibitor with IC50 of 15 nM. Phase 2.
价 格：￥电议型 号：T6420产 地：美洲
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T8847Fosravuconazole L-lysine ethanolate；化合物T8847BMS-379224 L-lysine ethanolate|||E-1224 L-lysine ethanol
Fosravuconazole L-lysine ethanolate (BMS-379224 L-lysine ethanolate) is a broad-spectrum antifungal agent. In Japan, it is approved for the treatment of onychomycosis, a fungal infection of the nail. It is a prodrug that is converted into ravuconazole.
价 格：￥电议型 号：T8847产 地：中国大陆
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T8730BMS986260；化合物BMS986260BMS986260
BMS-986260 is a selective, and orally bioavailable TGFβR1 inhibitor(IC50 = 1.6 nM).
价 格：￥电议型 号：T8730产 地：中国大陆
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T8710MSAB；化合物MSABMSAB
MSAB is a selective inhibitor of Wnt/β-catenin signaling. MSAB binds to β-catenin, promoting its degradation, and specifically downregulates Wnt/β-catenin target genes.
价 格：￥电议型 号：T8710产 地：中国大陆
