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产品数：86101
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T7939FingolimodLPL Receptor,Inhibitor,FTY 720,inhibit,PAK,FTY720,Fingolimod,Lysophospholipid Receptor,p21
Fingolimod is an antagonist of sphingosine 1-phosphate (S1P) (IC50 of 0.033 nM in K562 and NK cells).
价 格：￥电议型 号：T7939产 地：中国大陆
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T12821S1PR1 modulator 1S-1PR1 modulator 1,S1PR1 modulator 1,inhibit,LPL Receptor,Lysophospholipid Receptor
S1PR1 modulator 1 is a selective inhibitor of S1PR1 with a pIC50 of 7.6.
价 格：￥电议型 号：T12821产 地：中国大陆
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T10918NEP-IN-1NEP In 1,NEPIn1
NEP-IN-1 is an inhibitor of neutral endopeptidase (NEP, IC50 = 2 nM) and can be used in studies about female sexual arousal disorders.
价 格：￥电议型 号：T10918产 地：中国大陆
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T8450TCN 213glycine-dependentlly,Inhibitor,Ionotropic glutamate receptors,inhibit,iGluR,surmountable,TCN-
TCN213 is an antagonist of NMDA receptor that has a selective for NR1/NR2A over NR1/NR2B
价 格：￥电议型 号：T8450产 地：中国大陆
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T6704TG 100713PI3Kβ,Inhibitor,TG-100713,PI3Kα,PI3Kγ,TG 100713,inhibit,isoform,Phosphoinositide 3-kinase,P
TG100713 is a pan-PI3K inhibitor against PI3Kγ, PI3Kδ, PI3Kα and PI3Kβ with IC50 of 50 nM, 24 nM, 165 nM and 215 nM, respectively.
价 格：￥电议型 号：T6704产 地：中国大陆
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T7211Tyr-Gly-Gly-Phe-Met-OHInhibitor,Tyr Gly Gly Phe Met OH,Opioid Receptor,TyrGlyGlyPheMetOH,inhibit
Tyr-Gly-Gly-Phe-Met-OH, is a naturally occurring, endogenous opioid peptide that inhibits tumor growth via binding to the opioid receptor.
价 格：￥电议型 号：T7211产 地：中国大陆
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T8421TED-347PPI,irreversible,protein-protein,YAP,allosteric,TEAD4?Yap1,transcriptional,glioblastoma,TED 3
TED-347 is an irreversible and covalent inhibitor of TEAD4-Yap1 protein-protein interaction(EC50 of 5.9 μM), and inhibits glioblastoma cell viability.
价 格：￥电议型 号：T8421产 地：中国大陆
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TN12483-Epioleanolic acidInhibitor,3-Epioleanolic acid,inhibit,3 Epioleanolic acid,3Epioleanolic acid
3-Epioleanolic acid and oleanonic acid possess varying degrees of agonist activity on uterine smooth muscle with minor changes in the molecular structure affecting its intrinsic activity on uterine muscle.
价 格：￥电议型 号：TN1248产 地：中国大陆
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T9018JHU37160Inhibitor,hM4Di,Clozapine,hM3Dq,DREADD,inhibit,Muscarinic acetylcholine receptor,JHU-37160,J
JHU 37160 is a Designer Receptors Exclusively Activated by Designer Drug (DREADD) agonist with Ki of 1.9 nM and 3.6 nM for human muscarinic acetylcholine M3 receptors (hM3Dq) and hM4Di in vitro, respectively. And EC50 values are 18.5 nM and 0.2 nM for hM3Dq and hM4Di in fluorescent and BRET-based assays in HEK-293 cells, respectively.
价 格：￥电议型 号：T9018产 地：中国大陆
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TN1555Platycoside G1Inhibitor,Platycoside G 1,Platycoside G1,inhibit,Platycoside G-1
Deapi-platycoside E may have anti-inflammatory effects.
价 格：￥电议型 号：TN1555产 地：中国大陆
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T75791-BCP1 BCP,Inhibitor,inhibit,1BCP,iGluR,1-BCP,Ionotropic glutamate receptors
1-BCP is a centrally active drug that modulates AMPA receptor gated currents.
