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ѻƹ ȼ
(0 -40)ۣ
(41-90)ۣɽǢ̸
(91+ )ۣɳ
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עţ ֤
˴ ֤
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עʽ ֤
Ʒ86101
ι۴3793847
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Fr14500Compound Fr14500Compound Fr14500
ţFr14500 أй½
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TN1012LFebrifugine dihydrochlorideInhibitor,Parasite,Febrifugine dihydrochloride,antimalarial,alkaloid,Quin
Febrifugine dihydrochloride is a biochemical with therapeutic activity regarding malaria, cancer, fibrosis and inflammatory diseases.
ţTN1012L أй½
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PDK0380CarbazoleCarbazole
ţPDK0380 أй½
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Fr16683Compound Fr16683Compound Fr16683
ţFr16683 أй½
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TN6705GraveolineGraveoline
Graveoline is an apoptosis and autophagy inducer in skin melanoma cancer cells
ţTN6705 أй½
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Fr13901Compound Fr13901Compound Fr13901
ţFr13901 أй½
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TP1889MCL0020inhibit,Melanocortin Receptor,COS-1,Inhibitor,MCL0020,MC Receptor,anorexia,dose-dependently,s
Potent and selective melanocortin MC4 receptor antagonist (IC50 values are 11.63, 1115 and > 10 000 nM at MC4, MC3 and MC1 receptors respectively). Significantly reverses stress-induced anorexia but has no effect on food intake in free-feeding rats. Exhibits anxiolytic-like activity in vivo.
ţTP1889 أй½
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TP1018LUrechistachykinin II acetateUrechistachykinin II acetate
Urechistachykinin II acetate is an invertebrate rapid kinin-related peptide (TRPs) isolated from carotenoid worms, shows antimicrobial activities without a hemolytic effect
ţTP1018L أй½
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T7123AMG-47aInhibitor,signal,kinases,AMG 47a,JAK,Janus kinase,AMG-47a,transduction,Src,VEGFR,cytoplamic,p
AMG-47a is a potent inhibitor of Lck and T cell proliferation. AMG-47a could promote the degradation of the KRAS oncoprotein. AMG-47a selectively reduced the levels of EGFP-KRASG12V protein but did not affect EGFP protein in cells.
ţT7123 أй½
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TN71612,3-Dibromomaleinimide
2,3-Dibromomaleinimide is a marine derived natural products found in Axinella brevistyla.
ţTN7161 أй½
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TN66602-Ethylhexyl trans-4-methoxycinnamate2Ethylhexyl trans4methoxycinnamate,2 Ethylhexyl trans 4 methoxy
2-Ethylhexyl trans-4-methoxycinnamate is a sunscreen agent.
ţTN6660 أй½
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T11155Eg5 Inhibitor V, trans-24Eg5 Inhibitor V, trans 24,Eg-5 Inhibitor V, trans-24,Eg5 Inhibitor V, trans
Eg5 Inhibitor V, trans-24 is a specific and potent Eg5 inhibitor that can be used in cancer research with an IC50 value of 0.65 uM.
ţT11155 أй½
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T60889RP-6306
RP-6306 is a potent, selective and orally active PKMYT1 inhibitor (IC50= 14 nM). RP-6306 exhibits a high degree of selectivity for PKMYT1 over other kinases in cellular binding assays. RP-6306 exhibits anticancer effects.
ţT60889 أй½
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T4074GSK-872translocation,GSK-872,neurological,HMGB1,Receptor-interacting protein kinases,brain,GSK 872,c
GSK872 (GSK2399872A) is an effective and specific RIP3 kinase inhibitor. It binds RIP3 kinase domain with high affinity (IC50: 1.8 nM) and inhibits kinase activity (IC50: 1.3 nM).
ţT4074 أй½
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T7363Ibuprofen PiconolIbuprofen Piconol,U 75630,U-75630,Inhibitor,inhibit
Ibuprofen piconol is a non-steroidal, anti-inflammatory (NSAID) agent for the topical relief of primary thermal burns and sunburns.Ibuprofen piconol is a Pyridyl ester of ibuprofen.
ţT7363 أй½
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T7346Lodenafilinhibit,Phosphodiesterase (PDE),Lodenafil,Inhibitor
Lodenafil is a potent PDE5 inhibitor, with treatment of erectile dysfunction (ED)
ţT7346 أй½
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T7449o-Phenanthroline monohydrateInhibitor,inhibit,Matrix metalloproteinases,o-Phenanthroline,MMP,1,10-Ph
1,10-Phenanthroline monohydrate is an inhibitor of metallopeptidases, inhibits zinc-dependent hydrolysis of Fa-Gly-Leu-NH2 by B. subtilis neutral protease and B. thermoproteolyticus thermolysin.
ţT7449 أй½
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T8118BekanamycinBekanamycin,Gram-negative,inhibit,influx,action,Antibiotic,calcium,Inhibitor,presynaptic,
Bekanamycin is an aminoglycoside antibiotic.
ţT8118 أй½
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T14362LAY 9944 dihydrochloride1(2chlorophenyl)N[[4[(2chlorophenyl)methylaminomethyl]cyclohexyl]methyl]metha
AY 9944 dihydrochloride is a intermediate.
ţT14362L أй½