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T9009ICA-105574activator,KcsA,current amplitudes,ICA105574,ICA-105574,ICA 105574,Potassium Channel,inhibi
ICA-105574 is an activator of hERG that binds to the channel to remove inactivation, thus increasing peak current amplitude and shortening the action potential. It also modulates activation kinetics of the channel.
价 格：￥电议型 号：T9009产 地：中国大陆
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T95538-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-carboxylic acid8 [(2,6 dimethylbe
8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-car is a H+/K+ ATPase inhibitor with IC50 of 0.38μM.
价 格：￥电议型 号：T9553产 地：中国大陆
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T8351UBP551UBP551,UBP-551
UBP551 is a potent and selective NMDA receptors modulator.
价 格：￥电议型 号：T8351产 地：中国大陆
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TQ0139VU 0240551
VU 0240551 is a selective antagonist of neuronal K-Cl cotransporter KCC2 inhibitor with an IC50 of 560 nM. VU 0240551 inhibits L-type calcium channels and hERG.
价 格：￥电议型 号：TQ0139产 地：中国大陆
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T7557Guvacine hydrochlorideInhibitor,γ-Aminobutyric acid Receptor,GABA Receptor,inhibit,Guvacine hydrochl
Guvacine hydrochloride is an inhibits of GABA uptake (IC50 : 10 μM)
价 格：￥电议型 号：T7557产 地：中国大陆
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T35530IHMT-PI3Kδ-372IHMTPI3Kδ372,IHMT-PI-3Kδ-372,IHMT PI3Kδ 372
IHMT-PI3Kδ-372 is a selective inhibitor of PI3Kδ with an IC50 of 14 nM and can be used in studies about chronic obstructive pulmonary disease.
价 格：￥电议型 号：T35530产 地：中国大陆
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T27554HS38HS38
HS38 is a specific and ATP-competitive DAPK inhibitor with Kds of 300 nM, 200 nM, and 280 nM for DAPK1, PIM3, and ZIPK. HS38 can be used in studies about smooth muscle-related disorders.
价 格：￥电议型 号：T27554产 地：中国大陆
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T21855AMI-193
AMI-193 is an effective and selective antagonist of 5-HT2 and D2 receptor with Kis of 2, 3, 50, 2530, and 4300 nM for 5-HT2, D2 Receptor, 5-HT1A, D1 Receptor, and 5-HT1C Receptor. AMI-193 shows antipsychotic activity.
价 格：￥电议型 号：T21855产 地：中国大陆
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T13355XanthorrhizolXanthorrhizol,inhibit,Bacterial,Inhibitor
Xanthorrhizol is a natural product isolated from Curcuma xanthorrhiza Roxb. Xanthorrhizol is a potential antibacterial agent.
价 格：￥电议型 号：T13355产 地：中国大陆
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T7355IC87201IC 87201,IC87201,IC-87201,inhibit,iGluR,Inhibitor,Ionotropic glutamate receptors
IC87201 is a nNOS-PDZ/PSD-95-PDZ inhibitor. IC87201 showed great promise in cellular experiments and animal models of ischemic stroke and pain.
价 格：￥电议型 号：T7355产 地：中国大陆
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T9558KL-11743GLUT,inhibit,KL11743,Inhibitor,KL 11743,GLUT1,GLUT2,KL-11743,GLUT3,glucose,GLUT4,Glucose tra
KL-11743 specifically blocks glucose metabolism, triggering an acute collapse in NADH pools and a striking accumulation of aspartate, indicating a dramatic shift toward oxidative phosphorylation in the mitochondria.
价 格：￥电议型 号：T9558产 地：中国大陆
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T8542BMS-345541 hydrochlorideI kappa B kinase,BMS345541 hydrochloride,Inhibitor,BMS345541,BMS-345541,BMS
BMS-345541 hydrochloride is a selective IKK inhibitor (IKK2 and IKK1 with IC50 of 0.3 μM and 4 μM,respectively).
价 格：￥电议型 号：T8542产 地：中国大陆
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T12238NNC 55-0396NNC 55-0396,inhibit,Ca2+ channels,Inhibitor,NNC 550396,NNC 55 0396,Calcium Channel,Ca cha
NNC 55-0396 is a highly selective blocker of T-type calcium channel with IC50 of 6.8 μM. NNC 55-0396 can be used in studies about preventing human ovarian cancer cell proliferation.
价 格：￥电议型 号：T12238产 地：中国大陆
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T8255(±)-CatechinCyclooxygenase,(±)-Catechin,rel-Catechuic acid,(±)Catechin,COX,rel-Cianidanol,(±) Catech
(±)-Catechin hydrate is a natural product,has antioxidant activity and is effective in reducing oxidative stress.
价 格：￥电议型 号：T8255产 地：中国大陆
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T7416WS-12HEK293T,AVX 012,chronic neuropathic pain,TRP Channel,AR 15512,inhibit,AVX012,WS 12,WS12,WS-12,A
WS-12 is a potent TRPM8 agonist that acts as a cooling agent (EC50 : 193 nM)
价 格：￥电议型 号：T7416产 地：中国大陆
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T35529hSMG-1 inhibitor 11ehSMG 1 inhibitor 11e,hSMG1 inhibitor 11e
hSMG-1 inhibitor 11e is an effective and selective inhibitor of hSMG-1 (IC50 <0.05 nM) and can be used in studies about cancer treatment.
价 格：￥电议型 号：T35529产 地：中国大陆
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TN2268TetrahydromagnololMagnolignan,metabolite,Inhibitor,inhibit,Tetrahydromagnolol,Magnolol,CB2,GPR55,Can
Tetrahydromagnolol can activate cannabinoid (CB) receptors.
价 格：￥电议型 号：TN2268产 地：中国大陆
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T11961MBM-55SMBM 55S,MBM55S
MBM-55S is an effective inhibitor of Nek2 with an IC50 of 1 nM. MBM-55S indecus cell cycle arrest and apoptosis thereby inhibiting the proliferation of cancer cells. MBM-55S shows antitumor activities.
价 格：￥电议型 号：T11961产 地：中国大陆
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T60024CFT7455cereblon,CFT 7455,Ligands for E3 Ligase,anti-cancer agent,inhibit,CFT-7455,Inhibitor,CFT7455,
CFT7455 is an anti-cancer agent showing high affinity to the cereblon E3 ligase with a Kd of 0.9 nM. CFT7455 is an orally active degrader of zinc finger transcription factors Ikaros (IKZF1), and Aiolos (IKZF3).
价 格：￥电议型 号：T60024产 地：中国大陆
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T60390PI-55
PI-55 is a specific cytokinin receptor inhibitor. PI-55 is structurally related to 6-benzylaminopurine (BAP) and was shown to inhibit competitively BAP binding on Arabidopsis-specific receptors CRE1/AHK4 and AHK3. PI-55 inhibits cytokinins-induced haustorium formation and increased parasite aggressiveness [1].
价 格：￥电议型 号：T60390产 地：中国大陆
