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Agmatine sulfate
Catalog No. A20485 NO synthase inhibitorAgmatine sulfate exerts modulatory action at multiple molecular targets, such as neurotransmitter systems, ion channels and nitric oxide synthesis. It is an endogenous agonist at imidazoline receptor and a NO synthase inhibitor. 了解更多 -
TA-7552
Catalog No. A20473 -
Fumarate hydratase-IN-1
Catalog No. A20471 fumarate hydratase inhibitorFumarate hydratase-IN-1 (compound 2) is a cell-permeable fumarate hydratase inhibitor. Fumarate hydratase-IN-1 has antiproliferative activity against several cancer cell lines with a mean IC50 of 2.2 μM. 了解更多 -
CCR2 antagonist 3
Catalog No. A20467 -
Tiodazosin
Catalog No. A20463 ostsynaptic alpha adrenergic receptor antagonistTiodazosin is a potent competitive postsynaptic alpha adrenergic receptor antagonist. 了解更多 -
S1p receptor agonist 1
Catalog No. A20461 S1P receptor agonistS1p receptor agonist 1 is an S1P receptor agonist extracted from patent WO 2015039587 A1, compound example 2. 了解更多 -
Trifarotene
Catalog No. A20458 RAR agonistTrifarotene (CD5789) is a retinoic acid receptor (RAR) agonist with Kdapp of 2, 15 and 500 nM for RARγ, RARβ and RARα, respectively. 了解更多 -
TCS-OX2-29
Catalog No. A20457 OX2R antagonistTCS-OX2-29 is a potent, high affinities and selective orexin-2 receptor (OX2R) antagonist with an IC50 value of 40 nM and a pKI value of 7.5. TCS-OX2-29 displays ~250-fold selectivity for OX2 over OX1. 了解更多 -
mPGES1-IN-3
Catalog No. A20454 mPGES-1 inhibitormPGES1-IN-3 (Compound 17d) is a potent and selective microsomal prostaglandin E2 synthase-1 (mPGES-1) inhibitor, which exhibits excellent mPGES-1 enzyme (IC50: 8 nM), cell (A549 IC50: 16.24 nM) and human whole blood potency (IC50: 249.9 nM). 了解更多 -
CGP 25454A
Catalog No. A20448 dopamine autoreceptor antagonistCGP 25454A is a novel and selective presynaptic dopamine autoreceptor antagonist. 了解更多 -
WAY-200070
Catalog No. A20442 ERRβ agonistWAY-200070 is a selective estrogen receptor β (ERRβ) agonist with an IC50 of 2.3 nM. 了解更多 -
CCR5 antagonist 1
Catalog No. A20439 CCR5 antagonistCCR5 antagonist 1 is a CCR5 antagonist which can inhibit HIV replication extracted from WO 2004054974 A2. 了解更多 -
Urolithin A
Catalog No. A20426 Urolithin A, a gut-microbial metabolite of ellagic acid, exerts anti-inflammatory, antiproliferative, and antioxidant properties. Urolithin A induces autophagy and apoptosis, suppresses cell cycle progression, and inhibits DNA synthesis. 了解更多 -
Nitromifene
Catalog No. A20417 -
Chlordantoin
Catalog No. A20416 antifungal drugChlordantoin is an antifungal drug which can be used to treat vaginal candidiasis. 了解更多 -
Tomivosertib
Catalog No. A20407 MNK1/MNK2 inhibitorTomivosertib (eFT508) is a potent, highly selective, and orally bioavailable MNK1 and MNK2 inhibitor, with IC50s of 1-2 nM against both isoforms. 了解更多 -
LXRβ agonist-2
Catalog No. A20405 LXRβ agonistLXRβ agonist-2 is a highly potent and β-selective liver X receptor (LXRβ) agonist with EC50 of 7 nM, displays 28.5-fold selectivity over LXRα (EC50=200 nM) and used in the treatment of atherosclerosis. 了解更多 -
BMS-986020
Catalog No. A20393 LPA1 antagonistBMS-986020 is a high-affinity lysophosphatidic acid receptor 1 (LPA1) antagonist. 了解更多 -
AGN 194078
Catalog No. A20387 RARα agonistAGN 194078 is a selective RARα agonist with a Kd and EC50 of 3 and 112 nM, respectively. 了解更多 -
Closthioamide
Catalog No. A20385 DNA gyrase inhibitorClosthioamide is a potent inhibitor of bacterial DNA gyrase and highly active against Ec, MRSA, VRE and Mv), with MICs of 9.00 μM, 0.58 μM, 0.58 μM and 72.03 μM respectively. 了解更多 -
Adenosine antagonist-1
Catalog No. A20383 AA3R antagonistAdenosine antagonist-1 is an adenosine A3 receptor (AA3R) antagonist. 了解更多 -
9-Propenyladenine
Catalog No. A20357 9-Propenyladenine is a mutagenic impurity in tenofovir disoproxil fumarate. Tenofovir is an antiretroviral drug known as nucleotide analogue reverse transcriptase inhibitors, which block reverse transcriptase, a crucial virus enzyme in HIV-1 and HBV. 了解更多 -
Spaglumic Acid
Catalog No. A20356 Spaglumic Acid is a neuropeptide found in millimolar concentrations in brain. 了解更多 -
Thiazolidinone-Derivatives-1
Catalog No. A20355 Thiazolidinone-Derivatives-1 is an antiulcer agent which inhibits the secretion of gastric acid. 了解更多 -
(+)-Dihydrexidine hydrochloride
Catalog No. A20339 dopamine D1 receptor agonist(+)-Dihydrexidine hydrochloride ((+)-DAR-0100 hydrochloride) is a dopamine D1 receptor agonist with an EC50 of 72± 21 nM. 了解更多 -
2-(E-2-decenoylamino)ethyl 2-(cyclohexylethyl) sulfide
Catalog No. A20334 2-(E-2-decenoylamino)ethyl 2-(cyclohexylethyl) sulfide is a compound that inhibits stress-induced ulcer and low toxicity, and can maintain the content of phospholipase A2 and prostaglandin E2 in ulcerated rats induced by water immersed restrained stress. 了解更多 -
SYM 2081
Catalog No. A20332 kainate receptors agonistSYM 2081 is a high-affinity ligand and potent, selective agonist of kainate receptors, inhibits [3H]-kainate binding with an IC50 of 35 nM, almost 3000- and 200-fold selectivity for kainate receptors over AMPA and NMDA receptors respectively. 了解更多 -
GPR120-IN-1
Catalog No. A20328
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