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(0 -40)ۣ
(41-90)ۣɽǢ̸
(91+ )ۣɳ
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Ʒ86101
ι۴3793359
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TN2031-Terpinene
-Terpinene, a monoterpene, is an orally active antioxidant compound which can scavenge radicals directly. -Terpinene has potent antinociception activity.
ţTN2031 أй½
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T8915GlycylsarcosineInhibitor,Gly-Sar,Glycylsarcosine,inhibit
Glycylsarcosine is a dipeptide obtained by formal condensation of the carboxy group of glycine with the amino group of sarcosine
ţT8915 أй½
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TN2345Loureirin DLoureirin D
Loureirin D is a chalcone from the herbs of Dracaena cochinchinensis.
ţTN2345 أй½
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T10269AHR antagonist 2AHR antagonist 2
AHR antagonist 2 is an antagonist of the aryl hydrocarbon receptor. The IC50s for human AHR and mouse AHR are 0.885 and 2.03 nM, respectively.
ţT10269 أй½
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TN1539Cussosaponin CCussosaponin C,Inhibitor,inhibit
Cussosaponin C is a natural product isolated from Pulsatilla koreana Nakai.
ţTN1539 أй½
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TN1089Hydroxy--sanshool
Hydroxy--sanshool is a pungent compound obtained from Zanthoxylum piperitum.
ţTN1089 أй½
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T9084Cetirizine Impurity B dihydrochlorideinhibit,Cetirizine Impurity B,Inhibitor,Cetirizine Impurity B d
Cetirizine Impurity B dihydrochloride is an impurity of Cetirizine dihydrochloride. Cetirizine is a second-generation antihistamine. Cetirizine is a specific, orally active and long-acting histamine H1-receptor antagonist. Cetirizine marks antiallergic properties and inhibits eosinophil chemotaxis during the allergic response.
ţT9084 أй½
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T6965RG7112E1 activating enzyme,Inhibitor,RO-5045337,E1/E2/E3 Enzyme,RG7112,Ubiquitin conjugating enzyme,
RG7112 (RO5045337) is an orally bioavailable and selective p53-MDM2 inhibitor.
ţT6965 أй½
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TP1159LBoc-Gly-Gly-Phe-Gly-OH acetateBocGlyGlyPheGlyOH acetate,Boc Gly Gly Phe Gly OH acetate
Boc-Gly-Gly-Phe-Gly-OH acetate is a self-assembly of N- and C-protected tetrapeptide.
ţTP1159L أй½
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T6118NVP-HSP990HSP-990,NVP-HSP990,Apoptosis,Heat shock proteins,NVP HSP990,HSP,NVP-HSP-990,HSP 990,Inhibi
NVP-HSP990 (HSP990) is an effective and specific HSP90/ inhibitor (IC50: 0.6 /0.8 nM).
ţT6118 أй½
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T2738DehydroandrographolideiNOS,Dehydroandrographolide,Influenza Virus,Inhibitor,herbal,stress,oxidative,
Dehydroandrographolide is a natural compound extracted from herbal medicine Andrographis paniculata (Burm f) Nees.
ţT2738 أй½
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T12204NecroX-5NecroX 5,NecroX5
NecroX-5, a derivative of NecroX, exhibits anti-inflammatory and anti-cancer activities. NecroX-5 reduces intracellular calcium concentration.
ţT12204 أй½
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T6451Clodronic acid disodium saltClodronic acid disodium,inhibit,ADP,mitochondria,first-generation,metast
Clodronate Disodium, a bisphosphonate, is a potent antiosteolytic agent which inhibits bone resorption.
ţT6451 أй½
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T23074NNC 63-0532
NNC 63-0532 is a potentnociceptin receptor agonist, Ki=7.3 nM, EC50=305 nM.
ţT23074 أй½
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T14681BMS-935177BMS 935177,BMS935177
BMS-935177 is a reversible BTK inhibitor with IC50 value of 3 nM.
ţT14681 أй½
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TWO2727Propane-1,2,3-triyl tripalmitateInhibitor,Propane1,2,3triyl tripalmitate,inhibit,Endogenous Metaboli
Tripalmitin is a triacylglycerol found in dietary fats. Tripalmitin increases body weight and plasma LDL levels and reduces hepatic LDL receptor mRNA levels in hamsters fed a diet enriched with it. It inhibits glucose-stimulated insulin secretion and reduces viability of INS1 cells in a dose-dependent manner. Formulations containing tripalmitin are used in cosmetic products to condition skin and as a thickening agent. It is also used to form the lipid matrices of nanoparticles for drug delivery.
ţTWO2727 أй½
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T61150Oleyl Mesylate
Oleyl Mesylate is a derivative of oleyl alcohol that can be incorporated into various formulations.
ţT61150 أй½
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T36957BODIPY 493/503
BODIPY 493/503 is a lipophilic fluorescent probe with Ex/Em of 493/503 nm. BODIPY 493/503 localizes to polar lipids and can be used to label cellular neutral lipid contents and for live and fixed cell applications.
ţT36957 أй½
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T6695TasquinimodTasquinimod,ABR215050,Inhibitor,ABR 215050,inhibit,Histone deacetylases,HDAC
Tasquinimod is a quinoline-3-carboxamide linomide analog with antiangiogenic and potential antineoplastic activities. Tasquinimod has been shown to decrease blood vessel density but the exact mechanism of action is not known. This agent has also been shown to augment the antineoplastic effects of docetaxel and androgen ablation in a murine model of prostate cancer involving human prostate cancer xenografts.
ţT6695 أй½
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T6864IxabepiloneBMS247550,inhibit,Inhibitor,Aza-epothilone B,Apoptosis,Microtubule/Tubulin,Ixabepilone,BM
Ixabepilone is an orally bioavailable microtubule inhibitor. It binds to tubulin and promotes tubulin polymerization and microtubule stabilization, thereby arresting cells in the G2-M phase of the cell cycle and inducing tumor cell apoptosis.
ţT6864 أй½