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产品数：86101
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TJS03145,7-Dihydroxy-4-methylcoumarinBacterial,inhibit,Fungal,Inhibitor,5,7Dihydroxy4methylcoumarin,5,7 Dih
5,7-Dihydroxy-4-methylcoumarin inhibits human neutrophil oxidative metabolism and elastase activity. 5,7-Dihydroxy-4-methylcoumarin has in vitro platelet antiaggregatory property. 5,7-Dihydroxy-4-methylcoumarin shows inhibition of the cyclooxygenase pathway.
价 格：￥电议型 号：TJS0314产 地：中国大陆
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T9226CCG-143140CCG143140,CCG 143140
CCG-143140 is a GLP-1 receptor inverse agonists.
价 格：￥电议型 号：T9226产 地：中国大陆
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T6733WZ-3146EGFR,HER1,WZ-3146,Epidermal growth factor receptor,WZ 3146,ErbB-1,WZ3146,inhibit,Inhibitor
WZ3146 is a mutant-selective irreversible inhibitor of EGFR(L858R) and EGFR(E746_A750) with IC50 of 2 nM and 2 nM; does not inhibit ERBB2 phosphorylation (T798I).
价 格：￥电议型 号：T6733产 地：中国大陆
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T23889CID-663143CID 663143
CID-663143 inhibits cancer cell growth and shows microtubule-binding activity.
价 格：￥电议型 号：T23889产 地：中国大陆
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T8329AR 231453inhibit,GPR119,AR-231453,G Protein-Coupled Receptor 119,diabetes,AR231453,AR 231453,insulin
AR 231453 is a selective and orally available GPR119 agonist,can stimulate β-cell replication and improve islet graft function.
价 格：￥电议型 号：T8329产 地：中国大陆
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T25282CYM 50358 hydrochloride (1314212-39-9 free base)CYM 50358 hydrochloride (1314212 39 9 free base),CYM
CYM50358 HCl is an S1P4 antagonist.
价 格：￥电议型 号：T25282产 地：中国大陆
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T31425Dibenz[a,h]anthracene
Dibenz[a,h]anthracene has induced DNA damage and gene mutations in bacteria and gene mutations and transformation in several types of mammalian cell cultures.
价 格：￥电议型 号：T31425产 地：中国大陆
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T67844RBN-3143RBN3143
RBN-3143 is a potent and inhibitor of NAD+-competitive catalytic PARP14 (IC50= 4 nM). RBN-3143 inhibits ADP-ribosylation mediated by PARP14 and stabilizes PARP14 in cell lines. RBN-3143 exhibits research potential of lung inflammation.
价 格：￥电议型 号：T67844产 地：中国大陆
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T36200AZD 3147AZD 3147
AZD 3147 is an inhibitor of mTORC with IC50s of 40.7 and 5.75 nM for mTORC1 and mTORC2. AZD 3147 shows IC50s of 912, 5495, 9333, and 6310 nM for PI3Kα, PI3Kβ, PI3Kδ, and PI3Kγ, respectively.
价 格：￥电议型 号：T36200产 地：中国大陆
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T10314AM103
AM103 is an effective and selective inhibitor of FLAP (IC50 = 4.2 nM).
价 格：￥电议型 号：T10314产 地：中国大陆
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T8314RP-64477RP-64477,Diglyceride acyltransferase,RP 64477,inhibit,mono- acylglycerol acyltransferase,Acy
RP64477 is the cholesterol esterifying enzyme Acyl-coenzyme A:cholesterol O-acyltransferase (ACAT) inhibitor.
价 格：￥电议型 号：T8314产 地：中国大陆
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T23145PHA 543613PHA 543613 hydrochloride
PHA 543613 is a specific agonist of α7 nAChR (Ki = 8.8 nM) and can be used in studies about the cognitive deficits of Alzheimer´s disease and schizophrenia.
价 格：￥电议型 号：T23145产 地：中国大陆
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T7352PridopidineFR-310826,Dopamine Receptor,inhibit,Pridopidine,Inhibitor,ACR-16,ACR 16,ASP-2314,FR 31082
Pridopidine, a dopamine (DA) stabilizer, acts as a low affinity dopamine D2 receptor (D2R) antagonist, improves motor performance and shows neuroprotective effects in Huntington disease R6/2 mouse model.
价 格：￥电议型 号：T7352产 地：中国大陆
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T23143PG 01037 dihydrochloride
PG 01037 dihydrochloride is a potent and selective dopamine D3 receptor antagonist with a Ki of 0.7 nM.
价 格：￥电议型 号：T23143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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T9064LY3143921 hydrateLY-3143921 hydrate,LY3143921 hydrate
LY3143921 ((S)-Example 2) hydrate is an orally active CDC7 kinase inhibitor with broad in vitro anticancer activity [1].
价 格：￥电议型 号：T9064产 地：中国大陆
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T13314VTX-27Inhibitor,VTX27,VTX 27,PKC,Protein kinase C,inhibit,VTX-27
VTX-27 is a selective inhibitor of protein kinase C θ (PKC θ) (Kis: 0.08 nM and 16 nM for PKC θ and PKC δ).
价 格：￥电议型 号：T13314产 地：中国大陆
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T31488Dimethindene
Dimethindene is a selective antagonist of H1 receptor and blocks K+ current. Dimethindene exhibits antihistamine and anticholinergic effects.
价 格：￥电议型 号：T31488产 地：中国大陆
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T3148MK-571 sodiumMRP4,Lysophospholipid Receptor,human mast cells,LAD2,MK 571 sodium,MRP1,Leukotriene Rec
MK-571 is a selective, orally active antagonist of the CysLT1 receptor. MK571 is a multidrug resistance protein-2 (ABCC2, Mrp2) inhibitor used to demonstrate the role of Mrp2 in the cellular efflux of drugs, xenobiotics, and their conjugates. MK571 can inhibit the synthesis of K-4′-O-GlcA (19.7 μM). MK571 dose-dependently inhibits the intracellular biosynthesis of all flavonol sulphates and glucuronides by Caco-2 cells. MK571 significantly inhibits phase-2 conjugation of kaempferol by cell-free
价 格：￥电议型 号：T3148产 地：中国大陆
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T13140Umbralisib R-enantiomerUmbralisib Renantiomer,Umbralisib R enantiomer
Umbralisib R-enantiomer (TGR-1202 R-enantiomer) is an inhibitor of PI3Kδ, which is the less active enantiomer of TGR-1202.
价 格：￥电议型 号：T13140产 地：中国大陆
