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T8439Clobenpropit dihydrobromideApoptosis,inhibit,Clobenpropit dihydrobromide,histamine H3R,antagonist,in
Clobenpropit dihydrobromide is a potent antagonist and inverse agonist of histamine H3R (histamine H3LR,pEC50 of 8.07)
价 格：￥电议型 号：T8439产 地：中国大陆
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T8952bis(p-methoxyphenyl)iodonium bromidebis(pmethoxyphenyl)iodonium bromide,bis(p methoxyphenyl)iodonium
bis(p-methoxyphenyl)iodonium bromide is a chemical compound.
价 格：￥电议型 号：T8952产 地：中国大陆
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T4172Methoxy-PMS1-Methoxyphenazine,Methoxy PMS,MethoxyPMS,Methoxy-PMS,Reactive Oxygen Species,inhibit,Inh
1-Methoxy PMS is stable electron-transport mediator between NAD(P)H and tetrazolium dyes, can induce active oxygen formation.
价 格：￥电议型 号：T4172产 地：中国大陆
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T6457CTEPMetabotropic glutamate receptors,CTEP,RO4956371,inhibit,mGluR,Inhibitor,RO-4956371
CTEP (RO4956371) is a novel, long-acting, orally bioavailable allosteric antagonist of mGlu5 receptor with IC50 of 2.2 nM, shows >1000-fold selectivity over other mGlu receptors.
价 格：￥电议型 号：T6457产 地：中国大陆
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T9681MAK-683 hydrochlorideEED inhibitor,MAK 683 hyrochloride,embryonic ectoderm development,Histone Methy
MAK683 hydrochloride is an inhibitor of embryonic ectoderm development (EED) (patent US20160176882 A1, compound example 2). MAK683 exhibits IC50s of 59, 26, 89 nM in EED Alphascreen binding, ELISA and LC-MS assay.
价 格：￥电议型 号：T9681产 地：中国大陆
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T9048EcamsuleEcamsule,adiation,dimer,benzylidene camphor derivative,inhibit,Inhibitor,UVA filter,PMLE,pyr
Ecamsule is a benzylidene camphor derivative, many of which are known for their excellent photostability. Ecamsule is an organic compound which is added to many sunscreens to filter out UVA rays.
价 格：￥电议型 号：T9048产 地：中国大陆
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TP2334PMX 53 acetate(219639-75-5 free base)PMX 53 acetate(219639755 free base),PMX 53 acetate(219639 75 5
PMX-53 is a potent and orally active CD88 (C5aR) antagonist (IC50: 20 nM) and inhibits C5a-induced neutrophil myeloperoxidase release and chemotaxis with IC50 values of 22 nM and 75 nM, respectively. PMX-53 is also an agonist of Mas-related gene 2 (MrgX2).
价 格：￥电议型 号：TP2334产 地：中国大陆
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T6598MPEPMetabotropic glutamate receptors,inhibit,MPEP,mGluR,Inhibitor
MPEP is a selective mGlu5 receptor antagonist with IC50 of 36 nM, exhibits no appreciable activity at mGlu1b/2/3/4a/7b/8a/6 receptors.
价 格：￥电议型 号：T6598产 地：中国大陆
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T9229Pim-1/2 kinase inhibitor 12,4 Thiazolidinedione, 5 p methoxybenzylidene ,2,4Thiazolidinedione, 5pmet
Pim-1/2 kinase inhibitor 1 is an orally active pim-1/2 kinase inhibitor. Pim-1/2 kinase inhibitor 1 blocks the ability of Pim kinases to phosphorylate peptides, and inhibits the pim protein kinase directed phosphorylation of 4E-BP1 and p27 Kip1. Pim-1/2 kinase inhibitor 1 can be used in the cancer research, especially prostate cancer [1].
