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产品数：86101
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T8931LICCB-19 hydrochlorideICCB19,ubiquitination,cIAP2,TRADD,cIAP1,RDA,ICCB 19 hydrochloride,Receptor-inte
ICCB-19 HCl is an inhibitor of TRADD (TNFRSF1A Associated Via Death Domain). It binds to a pocket on the N-terminal TRAF2-binding domain of TRADD (TRADD-N), which interacts with the C-terminal domain (TRADD-C) and TRAF2 to modulate the ubiquitination of RIPK1 and beclin 1.
价 格：￥电议型 号：T8931L产 地：中国大陆
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T8416Capmatinib xHClApoptosis,c-Met/HGFR,ATP competitive,inhibit,INC-280,Inhibitor,Capmatinib,SNU-5,INCB-
Capmatinib xHCl is a potent, orally active, selective, and ATP competitive c-Met kinase inhibitor, potently blocking in vitro kinase activity (IC50 = 0.13 nM) as well as constitutive or HGF-stimulated activity in cells (IC50 values range from 0.3 to 1.1 nM).
价 格：￥电议型 号：T8416产 地：中国大陆
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T11227L1Eravacycline HCl
Eravacycline HCl is potent antibiotic with broad-spectrum antibacterial activity.
价 格：￥电议型 号：T11227L1产 地：中国大陆
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T34374RO5203648 HClRO5203648 HCl,RO-5203648 HCl
RO5203648 HCl is a partial agonist of trace amine-related receptor 1 (TAAR1) with antipsychotic and antidepressant-like activities. RO5203648 HCl can be used in studies about neuropsychiatric therapeutics.
价 格：￥电议型 号：T34374产 地：中国大陆
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T7401(S)-3-AMino-2-Methylpropanoic acid-HCl(S) 3 AMino 2 Methylpropanoic acid HCl,(S)3AMino2Methylpropano
(S)-3-AMino-2-Methylpropanoic acid-HCl is a chemical compound.
价 格：￥电议型 号：T7401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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T28145ND-322 HClND 322 HCl
ND-322 HCl is a selective inhibitor of MT1-MMP and MMP2 and reduces in vitro melanoma cell growth, migration and invasion.
价 格：￥电议型 号：T28145产 地：中国大陆
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T6441CGS 21680 HydrochlorideCGS-21680,Inhibitor,CGS 21680,inhibit,CGS21680,CGS 21680 Hydrochloride,Adenos
CGS 21680 HCl（ IC50=22 nM）, an adenosine receptor agonist, exhibits 140-fold potency in A2 receptor over A1 receptor.
价 格：￥电议型 号：T6441产 地：中国大陆
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T24579Oxyfedrine L-form HCl
Oxyfedrine L-form HCl is a partial agonist at beta-adrenergic receptors and acts as a coronary vasodilator and cardiotonic agent.
价 格：￥电议型 号：T24579产 地：中国大陆
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T9640Diethylnorspermine HCl
Diethylnorspermine HCl potently induces SSAT (spermidine/spermine N1-acetyltransferase) mRNA and effectively stabilizes SSAT enzyme activity.
价 格：￥电议型 号：T9640产 地：中国大陆
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T8738LUN42518 HCl 47142-51-8(free base)LUN-42518 HCl 47142-51-8(free base),LUN42518 HCl 47142 51 8(fre
LUN42518 HCl is an analogue of phentolamine. Phentolamine is a nonselective alpha-adrenergic antagonist.
价 格：￥电议型 号：T8738产 地：中国大陆
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T6961PX-478Inhibitor,Autophagy,HIFs,inhibit,PX-478,PX 478,HIF-PH,HIF/HIF Prolyl-Hydroxylase,PX478,Hypoxia
PX-478 2HCl is an orally active, and selective inhibitor of hypoxia-inducible factor-1α (HIF-1α).
价 格：￥电议型 号：T6961产 地：中国大陆
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T6782LBenzocaine xHCl(94-09-7(free base))Benzocaine xHCl(94 09 7(free base)),Benzocaine xHCl(94097(free ba
Benzocaine shares a common receptor with all othe rLAs in the voltage-gated Na+ channel(IC50 of 0.8 mM tested with a potential of +30 mV).
价 格：￥电议型 号：T6782L产 地：中国大陆
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T8825Capmatinib 2HCl.H2OS114,SNU-5,ATP competitive,Balb/c nu/nu mice,U-87MG,INCB-28060 dihydrochloride,or
Capmatinib 2HCl.H2O is an orally bioavailable inhibitor of the proto-oncogene c-Met (HGFR)with potential antineoplastic activity.
价 格：￥电议型 号：T8825产 地：中国大陆
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T8494NS-3-008 hydrochloriderenal,inhibit,Ccl2,NS3008 hydrochloride,Hsd17b4,Stat5,transcriptional,Inhibito
NS-3-008 HCl is a transcriptional G0/G1 switch 2 (G0s2) inhibitor( IC50 of 2.25 μM).
价 格：￥电议型 号：T8494产 地：中国大陆
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T60107N-0500 HCl
N-0500 HCl is a very potent centrally acting DA receptor agonist. N-0500 HCl is a potent displacer of the specific [3H]DP5,6-ADTN binding with IC50 of 3nM.
价 格：￥电议型 号：T60107产 地：中国大陆
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T22325EPZ020411 hydrochlorideEPZ-020411 hydrochloride,EPZ020411 hydrochloride
EPZ020411 hydrochloride is a selective and potent small molecule PRMT6 inhibitor with an IC50 value of 10 nM.
价 格：￥电议型 号：T22325产 地：中国大陆
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T6142PD128907 HClPD128907 HCl,PD-128907 HCl
PD128907 HCl is a potent and selective dopamine D3 receptor agonist, with EC50 of 0.64 nM, exhibits 53-fold selectivity over dopamine D2 receptor.
价 格：￥电议型 号：T6142产 地：中国大陆
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T6840LFRAX486 HCL(1232030-35-1 free base)FRAX486 HCL(1232030351 free base),FRAX486 HCL(1232030 35 1 free b
FRAX486 HCL is a potent p21-activated kinase (PAK) inhibitor with IC50 values of 14, 33, 39 and 575 nM for PAK1, PAK2, PAK3 and PAK4 respectively.
价 格：￥电议型 号：T6840L产 地：中国大陆
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T8857LJP-1586 HCl
LJP-1586 HCl, a highly selective inhibitor of vascular adhesion protein-1 (VAP-1), exhibits antiinflammation effect by reducing adhesion molecule expression and immune cell infiltration after intracerebral hemorrhage (ICH).
价 格：￥电议型 号：T8857产 地：中国大陆
