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Catalog | name | Description | price |
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R-C-2155 | Urolithin B CAS:1139-83-9 | Urolithin B is a metabolite of the polyphenolic antioxidant ellagic acid that has diverse biological activities.It is formed from ellagic acid via several intermediates by gut microbiota.Urolithin B reduces the levels of advanced glycation end products(AGEs)in a cell-free assay in a concentration-dependent manner.Urolithin B(1.18-4.7nM)inhibits testosterone-induced proliferation of MCF-7aro cells. | price> |
R-R-3855 | ADRA1D receptor antagonist 1 CAS No.1191908-14-1 | ADRA1D receptor antagonist 1/CAS No.1191908-14-1 is a potent, selective and orally active α1D adrenoceptor antagonist, with a Ki of 1.6 nM. | price> |
R-C-2156 | Licochalcone D CAS:144506-15-0 | Licochalcone D,a flavonoid compound mainly existing in the root of Glycyrrhiza inflate,is a potent inhibitor of NF-kappaB(NF-κB)p65.Licochalcone D possesses antioxidant,anti-inflammatory,anti-cancer properties. | price> |
R-R-3856 | Propranolol-d7 CAS No.98897-23-5 | Propranolol-d7/CAS No.98897-23-5 is the deuterium labeled Propranolol. Propranolol 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-2157 | Licochalcone B CAS:58749-23-8 | Licochalcone B has antitumor,antimetastatic,cardioprotective,antioxidant, antiapoptotic,and anti-inflammatory effects,it can significantly inhibit LPS-induced phosphorylation at serine 276 and transcriptional activation of NF-KB. Licochalcone B can protect the liver from carbon tetrachloride(CCl4)-induced injury,the protection may be due to inhibition of p38 and NFκB signaling,which subsequently reduces inflammation in the liver. | price> |
R-R-3857 | Aposcopolamine CAS No.535-26-2 | Aposcopolamine/CAS No.535-26-2 is an alkaloid that can be isolated from Datura ferox. Aposcopolamin can closely binds with ACHE, ADRA2A and CHRM2. Aposcopolamine can be used for the research of Alzheimer disease. | price> |
R-C-2158 | Myrislignan CAS: 171485-39-5 | Myrislignan has anti-inflammatory,and anti-cancer activities,it inhibited NF-κB signalling pathway activation,inhibited the proliferation of A549 cells in a dose-and time-dependent manner,it also significantly induced apoptosis and cell cycle arrest in A549 cells. | price> |
R-R-3858 | Tamsulosin hydrochloride CAS No.106463-17-6 | Tamsulosin hydrochloride ((R)-(-)-YM12617)/CAS No.106463-17-6 is an inhibitor of α1-adrenergic receptor. Tamsulosin hydrochloride is used for the research of prostatic hyperplasia. Tamsulosin hydrochloride attenuates abdominal aortic aneurysm growth in animal models. | price> |
R-C-2159 | E3330 CAS:136164-66-4 | E3330(APX-3330)is a direct,orally active and selective AP endonuclease 1(APE1; REF-1)inhibitor,which suppresses NF-κB DNA-binding activity.E3330(APX-3330) blocks TNF-α-induced activation of IL-8 production in liver cancer cell lines. E3330(APX-3330)shows anticancer properties,such as inhibition of cancer cell growth and migration. | price> |
R-R-3859 | Medroxalol CAS No.56290-94-9 | Medroxalol (RMI81968)/CAS No.56290-94-9 is an orally active adrenergic receptor antagonist, blocks α- and β-adrenergic receptors. Medroxalol shows antihypertensive and vasodilating effects. | price> |
R-C-2160 | Withaferin A CAS:5119-48-2 | Withaferin A is a steroidal lactone present in W.somnifera that at 2-25μM has been shown to bind to and induce aggregation of vimentin intermediate filaments in cultured endothelial cells and fibroblasts,causing apoptosis. | price> |
R-R-3860 | Bupranolol CAS No.14556-46-8 | Bupranolol/CAS No.14556-46-8 is an orally active, competitive and non-selective β-adrenoceptor antagonist without intrinsic sympathomimetic activity. | price> |
R-C-2161 | AZD7648 CAS:2230820-11-6 | AZD7648 is a potent inhibitor of DNA-PK with an IC50 of 0.6nM in biochemical assay and more than 100-fold selective against 396 other kinases. | price> |
R-R-3861 | BMS-466442 CAS No.1598424-76-0 | BMS-466442/CAS No.1598424-76-0 is a potent and selective inhibitor of asc-1 (alanine serine cysteine transporter-1), with an IC50 of 11 nM. BMS-466442 inhibits [3H] D-serine uptake into rat brain synaptosomes, with an IC50 of 400 nM. BMS-466442 can be used for schizophrenia research. | price> |
R-C-2162 | AZD1480 CAS:935666-88-9 | AZD1480 is an orally bioavailable inhibitor of Janus-associated kinase 2(JAK2)with potential antineoplastic activity.JAK2 inhibitor AZD1480 inhibits JAK2 activation,leading to the inhibition of the JAK/STAT(signal transducer and activator of transcription)signaling including activation of STAT3. | price> |
R-R-3862 | Desglymidodrine CAS No.3600-87-1 | Desglymidodrine (ST 1059)/CAS No.3600-87-1, the active metabolite of Midodrine (HY-12749), is a selective α1-adrenoceptor agonist. Desglymidodrine is an effective arterial and venous vasoconstrictor and can be used to regulate blood pressure. | price> |
R-C-2163 | Linderalactone CAS:728-61-0 | Linderalactone inhibits human lung cancer growth by modulating the expression of apoptosis-related proteins(Bax and Bcl-2)with an IC50 of 15µM in A-549 cells. Linderalactone induces G2/M cell cycle arrest and could also suppress the JAK/STAT signalling pathway. | price> |
R-R-3863 | Metipranolol hydrochloride CAS No.36592-77-5 | Metipranolol hydrochloride/CAS No.36592-77-5 is a non-selective β adrenergic receptor blocking agent. | price> |
R-C-2164 | PF-06826647 CAS:2127109-84-4 | PF-06826647 is an orally active and selective TYK2 inhibitor(IC50=17nM),which binds to TYK2 catalytically active JH1 domain.PF-06826647 displays selectivity for TYK2 over JAK1(IC50=383nM)and JAK2(74nM).PF-06826647 can be used for the research of psoriasis,ulcerative colitis, and hidradenitis suppurativa. | price> |
R-R-3864 | Dicentrine CAS No.517-66-8 | Dicentrine/CAS No.517-66-8 is a natural product isolated from the plant Stephania epigaea Lo with antihypertensive effect. Dicentrine is an α1-adrenoceptor antagonist which has effective against human hyperplastic prostates. | price> |