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产品数：86101
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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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T7506Yoda 1KcsA,Potassium Channel,Akt,Yoda-1,PKB,Inhibitor,A431 cells,Yoda 1,HCAECs,inhibit,Protein kinas
Yoda1 is a Piezo1 ion channel agonist (EC50s = 17.1 and 26.6 μM for murine and human Piezo1-transfected HEK293T cells, respectively)
价 格：￥电议型 号：T7506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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T73457-Hydroxy-4H-chromen-4-oneSrc,7Hydroxy4Hchromen4one,inhibit,7 Hydroxy 4H chromen 4 one,Inhibitor
7-Hydroxychromone is a Src kinase inhibitor (IC50 of <300 μM).
价 格：￥电议型 号：T7345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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T7203OglufanideM21 human melanoma,anti-angiogenesis,Vascular endothelial growth factor receptor,HCV,inhib
Oglufanide is a naturally occurring thymic immunomodulator,and inhibits vascular endothelial growth factor (VEGF).
价 格：￥电议型 号：T7203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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T8236RHC 80267COX,mAChR,Platelet,mono- acylglycerol acyltransferase,Cyclooxygenase,Acyltransferase,Phosph
RHC 80267 is a selective inhibitor of DAGL (IC50 : 4 μM in canine platelets)
价 格：￥电议型 号：T8236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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T9696β-catenin-IN-2HCT116,inhibit,cancer,β-catenin,cell,Beta catenin,HT-29,Tcf/4,Colorectal,Inhibitor,β c
β-catenin-IN-2 is a potent inhibitor of β-catenin that can be used in colorectal cancer research.
价 格：￥电议型 号：T9696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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T9341Bemnifosbuvirguanosine,pangenotypic,Hepatitis C virus,SARS coronavirus,inhibit,HCV,Bemnifosbuvir,Inh
Bemnifosbuvir is a novel phosphoramidate prodrug of 2´-fluoro-2´-C-methylguanosine-5´-monophosphate that has potent in vitro activity against HCV.
价 格：￥电议型 号：T9341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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TQ0064Peretinoininhibit,NIK-333,NIK 333,Retinoic acid receptors,SphK,Peretinoin,Retinoid X receptors,HCV,I
Peretinoin is an oral acyclic retinoid with a vitamin A-like structure that targets retinoid nuclear receptors such as RXR and RAR.
价 格：￥电议型 号：TQ0064产 地：中国大陆
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TQ0108MK-6892HCAR2,PUMA-G,MK-6892,HM74A,HCA2,Inhibitor,GPR109A,MK6892,inhibit,MK 6892
MK-6892 is a selective and full agonist for the high-affinity nicotinic acid receptor GPR109A (Ki: 4 nM; GTPγS EC50: 16 nM).
价 格：￥电议型 号：TQ0108产 地：中国大陆
