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T7311Oxyphenisatin acetateAutophagy,Oxyphenisatin acetate,inhibit,Inhibitor,Oxyphenisatin
Oxyphenisatin acetate inhibits the growth of the breast cancer cell lines MCF7, T47D, HS578T, and MDA-MB-468.
价 格：￥电议型 号：T7311产 地：中国大陆
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TN3748D-AsparagineEndogenous Metabolite,D-Asparagine,L-Asparagine,D Asparagine,DAsparagine,asparaginase,ni
D-Asparagine is a source of nitrogen for yeast strains. D-Asparagine is a competitive inhibitor of L-Asparagine hydrolysis (Ki = 0.24 mM).
价 格：￥电议型 号：TN3748产 地：中国大陆
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T8328STING agonist-1inhibit,TMEM173,Inhibitor,STING agonist 1,G 10,G-10,Stimulator of Interferon Genes,ST
STING agonist-1 is a human-specific STING agonist,elicits antiviral activity against emerging Alphaviruses.
价 格：￥电议型 号：T8328产 地：中国大陆
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T7101Tyrphostin AG30HER1,ErbB-1,Inhibitor,EGFR,Tyrphostin AG30,Epidermal growth factor receptor,Tyrphosti
Tyrphostin AG30 (AG30) is a potent protein tyrosine kinases (PTK) inhibitor.
价 格：￥电议型 号：T7101产 地：中国大陆
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T60145CCR6 antagonist 1CCR6antagonist1
CCR6 antagonist 1 is a CCR6 antagonist. CCR6 antagonist 1 inhibits the CCL20/CCR6 axis. CCR6 antagonist 1 can be used in the research of autoimmune-mediated inflammatory diseases, such as inflammatory bowel diseases (IBDs).
价 格：￥电议型 号：T60145产 地：中国大陆
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T38622Bcl-xL antagonist 2Bcl xL antagonist 2,BclxL antagonist 2
Bcl-xL antagonist 2 is an effective and selective antagonist of Bcl-xL with an IC50 of 91 nM and a Ki of 65 nM. Bcl-xL antagonist 2 induces apoptosis in cancer cells and can be used in studies about chronic lymphocytic leukemia and non-Hodgkin’s lymphoma.
价 格：￥电议型 号：T38622产 地：中国大陆
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TQ0025E7046Inhibitor,E-7046,Prostaglandin Receptor,E7046,E 7046,inhibit
E7046 is a specific, orally bioavailable EP4 antagonist (IC50: 13.5 nM, Ki: 23.14 nM), exhibiting anti-tumor activities.
价 格：￥电议型 号：TQ0025产 地：中国大陆
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TP1865LRhodopsin Epitope Tag acetateRhodopsin Epitope Tag acetate
Rhodopsin Epitope Tag acetate is a 9-amino acid peptide representing C terminus of bovine rhodopsin widely used as an epitope tag. A number of anti-rhodopsin antibodies can recognize this epitope.
价 格：￥电议型 号：TP1865L产 地：中国大陆
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TN71857-Cyano-7-deazaguanine
3H-Pyrrolo[2,3-d]pyrimidine-5-carbonitrile, 2-amino-4,7-dihydro-4-oxo- is a marine derived natural products found in Streptomyces qinglanensis.
价 格：￥电议型 号：TN7185产 地：中国大陆
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T7964Isomaltoral,food,stabilizing,Inhibitor,Lactate Dehydrogenase,inhibit,agent,LDH,Isomalt,industry,exci
Palatinitol is a mixture of 1,6-mannitol glucopyranoside and 1,6-sorbitol glucopyranoside
价 格：￥电议型 号：T7964产 地：中国大陆
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T9541CTBHATs,Inhibitor,neurons,CTB,Apoptosis,MCF-7 cell,cancer,potent,HAT,autophagic flux,inhibit,Histone
CTB (Cholera Toxin B subunit) is an activator of p300 histone acetyltransferase and induces apoptosis in MCF-7 cells.
