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Catalog | name | Description | price |
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R-C-1108 | ANA-12 CAS: 219766-25-3 | ANA-12 is a potent and selective TrkB antagonist with IC50s of 45.6 nM and 41.1 μM for the high and low affinity sites,respectively. | price> |
R-R-2808 | Emicerfont CAS No.786701-13-1 | Emicerfont/CAS No.786701-13-1 is a corticotropin-releasing factor type 1 (CRF1) receptor antagonist with an IC50 of 66 nM. | price> |
R-C-1109 | ITD1 CAS:1099644-42-4 | ITD 1 is an inhibitor of TGF-β(IC50=0.85 µM).It is selective for TGF-β in an SBE4/Smad reporter assay,providing 83% inhibition when used at a concentration of 2.5 µM,over activin A,which is inhibited by 51% when used at the same concentration.ITD 1 inhibits TGF-β signaling by induction of TGF-β receptor type II degradation.It stimulates differentiation of mouse embryonic stem cells (mESCs)into cardiomyocytes. | price> |
R-R-2809 | GLP-1(7-36), amide acetate CAS No.1119517-19-9 | GLP-1(7-36), amide acetate/CAS No.1119517-19-9 is a major intestinal hormone that stimulates glucose-induced insulin secretion from β cells. | price> |
R-C-1110 | MK0822 CAS:603139-19-1 | Odanacatib is a potent,selective,and neutral inhibitor of cathepsin K(IC50s=0.2 and 1 nM for human and rabbit enzymes,respectively),a protease involved in osteoclastic bone resorption.It demonstrates high selectivity for cathepsin K over cathepsins B,L,and S.Formulations containing odanacatib reduce bone resorption,with lesser reductions in bone formation,resulting in increased bone mineral density. | price> |
R-R-2810 | Orforglipron CAS No.2212020-52-3 | Orforglipron (LY3502970) (GLP-1 receptor agonist 1)/CAS No.2212020-52-3 is a GLP-1 receptor agonist extracted from patent WO2018056453A1, Compound 67. | price> |
R-C-1111 | Sunitinib (SU 11248) CAS:557795-19-4 | Sunitinib(SU 11248)is a multi-targeted receptor tyrosine kinase inhibitor with IC50s of 80 nM and 2 nM for VEGFR2 and PDGFRβ,respectively.Sunitinib, an ATP-competitive inhibitor,effectively inhibits autophosphorylation of Ire1α by inhibiting autophosphorylation and consequent RNase activation. | price> |
R-R-2811 | MK 0893 CAS No.870823-12-4 | MK 0893/CAS No.870823-12-4 is a potent and selective glucagon receptor antagonist with an IC50 of 6.6 nM. | price> |
R-C-1112 | ML234 CAS: 1222800-79-4 | ML-324 is a potent JMJD2 demethylase inhibitor with demonstrated antiviral activity. | price> |
R-R-2812 | Adomeglivant CAS No.1488363-78-5 | Adomeglivant (LY2409021)/CAS No.1488363-78-5 is a potent, selective glucagon receptor (GluR) allosteric antagonist. Adomeglivant is widely used in the research for type 2 diabetes mellitus. | price> |
R-C-1113 | AC710 CAS:1351522-04-7 | AC710 is a potent,orally active,and selective platelet-derived growth factor receptor-family kinase inhibitor with potential anticancer activity. | price> |
R-R-2813 | GLP-1(7-37) acetate CAS No.1450806-98-0 | GLP-1(7-37) acetate/CAS No.1450806-98-0 is an intestinal insulinotropic hormone that augments glucose induced insulin secretion. | price> |
R-C-1114 | AC5216 CAS:226954-04-7 | Emapunil(AC-5216,18 kiloDalton Translocator Protein,XBD173)is a novel mitochondrial benzodiazepine receptor/translocator protein (MBR/TSPO)ligand. Emapunil(AC-5216)showes high affinity for MBRs prepared from rat whole brain with Ki of 0.297 nM and IC50 of 3.04 nM and 2.73 nM at rat glioma cells and human glioma cells,respectively. | price> |
R-R-2814 | Semaglutide TFA | Semaglutide TFA, a long-acting GLP-1 analogue, is a glucagon-like peptide-1 (GLP-1) receptor agonist. Semaglutide TFA has the potential for type 2 diabetes treatment. | price> |
R-C-1115 | SD208 CAS:627536-09-8 | SD-208 is a potent,orally active ATP-competitive transforming growth factor-β receptor 1(TGF-βRI)inhibitor(IC50=49 nM);displays>100-fold and>17-fold selectivity over TGF-βRII and other common kinases respectively. | price> |
R-R-2815 | BETP CAS No.1371569-69-5 | BETP/CAS No.1371569-69-5 is an agonist of glucagon-like peptide-1 (GLP-1) receptor, with EC50s of 0.66 and 0.755 μM for human and rat GLP-1 receptor, respectively. | price> |
R-C-1116 | RGB-286638 CAS: 784210-87-3 | RGB-286638 is a CDK inhibitor that inhibits the kinase activity of cyclin T1-CDK9,cyclin B1-CDK1,cyclin E-CDK2,cyclin D1-CDK4,cyclin E-CDK3,and p35-CDK5 with IC50s of 1,2,3,4,5 and 5 nM,respectively;also inhibits GSK-3β,TAK1,Jak2 and MEK1,with IC50s of 3,5,50,and 54 nM. | price> |
R-C-2816 | mPEG-Hyd-PLGA | PEG-PLGA is an amphiphilic AB diblock copolymer whose axis is hydrophilic(block glycolide)(PLGA)composition Peg polymer was terminated with methyl ether group and hydrophobic block was terminated with hydroxyl group.It has biological characteristics. | price> |
R-R-2816 | GLP-1(9-36)amide CAS No.161748-29-4 | GLP-1(9-36)amide/CAS No.161748-29-4 is a major metabolite of glucagon-like peptide-1-(7-36) amide formed by the enzyme dipeptidyl peptidase-4 (DPP-4). GLP-1(9-36)amide acts as an antagonist to the human pancreatic GLP-1 receptor. | price> |
R-C-1117 | HTH-01-015 CAS:1613724-42-7 | HTH-01-015 is a selective NUAK1/ARK5 inhibitor(IC50 is 100 nM).HTH-01-015 inhibits NUAK1 with>100-fold higher potency than NUAK2(IC50 of >10μM). | price> |