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产品数：86101
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TN1403Arjunolic acidhepatocyte injury,hyperglycemia,Inhibitor,type 1 diabetes,antimicrobial,antioxidant,Re
Arjunolic acid has antioxidant, anti-inflammatory, antinociceptive and anticholinesterasic (AChE and BuChE) activities, it may as promising targets for the development of innovative multi-functional medicines for Alzheimer desease treatment.
价 格：￥电议型 号：TN1403产 地：中国大陆
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TQ0009UCB9608Phosphatidylinositol 4 kinases,UCB-9608,Inhibitor,UCB 9608,UCB9608,PI4 kinases,PI4K,inhibit
UCB9608 is a selective and orally active PI4KIIIβ inhibitor (IC50: 11 nM), selective over PI3KC2 α, β, and γ lipid kinases.
价 格：￥电议型 号：TQ0009产 地：中国大陆
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T37662Pregabalin Diacid Impurity
Pregabalin Diacid Impurity is an impurity found in commercial preparations of pregabalin which is an analog of GABA.
价 格：￥电议型 号：T37662产 地：中国大陆
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TP1216CaM kinase II inhibitor TFA saltCaM kinase II inhibitor TFA salt
Autocamtide-2-Related Inhibitory Peptide is a highly specific and potent inhibitor of CaMKII with an IC50 of 40 nM.
价 格：￥电议型 号：TP1216产 地：中国大陆
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T22783FGIN-1-43FGIN143,FGIN 1 43
FGIN-1-43 is a potent and specific ligand for the mitochondrial DBI receptor.
价 格：￥电议型 号：T22783产 地：中国大陆
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TN1521ColutehydroquinoneFungal,isoflavonoid,Colutehydroquinone,inhibit,Inhibitor,antifungal
Colutehydroquinone is an antifungal isoflavonoid from Colutea arborescens.
价 格：￥电议型 号：TN1521产 地：中国大陆
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T8457NPS2390Inhibitor,NPS2390,Calcium-sensing receptor,NPS-2390,mGluR,inhibit,Metabotropic glutamate rece
NPS2390 is a first generation quinoxaline derivative that acts as a noncompetitive antagonist of mGluR1 and mGluR5 (IC50 of 5.2 and 82 nM, respectively)
价 格：￥电议型 号：T8457产 地：中国大陆
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T9379L-Threonic acid magnesium saltL Threonic acid magnesium salt,LThreonic acid magnesium salt
L-Threonic acid magnesium salt (L-TAMS) increases synapse density and memory ability in both aged rats and late stage Alzheimer’s disease (AD) model mice.
价 格：￥电议型 号：T9379产 地：中国大陆
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T9235GW604714XInhibitor,mitochondrial respiration,Mitochondrial Metabolism,Parkinson’s Disease,MCT1,GW604
GW604714X were found to be potent inhibitors of mitochondrial respiration supported by pyruvate
价 格：￥电议型 号：T9235产 地：中国大陆
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T7320TozadenantP1 receptor,SYN-115,Adenosine Receptor,SYN 115,Tozadenant,Inhibitor,inhibit
Tozadenant is an adenosine A2A receptor antagonist(Ki of 11.5 nM and 6 nM on human and rhesus,respectively)
价 格：￥电议型 号：T7320产 地：中国大陆
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T16687Pyr3Pyr3,Pyr-3
Pyr3 is a selective transient receptor potential canonical channel 3 inhibitor. Pyr3 inhibits TRPC3-mediated Ca2+ influx in a dose-dependent manner(IC50 = 700 nM).
价 格：￥电议型 号：T16687产 地：中国大陆
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T10824cis-Urocanic acid
cis-Urocanic acid is a 5-HT2A receptor agonist (Kd: 4.6 nM). It is an immune modulator that induces immunosuppression by binding to the 5-HT2A receptor.
价 格：￥电议型 号：T10824产 地：中国大陆
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T9593Senaparibinhibit,poly ADP ribose polymerase,IMP 4297,Inhibitor,breast,pancreatic,IMP-4297,Senaparib,
Senaparib is a novel highly potent and selective oral PARP1/2 inhibitor with strong antitumor activity.
价 格：￥电议型 号：T9593产 地：中国大陆
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T88332-chloro-5-(16,18-dioxo-17-azapentacyclo[6.6.5.0~2,7~.0~9,14~.0~15,19~]nonadeca-2,4,6,9,11,13-hexaen
2-chloro-5-(16,18-dioxo-17-azapentacyclo[6.6.5.0~2,7~.0~9,14~.0~15,19~]nonadeca-2,4,6,9,11,13-hexaen-17-yl)benzoic acid is a chemical compound
价 格：￥电议型 号：T8833产 地：中国大陆
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TN1455Bryodulcosigenininhibit,Bryodulcosigenin,Inhibitor
Bryodulcosigenin has anti-inflammatory effect, it shows potent inhibitory effects on EBV-EA induction.
价 格：￥电议型 号：TN1455产 地：中国大陆
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T7206L2-Iminobiotin hydrobromideNitric oxide synthases,NOS,NO Synthase,2-Iminobiotin,2Iminobiotin hydrobro
2-Iminobiotin hydrobromide is a cyclic guanidino analog of biotin that acts as a reversible inhibitor of inducible nitric oxide synthase (iNOS) and neuronal NOS (nNOS; Ki of 21.8 and 37.5 μM for mouse iNOS and rat nNOS, respectively).
价 格：￥电议型 号：T7206L产 地：中国大陆
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T7659Bisindolylmaleimide IVdisease,Protein kinase C,Bisindolylmaleimide IV,CMV,inhibit,selective,human,DM
Bisindolylmaleimide IV is a protein kinase C (PKC) cell permeable inhibitor( IC50 : 0.10 - 0.55 μM)
价 格：￥电议型 号：T7659产 地：中国大陆
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T9271RAD51-IN-1cancer,inhibit,tumor cell,chemotherapy,RAD51 IN 1,Inhibitor,RAD51,DNA damage,RAD-51-IN-1,R
Rad51-in-1 is a derivative of B02 and an effective inhibitor of Rad51.
价 格：￥电议型 号：T9271产 地：中国大陆
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T8742G5-7antiangiogenic,inhibit,Apoptosis,JAK,Glioma,G-5-7,cycle,G5 7,phase,G57,STAT3,cell,Inhibitor,EGFR
JAK2 inhibitor G5-7 is an orally active JAK2 inhibitor, selectively inhibits JAK2–mediated phosphorylation and activation of EGFR (Tyr1068) and STAT3 by binding to JAK2. G5-7 has the potential for glioma study
价 格：￥电议型 号：T8742产 地：中国大陆
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TN1878Loureirin D
Loureirin D is isolated from the stem wood of Dracaena loureiri.
价 格：￥电议型 号：TN1878产 地：中国大陆
