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￥ 0.00 “AG 013736”的搜索结果
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Maytansinol
Catalog No. A20767 microtubule depolymerizing agentMaytansinol, also known as Ansamitocin P-0, is a potent microtubule depolymerizing agent. 了解更多 -
SB-616234A
Catalog No. A20764 5-HT1B receptor antagonistSB-616234A is a selective and orally bioavailable 5-HT1B receptor antagonist, with anxiolytic and antidepressant activity. 了解更多 -
GSK2018682
Catalog No. A20752 S1P1/S1P5 receptor agonistGSK2018682 is an agonist for S1P1 and S1P5 receptor with pEC50s of 7.7 and 7.2, respectively, and has no agonist activity towards human S1P2, S1P3, or S1P4. GSK2018682 is used in the research of multiple sclerosis. 了解更多 -
Seladelpar
Catalog No. A20744 PPAR-δ agonistSeladelpar (MBX-8025) is an orally active, potent (50% effect concentration EC50 2 nM), and specific PPAR-δ agonist. 了解更多 -
9-Azido-Neu5DAz
Catalog No. A20741 imaging agent9-Azido-Neu5DAz is a non-natural bifunctional carbohydrates as imaging agent. 了解更多 -
Duocarmycin MA
Catalog No. A20738 antibody drug conjugates (ADCs) toxinDuocarmycin MA is an antibody drug conjugates (ADCs) toxin. Duocarmycin is a DNA alkylating agent that binds in the minor groove. Duocarmycin MA can be used against multi-drug resistant cell lines. 了解更多 -
FPR Agonist 43
Catalog No. A20720 dual FPR1/FPR2/ALX agonistFPR Agonist 43 (compound 43) is a dual formyl peptide receptor 1 (FPR1) and formyl peptide receptor 2 (FPR2)/ALX agonist. 了解更多 -
Ro-24-0238
Catalog No. A20719 thromboxane synthesis inhibitorRo-24-0238 is an antagonist of platelet activating factor (PAF) and inhibitor of thromboxane synthesis, used for lessening the inflammation and damage resulting from a local release of PAF. 了解更多 -
Ro-24-4736
Catalog No. A20717 PAF antagonistRo 24-4736 is a potent, selective, p.o.-active platelet-activating factor (PAF) antagonist with a long duration of action. 了解更多 -
Perzinfotel
Catalog No. A20708 NMDA receptor antagonistPerzinfotel (EAA-090) is a potent, selective, and competitive NMDA receptor antagonist with neuroprotective effects. Perzinfotel (EAA-090) shows high affinity (IC50=30 nM) for the glutamate site. 了解更多 -
Fezolinetant
Catalog No. A20706 NK3R antagonistFezolinetant is an antagonist of the neurokinin 3 receptor (NK3R), used for the treatment of menopausal hot flushes. 了解更多 -
CS-003 Free base
Catalog No. A20704 triple tachykinin receptor antagonistCS-003 Free base (CS-003), a triple tachykinin receptor antagonist, shows high affinities for human (Neurokinin) NK1, NK2 and NK3 receptors with Ki values of 2.3 nM, 0.54 nM and 0.74 nM, respectively. 了解更多 -
GSK2256294A
Catalog No. A20696 recombinant human sEH inhibitorGSK2256294A is a potent, reversible, tight binding inhibitor of isolated recombinant human sEH (soluble epoxide hydrolase) (IC50 = 27 pM; t1/2 = 121 min) and displays potent inhibition against the rat (IC50 = 61 pM) and murine (IC50 = 189 pM) orthologs of sEH. 了解更多 -
Pumaprazole
Catalog No. A20693 -
Pumosetrag Hydrochloride
Catalog No. A20692 5-HT3 partial agonistPumosetrag Hydrochloride (MKC-733; DDP-733) is an orally available 5-HT3 partial agonist developed for the treatment of irritable bowel syndrome and gastroesophageal reflux disease. 了解更多 -
Setmelanotide
Catalog No. A20689 MC4R agonistSetmelanotide (RM-493; BIM-22493; IRC-022493) is a selective melanocortin 4 receptor (MC4R) agonist with EC50s of 0.27 nM and 0.28 nM for human and rat MC4R, respectively. 了解更多 -
GLP-1R Antagonist 1
Catalog No. A20679 glucagon-like peptide 1 receptor antagonistGLP-1R Antagonist 1 (compound 5d) is an orally active, CNS penetrant and non-competitive antagonist of glucagon-like peptide 1 receptor (GLP-1R), with an IC50 of 650 nM. 了解更多 -
Nucleoside-Analog-1
Catalog No. A20671 Nucleoside-Analog-1 is a 4??-Azidocytidine analogue against Hepatitis C virus replication. 了解更多 -
Nucleoside-Analog-2
Catalog No. A20666 Nucleoside-Analog-2 is a 4'-Azidocytidine analogue against Hepatitis C virus (HCV) replication. 了解更多 -
Sultopride
Catalog No. A20663 dopamine D2 receptor antagonistSultopride (LIN-1418) is a selective antagonist of dopamine D2 receptor. 了解更多 -
5-FAM
Catalog No. A20660 fluorescent derivatization reagent5-FAM (5-Carboxyfluorescein) contains a carboxylic acid that can be used to react with primary amines via carbodiimide activation of the carboxylic acid. Fluorescein is the most common fluorescent derivatization reagent for labeling biomolecules. 了解更多 -
JNJ-18038683
Catalog No. A20659 5-HT7 receptor antagonistJNJ-18038683 is a 5-Hydroxytryptamine Type 7 (5-HT7) receptor antagonist, with pKis of 8.19, 8.20 for rat and human 5-HT7 in HEK293 cells, respectively. 了解更多
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