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T9786Lu AF27139Inhibitor,P2XRs,oral,P2X7,rodent-active,Lu AF 27139,CNS-penetrant,CNS,Lu AF27139,Lu AF-271
Lu AF27139 is an effective and selective antagonist of P2X7 receptor (IC50s of 12 and 2.4 nM for human and rat, Kis of 22, 54, and 13 nM for mouse, human, and rat, respectively). Lu AF27139 can be used in CNS diseases studies.
价 格：￥电议型 号：T9786产 地：中国大陆
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T9239RS-25344RS25344,RS 25344
RS-25344 is a potent and selective phosphodiesterase (PDE) 4 inhibitor. It inhibits eosinophil chemotaxis and increases progressive motility of spermatozoa in vitro.
价 格：￥电议型 号：T9239产 地：中国大陆
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TN3669Cis-N-FeruloyltyramineCis N Feruloyltyramine,CisNFeruloyltyramine
Cis-N-Feruloyltyramine shows cytotoxicity against the P-388 cancer cell line. N-cis-Feruloyltyramine and N-trans-Feruloyltyramine are the inhibitors of in vitro prostaglandin (PG) synthesis.
价 格：￥电议型 号：TN3669产 地：中国大陆
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T8851I3MT-3EA.hy926 cells,Hippo (MST),inhibit,I3MT-3,3MST,HEK293,I3MT3,cell-membrane,COS-7,I-3MT-3,I3MT 3
I3MT-3 (HMPSNE) is a potent, selective and cell membrane permeability inhibitor of 3-mercaptopyruvate sulfur transferase (3MST), which targets the persulfated cysteine residues located at the active site of 3MST.
价 格：￥电议型 号：T8851产 地：中国大陆
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T9073SRS16-86IRI,SRS16-86,Inhibitor,ferrostatin,SRS-16-86,ischemia-reperfusion injury,SCI,spinal cord inj
SRS16-86 is a novel third-generation ferrostatin, is an inhibitor of?ferroptosis.
价 格：￥电议型 号：T9073产 地：中国大陆
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TN2282trans-Stilbenetrans Stilbene,inhibit,transStilbene,trans-Stilbene,Inhibitor
trans-Stilbene is a natural product used in the manufacture of dye lasers, optical brighteners, and non-steroidal synthetic estrogens.
价 格：￥电议型 号：TN2282产 地：中国大陆
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T6729LomibuvirRdRp,Lomibuvir,cis-Lomibuvir,cis-isomer,DNA/RNA Synthesis,HCV,inhibit,Inhibitor,non-nucleos
Lomibuvir (VX-222) is a selective, non-nucleoside allosteric inhibitor of HCV NS5B polymerase (RdRp) with a Kd of 17 nM. Lomibuvir inhibits the 1b/Con1 HCV subgenomic replicon with an EC 50 of 5.2 nM. Lomibuvir preferentially inhibits elongative RNA synthesis rather than de novo -initiated RNA synthesis [1].
价 格：￥电议型 号：T6729产 地：中国大陆
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T12821S1PR1 modulator 1S-1PR1 modulator 1,S1PR1 modulator 1,inhibit,LPL Receptor,Lysophospholipid Receptor
S1PR1 modulator 1 is a selective inhibitor of S1PR1 with a pIC50 of 7.6.
价 格：￥电议型 号：T12821产 地：中国大陆
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T6901N6022N6022,Inhibitor,inhibit,N 6022,S-nitrosoglutathione reductase,N-6022,GSNOR
N6022(IC50 of 8 nM) is an effective, reversible, and selective S-Nitrosoglutathione reductase(GSNOR) inhibitor.
价 格：￥电议型 号：T6901产 地：中国大陆
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T6609NMS-E973NMS-E973,Leukemia,NMS E973,inhibit,HSP,Heat shock proteins,Adenocarcinoma,Hsp90α,ovary,colon
NMS-E973 is a potent and selective Hsp90 inhibitor with DC50 of <10 nM for Hsp90 binding, no activiy against a panel of 52 diverse protein kinases.
价 格：￥电议型 号：T6609产 地：中国大陆
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T67783trans-isrib A17
trans-isrib A17 is an potent inhibitor of the integrated stress response with EC50 of 0.6 nM.
价 格：￥电议型 号：T67783产 地：中国大陆
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T62209HS-276
HS-276 is an orally active, potent and highly selective TAK1 inhibitor (Ki= 2.5 nM). HS-276 exhibits significant inhibition of TAK1, CLK2, GCK, ULK2, MAP4K5, IRAK1, NUAK, CSNK1G2, CAMKKβ-1, and MLK1, with IC50 values of 8.25, 29, 33, 63, 125, 264, 270, 810, 1280, and 5585 nM, respectively. HS-276 exhibits research potential for rheumatoid arthritis (RA) research.
价 格：￥电议型 号：T62209产 地：中国大陆
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T60220ROS kinases-IN-1ROSkinasesIN1
ROS kinases-IN-1 is a ROS tyrosine kinase inhibitor with IC50 value of 1.22 μM. ROS kinases-IN-1 shows anti-tumor activity.
价 格：￥电议型 号：T60220产 地：中国大陆
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T8688(Rac)-X77SARS-CoV,(Rac)-X77,protease,SARS coronavirus,inhibit,Inhibitor,(Rac) X77,(Rac)-X-77,coronav
CPD77 is a potent SARS- CoV- 2 main protease inhibitor.
价 格：￥电议型 号：T8688产 地：中国大陆
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T8378AS2863619Cyclin dependent kinase,AS2863619,STAT,AS 2863619,Inhibitor,inhibit,CDK,AS-2863619
AS2863619 is an orally active inhibitor of cyclin-dependent kinase 8 (CDK8) and CDK19 (IC50s of 0.61 nM and 4.28 nM, respectively).
价 格：￥电议型 号：T8378产 地：中国大陆
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TN7028Picras-3-en-16-one, 11,20-epoxy-2-(β-D-glucopyranosyloxy)-1,11,12,14,15-pentahydroxy-, (1β,2α,11β,12
Picras-3-en-16-one, 11,20-epoxy-2-(β-D-glucopyranosyloxy)-1,11,12,14,15-pentahydroxy-, (1β,2α,11β,12α,15β)- is a chemical compound.
价 格：￥电议型 号：TN7028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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T7787BMS817378BMS817378,BMS-817378
BMS817378 is a potent and selective inhibitor of MET(IC50 : 1.7 nM).
价 格：￥电议型 号：T7787产 地：中国大陆
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T22119NS3694NS 3694,Inhibitor,Apaf-1,Apoptosis,inhibit,caspase-9,NS-3694,apoptosome inhibitor,NS3694,cytoc
NS3694 is an inhibitor of apoptosis and inhibits apoptosome formation and caspase activation.
价 格：￥电议型 号：T22119产 地：中国大陆
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T7938QuinidineMES-SA,Inhibitor,CYPs,Potassium Channel,Parasite,Cytochrome P450,MESSA/DX5,Apoptosis,oral a
Quinidine is a stereoisomer of the antimalarial agent quinine and a class Ia antiarrhythmic agent. for the treatment of abnormal heart rhythms and also malaria.
价 格：￥电议型 号：T7938产 地：中国大陆
