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T22671CJ 0334665-HT Receptor,Inhibitor,inhibit,gastroprokinetic,CJ-033466,CJ033466,Serotonin Receptor,gast
CJ 033466 is a selective partial agonist of 5-HT4 receptor (EC50 = 9 nM) with gastroprokinetic effect.
价 格：￥电议型 号：T22671产 地：中国大陆
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T4346SPDB
SPDB is a small fragment linked to DM4 conjugates. It conjugates to antibodies utilizing disulfide linkers: anti-EGFR-SPDB-DM4 has been widely used.
价 格：￥电议型 号：T4346产 地：中国大陆
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T4074LGSK872 HCl（1346546-69-7 free base）GSK2399872A
GSK872 HCl is an effective and specific RIP3 kinase inhibitor. It binds RIP3 kinase domain with high affinity (IC50: 1.8 nM) and inhibits kinase activity (IC50: 1.3 nM).
价 格：￥电议型 号：T4074L产 地：中国大陆
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T4049Genz-123346 free base
Genz 123346 is an inhibitor of GL1 synthase that blocks the conversion of ceramide to GL1.
价 格：￥电议型 号：T4049产 地：中国大陆
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T3468TomivosertibeFT508
eFT508 is a potent, highly selective MNK1 and MNK2 inhibitor with IC50 value of 1-2 nM.
价 格：￥电议型 号：T3468产 地：中国大陆
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T3467MiransertibAKT inhibitor 2；ARQ-092
ARQ-092 is an orally bioavailable, selective, and potent allosteric Akt inhibitor.
价 格：￥电议型 号：T3467产 地：中国大陆
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T3465Vesnarinone维司力农；Piteranometozine；OPC-8212；Arkin
Vesnarinone (INN) is a mixed phosphodiesterase 3 inhibitor and ion-channel modifier that has modest, dose-dependent, positive inotropic activity, but minimal negative chronotropic activity. It also suppresses cell proliferation and induces apoptosis by in
价 格：￥电议型 号：T3465产 地：中国大陆
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T3464PHCCC(-) PHCCC
PHCCC is a Group I metabotropic glutamate receptor antagonist and a positive allosteric modulator of mGluR4. It also is a potent to antagonism for mGluR2 and mGluR8.
价 格：￥电议型 号：T3464产 地：中国大陆
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T3463NVP-ACC789ZK202650；ACC-789
ACC-789 (NVP-ACC789; ZK-202650) is an effective, specific and orally active inhibitor of the VEGF receptor tyrosine kinases.
价 格：￥电议型 号：T3463产 地：中国大陆
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T3462BMS-582949 hydrochlorideBMS-582949 HCl
The BMS-582949 hydrochloride is a highly specific p38α MAPK inhibitor (IC50: 13 nM).
价 格：￥电议型 号：T3462产 地：中国大陆
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T3461Losartan Carboxylic AcidE-3174；EXP-3174
EXP-3174 is a potent AT1 antagonist (Kis: 0.57 nM, rat; 0.67 nM, human), producing a depressor response and vasodilatation. EXP3174, a metabolite of losartan, is more potent than losartan in blocking the angiotensin II-induced responses in vascular smooth
价 格：￥电议型 号：T3461产 地：中国大陆
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T34603L-SelenocystineL-Selenocystine
L-Selenocystine can be used as a building block in biologically active selenol compounds.
价 格：￥电议型 号：T34603产 地：中国大陆
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T3460HhAntag
HhAntag is a small molecule inhibitor of GLI1-mediated transcription, an essential down-stream element of the Hedgehog (Hh) pathway with the anti-tumor activity.
价 格：￥电议型 号：T3460产 地：中国大陆
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T33467MOMIPP
MOMIPP is a PIKfyve inhibitor and a macropinocytosis inducer. MOMIPP readily penetrates the blood-brain barrier and is moderately effective in suppressing progression of intracerebral glioblastoma xenografts[1][2].
价 格：￥电议型 号：T33467产 地：中国大陆
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T3346AKT inhibitor VIIIAKTi-1/2
AKT inhibitor VIII is a highly specific Akt1/2 inhibitor (IC50: 58/210 nM). The selectivity for Akt1 is higher about 36-fold than Akt3.
价 格：￥电议型 号：T3346产 地：中国大陆
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T23469TQS4-Naphthalen-1-yl-3a,4,5,9b-tetrahydro-3H-cyclopenta[c]quinoline-8-sulfonamide
TQS is a positive allosteric modulator of α7 nACh receptors.
价 格：￥电议型 号：T23469产 地：中国大陆
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T2346Enasidenib恩西地平；AG-221
Enasidenib is an orally available inhibitor of specific mutant forms of the mitochondrial enzyme isocitrate dehydrogenase type 2 (IDH2), with potential antineoplastic activity.
价 格：￥电议型 号：T2346产 地：中国大陆
