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T6767TCS7010Aurora Kinase,inhibit,TCS 7010,Apoptosis,TCS-7010,TCS7010,Inhibitor
Aurora A Inhibitor I is a novel, potent, and selective inhibitor of Aurora A with IC50 of 3.4 nM in a cell-free assay. It is 1000-fold more selective for Aurora A than Aurora B.
价 格：￥电议型 号：T6767产 地：中国大陆
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T24905TT01001
TT01001 is a selective agonist of mitoNEET and reduces oxidative stress injury and neuronal apoptosis by improving mitochondrial dysfunction. TT01001 can be used in studies about the treatment of type II diabetes.
价 格：￥电议型 号：T24905产 地：中国大陆
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T6S1010Allomatrinealkaloid,antinociceptive,κ-opioid,Allomatrine,receptors,inhibit,(+)-Allomatrine,Inhibitor
Allomatrine is a natural product from Sophora alopecuroides L. Allomatrine, when given i.c.v., may stimulate the descending dynorphinergic neuron, resulting in the stimulation of KORs in the spinal cord.
价 格：￥电议型 号：T6S1010产 地：中国大陆
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T6S0105PeiminineInhibitor,inhibit,Peiminine,Autophagy
1. Peiminine is an effective inhibitor for lung inflammation and pulmonary fibrosis in a rat model of bleomycin-induced lung injury.
价 格：￥电议型 号：T6S0105产 地：中国大陆
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TCS0102PulegoneEndogenous Metabolite,Transient receptor potential channels,TRP Channel,Pulegone,Inhibitor,i
1. Pulegone has cytotoxicity followed by regenerative cell proliferation is the MOA for Pulegone-induced urothelial tumors in female rats. 2. Pulegone induces a verapamil-sensitive psychostimulant effect that appears to independ on the opening of L-type calcium channels. 3. Pulegone has negative reinforcing properties and seems to possess anxiolytic-like actions unrelated to the benzodiazepine site of the γ-aminobutyric acid type A (GABAA) receptor.
价 格：￥电议型 号：TCS0102产 地：中国大陆
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TQ0289LY450108Inhibitor,inhibit,AMPA,Parkinson’s,LY 450108,depression,iGluR,LY-450108,LY450108,Ionotropic
LY450108 is a potentiator of the AMPA receptor that can be used in Parkinson´s disease studies.
价 格：￥电议型 号：TQ0289产 地：中国大陆
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TL0010CONIFERYL ALCOHOLinhibit,CONIFERYL ALCOHOL,Fungal,Inhibitor,Endogenous Metabolite
Coniferyl alcohol is a fungal growth inhibitor.
价 格：￥电议型 号：TL0010产 地：中国大陆
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T36010p38 MAPK Inhibitorp-38 MAPK Inhibitor,p38 MAPK Inhibitor
p38 MAPK inhibitor is a potent inhibitor of p38 MAP kinase (IC50 = 35 nM). It inhibits senescence induced by the oncogene RAS.
价 格：￥电议型 号：T36010产 地：中国大陆
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T23010MNI 137MNI 137
MNI 137 is a negative allosteric modulator of mGlu2. MNI 137 inhibits glutamate-induced calcium mobilization with IC50s of 8.3 and 12.6 nM for human and rat.
价 格：￥电议型 号：T23010产 地：中国大陆
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T9765TJ-M2010-5ischemia,MIRI,Anoxia,factor,MyD88,injury,reoxygenation,inhibit,reperfusion,differentiation
TJ-M2010-5 is a MyD88 inhibitor that binds to the TIR domain to interfere with its homodimerization and suppress MyD88 signaling. TJ-M2010-5 can be used in myocardial ischemia/reperfusion injury studies.
