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产品数：86101
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T7323BCI-215specificity,Phosphatase,DUSP-MKP,inhibit,Inhibitor,MAPK,BCI-215,BCI215,BCI 215,dual
BCI-215 causes selective cancer cell cytotoxicity in part through non-redox-mediated activation of MAPK signaling
价 格：￥电议型 号：T7323产 地：中国大陆
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T6738Z-FA-FMKSARS coronavirus,SARS-CoV,RRMs,DNA fragmentation,DEVDase,Caspase,Cathepsin,Inhibitor,externa
Z-FA-FMK can irreversibly inhibit cysteine protease and also inhibit effector caspases.
价 格：￥电议型 号：T6738产 地：中国大陆
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T7112Ibutamoren MesylateMK 0677,MK 677,Inhibitor,Ibutamoren,MK677,inhibit,Ibutamoren Mesylate,Growth horm
Ibutamoren Mesylate is a potent, non-peptide Growth hormone secretagogue receptor (GHSR) agonist.
价 格：￥电议型 号：T7112产 地：中国大陆
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TQ0286MK-0557MK0557,Neuropeptide Y Receptor,inhibit,MK 0557,Inhibitor,NPY receptor,MK-0557
MK-0557 is a selective and orally available antagonist of the neuropeptide Y5 receptor (Ki: 1.6 nM).
价 格：￥电议型 号：TQ0286产 地：中国大陆
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TP1466Z-YVAD-FMKCaspase 4,Inhibitor,Anti-inflammatory,ZYVADFMK,Caspase 1,Z YVAD FMK,Caspase,inhibit,anti-t
AA-Z-YVAD-FMK is a Irreversible caspase-1 inhibitor,with anti-inflammatory and anti-tumor activities.
价 格：￥电议型 号：TP1466产 地：中国大陆
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T6891MK-4101Apoptosis,inhibit,MK4101,Smoothened,MK-4101,MK 4101,Hedgehog,Inhibitor,Smo
MK-4101, an effective inhibitor of the Hedgehog pathway, has anti-tumor activity through the induction of extensive apoptosis and inhibition of proliferation in tumor cells.
价 格：￥电议型 号：T6891产 地：中国大陆
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T9034MK2-IN-3MAPK activated protein kinase 2,Mitogen-activated protein kinase activated protein kinase 2,
MK2-IN-3 is a potent, cell-permeable inhibitor of mitogen-activated protein kinase-activated protein kinase 2 (MAPKAP-K2 or MK-2) and can be used for the treatment of rheumatoid arthritis
价 格：￥电议型 号：T9034产 地：中国大陆
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T41345AFMK
AFMK is an active metabolite of Melatonin with antioxidant and free radical scavenging activity. AFMK is a modulator of apoptosis and improves the anti-tumor effect of Gemcitabine in PANC-1 cells.
价 格：￥电议型 号：T41345产 地：中国大陆
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T7130Navarixininhibit,CXC chemokine receptors,Inhibitor,MK 7123,Navarixin,SCH527123,SCH-527123,MK7123,CXC
Navarixin(SCH527123) is a novel, selective CXC chemokine receptor 2(CXCR2) antagonist that inhibits neutrophil activation and modulates neutrophil trafficking in animal models, characteristics that may be beneficial in the treatment of conditions with unbalanced pulmonary neutrophilia.
价 格：￥电议型 号：T7130产 地：中国大陆
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TQ0101MKC3946Inositol requiring enzyme 1,inhibit,IRE1,MKC3946,Inhibitor,MKC 3946,MKC-3946
MKC3946 is an effective and soluble IRE1α inhibitor which triggered modest growth inhibition in multiple myeloma cell lines.
价 格：￥电议型 号：TQ0101产 地：中国大陆
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T7020Z-VAD-FMKinhibit,Inhibitor,ZVADFMK,Hela,Z VAD FMK,Caspase,Antiapoptosis,cells,pan-caspase
Z-VAD-FMK (Caspase Inhibitor VI) is an irreversible pan-caspase inhibitor.
价 格：￥电议型 号：T7020产 地：中国大陆
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T7011Verubecestatorally,Beta-secretase,β-Secretase,inhibit,Aβ40,BACE1,MK8931,Alzheimer’s,BACE,Inhibitor,M
Verubecestat (MK-8931) is an effective and specific β-secretase inhibitor and β-site APP-cleaving enzyme 1 inhibitor or BACE1 protein inhibitor.
价 格：￥电议型 号：T7011产 地：中国大陆
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T7841MK 571MK 571
MK 571 is an orally active antagonist of CysLT1 receptor .
价 格：￥电议型 号：T7841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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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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TP1891L1MMK 1 acetateMMK 1 acetate
MMK1 is an agonist of formyl peptide receptor 2 (FPR2), which was previously known as formyl peptide receptor-like 1 (FPRL1) [1].
价 格：￥电议型 号：TP1891L1产 地：中国大陆
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T9497Niraparib tosylate monohyrateNiraparib tosylate,Apoptosis,cancer,MK-4827 tosylate,inhibit,breast,PAR
Niraparib, also know as MK-4827, is an inhibitor of poly (ADP-ribose) polymerase (PARP) with potential antineoplastic activity. MK4827 inhibits PARP activity, enhancing the accumulation of DNA strand breaks and promoting genomic instability and apoptosis. The PARP family of proteins detect and repair single strand DNA breaks by the base-excision repair (BER) pathway.
价 格：￥电议型 号：T9497产 地：中国大陆
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T7591ColuracetamInhibitor,iGluR,inhibit,MKC 231,Coluracetam,MKC231,Ionotropic glutamate receptors
Coluracetam(MKC-231) is a Choline Uptake Enhancer.
价 格：￥电议型 号：T7591产 地：中国大陆
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T6352(-)-Dizocilpine maleate(-)-MK 801 (Maleate)；C13737；(-)-MK 801 Maleate；(-)-MK 801马来酸
MK-801 is a potent, selective and non-competitive NMDA receptor antagonist with Kd of 37.2 nM in rat brain membranes.
价 格：￥电议型 号：T6352产 地：中国大陆
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T6340Enalaprilat Dihydrate依那普利拉二水合物；MK-422 Dihydrate；MK-422
Enalaprilat（IC50=1.94 nM） is a potent angiotensin-converting enzyme (ACE) inhibitor.
价 格：￥电议型 号：T6340产 地：中国大陆
