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TP1898HS024selective,melanocortin,intake,Inhibitor,Melanocortin Receptor,MC Receptor,HS-024,food,HS024,inh
Highly potent melanocortin MC4 receptor antagonist (Ki values are 0.29, 18.6, 5.45 and 3.29 nM for cloned human MC4, MC1, MC3 and MC5 receptors respectively). Increases food intake, and blocks α-MSH- and MTII-induced hypotension and bradycardia in rats, following central administration in vivo.
价 格：￥电议型 号：TP1898产 地：中国大陆
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T67777Flaviviruses-IN-3
Flaviviruses-IN-3 (compound 87) is a potent inhibitor of flaviviruse. Flaviviruses-IN-3 could reduce the WNV (West Nile virus) protease activity, with a inhibition of 54%.
价 格：￥电议型 号：T67777产 地：中国大陆
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T7741DS-1001binhibit,DS 1001b,Inhibitor,Isocitrate Dehydrogenase (IDH),DS-1001b,DS1001b
DS-1001b is an inhibitor of mutant IDH-1 (Isocitrate Dehydrogenase-1)
价 格：￥电议型 号：T7741产 地：中国大陆
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TQ0283RS102895CC chemokine receptor,CCR,Inhibitor,RS102895,inhibit,RS-102895,RS 102895
RS102895 is a potent CCR2 antagonist (IC50: 360 nM) and shows no effect on CCR1.
价 格：￥电议型 号：TQ0283产 地：中国大陆
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T9041AES-350Histone deacetylases,AES 350,MV4-11,AES-350,Apoptosis,acute myeloid leukemia,AML,Inhibitor,in
AES-350 is a potent and orally active HDAC6 inhibitor(IC50 and a Ki of 0.0244 μM and 0.035 μM, respectively). It is also against HDAC-3, -8, and -11 in an enzymatic activity assay with IC50 values of 0.187 μM, 0.245 μM, and >1μM, respectively. AES-350 triggers apoptosis in AML cells through HDAC inhibition and can be used for acute myeloid leukemia (AML) research.
价 格：￥电议型 号：T9041产 地：中国大陆
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T6767TCS7010Aurora Kinase,inhibit,TCS 7010,Apoptosis,TCS-7010,TCS7010,Inhibitor
Aurora A Inhibitor I is a novel, potent, and selective inhibitor of Aurora A with IC50 of 3.4 nM in a cell-free assay. It is 1000-fold more selective for Aurora A than Aurora B.
价 格：￥电议型 号：T6767产 地：中国大陆
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TP1180Dolastatin 10ADC Cytotoxin,Dolastatin-10,Dolastatin 10,DLS10,inhibit,NSC376128,DLS-10,NSC-376128,Dol
Dolastatin 10 is a potent antimitotic peptide that inhibits tubulin polymerization.
价 格：￥电议型 号：TP1180产 地：中国大陆
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TQ0230BTK IN-1Btk,SNS062,Inhibitor,SNS-062,BTK IN 1,Bruton tyrosine kinase,SNS 062,inhibit,BTK IN-1,BTK IN
BTK IN-1 (SNS062 analog) is an effective BTK inhibitor (IC50: <100 nM).
价 格：￥电议型 号：TQ0230产 地：中国大陆
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TN1030N-p-trans-CoumaroyltyramineInhibitor,Cholinesterase (ChE),Parasite,inhibit,N p trans Coumaroyltyrami
N-p-trans-Coumaroyltyramine is a natural product, is an acetylcholinesterase (AChE) inhibitor with an an IC50 of 122 μM. N-p-trans-Coumaroyltyramine exhibits anti-trypanosomal activity with an IC50 of 13.3 μM for T. brucei rhodesiense.
价 格：￥电议型 号：TN1030产 地：中国大陆
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TN6457N-trans-caffeoyltyramine
N-trans-caffeoyltyramine is a modulator of inflammatory responses and can be used in studies about treatment for chronic inflammatory diseases.
价 格：￥电议型 号：TN6457产 地：中国大陆
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TP1889MCL0020inhibit,Melanocortin Receptor,COS-1,Inhibitor,MCL0020,MC Receptor,anorexia,dose-dependently,s
Potent and selective melanocortin MC4 receptor antagonist (IC50 values are 11.63, 1115 and > 10 000 nM at MC4, MC3 and MC1 receptors respectively). Significantly reverses stress-induced anorexia but has no effect on food intake in free-feeding rats. Exhibits anxiolytic-like activity in vivo.
价 格：￥电议型 号：TP1889产 地：中国大陆
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TN66602-Ethylhexyl trans-4-methoxycinnamate2Ethylhexyl trans4methoxycinnamate,2 Ethylhexyl trans 4 methoxy
2-Ethylhexyl trans-4-methoxycinnamate is a sunscreen agent.
价 格：￥电议型 号：TN6660产 地：中国大陆
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T11155Eg5 Inhibitor V, trans-24Eg5 Inhibitor V, trans 24,Eg-5 Inhibitor V, trans-24,Eg5 Inhibitor V, trans
Eg5 Inhibitor V, trans-24 is a specific and potent Eg5 inhibitor that can be used in cancer research with an IC50 value of 0.65 uM.
价 格：￥电议型 号：T11155产 地：中国大陆
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T14681BMS-935177BMS 935177,BMS935177
BMS-935177 is a reversible BTK inhibitor with IC50 value of 3 nM.
价 格：￥电议型 号：T14681产 地：中国大陆
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T37082HS271HS271,HS-271
HS271 is a selective, highly potent and orally active IRAK4 inhibitor (IC50= 7.2 μM). HS271 shows excellent enzymatic and cellular activities, as well as excellent pharmacokinetic properties.
价 格：￥电议型 号：T37082产 地：中国大陆
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T10643c-Fms-IN-1cFmsIN1,c Fms IN 1
c-Fms-IN-1 is an inhibitor of c-FMS kinase (IC50 = 0.8 nM).
价 格：￥电议型 号：T10643产 地：中国大陆
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TN7110Ginsenoside Rs2Ginsenoside Rs2,Ginsenoside Rs-2
Ginsenoside Rs2 is a natural product isolated from the leaves of Panax japonicus var..
价 格：￥电议型 号：TN7110产 地：中国大陆
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T7015Vps34-IN-1inhibit,Autophagy,Vps34IN1,PI3K,Vps-34-IN-1,Inhibitor,Phosphoinositide 3-kinase,Vps34 IN 1
Vps34-IN1 is a potent and highly selective Vps34 inhibitor with IC50 of 25 nM invitro, which does not significantly inhibit the isoforms of class I as well as class II PI3Ks.
价 格：￥电议型 号：T7015产 地：中国大陆
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T10775c-Fms-IN-2c Fms IN 2,cFmsIN2
c-Fms-IN-2 is an inhibitor of c-FMS kinase (IC50 = 24 nM).
价 格：￥电议型 号：T10775产 地：中国大陆