价 格：￥电议型 号：T9229产 地：中国大陆
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T9776TRPM4 inhibitor 8hippocampal neurons,Ionotropic glutamate receptors,ERK,Inhibitor,neuroprotective ac
TRPM4 inhibitor 8 is an inhibitor of Transient receptor potential melastatin 4(TRPM4) which contributes to viability, migration, cell cycle shift, and adhesion.
价 格：￥电议型 号：T9776产 地：中国大陆
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T9709TRPM8 antagonist 3TRPM8 antagonist 3,TRP Channel,Transient receptor potential channels,inhibit,TRPM-
TRPM8 antagonist 3 is a blocker of TRPM8 (IC50 = 11 nM).
价 格：￥电议型 号：T9709产 地：中国大陆
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T9615CK7Inhibitor,Nek1,CDK,CK-7,Cdk9,CK 7,kidney development,CK7,inhibit,Cyclin dependent kinase,Cdk2
CK7, a?Cdk2/9?inhibitor, can be used for the synthesis of Nek1 inhibitor BSc5231 and BSc5367.
价 格：￥电议型 号：T9615产 地：中国大陆
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T9104TJ191cancer,TJ 191,Apoptosis,PMBC,MOLT-3,CEM,inhibit,C8166,Inhibitor,MOLT-4,MT-2,TJ191,HSB-2,TJ-191,
TJ191 is a selective anti-cancer agent, targeting low TβRIII-expressing malignant T-cell leukemia/lymphoma cells.
价 格：￥电议型 号：T9104产 地：中国大陆
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T8416Capmatinib xHClApoptosis,c-Met/HGFR,ATP competitive,inhibit,INC-280,Inhibitor,Capmatinib,SNU-5,INCB-
Capmatinib xHCl is a potent, orally active, selective, and ATP competitive c-Met kinase inhibitor, potently blocking in vitro kinase activity (IC50 = 0.13 nM) as well as constitutive or HGF-stimulated activity in cells (IC50 values range from 0.3 to 1.1 nM).
价 格：￥电议型 号：T8416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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TN31315-O-Cinnamoylquinic acidstable blue solution,isomer,blue sepal-color development,5OCinnamoylquinic a
5-O-Cinnamoylquinic acid is a nature product.
价 格：￥电议型 号：TN3131产 地：中国大陆
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T36683VedaprofenVedaprofen,Inhibitor,nonsteroidal,PM150,PM-150,Escherichia coli,inhibit,CERM-10202,CERM102
Vedaprofen inhibits COX-1 and reduces prostaglandin H2 synthesis with anti-inflammatory activities. Vedaprofen is an inhibitor of Escherichia coli sliding clamp with the IC50 of 222 μM and Ki of 131 μM.
价 格：￥电议型 号：T36683产 地：中国大陆
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T8825Capmatinib 2HCl.H2OS114,SNU-5,ATP competitive,Balb/c nu/nu mice,U-87MG,INCB-28060 dihydrochloride,or
Capmatinib 2HCl.H2O is an orally bioavailable inhibitor of the proto-oncogene c-Met (HGFR)with potential antineoplastic activity.
价 格：￥电议型 号：T8825产 地：中国大陆
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T9419FesoterodineDesfesoterodine,Fesoterodine,OAB,muscarinic,overactive,Inhibitor,SPM7605,mAChR,orally,5-
Fesoterodine is an orally active, competitive mAChR antagonist with pKi values of 8.0, 7.7, 7.4, 7.3, 7.5 for M1, M2, M3, M4, M5 receptors, respectively. It is used for the overactive bladder (OAB).
价 格：￥电议型 号：T9419产 地：中国大陆
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T9245TRPM4-IN-1TRP Channel,Transient receptor potential channels,non-selective,TRPM4IN1,diseases,TRPM4,in
TRPM4-IN-1 is a potent and selective inhibitor of TRPM4 with an IC50 of 1.5 μM.
价 格：￥电议型 号：T9245产 地：中国大陆
