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(0 -40)ۣ
(41-90)ۣɽǢ̸
(91+ )ۣɳ
ƹԱ5
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עţ ֤
˴ ֤
ҵͣ ֤
עʽ ֤
Ʒ86101
ι۴3792089
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Fr14534Compound Fr14534Compound Fr14534
ţFr14534 أй½
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T8234ML401ML401,Inhibitor,ML 401,EBI2/GPR183,inhibit,ML-401
ML401 is a selectively EBI2(GPR183) receptor antagonist(IC50 of 1.03 nM) .
ţT8234 أй½
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TN6732Oenothein Bantitumor,HCV,Hepatitis C virus,ellagitannin,antifungal,antioxidant,Bacterial,inhibit,Oen
Oenothein B is a specific inhibitor of poly(ADP-ribose) glycohydrolase. Oenothein B shows antioxidant, anti-inflammatory, antifungal, anti-HCV, and antitumor properties.
ţTN6732 أй½
-
TD0094Azomethine-H monosodiumInhibitor,inhibit,Azomethine H monosodium,AzomethineH monosodium,Azomethine-H
Azomethine-H monosodium is a colour-forming reagent and a boron determinations reagent.
ţTD0094 أй½
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T6944Thiophanate-MethylThiophanate-Methyl,inhibit,Inhibitor,Thiophanate Methyl,ThiophanateMethyl,Fungal
Thiophanate-Methyl (TM), a methyl benzimidazole carbamate (MBC) fungicide,
ţT6944 أй½
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T9459GR103545Inhibitor,Opioid Receptor,imaging,GR103545,inhibit,-OR,GR 103545,-opioid receptor,GR-10354
(R)-(-)-GR103545 fumarate is a chemical compound.
ţT9459 أй½
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T79823,6-Dihydroxyflavoneinhibit,Inhibitor,caspase cascade,cell viability,oxidative stress,3,6-DHF,Apopto
3,6-Dihydroxyflavone suppresses the epithelial-mesenchymal transition in breast cancer cells by inhibiting the Notch signaling pathway.
ţT7982 أй½
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T9306EST64454 Maleic acid saltEST-64454 Maleic acid salt,EST64454 Maleic acid salt
EST64454 Maleic acid salt is a compound.
ţT9306 أй½
-
T63812MrgprX2 antagonist-8
MrgprX2 antagonist-8 is an MrgprX2 antagonist that can be used to study inflammatory diseases.
ţT63812 أй½
-
T30577BRD0418
BRD0418 acts as an upregulator of TRIB1 expression by leading to reprogramming of hepatic lipoprotein metabolism from adipogenesis to clearance it.
ţT30577 أй½
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T10643c-Fms-IN-1cFmsIN1,c Fms IN 1
c-Fms-IN-1 is an inhibitor of c-FMS kinase (IC50 = 0.8 nM).
ţT10643 أй½
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T60147BAY-091BAY091
BAY-091 is a novel potent and highly selective PIP4K2A kinase inhibitor.
ţT60147 أй½
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T9753LEI110HepG2 cells,inhibit,thiol hydrolases,LEI110,Inhibitor,LEI-110,lipolysis,Phospholipase,LEI 110
LEI110 is a potent Phospholipase A2, group XVI (PLA2G16) inhibitor with an Ki value of 20 nM. LEI110 is a selective pan-inhibitor of the HRASLS family of thiol hydrolases (i.e., PLA2G16, HRASLS2, RARRES3 and iNAT).
ţT9753 أй½
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TN1041Quercimeritrinactivity,dentatum,amylase,Quercimeritrin,Ixeridium,Inhibitor,inhibit
Quercimeritrin has antibacterial activity, it shows promising activity against Staphylococcus aureus.
ţTN1041 أй½
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T9519EliapixantInhibitor,chronic,Eliapixant,cough,refractory,BAY-1817080,P2X Receptor,BAY1817080,P2X3,inh
Eliapixant (BAY 1817080) is a potent and selective P2X3 receptor antagonist, with an IC50 of 8 nM. Eliapixant can be used for the research of refractory chronic cough.
ţT9519 أй½
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T9834(3Z)-1-methyl-3-[2-(4-methylphenyl)-2-oxo-ethylidene]piperazin-2-one(3Z) 1 methyl 3 [2 (4 methylphen
(3Z)-1-methyl-3-[2-(4-methylphenyl)-2-oxo-ethylidene]piperazin-2-one is a chemical agent.
ţT9834 أй½
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T7529Yamogenintriacylglyceride,Inhibitor,fatty acid synthesis,Diastereomer,Yamogenin,Liver X receptor,LXR
Yamogenin is a diastereomer of diosgenin, which we have identified as the compound responsible for the anti-hyperlipidemic effect of fenugreek.
ţT7529 أй½
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T7303LIXIVAPTANVPA 985,LIXIVAPTAN,VPA985,inhibit,Inhibitor,Vasopressin Receptor
Lixivaptan is an orally active and selective vasopressin receptor V2 antagonist(Ki = 2.3 nM)
ţT7303 أй½
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T6703Tetrahydrozoline hydrochloridecongestion,conjunctival,Beta Receptor,Tetryzoline,Tetrahydrozoline hyd
Tetrahydrozoline HCl is an imidazoline derivative with alpha receptor agonist activity.
ţT6703 أй½