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产品数：86101
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T6908NSC 228155Epidermal growth factor receptor,Histone Acetyltransferase,EGFR,HER1,HATs,inhibit,Inhibito
NSC228155 is an activator of EGFR, binding to the sEGFR dimerization domain II and modulate EGFR tyrosine phosphorylation.
价 格：￥电议型 号：T6908产 地：中国大陆
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T7083GLPG1837GLPG-1837,ABBV 974,Cystic fibrosis transmembrane conductance regulator,Inhibitor,CFTR,Autoph
GLPG1837 is an effective CFTR potentiator, with EC50s of 3 nM and 339 nM for F508del and G551D CFTR, respectively.
价 格：￥电议型 号：T7083产 地：中国大陆
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TN1118Tormentic aciddiabetes,transporter,glucose,Tormentic acid,phosphorylation,RAW 264.7,inhibit,Inhibito
Tormentic acid is a natural product. It has anticancer, anti-inflammatory, anti-atherogenic , anti-allodynic, and hepatoprotective properties,
价 格：￥电议型 号：TN1118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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TN1417Azadirachtinpest,inhibit,cytoskeleton,cellular,transduction,signal,insecticides,Apoptosis,Azadiracht
Azadirachtin has antifungal activity, used as an insecticide.
价 格：￥电议型 号：TN1417产 地：中国大陆
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T12218NFAT Transcription Factor Regulator-1NFAT Transcription Factor Regulator 1,NFAT Transcription Factor
NFAT Transcription Factor Regulator-1 is an synthesis inhibitor of IL-2 (IC50 of 182 nM).
价 格：￥电议型 号：T12218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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T7123AMG-47aInhibitor,signal,kinases,AMG 47a,JAK,Janus kinase,AMG-47a,transduction,Src,VEGFR,cytoplamic,p
AMG-47a is a potent inhibitor of Lck and T cell proliferation. AMG-47a could promote the degradation of the KRAS oncoprotein. AMG-47a selectively reduced the levels of EGFP-KRASG12V protein but did not affect EGFP protein in cells.
价 格：￥电议型 号：T7123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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T4074GSK-872translocation,GSK-872,neurological,HMGB1,Receptor-interacting protein kinases,brain,GSK 872,c
GSK872 (GSK2399872A) is an effective and specific RIP3 kinase inhibitor. It binds RIP3 kinase domain with high affinity (IC50: 1.8 nM) and inhibits kinase activity (IC50: 1.3 nM).
价 格：￥电议型 号：T4074产 地：中国大陆
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T7430AM-0902Transient receptor potential channels,TRP Channel,AM 0902,AM-0902,Inhibitor,inhibit,AM0902
AM-0902 is a potent and specific TRPA1 antagonist (IC50s: 71/131 nM for rTRPA1 and hTRPA1).
价 格：￥电议型 号：T7430产 地：中国大陆
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TCS0102PulegoneEndogenous Metabolite,Transient receptor potential channels,TRP Channel,Pulegone,Inhibitor,i
1. Pulegone has cytotoxicity followed by regenerative cell proliferation is the MOA for Pulegone-induced urothelial tumors in female rats. 2. Pulegone induces a verapamil-sensitive psychostimulant effect that appears to independ on the opening of L-type calcium channels. 3. Pulegone has negative reinforcing properties and seems to possess anxiolytic-like actions unrelated to the benzodiazepine site of the γ-aminobutyric acid type A (GABAA) receptor.
价 格：￥电议型 号：TCS0102产 地：中国大陆
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T6788Bitopertininhibit,Bitopertin,RG 1678,RO-4917838,RG-1678,GlyT,Inhibitor,RO 4917838,Glycine transporte
Bitopertin (RG1678, RO-4917838) is a potent inhibitor of glycine transporter 1 (GlyT1), with Ki of 8.1 nM for human hGlyT1b and IC50 of 22-25 nM in Chinese hamster ovary cells.
价 格：￥电议型 号：T6788产 地：中国大陆
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T21807INCA-6factors,inhibit,INCA-6,NFAT,microvascular,INCA 6,transcription,endothelial,Inhibitor,retinopat
INCA-6 is a cell-permeable NFAT inhibitor. INCA-6 inhibits of CN-NFAT signaling by targeting of NFAT(P) substrate to the calcineurin (CN) phosphatase site.
价 格：￥电议型 号：T21807产 地：中国大陆
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T6668SGC-CBP30inhibit,IL-17A,HAT,HATs,BRD,Histone Acetyltransferase,ankylosing,SGCCBP30,cells,epigenetic,
SGC-CBP30 is an effective CREBBP/EP300 inhibitor (IC50: 21/38 nM).
价 格：￥电议型 号：T6668产 地：中国大陆
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TN2081Maohuoside Aorally,MAPK,osteogenesis,Maohuoside A,inhibit,Transforming growth factor beta receptors,
Maohuoside A promotes osteogenesis of rat mesenchymal stem cells via BMP and MAPK signaling pathways.
价 格：￥电议型 号：TN2081产 地：中国大陆
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T88684BP-TQS4BP TQS,allosteric agonist,transmembrane site,Inhibitor,α7 nAChR,inhibit,Nicotinic acetylchol
4BP-TQS is an allosteric agonist of α7 nAChRs.
价 格：￥电议型 号：T8868产 地：中国大陆
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T6848GSK1016790Ainhibit,Ca2+ channels,Inhibitor,embryonic,GSK-1016790A,Ca channels,HEK,vanilloid,transien
GSK1016790A (GSK101) is a novel, potent activator of TRPV4 (transient receptor potential vanilloid 4) with EC50 of 34 nM in choroid plexus epithelial cells.
价 格：￥电议型 号：T6848产 地：中国大陆
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T8890653-47 hydrochlorideInhibitor,transcription,65347 hydrochloride,Epigenetic Reader Domain,inhibit,CRE
653-47 hydrochloride is a potentiator, significantly potentiates the cAMP-response element binding protein (CREB) inhibitory activity of 666-15. It is also a very weak CREB inhibitor with IC50 of 26.3 μM.
价 格：￥电议型 号：T8890产 地：中国大陆
