Home > Keywords >
Catalog | name | Description | price |
---|---|---|---|
R-C-1613 | Pluripotin (SC1) CAS:839707-37-8 | Pluripotin(SC1)is a dual inhibitor of extracellular signal-regulated kinase 1(ERK1,MAPK3)and RasGAP.Maintains embryonic stem cell(ESC)self-renewal.Pluripotin also inhibits RSK1,RSK2,RSK3 and RSK4 with IC50 of 0.5 µM,2.5 µM,3.3µM and 10.0µM,respectively. | price> |
R-R-3313 | Amperozide CAS No.75558-90-6 | Amperozide/CAS No.75558-90-6 is an atypical antipsychotic that acts as an antagonist of the 5-HT2 receptor with a Ki value of 26 nM. Amperozide has a low affinity for D2 receptors. | price> |
R-C-1614 | BMS309403 CAS:300657-03-8 | BMS-309403 is a potent,orally active and selective adipocyte fatty acid binding protein(also known as FABP4,aP2)inhibitor with Kis of <2,250,and 350 nM for FABP4,FABP3,and FABP5,respectively.BMS-309403 interacts with the fatty-acid-binding pocket within the interior of the protein and competitively inhibits the binding of endogenous fatty acids.BMS-309403 improves endothelial function in apolipoprotein E-deficient mice and in cultured human endothelial cells. | price> |
R-R-3314 | BMY 14802 CAS No.105565-56-8 | BMY 14802/CAS No.105565-56-8 is a sigma-1 receptor (σ1R) antagonist, as well as an agonist at serotonin (5-HT) 1A and adrenergic alpha-1 receptors. | price> |
R-C-1615 | SIS3 HCL CAS:521984-48-5 | SIS3 is a novel specific inhibitor of Smad3.It has effect on transforming growth factor-beta1-induced extracellular matrix expression. | price> |
R-R-3315 | LY 165163 CAS No.1814-64-8 | LY 165163/CAS No.1814-64-8 is a potent 5-HT presynaptic receptor agonist. LY 165163 significantly decreases 5-HTP accumulation and increases DOPA accumulation in the cortex and striatum. | price> |
R-C-1616 | A804598 CAS:1125758-85-1 | A-804598 is a CNS penetrant,competitive and selective P2X7 receptor antagonist with IC50s of 9 nM,10nM and 11 nM for mouse,rat and human P2X7 receptors, respectively. | price> |
R-R-3316 | Iferanserin CAS No.58754-46-4 | Iferanserin (S-MPEC)/CAS No.58754-46-4 is a selective 5-HT receptor (serotonin receptor) antagonist with an affinity for 5-HT2A receptor. Iferanserin has the potential for internal hemorrhoid disease treatment. | price> |
R-C-1617 | GW4869 CAS:6823-69-4 | GW4869(GW69A,GW554869A)is a neutral,noncompetitive inhibitor of sphingomyelinase (SMase)with an IC50 of 1μM.It is selective for N-SMase,and does not inhibit acid SMase at up to at least 15μM. | price> |
R-R-3317 | Olanzapine-d3 CAS No.786686-79-1 | Olanzapine-d3/CAS No.786686-79-1 is the deuterium labeled Olanzapine. Olanzapine is a selective, orally active monoaminergic antagonist with high affinity binding to serotonin H1, 5HT2A/2C, 5HT3, 5HT6 (Ki=7, 4, 11, 57, and 5 nM, respectively), dopamine D1-4 (Ki=11 to 31 nM), muscarinic M1-5 (Ki=1.9-25 nM), and adrenergic α1 receptors (Ki=19 nM). Olanzapine is an atypical antipsychotic. | price> |
R-C-1618 | BAW2881 CAS: 861875-60-7 | NVP-BAW2881(BAW2881)is a potent and selective VEGFR2 inhibitor with an IC50 of 4nM. | price> |
R-R-3318 | Keto Ziprasidone CAS No.884305-07-1 | Keto Ziprasidone/CAS No.884305-07-1 is an impurity of Ziprasidone. Ziprasidone, an antipsychotic agent, is a combined 5-HT (serotonin) and dopamine receptor antagonist. | price> |
R-C-1619 | BFH772 CAS :890128-81-1 | BFH772,a structure analogue of BAW2881,is a potent and selective VEGF inhibitor.BFH772 is highly effective at targeting VEGFR2 kinase with an IC50 value of 3 nM.BFH772 inhibits the ligand induced autophosphorylation of RET, PDGFR,and KIT kinases,with IC50 values ranging between 30 and 160 nM. | price> |
R-R-3319 | (R)-Mirtazapine CAS No.61364-37-2 | (R)-Mirtazapine ((R)-Org3770)/CAS No.61364-37-2 is a R(−)-enantiomer of Mirtazapine with antinociceptive properties in an animal model of acute thermal nociception. (R)-Mirtazapine is a 5-HT3 receptor antagonist. (R)-Mirtazapine is mainly metabolized by CYP3A4. | price> |
R-C-1620 | HMN-214 CAS No. 173529-46-9 | HMN-214 inhibits polo-like and cyclin-dependent kinase activity,has potent antimicrotubular effects and results in profound apoptosis and antitumor activity in a broad spectrum of human xenografts. | price> |
R-R-3320 | OPC-14523 hydrochloride CAS No.145969-31-9 | OPC-14523 hydrochloride/CAS No.145969-31-9 is an orally active sigma and 5-HT1A receptor agonist, with high affinity for sigma receptors (σ1/2 IC50=47/56 nM), the 5-HT1A receptor (IC50=2.3 nM), and the 5-HT transporter (IC50=80 nM). OPC-14523 hydrochloride shows antidepressant-like activity. | price> |
R-C-1621 | HMN-176 CAS No. 173529-10-7 | HMN-176 is an active metabolite of HMN-214,which has a potent antitumor activity in mouse xenograft models.HMN-176 effectively inhibits PLK-1 by interference with its normal subcellular spatial distribution at centrosomes and along the cytoskeletal structure. | price> |
R-R-3321 | Clozapine-d4 CAS No.204395-52-8 | Clozapine-d4/CAS No.204395-52-8 is the deuterium labeled Clozapine. Clozapine is an antipsychotic used for the research of schizophrenia. Clozapine has high affinity for a number of neuroreceptors. | price> |
R-C-1622 | U93631 CAS:152273-12-6 | U93631 is a GABAA receptor ligand of novel chemical structure with IC50 of 100 nM,and has been shown to induce a rapid,time-dependent decay of GABA-induced whole-cell Cl-currents in recombinant GABAA receptors. | price> |
R-R-3322 | F 13714 fumarate CAS No.208109-39-1 | F13714 fumarate/CAS No.208109-39-1, a selective 5-HT1A receptor biased agonist, shows antidepressant-like properties after a single administration in the mouse model of chronic mild stress. | price> |