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T26856BMS-764459；化合物 T26856BMS-764459
BMS-764459 is a potent antagonist of corticotropin-releasing factor/hormone receptor 1 (CRHR-1).
价 格：￥电议型 号：T26856产 地：中国大陆
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T26855BMS-665053；化合物 T26855BMS665053；BMS665053
BMS-665053 is a corticotropin-releasing factor-1 (CRF1) receptor antagonist (IC50 = 1.0 nM). BMS-665053)11 is a potent inhibitor of CRF-stimulated cyclic adenosine monophosphate (cAMP) production in human Y-79 retinoblastoma cells (IC50 = 4.9 nM). In addition, BMS-665053 is efficacious in the Defensive Withdrawal model of anxiety in rats and has low in vivo clearance (Cl = 17 mL/min/kg, t? = 7.8 h) in rats.
价 格：￥电议型 号：T26855产 地：中国大陆
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T26854BMS641；化合物BMS641BMS-641|||BMS-209641|||BMS 641；BMS-641|||BMS-209641|||BMS 641
BMS641 (BMS-209641) is a selective and potent RARβ agonist.BMS641 has a high affinity for RARβ and synergistically activates RARβ and RARgamma to induce cellular maturation into specialized neuronal subtypes.
价 格：￥电议型 号：T26854产 地：中国大陆
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T26852BMS-605541；化合物BMS-605541BMS605541|||BMS 605541；BMS605541|||BMS 605541
BMS-605541 is a potent and selective inhibitor of vascular endothelial growth factor receptor-2 (VEGFR-2) kinase activity(Ki=49 nM).
价 格：￥电议型 号：T26852产 地：中国大陆
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T26851BMS-561390；化合物 T26851DPC083|||DPC 083|||DPC-083；DPC083|||DPC 083|||DPC-083
BMS-561390, a reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.
价 格：￥电议型 号：T26851产 地：中国大陆
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T26850BMS-538305 HCl；化合物 T26850BMS-538305|||BMS538305|||BMS 538305|||BMS-538305 hydrochloride；BMS-538305||
BMS-538305 is a potent, selective inhibitor of dipeptidyl peptidase IV (DPP-IV).
价 格：￥电议型 号：T26850产 地：中国大陆
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T26849BMS-457；化合物 T26849BMS-457
BMS-457 is a potent, CCR1-selective antagonist.
价 格：￥电议型 号：T26849产 地：中国大陆
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T26848BMS-433771 free base；化合物 T26848BMS-433771|||BMS 433771|||BMS433771；BMS-433771|||BMS 433771|||BMS4337
BMS-433771, a novel inhibitor of respiratory syncytial virus (RSV), binds the RSV F glycoprotein and inhibits membrane fusion.
价 格：￥电议型 号：T26848产 地：中国大陆
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T26847BMS-281384；化合物 T26847BMS-281384
BMS-281384 is a highly potent, phosphodiesterase 5 (PDE 5)-selective inhibitor.
价 格：￥电议型 号：T26847产 地：中国大陆
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T26846BMS270394；化合物 T26846BMS 189961|||BMS-270394|||BMS 270394；BMS 189961|||BMS-270394|||BMS 270394
BMS270394 is an agonist of nuclear retinoic acid receptor (RAR-γ).
价 格：￥电议型 号：T26846产 地：中国大陆
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T26845BMS-250749；化合物 T26845BMS 250749|||BMS250749；BMS 250749|||BMS250749
BMS-250749 is a fluoroglycosylated fluoroindolocarbazole, it has antitumor activity.
价 格：￥电议型 号：T26845产 地：中国大陆
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T26844BMS-199945；化合物 T26844BMS199945|||BMS 199945；BMS199945|||BMS 199945
BMS-199945 is an Influenza H1N1 Virus inhibitor.
价 格：￥电议型 号：T26844产 地：中国大陆
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T26843BMS-199264 hydrochloride；化合物 T26843BMS-199264 hydrochloride
BMS-199264 hydrochloride potently inhibits the ATP hydrolase activity of mitochondrial F1F0 ATP synthase.
价 格：￥电议型 号：T26843产 地：中国大陆
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T26842Bms 188107；化合物 T26842Bms188107|||Bms-188107；Bms188107|||Bms-188107
Bms 188107 is a calcium antagonist, it has cardioprotective effects.
价 格：￥电议型 号：T26842产 地：中国大陆
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T26841BMS 182874；化合物BMS 182874BMS182874|||BMS-182874；BMS182874|||BMS-182874
BMS 182874 is an orally effective and highly selective endothelin receptor ETA antagonist with an IC50 value of 0.150 μM for ETA and a Ki value of 0.055 μM for ETA.BMS 182874 is able to reduce arterial pressure in a rat hypertension model induced by Deoxycorticosterone acetate. BMS 182874 was able to reduce Deoxycorticosterone-induced arterial pressure in a rat model of hypertension and can be used to study cardiovascular disease.
价 格：￥电议型 号：T26841产 地：中国大陆
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T2679BMS-265246；化合物BMS-265246BMS265246；BMS265246
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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T26641Apadenoson；化合物 T26641ATL 146e|||BMS 068645|||ATL146e|||BMS-068645|||ATL-146e|||BMS068645；ATL 146e|||
Apadenoson is a potent Adenosine A2 receptor agonist with inhibitory effects on Adenosine A3 receptors with an IC of 45 nM. Apadenoson has anti-inflammatory activity and can be used to study neurological diseases.
价 格：￥电议型 号：T26641产 地：中国大陆
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T26361LBrasofensine Maleate；化合物 T26361LNS-2214|||NS 2214|||BMS-204756-07|||NS2214；NS-2214|||NS 2214|||BMS-2
Brasofensine Maleate inhibits the monoamine re-uptake.
价 格：￥电议型 号：T26361L产 地：中国大陆
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T26361Brasofensine sulfate；化合物 T26361NS 2214|||BMS 204756|||NS2214|||NS-2214|||BMS-204756；NS 2214|||BMS 20
Brasofensine sulfate is a dopamine reuptake inhibitor.
价 格：￥电议型 号：T26361产 地：中国大陆
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T2610LBMS-599626 2HCL(714971-09-2 Free base)；化合物 BMS-599626 2HCL(714971-09-2 Free base)BMS 599626 dihydroc
BMS-599626 2HCL (AC480 2HCl) is a BMS-599626 derivative. BMS-599626 is an orally available and selective dual inhibitor of HER1 and HER2 with IC50s of 20 and 30 nM, respectively. BMS-599626 inhibits tumor cell proliferation and has the potential to increase tumor BMS-599626 inhibits tumor cell proliferation and has the potential to increase tumor response to radiotherapy.
价 格：￥电议型 号：T2610L产 地：中国大陆
