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产品数：86101
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T7194CM-272DNMT1,anti-tumour,DNMTs,immunogenic,DNA MTases,CM272,DNMT3A,CM 272,G9a,H3K9me2,Inhibitor,epige
CM-272 is a dual G9a/DNA methyltransferases (DNMTs) inhibitor.
价 格：￥电议型 号：T7194产 地：中国大陆
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T7679UBCS039Autophagy,UBCS039,UBCS 039,inhibit,Sirtuin,Inhibitor,UBCS-039
UBCS039 is the first synthetic Sirt6 activator(EC50 : 38 μM)
价 格：￥电议型 号：T7679产 地：中国大陆
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TQ0097AGN 193109AGN193109,Autophagy,Inhibitor,Retinoic acid receptors,Retinoid X receptors,RAR/RXR,AGN 193
AGN 193109, a retinoid analog, is a potent and specific antagonist of RARs (Kds: 2 nM, 2 nM, and 3 nM for RARα, RARβ, and RARγ).
价 格：￥电议型 号：TQ0097产 地：中国大陆
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T7197Fadrozole(Rac)-FAD286,inhibit,Fadrozole,CGS 16949A,Inhibitor,Aromatase
Fadrozole is a nonsteroidal aromatase inhibitor with potential antineoplastic activity(IC50 : 6.4 nM)
价 格：￥电议型 号：T7197产 地：中国大陆
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T7378BRD9539Histone Methyltransferase,chromatin,PRC2,BRD9539,G9a,senescent,BRD-9539,BRD 9539,inhibit,H3K9
BRD9539 is an inhibitor of euchromatin histone methyltransferase 2 (EHMT2), also known as G9a, with an IC50 value of 6.3 μM
价 格：￥电议型 号：T7378产 地：中国大陆
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T7317CU-CPT-9aToll-like Receptor (TLR),inhibit,Inhibitor,CU CPT 9a,CUCPT9a
CU-CPT-9a is a potent TLR8 inhibitor (IC50 : 0.5 nM), that suppresses TLR8-mediated proinflammatory signaling in various cell lines and human primary cells-
价 格：￥电议型 号：T7317产 地：中国大陆
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TQ0232UNC0646H3K9me2,KMT1D,chromatin,EHMT1,Histone Methyltransferase,UNC-0646,SAR,inhibit,G9a,GLP,PKMT,UNC
UNC 0646 is a potent and selective inhibitor of the homologous protein lysine methyltransferases, G9a and GLP (IC50s: 6 nM/15 nM for G9a/GLP). UNC0646 potently blocks G9a/GLP methyltransferase activity in cells (IC50: 10 nM in MCF7 cells); exhibits low cellular toxicity (EC50: 4.7 μM in MCF7 cells).
价 格：￥电议型 号：TQ0232产 地：中国大陆
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T14087ABT-239ABT239,ABT 239
ABT-239 is a novel, highly efficacious, non-imidazole?class of H3R antagonist. Its a transient receptor potential vanilloid type 1 (TRPV1) antagonist.
价 格：￥电议型 号：T14087产 地：中国大陆
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T6757AMG319AMG-319,AMG 319,Inhibitor,inhibit,PI3K,AMG319,Phosphoinositide 3-kinase
AMG319 is a potent and selective PI3Kδ inhibitor with IC50 of 18 nM, >47-fold selectivity over other PI3Ks. Phase 2.
价 格：￥电议型 号：T6757产 地：中国大陆
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TQ0028EX229AMP-activated protein kinase,inhibit,EX 229,AMPK,Inhibitor,EX-229,EX229
EX229 is an allosteric activator of AMPK, with Kds of 0.06 μM, 0.06 μM and 0.51 μM for α1β1γ1, α2β1γ1, and α1β2γ1, respectively.
价 格：￥电议型 号：TQ0028产 地：中国大陆
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T9520ALC-0159ALC0159,conjugate,lipid,vaccine,ALC 0159,ALC-0159,inhibit,excipient,Inhibitor
ALC-0159 is a polyethylene glycol (PEG) lipid conjugate that could be used as a vaccine excipient[1].
价 格：￥电议型 号：T9520产 地：中国大陆
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T14090AC-55649AC55649,AC 55649
AC-55649 is a potent, highly isoform-selective agonist of human RARβ2 receptor, with a pEC50 of 6.9.
价 格：￥电议型 号：T14090产 地：中国大陆
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T9196IACS-13909antiproliferative,RTK,IACS13909,inhibit,SHP2,pMEK,anticancer,Inhibitor,MAPK,IACS 13909,pER
IACS-13909, a specific and potent allosteric inhibitor of SHP2, that suppresses signaling through the MAPK pathway.
价 格：￥电议型 号：T9196产 地：中国大陆
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T10341Antitumor agent-19Antitumor agent 19,Antitumor agent19
Antitumor agent-19 is a modulator of tumor-associated macrophages with EC50s of 17.18 μM and 18.87 μM in the RAW 264.7 cells and the BMDM cells.
价 格：￥电议型 号：T10341产 地：中国大陆
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T60065WAY-118959-AWAY 118959 A,WAY118959A
WAY-118959-A is a potential microtubule acetylation inhibitor.
价 格：￥电议型 号：T60065产 地：中国大陆
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T10316AN3199AN3199,AN-3199
AN3199 is a selective inhibitor of PDE4 with an IC50 of 94.5 nM.
价 格：￥电议型 号：T10316产 地：中国大陆
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T9966GSK-1520489AGSK1520489A,inhibit,GSK 1520489A,HT29,GSK-1520489A,Inhibitor,active protein kinase
GSK-1520489A is an active PKMYT1 inhibitor.
价 格：￥电议型 号：T9966产 地：中国大陆
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T7375A-836339A-836339,A 836339,Cannabinoid Receptor,A836339,inhibit,Inhibitor
A-836339 acts as a potent cannabinoid receptor full agonist which has a higher affinity for the peripheral CB2 receptor (Ki = 0.64 nM) over the central CB1 receptor (Ki = 270 nM). It displays analgesic, anti-inflammatory, and anti-hyperalgesic effects in mice.
价 格：￥电议型 号：T7375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
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