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Catalog | name | Description | price |
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R-C-1852 | TP-4748 CAS:1150114-62-7 | TP-4748 is a biochemical. | price> |
R-R-3552 | PSB 0777 ammonium hydrate | PSB 0777 ammonium hydrate is a potent and selective adenosine A2A receptor full agonist with Ki values of 44.4 nM, 360 nM for rat and human A2A receptors, respectively. PSB 0777 ammonium hydrate has Ki values of ≥10000 nM, 541 nM for rat and human A1 receptors, respectively. PSB 0777 ammonium hydrate shows poor brain penetrant and perorally non-absorbable effect. PSB 0777 ammonium hydrate has the potential for inflammatory bowel disease (IBS) research research. | price> |
R-C-1853 | DBPR114 CAS:2443767-35-7 | DBPR114 is a potent multi-kinase inhibitor with potent activities against more than 57 oncogenic kinases,including Aurora-A,FLT3,CSF1R,MET,etc.DBPR114 exhibited favorable PK profiles:a long half-life(t1/2 =23.5h),moderate clearance and high volume of distribution.Also DBPR114 can effectively inhibit the growth of human acute myeloid leukemia MOLM-13 and MV4-11,MIA PaCa-2,Hep3B, MKN45,Colo205,and NTUB1 solid tumor xenografts in vivo without causing significant body weight loss. | price> |
R-R-3553 | ANR94 CAS No.634924-89-3 | ANR94/CAS No.634924-89-3 is a potent and selective adenosine A2A receptor (AA2AR) antagonist with an Ki of 46 nM for hAA2AR. ANR94 has the potential for the research of Parkinson disease. | price> |
R-C-1854 | TP748 CAS:951698-15-0 | TP748 is a bioactive chemical. | price> |
R-R-3554 | Xanthine amine congener hydrochloride CAS No.1783977-95-6 | Xanthine amine congener (XAC) hydrochloride/CAS No.1783977-95-6 is a non-selective adenosine receptor antagonist. Xanthine amine congener hydrochloride induces convulsions in mice. | price> |
R-C-1855 | THZ2 CAS:1604810-84-5 | THZ2,a THZ1 analog,is a selective inhibitor of CDK7 with IC50 of 13.9 nM.THZ2 efficiently suppresses the clonogenic growth of TNBC cells with IC50 of ~10nM. | price> |
R-R-3555 | MRS1334 CAS No.192053-05-7 | MRS1334/CAS No.192053-05-7 is a potent and selective human adenosine A3 receptor antagonist with Kis of 2.69 nM, >100 nM, >100 nM for hA3, rA1, rA2A, respectively. MRS1334 blocks the protective effect of Cl-IB-MECA leading to significant bradycardia and elevated ST segment. MRS1334 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. | price> |
R-C-1856 | THZ531 CAS:1702809-17-3 | THZ531 is a selective and covalent inhibitor of both CDK12 and CDK13 with IC50s of 158 nM and 69 nM. | price> |
R-R-3556 | 8-Cyclopentyl-1,3-dimethylxanthine CAS No.35873-49-5 | 8-Cyclopentyl-1,3-dimethylxanthine (Compound 2a)/CAS No.35873-49-5 is a selective adenosine A1 receptor antagonist with Kis of 10.9 nM and 1440 nM for A1 receptor and A2 receptor, respectively. | price> |
R-C-1857 | FM-381 CAS:2226521-65-7 | FM-381 is a potent covalent reversible inhibitor of JAK3 targeting the unique Cys909.FM-381 has an IC50 of 127 pM for JAK3,with 410,2700 and 3600-fold selectivity over JAK1,JAK2 and TYK2,respectively. | price> |
R-R-3557 | Norisoboldine CAS No.23599-69-1 | Norisoboldine/CAS No.23599-69-1 is an orally active natural aryl hydrocarbon receptor (AhR) agonist. Norisoboldine, as a major isoquinoline alkaloid present in Radix Linderae, can be used for the research of Rheumatoid arthritis and Ulcerative colitis. | price> |
R-C-1858 | Bafetinib (INNO-406) CAS:859212-16-1 | Bafetinib(INNO-406,NS-187)is a potent and selective dual Bcr-Abl/Lyn inhibitor with IC50 of 5.8nM/19nM in cell-free assays,does not inhibit the phosphorylation of the T315I mutant and is less potent to PDGFR and c-Kit. | price> |
R-R-3558 | Cirazoline hydrochloride CAS No.40600-13-3 | Cirazoline hydrochloride (LD 3098 hydrochloride)/CAS No.40600-13-3 is a potent competitive full α1A-adrenergic receptor (α1A-AR) agonist (Ki=120 nM) and only a partial agonist at α1B-AR (Ki= 960 nM) and α1D-AR (Ki=660 nM). | price> |
R-C-1859 | IOX4 CAS:1154097-71-8 | IOX4 is a selective HIF prolyl-hydroxylase 2(PHD2)inhibitor with an IC50 value of 1.6nM,induces HIFα in cells and in wildtype mice with marked induction in the brain tissue.IOX4 competes with and displaces 2-oxoglutarate(2OG)at the active site of PHD2. | price> |
R-R-3559 | MRS-3777 hemioxalate CAS No.1186195-57-2 | MRS-3777 hemioxalate/CAS No.1186195-57-2 is a selective adenosine A3 receptor antagonist. | price> |
R-C-1860 | Autophinib CAS:1644443-47-9 | Autophinib is a potent autophagy inhibitor with a novel chemotype with IC50 values of 90 and 40nM for autophagy in starvation induced autophagy assay and rapamycin induced autophagy assay.The IC50 value for Vps34 is 19nM in vitro. | price> |
R-R-3560 | Adenosine receptor antagonist 2 CAS No.2703054-47-9 | Adenosine receptor antagonist 2/CAS No.2703054-47-9 is an orally active A2a/A2b adenosine receptor antagonist with IC50s of 1 nM and 3 nM, respectively. Adenosine receptor antagonist 2 has anti-tumor activity. | price> |
R-C-1861 | SGI-1776 CAS:1025065-69-3 | SGI-1776 is a small-molecule pan-Pim protein kinase inhibitor with potential antineoplastic activity.Pim kinase inhibitor SGI-1776 binds to and inhibits the activities of Pim-1,-2 and -3,serine-threonine kinases,which may result in the interruption of the G1/S phase cell cycle transition,the expression of pro-apoptotic Bcl2 proteins and tumor cell apoptosis.PIM kinases play key roles in cell cycle progression and apoptosis inhibition and may be overexpressed in various malignancies. | price> |
R-R-3561 | Adenosine A1 receptor activator T62 CAS No.40312-34-3 | Adenosine A1 receptor activator T62/CAS No.40312-34-3 is an allosteric enhancer of adenosine A1 receptor. Adenosine A1 receptor activator T62 produces antinociception in animal models of acute pain and also reduces hypersensitivity in models of inflammatory and nerve-injury pain. | price> |