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T9194UMB298UMB-298,UMB298,inhibit,MOLM13,Inhibitor,bromodomain,UMB 298,selective,potent,Epigenetic Reader
UMB298 is a potent and selective CBP/P300 bromodomain inhibitor. UMB298 inhibits BRD4 with IC50 of 5193nM.
价 格：￥电议型 号：T9194产 地：中国大陆
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T8295Sclareol glycolSclareol glycol,Inhibitor,Precursor,20624,ambroxide,Hyphozyma,inhibit,ATCC,roseonigra
Sclareol glycol is the precursor of ambroxide.
价 格：￥电议型 号：T8295产 地：中国大陆
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T80291-Methylpyrrolidine1Methylpyrrolidine,1 Methylpyrrolidine,Inhibitor,inhibit,1-Methylpyrrolidine
1-Methylpyrrolidine is extensively used in the synthesis of pyrrolidine based ionic liquids.
价 格：￥电议型 号：T8029产 地：中国大陆
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T22947LY266097 hydrochlorideLY-266097 hydrochloride,LY266097 hydrochloride
LY266097 hydrochloride is an antagonist of 5-HT2 with pKis of 7.7, 9.8, and 7.6 for human 5-HT2A, 5-HT2B, and 5-HT2C and can be used in studies about depression.
价 格：￥电议型 号：T22947产 地：中国大陆
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TN7029(2S)-1-O-p-coumaroyl-2-O-acetyl-3-O-β-D-glucopyranosylglycerol(2S)1Opcoumaroyl2Oacetyl3OβDglucopyran
(2S)-1-O-p-coumaroyl-2-O-acetyl-3-O-β-D-glucopyranosylglycerol is a chemical compound.
价 格：￥电议型 号：TN7029产 地：中国大陆
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T41291MS-PPOHMS PPOH,MSPPOH
MS-PPOH is a potent and selective inhibitor of cytochrome P450 (CYP) epoxygenase. MS-PPOH inhibits CYP2C8 and CYP2C9 with IC50s of 15 and 11 ?M, respectively
价 格：￥电议型 号：T41291产 地：中国大陆
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TP1217LAutocamtide 2 TFA(129198-88-5 free base)Autocamtide 2 TFA(129198885 free base),Autocamtide 2 TFA(129
Autocamtide 2 TFA is a highly selective peptide substrate of calcium/calmodulin-dependent protein kinase II (CaMKII). Autocamtide 2 TFA can be used in the CaMKII activity assay.
价 格：￥电议型 号：TP1217L产 地：中国大陆
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T9629WAY-309060Inhibitor,WAY309060,MCF7,BRD4 Inhibitor-24,antitumor,Epigenetic Reader Domain,inhibit,brea
WAY-309060 is a BRD4 small molecule inhibitor with antitumor activity.
价 格：￥电议型 号：T9629产 地：中国大陆
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T27629ISAM-140ISAM 140
ISAM-140 is a potent and highly selective antagonist of A2B adenosine receptor.
价 格：￥电议型 号：T27629产 地：中国大陆
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TP2314Tripeptide-1 Acetate（72957-37-0，free）Tripeptide1 Acetate（72957370，free）,Tripeptide 1 Acetate（72957 3
Tripeptide-1 Acetate is a biologically active peptide
价 格：￥电议型 号：TP2314产 地：中国大陆
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TN10253,29-O-Dibenzoyloxykarounidiolvirus,promoters,early,chemopreventive,inhibit,3,29 O Dibenzoyloxykarou
3,29-O-Dibenzoyloxykarounidiol is a natural product with regulate blood sugar level, has potent inhibitory effects on Epstein-Barr virus early antigen (EBV-EA) induced by tumor promoter 12-O-tetradecanoylphorbol-13-acetate (TPA).
价 格：￥电议型 号：TN1025产 地：中国大陆
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TP13782-Furoyl-LIGRLO-amide TFA(729589-58-6 free base)2 Furoyl LIGRLO amide TFA(729589 58 6 free base),2Fu
2-Furoyl-LIGRLO-amide is a potent and selective protease-activated receptor 2 (PAR2) agonist.
价 格：￥电议型 号：TP1378产 地：中国大陆
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T7394Toceranib PhosphateSU11654,inhibit,SU-11654,Toceranib,Toceranib Phosphate,VEGFR,PHA 291639E,Platelet
Toceranib phosphate, is a selective inhibitor of the tyrosine kinase activity of several members of the split kinase RTK family, including Flk-1/KDR, PDGFR
价 格：￥电议型 号：T7394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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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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T7829FK962Alzheimer,somatostatin,FK-962,FK 962,inhibit,FK962,Inhibitor,cognitive
FK962 is an somatostatin release enhancer , exerts cognitive-enhancing actions.
价 格：￥电议型 号：T7829产 地：中国大陆
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T37042SCH529074
SCH529074 is a selective activator of p53 (Ki = 1 μM) and can be used in studies about non-small-cell lung carcinoma. SCH529074 restores mutant p53 function and interrupts HDM2-mediated ubiquitination of wild Type p53.
价 格：￥电议型 号：T37042产 地：中国大陆
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T6629PYR-41E3 ligating enzyme,E1 activating enzyme,E1/E2/E3 Enzyme,Inhibitor,PYR-41,Ubiquitin conjugating
PYR-41 is the first cell-permeable inhibitor of ubiquitin-activating enzyme E1, with no activity at E2.
价 格：￥电议型 号：T6629产 地：中国大陆
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T40229SR-0813SR0813,SR 0813
SR-0813 is a potent and selective ENL/AF9 YEATS domain inhibitor. SR-0813 has IC 50 and EC 50 values of 25 nM and 205 nM for ENL YEATS domain, respectively. SR-0813 has IC 50 and EC 50 values of 311 nM and 76 nM (CETSA) for AF9 YEATS domain, respectively. SR-0813 binds MAP3K19 with over 100-fold lower affinity ( K d =3.5 μM) than ENL YEATS ( K d =30 nM). SR-0813 can be used for the research of acute leukemia.
价 格：￥电议型 号：T40229产 地：中国大陆
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T16401Org-12962Org 12962,Org12962
Org-12962 is an effective and selective 5-HT2C?receptor agonist pEC50: 7.01). Org-12962 shows antiaversive effects in a rat model of panic-like anxiety. Org-12962 also shows high effacy for the 5-HT2A?and 5-HT2B receptors (pEC50s: 6.38 and 6.28, respectively).
价 格：￥电议型 号：T16401产 地：中国大陆
