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(0 -40)ۣ
(41-90)ۣɽǢ̸
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Ʒ86101
ι۴3804434
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T8320J14cancer,inhibit,damage,Sulfiredoxin,J14,cytotoxicity,Reactive Oxygen Species,J 14,death,adenocarci
J-14 is an inhibitor of reversible sulfiredoxin(IC50 : 8.1 M). J14 induces oxidative stress (intracellular ROS accumulation) by inhibiting sulfiredoxin, leading to cytotoxicity and cancer cell death
ţT8320 أй½
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TN1121EvocarpineEvocarpine,Ca2+,HL-60,inhibit,antimycobacterial,Inhibitor,leukaemia,Bacterial,Apoptosis,In
Evocarpine shows antimycobacterial, and vasorelaxant effects, it can inhibit Ca2+ influx through voltage-dependent calcium channels.
ţTN1121 أй½
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T95712,4,5-Trichloro-7H-pyrrolo[2,3-d]pyrimid2,4,5Trichloro7Hpyrrolo[2,3d]pyrimid,2,4,5 Trichloro 7H pyrr
2,4,5-Trichloro-7H-pyrrolo[2,3-d]pyrimid is a chemical agent.
ţT9571 أй½
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T8948Ferrohemeinhibit,Inhibitor,Ferroheme
protoheme used as nutrient fortifier, blood tonic and food additive for iron
ţT8948 أй½
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T25534Indazole-Cl
Indazole-Cl is a selective ER? agonist and a selective estrogen receptor modifier (SERM).
ţT25534 أй½
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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).
ţT6733 أй½
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TQ0062NastorazepideZ360,CCK Receptor,Cholecystokinin Receptor,Inhibitor,Z 360,Nastorazepide,inhibit
Nastorazepide is a selective, orally available antagonist of gastrin/cholecystokinin 2 (CCK-2) receptor with potential antineoplastic activity.
ţTQ0062 أй½
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TP1358LPeptide M acetate
Peptide M acetate is a synthetic amino acid (18 amino acids in length which correspond to the amino acid positions 303-322 of bovine S-antigen: DTNLASSTIIKEGIDKTV). Peptide M acetate is capable of inducing experimental autoimmune uveitis in monkeys and Hartley guinea pigs as well as Lewis rats.
ţTP1358L أй½
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TMA0958Forsythoside Finhibit,Xanthine Oxidase,Forsythoside F,antihyperuricemic,Inhibitor
Arenarioside is a natural product, and GI50 values of 10-16 microM against B16F10 cell.
ţTMA0958 أй½
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T50125Compound C749Compound C749
ţT50125 أй½
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T11986Mebeverine acidDrug Metabolite,inhibit,Mebeverine acid,Inhibitor
Mebeverine acid is a secondary metabolite of Mebeverine and can be used as a marker of oral exposure to Mebeverine.
ţT11986 أй½
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T69811-Methyl-6-oxo-1,6-dihydropyridine-3-carboxylic acid1Methyl6oxo1,6dihydropyridine3carboxylic acid,In
Nudifloric Acid is from Cordyceps bassiana. Nudifloric Acid targets to block AP-1-mediated luciferase activity, implying it has an anti-inflammatory function.
ţT6981 أй½
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T6470Diclofenac PotassiumApoptosis,Diclofenac Potassium,COX,CHO,caspase,COX-1,cascade,anti-inflammatory,n
Diclofenac potassium is a nonsteroidal anti-inflammatory drug taken to reduce inflammation and as an analgesic reducing pain in certain conditions.
ţT6470 أй½
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T72345-Amino-2-chloropyridine5 Amino 2 chloropyridine,5Amino2chloropyridine
5-Amino-2-chloropyridine is Pyridine intermediates
ţT7234 أй½
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TP1071NociceptinInhibitor,inhibit,Nociceptin,Opioid Receptor
Nociceptin is a 17-amino-acid polypeptide that is structurally related to the opioid peptide dynorphin A.
ţTP1071 أй½
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T40659L-Acetylenic GABA hydrochloride
-Acetylenic GABA hydrochloride is a GABA transaminase inhibitor.
ţT40659L أй½
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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.
ţT6S0105 أй½
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T5467SAR125844Inhibitor,SAR125844,c-Met/HGFR,inhibit,SAR 125844,SAR-125844,Apoptosis
SAR125844, a potent and highly selective inhibitor of the MET receptor tyrosine kinase (RTK), for intravenous administration. (IC50 value of 4.2 nmol/L)
ţT5467 أй½
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PDK0168Compound PDK0168Compound PDK0168
ţPDK0168 أй½
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T17875Pomalidomide-C2-NH2Inhibitor,E3 Ligase Ligand-Linker Conjugates,PomalidomideC2NH2,Pomalidomide-C-2-N
Pomalidomide-C2-NH2 is a synthesized E3 ligase ligand-linker conjugate containing a Pomalidomide-based cereblon ligand and a linker.
ţT17875 أй½