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| Catalog | name | Description | price |
|---|---|---|---|
| R-C-1487 | Pazopanib (GW786034) CAS:444731-52-6 | Pazopanib(GW786034)is a novel multi-target inhibitor of VEGFR1,VEGFR2,VEGFR3,PDGFRβ,c-Kit,FGFR1,and c-Fms with IC50s of 10,30,47, 84,74,140 and 146 nM,respectively. | price> |
| R-R-3187 | Dolasetron CAS No.115956-12-2 | Dolasetron(MDL-73147)/CAS No.115956-12-2 is a serotonin 5-HT3 receptor antagonist used to treat nausea and vomiting following chemotherapy. | price> |
| R-C-1488 | U0126-EtOH CAS:1173097-76-1 | U0126-EtOH is a highly selective inhibitor of MEK1/2 with IC50 of 0.07 μM/0.06 μM in cell-free assays,100-fold higher affinity for N3-S218E/S222D MEK than PD98059.U0126 inhibits autophagy and mitophagy with antiviral activity. | price> |
| R-R-3188 | Tandospirone citrate CAS No.112457-95-1 | Tandospirone citrate/CAS No.112457-95-1 is a potent and selective 5-HT1A receptor partial agonist (Ki = 27 nM) that displays selectivity over SR-2, SR-1C, α1, α2, D1 and D2 receptors (Ki values ranging from 1300-41000 nM). | price> |
| R-C-1489 | Fulvestrant (ICI-182780) CAS:129453-61-8 | Fulvestrant(ICI-182780,ZD 9238,ZM 182780)is an estrogen recepto(ER)antagonist with IC50 of 0.94 nM in a cell-free assay.Fulvestrant also induces autophagy and apoptosis and has antitumor activity. | price> |
| R-R-3189 | Tropisetron Hydrochloride CAS No.105826-92-4 | Tropisetron Hydrochloride (SDZ-ICS-930)/CAS No.105826-92-4 is a selective 5-HT3 receptor antagonist and α7-nicotinic receptor agonist with an IC50 of 70. | price> |
| R-C-1490 | Decitabine (NSC 127716) CAS:2353-33-5 | Decitabine(NSC 127716,Deoxycytidine,Dacogen,5-aza-2-deoxycytidine,5-AZA-dC, 5-aza-CdR)is a DNA methyltransferase inhibitor,incorporating into DNA and resulting in hypomethylation of DNA and intra-S-phase arrest of DNA replication. It is used to treat myelodysplastic syndrome(MDS).Decitabine induces cell cycle arrest and apoptosis in various cancer cell lines. | price> |
| R-R-3190 | Nelotanserin CAS No.839713-36-9 | Nelotanserin/CAS No.839713-36-9 is a potent 5-HT2A inverse agonist, a moderately potent 5-HT2C partial inverse agonist and a weak 5-HT2B inverse agonist, with IC50s of 1.7, 79, 791 nM in IP accumulation assays, respectively. | price> |
| R-R-3191 | Pumosetrag Hydrochloride CAS No.194093-42-0 | Pumosetrag Hydrochloride (MKC-733; DDP-733)/CAS No.194093-42-0 is an orally available 5-HT3 partial agonist developed for the treatment of irritable bowel syndrome and gastroesophageal reflux disease. | price> |
| R-C-1492 | Bicalutamide (ICI-176334) CAS:90357-06-5 | Bicalutamide is a synthetic,nonsteroidal antiandrogen.Bicalutamide competitively binds to cytosolic androgen receptors in target tissues,thereby inhibiting the receptor binding of androgens.This agent does not bind to most mutated forms of androgen receptors. | price> |
| R-R-3192 | Befiradol hydrochloride CAS No.2436760-81-3 | Befiradol hydrochloride (NLX-112 hydrochloride)/CAS No.2436760-81-3 is a selective 5-HT1A receptor agonist. | price> |
| R-C-1493 | Letrozole (CGS 20267) CAS:112809-51-5 | Letrozole(CGS 20267)is a third generation inhibitor of aromatase with IC50 of 0.07-20 nM in cell-free assays.It has no effect on the plasma levels of 17α-OH progesterone,thyroid-stimulating hormone(TSH),luteinizing hormone(LH),follicle-stimulating hormone(FSH),or androstenedione and does not affect normal urine electrolyte excretion or thyroid function in clinical studies.Letrozole induces autophagy. | price> |
| R-R-3193 | Xaliproden hydrochloride CAS No.90494-79-4 | Xaliproden hydrochloride (SR57746A)/CAS No.90494-79-4 is a potent, selective and orally active agonist of 5-HT1A receptor, shows a high affinity for 5-HT1A specific binding sites in the rat hippocampus (IC50=3 nM). Xaliproden hydrochloride is also a selective antagonist of dopamine D2 receptor, has moderate affinity (IC50=0.1-1 μM). Xaliproden hydrochloride exhibits anti-depression and anti-anxiety effects, and it may possess therapeutic potential for the research of neurodegenerative diseases. | price> |
| R-C-1494 | Enalaprilat Dihydrate CAS: 84680-54-6 | Enalaprilat is the active metabolite of enalapril.It is the first dicarboxylate-containing ACE inhibitor and was developed partly to overcome these limitations of captopril. | price> |
| R-R-3194 | GR 125743 CAS No.148547-33-5 | GR 125743/CAS No.148547-33-5 is a selective 5-HT1B/1D receptor antagonist, with pKis of 8.85 and 8.31 for wild-type h5-HT1B and wild-type h5-HT1D, respectively. | price> |
| R-C-1495 | Daptomycin CAS:103060-53-3 | Daptomycin is a lipopeptide antibiotic used in the treatment of certain infections caused by Gram-positive organisms. | price> |
| R-R-3195 | Ecopipam hydrochloride CAS No.190133-94-9 | Ecopipam (SCH 39166) hydrochloride/CAS No.190133-94-9 is a potent, selective and orally active antagonist of dopamine D1/D5 receptor, with Kis of 1.2 nM and 2.0 nM, respectively. Ecopipam hydrochloride shows more than 40-flod selectivity over D2, D4, 5-HT, and α2a receptor (Ki=0.98, 5.52, 0.08, and 0.73 μM, respectively). Ecopipam hydrochloride can be used for the research of schizophrenia and obesity. | price> |
| R-C-1496 | BI-78D3 CAS:883065-90-5 | BI-78D3(JNK Inhibitor X),is a potent JNK inhibitor.BI-78D3 dose-dependently inhibits the phosphorylation of JNK substrates both in vitro and in cell.BI-78D3 not only blocks JNK dependent Con A-induced liver damage but also restores insulin sensitivity in mouse models of type 2 diabetes. | price> |
| R-R-3196 | A-582941 dihydrochloride CAS No.848591-90-2 | A-582941 dihydrochloride/CAS No.848591-90-2 is a potent, selective and brain-penetrant partial agonist of α7 nAChR, with Kis of 10.8 and 16.7 nM in rat brain membranes and human frontal cortex, respectively. A-582941 dihydrochloride also binds to human 5-HT3 receptor with a Ki of 150 nM. A-582941 has the potential for cognitive deficits associated with various neurodegenerative and psychiatric disorders research. | price> |
| R-C-1497 | SKF96365 CAS:130495-35-1 | SKF96365,originally identified as a blocker of receptor-mediated calcium entry, is widely used diagnostically,as a blocker of transient receptor potential canonical type(TRPC)channels. | price> |

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