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Catalog | name | Description | price |
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R-R-3579 | SDZ-WAG994 CAS No.130714-47-5 | SDZ-WAG994 (WAG-994)/CAS No.130714-47-5 is a stable, long-acting, selective and orally active A1-adenosine receptor agonist with a KD of 23 nM. SDZ-WAG994 can be used for the research of atrial fibrillation. | price> |
R-C-1880 | LX-2343 CAS:333745-53-2 | LX2343 is a BACE1 enzyme inhibitor with an IC50 value of 11.43±0.36 μM.LX2343 acts as a non-ATP competitive PI3K inhibitor with an IC50 of 15.99±3.23μM.LX2343 stimulates autophagy in its promotion of Aβ clearance. | price> |
R-R-3580 | Alloxazine CAS No.490-59-5 | Alloxazine/CAS No.490-59-5 is a selective A2b antagonist. Alloxazine completely block 5 N-Ethylcarboxamido adenosine (NECA)-mediated cyclic AMP accumulation with an IC50 of 2.9 μM. Alloxazine can be used for the research of cancer. | price> |
R-C-1881 | ML355 CAS:1532593-30-8 | ML355 is a potent and selective inhibitor of 12-Lipoxygenase(12-LOX)with an IC50 of 0.34μM,shows excellent selectivity over related lipoxygenases and cyclooxygenases,and possesses favorable ADME properties. | price> |
R-R-3581 | ST 1535 CAS No.496955-42-1 | ST 1535/CAS No.496955-42-1 is a potent and orally active A2A adenosine receptor antagonist. ST 1535 shows antiparkinsonian activity and antitremorigenic effects. ST 1535 has the potential for the research of Parkinson disease. | price> |
R-C-1882 | Evobrutinib (M-2951) CAS:1415823-73-2 | Evobrutinib(M-2951,MSC-2364447C)is a highly selective BTK inhibitor with an IC50 of 37.9 nM.It has potential anti-neoplastic activity. | price> |
R-R-3582 | Binodenoson CAS No.144348-08-3 | Binodenoson (MRE-0470)/CAS No.144348-08-3 is a potent and selective A2A adenosine receptor agonist (KD=270 nM). Binodenoson is being developed as a short-acting coronary vasodilator as an adjunct to radiotracers for use in myocardial stress imaging. | price> |
R-C-1883 | SSR240612 CAS:464930-42-5 | SSR240612 is a potent,and orally active specific non-peptide bradykinin B1 receptor antagonist,with Kis of 0.48 nM and 0.73nM for B1 kinin receptors of human fibroblast MRC5 and HEK cells expressing human B1 receptors,481nM and 358 nM for B2 receptors of guinea pig ileum membranes and CHO cells expressing human B1 receptor,respectively. | price> |
R-R-3583 | CL 316243 CAS No.138908-40-4 | CL316243/CAS No.138908-40-4 is a highly potent selective β3-adrenoceptor agonist with a EC50 of 3 nM, but is an extremely poor to β1/2- receptors.CL316243 is a effective stimulant of adipocyte lipolysis and increases brown adipose tissue thermogenesis and metabolic rate. CL316243 has the potential for the treatment obesity, diabetes and urge urinary incontinence. | price> |
R-C-1884 | FH1(BRD-K4477) CAS: 2719-05-3 | FH1(NSC 12407)enhances hepatocyte functions,and promotes the differentiation of induced pluripotent stem(iPS)-derived hepatocytes toward a phenotype more mature and the maturation of well-differentiated cultures of hepatocyte-like cells (iHeps). | price> |
R-R-3584 | Propranolol CAS No.525-66-6 | Propranolol/CAS No.525-66-6 is a nonselective β-adrenergic receptor (βAR) antagonist, has high affinity for the β1AR and β2AR with Ki values of 1.8 nM and 0.8 nM, respectively. Propranolol inhibits [3H]-DHA binding to rat brain membrane preparation with an IC50 of 12 nM. Propranolol is used for the study of hypertension, pheochromocytoma, myocardial infarction, cardiac arrhythmias, angina pectoris, and hypertrophic cardiomyopathy. | price> |
R-C-1885 | Saquinavir mesylate CAS:149845-06-7 | Saquinavir mesylate is an HIV Protease Inhibitor used in antiretroviral therapy. | price> |
R-R-3585 | Zenidolol hydrochloride CAS No.72795-01-8 | Zenidolol (ICI-118551) hydrochloride/CAS No.72795-01-8 is a highly selective β2 adrenergic receptor antagonist, with Kis of 0.7, 49.5 and 611 nM for β2, β1 and β3 receptors, respectively. | price> |
R-C-1886 | Crenigacestat (LY3039478) CAS:1421438-81-4 | LY3039478 is a orally bioavailable,novel small molecule Notch inhibitor with an IC50 of ~1nM in most of the tumor cell lines tested. | price> |
R-R-3586 | BRL-44408 maleate CAS No.681806-46-2 | BRL-44408 maleate/CAS No.681806-46-2 is an α2A-adrenoceptor antagonist (Ki: 8.5 nM). BRL-44408 maleate has antidepressant and analgesic activity. BRL-44408 also improves cecal ligation puncture (CLP)-induced acute lung injury. | price> |
R-C-1887 | Opaganib (ABC294640) CAS:915385-81-8 | ABC294640 is an orally available,aryladamantane compound and selective inhibitor of sphingosine kinase-2(SK2)with potential antineoplastic activity. | price> |
R-R-3587 | Adenosine receptor antagonist 4 CAS No.133240-06-9 | Adenosine receptor antagonist 4 (compound 2)/CAS No.133240-06-9 is an adenosine A1 receptor antagonist with a Ki of 101 nM for human A1 receptor. | price> |
R-C-1888 | CB-03-01 CAS:19608-29-8 | Clascoterone(Winlevi,Cortexolone 17 alpha-propionate,Cortexolone 17α-propionate, CB-03-01)is a topical and peripherally selective antagonist of androgen receptor(AR). | price> |
R-R-3588 | FSCPX CAS No.156547-56-7 | FSCPX/CAS No.156547-56-7 is a potent and selective irreversible antagonist of A1 adenosine receptor (A1AR), with low nanomolar potency for binding to the A1AR. FSCPX could modify the effect of NBTI, a nucleoside transport inhibitor, by reducing the interstitial adenosine level in the guinea pig atrium. | price> |
R-C-1889 | Sapacitabine CAS:151823-14-2 | Sapacitabine is hydrolyzed by amidases to the deoxycytosine analogue CNDAC(2-Cyano-2-deoxyarabinofuranosylcytosine),which is then phosphorylated into the active triphosphate form.As an analogue of deoxycytidine triphosphate,CNDAC triphosphate incorporates into DNA strands during replication,resulting in single-stranded DNA breaks during polymerization due to beta-elimination during the fidelity checkpoint process; cell cycle arrest in the G2 phase and apoptosis ensue. | price> |