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T26880BNS；化合物 T26880BNS
BNS is a potent, prolyl-hydroxylase 2 (PHD2)-selective inhibitor.
价 格：￥电议型 号：T26880产 地：中国大陆
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T2688LY310762；化合物LY310762LY310762 HCl；LY310762 HCl
LY310762 is a 5-HT1D receptor antagonist with Ki of 249 nM.
价 格：￥电议型 号：T2688产 地：中国大陆
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T26879BNC-1；化合物 T26879BNC 1；BNC 1
BNC-1 is a modulator of amyloid pathology. BNC-1 significantly decreases amyloid burden and improves markers of synaptic integrity in well-established mouse models of amyloid deposition by promoting phosphorylation and activation of Elk-1.
价 格：￥电议型 号：T26879产 地：中国大陆
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T26878BN-82451 2HCl；BN-82451 盐酸盐BN-82451B 2HCl|||BN 82451B 2HCl；BN-82451B 2HCl|||BN 82451B 2HCl
BN-82451 2HCl is a dual inhibitor of COX-1 and COX-2 and can be used to study Huntington´s chorea and Parkinson´s disease.
价 格：￥电议型 号：T26878产 地：中国大陆
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T26877BN 52115；化合物 T26877BN-52115|||BN52115；BN-52115|||BN52115
BN 52115, a platelet activating factor antagonist, has been found to inhibit in vivo bronchopulmonary alteration.
价 格：￥电议型 号：T26877产 地：中国大陆
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T26876BN 52111；化合物 T26876BN-52111|||BN52111；BN-52111|||BN52111
BN 52111 is a platelet activating factor antagonist.
价 格：￥电议型 号：T26876产 地：中国大陆
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T26875BN 50739；化合物 T26875BN50739|||BN-50739；BN50739|||BN-50739
BN 50739 is an antagonist of platelet-activating factor (PAF). BN 50739 suppresses certain cardiac arrhythmias. PAF is released from ischaemic myocardium and may contribute to initiation of ischaemia-induced ventricular fibrillation (VF)
价 格：￥电议型 号：T26875产 地：中国大陆
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T26874BN 50341；化合物 T26874BN50341|||BN-50341；BN50341|||BN-50341
BN 50341 is an inhibitor of antithrombotic platelet activating factor.
价 格：￥电议型 号：T26874产 地：中国大陆
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T26873BMY-27709；化合物BMY-27709BMY 27709|||BMY27709；BMY 27709|||BMY27709
BMY-27709 is an influenza virus growth inhibitor with an IC50 value of 3-8 μM against A/WSN/33 virus growth, and also exhibits inhibitory activity against some subtypes of influenza viruses.BMY-27709 acts early in the course of H1 and H2 virus infections, and exhibits antiviral activity through inhibition of hemagglutinin proteins. However, BMY-27709 has no effect on H3 subtype viruses and influenza B/Lee/40 viruses.
价 格：￥电议型 号：T26873产 地：中国大陆
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T26872BMVC4；化合物 T26872BMVC 4|||BMVC-4；BMVC 4|||BMVC-4
BMVC4 is a G-quadruplex stabilizer. BMVC4 induces senescence by activation of pathways of response to DNA damage that was independent of its telomerase inhibitory activity.
价 格：￥电议型 号：T26872产 地：中国大陆
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T26871BMT-052；化合物 T26871BMT052；BMT052
BMT-052 is a potent and selective Pan-genotypic HCV NS5B Polymerase Inhibitor (EC50 = 7 nM).
价 格：￥电议型 号：T26871产 地：中国大陆
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T26870BMS-986124；化合物 T26870BMS 986124|||BMS-986122；BMS 986124|||BMS-986122
BMS-986124 is an allosteric modulator of the μ-Opioid Receptor.
价 格：￥电议型 号：T26870产 地：中国大陆
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T2687Omeprazole sulfide；奥美拉唑硫醚Omeprazole metabolite Omeprazole sulfide|||Ufiprazole；Omeprazole metabolite
Omeprazole sulfide (Ufiprazole), a metabolite of Omeprazole, functions as a proton pump inhibitor.
价 格：￥电议型 号：T2687产 地：中国大陆
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T2686LEsomeprazole Sodium埃索美拉唑钠埃索美拉唑钠|||(S)-Omeprazole sodium
Esomeprazole Sodium ((S)-Omeprazole sodium) is the S-isomer of omeprazole with selective and irreversible proton pump inhibitor activity.Esomeprazole acts as an exosome inhibitor by blocking the exosome release via the inhibition of V-H+-ATPases
价 格：￥电议型 号：T2686L产 地：中国大陆
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T26869BMS-986122；化合物BMS-986122BMS 986122；BMS 986122
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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T26868BMS-986118；化合物 T26868BMS 986118；BMS 986118
BMS-986118 is a full agonist of GPR40, is a G-protein-coupled receptor expressed primarily in pancreatic islets and intestinal L-cells that has been a target of significant recent therapeutic interest for type II diabetes. Activation of GPR40 by partial agonists elicits insulin secretion only in the presence of elevated blood glucose levels, minimizing the risk of hypoglycemia.
价 格：￥电议型 号：T26868产 地：中国大陆
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T26867BMS-986104 HCl；化合物 T26867BMS986104|||BMS-986104|||BMS 986104；BMS986104|||BMS-986104|||BMS 986104
BMS-986104 is a potent and selective S1P1 receptor modulator.
价 格：￥电议型 号：T26867产 地：中国大陆
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T26866BMS-960；化合物BMS-960BMS 960|||BMS960；BMS 960|||BMS960
BMS-960 is an S1P agonist with potential anti-tumour activity for cancer research.
价 格：￥电议型 号：T26866产 地：中国大陆
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T26865BMS-933043；化合物 T26865BMS933043；BMS933043
BMS-933043 is a Selective α7 nAChR partial agonist. BMS-933043 showed potent binding affinity to native rat (Ki = 3.3 nM) and recombinant human alpha7 nicotinic acetylcholine receptors (Ki = 8.1 nM). BMS-933043 shows agonist activity in a calcium fluorescence assay (EC50 = 23.4 nM) and whole cell voltage clamp electrophysiology (EC50 = 0.14 μM (rat) and 0.29 μM (human)).
价 格：￥电议型 号：T26865产 地：中国大陆
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T26864BMS-932481；化合物 T26864BMS932481；BMS932481
BMS-932481 is a γ-secretase modulator.
价 格：￥电议型 号：T26864产 地：中国大陆