价 格：￥电议型 号：T7579产 地：中国大陆
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T8367TerpineolTerpineol
Terpineol is a natural product,used for making essence
价 格：￥电议型 号：T8367产 地：中国大陆
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T7064Valproic AcidHistone deacetylases,Mitochondrial Autophagy,bipolar disorder,epilepsy,Autophagy,Apopto
Valproic Acid is a branched chain fatty acid which potentially enhances central GABAergic neurotransmission and inhibits Na+ channels. Currently, the various molecular mechanisms of action of Valproic Acid have not been completely elucidated. Valproic Acid has been reported to be a potent inhibitor of histone deacetylases (HDACs) in vitro. Valproic Acid is also noted to relieve HDAC-dependent transcriptional repression and causes the hyperacetylation of histones in cultured cells. Additionally,
价 格：￥电议型 号：T7064产 地：中国大陆
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T7218Endomorphin 2Endomorphin2,inhibit,Inhibitor,Endomorphin-2,Endomorphin 2,Opioid Receptor
Endomorphins-2 (EM-2) could decrease both the frequency and amplitude of the sEPSC of the motoneurons in lamina IX, which was reversed by the MOR antagonist CTOP. EM-2-IR fibers originated from primary afferent fibers form symmetric synaptic connections with motoneurons innervating skeletal muscles of the lower limbs in lamina IX of the spinal ventral horn and EM-2 might exert inhibitory effects on the activities of these motoneurons through both presynaptic and postsynaptic mechanisms.
价 格：￥电议型 号：T7218产 地：中国大陆
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T7811Pilsicainide HClatrial tachyarrhythmias,SUN-1165,Pilsicainide HCl,antiarrhythmic,inhibit,orally acti
Pilsicainide HCl is a pure sodium channel blocker
价 格：￥电议型 号：T7811产 地：中国大陆
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T6559Rhamnose monohydrateRhamnose monohydrate,Rhamnose,Inhibitor,immunotherapies,cancer,monosaccharide,in
L(+)-Rhamnose (Rham) is a naturally-occurring deoxy sugar that is found primarily in plants and some bacteria.
价 格：￥电议型 号：T6559产 地：中国大陆
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T95251,2-Dimyristoyl-sn-glycero-3-phosphocholineInhibitor,inhibit,lipid,bilayer,Dimyristoyl phosphatidylc
1,2-Dimyristoyl-sn-glycero-3-phosphocholine (DMPC) is a synthetic phospholipid used in liposomes which is used for the study of lipid monolayers and bilayers[1].
价 格：￥电议型 号：T9525产 地：中国大陆
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TQ0229ETP-46321Inhibitor,ETP-46321,Phosphoinositide 3-kinase,ETP46321,inhibit,PI3K,ETP 46321
ETP-46321 is an effective and orally bioavailable PI3Kα/PI3Kδ inhibitor (Ki: 2.3/14.2 nM).
价 格：￥电议型 号：TQ0229产 地：中国大陆
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T12871Talmapimodcytotoxicity,multiple,inhibit,tumor,SCIO 469,SCIO469,cells,Hsp27,Inhibitor,phosphorylation
Talmapimod is an selective, orally active, and ATP-competitive p38α inhibitor with IC50 of 9 nM and 90 nM for p38α and p38β, respectively. Talmapimod exhibits at least 2000-fold selectivity over a panel of 20 kinases, including other MAPKs.
价 格：￥电议型 号：T12871产 地：中国大陆
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TN7028Picras-3-en-16-one, 11,20-epoxy-2-(β-D-glucopyranosyloxy)-1,11,12,14,15-pentahydroxy-, (1β,2α,11β,12
Picras-3-en-16-one, 11,20-epoxy-2-(β-D-glucopyranosyloxy)-1,11,12,14,15-pentahydroxy-, (1β,2α,11β,12α,15β)- is a chemical compound.
价 格：￥电议型 号：TN7028产 地：中国大陆