价 格：￥电议型 号：T9765产 地：中国大陆
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TQ0010Brepocitinibinhibit,Janus kinase,PF06700841,JAK,Brepocitinib,Inhibitor,PF 06700841
Brepocitinib is a potent dual JAK1/TYK2 inhibitor (IC50s: 17 nM/23 nM). Brepocitinib also inhibits JAK2/3 (IC50s: 77 nM/6.49 μM).
价 格：￥电议型 号：TQ0010产 地：中国大陆
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T101083-Bromocytisine
3-Bromocytisine is an effective agonist of nAChR (IC50s: 0.28, 0.30 and 31.6 nM for hα4β4, hα4β2, and hα7).
价 格：￥电议型 号：T10108产 地：中国大陆
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T60108PDGFR Tyrosine Kinase Inhibitor III
PDGFR Tyrosine Kinase Inhibitor III (PDGF Receptor Tyrosine Kinase Inhibitor III) is a multikinase inhibitor that inhibits PDGFR, EGFR, FGFR, PKA, and PKC, respectively. PDGFR Tyrosine Kinase Inhibitor III can be used for the research of amyotrophic lateral sclerosis [1].
价 格：￥电议型 号：T60108产 地：中国大陆
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T9010IMM-H007JNK,Nuclear factor-κB,WS 070117,IMM H007,AP-1,inflammatory,WS070117,inhibit,AMPK,atheroscler
IMM-H007 is a novel lipid-lowering agent, increasing abca1 protein expression
价 格：￥电议型 号：T9010产 地：中国大陆
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T60103N6-(p-Hydroxyphenethyl)-Adenosine)N6 (P HYDROXYPHENETHYL) ADENOSINE),N6(PHYDROXYPHENETHYL)ADENOSINE)
N6-(p-Hydroxyphenethyl)-Adenosine) is an adenosine analogue.
价 格：￥电议型 号：T60103产 地：中国大陆
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TQ0046BavisantJNJ31001074,JNJ 31001074,Neurological disorders,inhibit,Histamine Receptor,attention-deficit
Bavisant is a selective and orally active Human H3 receptor antagonist. Bavisant can be used in research on mechanisms of action, involving wakefulness and cognition and the treatment for ADHD.
价 格：￥电议型 号：TQ0046产 地：中国大陆
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TD0105Sulfobromophthalein disodium saltinhibit,Sulfobromophthalein disodium salt,MDR2,Sulfobromophthalein
Sulfobromophthalein disodium salt is an organic anion dye, it is used in the study of a variety of membrane carriers expressed in animal tissues and involved in transport of drugs and metabolites.
价 格：￥电议型 号：TD0105产 地：中国大陆
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T9906IpilimumabBMS734016,MDX010,Ipilimumab,inhibit,BMS-734016,BMS 734016,Inhibitor,MDX 010,MDX-010
Ipilimumab anti-CTLA-4) is an immunomodulatory monoclonal antibody directed against the cell surface antigen CTLA-4 and also a type of immune checkpoint inhibitor.
价 格：￥电议型 号：T9906产 地：中国大陆
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TQ0104CRT0066101 dihydrochlorideInhibitor,CRT-0066101 dihydrochloride,CRT0066101,CRT0066101 dihydrochlorid
CRT0066101 dihydrochloride is an effective and selective PKD inhibitor (IC50s: 1, 2.5 and 2 nM for PKD1, 2, and 3).
价 格：￥电议型 号：TQ0104产 地：中国大陆
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T0105Carbachol
Carbachol is used to study responses mediated by nAChR and mAChR, including smooth muscle contraction, gut motility, and neuronal signaling. IC50 value: 10 to 10,000 nM (Ki) Target: nAChR, mAChR Carbamoylcholine is an analog of acetylcholine that activates acetylcholine receptors (AChR). Carbamoylcholine is an agonist of both nicotinic (nAChR) and muscarinic (mAChR) receptors, with reported Ki values ranging from 10 to 10,000 nM for different receptors and different preparations.
价 格：￥电议型 号：T0105产 地：中国大陆