价 格：￥电议型 号：T9541产 地：中国大陆
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T6541Ibutilide FumarateIbutilide,antiarrhythmia agent,Potassium Channel,inhibit,Inhibitor,long QT syndrom
Ibutilide Fumarate is the fumarate salt form of ibutilide, a class III antiarrhythmic agent. Ibutilide exerts its effect by activating a slow, inward, predominately sodium current rather than by blocking outward potassium currents. This results in prolongation of atrial and ventricular action potential duration and refractory periods. Ibutilide slightly decreases the sinus rate and atrioventricular (AV) conduction and produces a dose-related prolongation of the QT interval.
价 格：￥电议型 号：T6541产 地：中国大陆
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T9623RORγt inverse agonist 13RORγt inverse agonist 13,ROR,RORγt inverse agonist-13,RAR-related orphan rec
RORγt inverse agonist 13 (Compound 3i) is a potent, orally active and selective RORγt inverse agonist (IC50=63.8 nM), with improved drug-like properties[1].
价 格：￥电议型 号：T9623产 地：中国大陆
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T7364NNC-0640NNC-0640,Glucagon Receptor,NNC0640,GCGR,inhibit,Inhibitor,NNC 0640
NNC-0640 is a negative allosteric modulator of Human Glucagon Receptor with an IC50 of 69.2 nM.
价 格：￥电议型 号：T7364产 地：中国大陆
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T9729AGI-43192AGI 43192,AGI43192
AGI-43192 is a potent methionine adenosyltransferase 2A ( MAT2A ) inhibitor. AGI-43192 is a potent, but limited brain-penetrant compound. AGI-43192 has the potential for exploring the effects of SAM modulation in the central nervous system (CNS) and research of cancer disease [1].
价 格：￥电议型 号：T9729产 地：中国大陆
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T6422Brimonidine TartrateUK-14304,UK14304,AGN190342,Brimonidine,Adrenergic Receptor,AGN-190342,AGN 190342
Brimonidine tartrate is a quinoxaline derivative and adrenergic α-2 receptor agonist (EC50: 0.45 nM) that is used to manage intraocular pressure associated with open-angle glaucoma or ocular hypertension.
价 格：￥电议型 号：T6422产 地：中国大陆
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T6450ClinofibrateClinofibrate,HMG-CoA Reductase (HMGCR),Autophagy,inhibit,Inhibitor,S 8527,S8527
Clinofibrate（IC50 of 0.47 mM）, a lipid-lowering agent, inhibits hydroxymethylglutaryl coenzyme A reductase (HMGCR). It is utilized to control high cholesterol and triacylglyceride levels in the blood.
价 格：￥电议型 号：T6450产 地：中国大陆
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T6473DioscinAutophagy,CCRIS-4123,CCRIS4123,Apoptosis,Dioscin,inhibit,Inhibitor
Dioscin is a saponin with antitumor activities.
价 格：￥电议型 号：T6473产 地：中国大陆
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T23445Anxiolytic/nonsedative agent-1
Anxiolytic/nonsedative agent-1 is a potent and selective GABAA agonist. Anxiolytic/nonsedative agent-1 shows appreciable affinity for the BzR in bovine brain membranes with Kis of 14, 121, 239 nM for α1β2γ2, α2β2γ2, α5β3γ2, respectively. Anxiolytic/nonsedative agent-1 shows α2 selective efficacy in vitro and anxioselective effects in vivo.
价 格：￥电议型 号：T23445产 地：中国大陆
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T38287C3a Receptor Agonist
C3a Receptor Agonist binds the G protein-coupled C3a receptors (C3aRs) in the immune system complement pathway. Activation of C3aR prevents neutrophils from being mobilized in a model of intestinal ischemia-reperfusion injury. C3aRs are expressed on neural progenitor cells and immature neurons in adult mice. C3a stimulates differentiation of neural progenitor cells in vitro.
价 格：￥电议型 号：T38287产 地：中国大陆
