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| Catalog | name | Description | price |
|---|---|---|---|
| R-C-1598 | BMS582949(HCl) CAS:912806-16-7 (HCl) | BMS-582949(PS540446)is a potent and selective p38 mitogen-activated protein kinase(p38 MAPK)inhibitor with IC50 of 13nM,inhibiting both p38 kinase activity and activation of p38. | price> |
| R-R-3298 | LP 12 hydrochloride hydrate | LP 12 hydrochloride hydrate is a potent and selective 5-HT7 receptor agonist with a Ki of 0.13 nM. LP 12 hydrochloride hydrate displays selectivity for 5-HT7 over D2, 5-HT1A and 5-HT2A receptors (Ki values are 224 nM, 60.9 nM and >1000 nM, respectively). | price> |
| R-C-1599 | ADX 47273 CAS:851881-60-2 | ADX-47273 is a potent,selective and brain-penetrant mGluR5 positive allosteric modulator(PAM),with an EC50 of 0.17 μM for potentiation of glutamate(50nM) response.ADX-47273 has antipsychotic and procognitive activities. | price> |
| R-R-3299 | Temanogrel CAS No.887936-68-7 | Temanogrel/CAS No.887936-68-7 is a highly selective 5-HT2A receptor antagonist with a Ki of 4.9 nM. | price> |
| R-C-1600 | ozanimod CAS:1306760-87-1 | Ozanimod(RPC-1063)is a potent and selective S1P1 and S1P5 receptor agonist with EC50s of 410 pM and 11 nM in [35S]-GTPγS binding,respectively. | price> |
| R-R-3300 | Cariprazine-d8 CAS No.1308278-50-3 | Cariprazine-d8/CAS No.1308278-50-3 is a deuterium labeled Cariprazine. Cariprazine is a novel antipsychotic agent candidate that exhibits high affinity for the D3 (Ki=0.085 nM) and D2 (Ki=0.49 nM) receptors, and moderate affinity for the 5-HT1A receptor (Ki=2.6 nM). | price> |
| R-C-1601 | K-Ras-IN-1 CAS:84783-01-7 | K-Ras-IN-1 is a K-Ras inhibitor.K-Ras-IN-1 binds to K-Ras(WT),K-Ras(G12D),K-Ras(G12V),and H-Ras.K-Ras-IN-1 has potential for the research of pancreatic, colon and lung carcinomas. | price> |
| R-R-3301 | GR127935 hydrochloride CAS No.148642-42-6 | GR127935 hydrochloride/CAS No.148642-42-6 is a potent and orally active 5-HT1D and 5-HT1B receptor antagonist with pKis of 8.5 for both isoforms. GR127935 hydrochloride has 100-fold selectivity for 5-HT1B/1D receptors over 5-HT1A, 5-HT2A, and 5-HT2C receptors. GR127935 hydrochloride can be used in neurological disease research. | price> |
| R-C-1602 | Tolvaptan CAS:150683-30-0 | Tolvaptan(OPC-41061)is an orally effective nonpeptide arginine vasopressin V2 receptor antagonist with IC50 of 3 nM,used to treat hyponatremia. | price> |
| R-R-3302 | Trazodone CAS No.19794-93-5 | Trazodone (AF-1161 free base)/CAS No.19794-93-5 is a serotonin receptor antagonist and reuptake inhibitor. Trazodone can be used for the research of major depressive disorder. Trazodone also has potential for sleep disorder research. | price> |
| R-C-1603 | Mozavaptan CAS:137975-06-5 | Mozavaptan(OPC-31260)is a novel competitive vasopressin receptor antagonist for both V1 and V2 receptors with IC50 of 1.2 μM and 14 nM,respectively. | price> |
| R-R-3303 | 4,4-Diphenylbutylamine hydrochloride CAS No.22101-90-2 | 4,4-Diphenylbutylamine/CAS No.22101-90-2 shows affinity for the 5-HT2A and H1 receptors with Kis of 2589 and 1670 nM, respectively. | price> |
| R-C-1604 | Conivaptan hydrochloride CAS:168626-94-6 | Conivaptan(hydrochloride)is a non-peptide antagonist of vasopressin receptor, with Ki values of 0.48 and 3.04 nM for rat liver V1A receptor and rat kidney V2 receptor respectively. | price> |
| R-R-3304 | Cyamemazine CAS No.3546-03-0 | Cyamemazine/CAS No.3546-03-0 is a neuroleptic agent that contains the phenothiazine chromophore. Cyamemazine is often used as an anxiolytic. Cyamemazine is a potent 5-HT3 (Ki of 12 nM), 5-HT2A (Ki = 1.5 nM) and 5-HT2C (Ki of 75 nM) receptors antagonist with antipsychotic activity. | price> |
| R-C-1605 | Lixivaptan CAS:168079-32-1 | Lixivaptan(VPA-985,WAY-VPA985)is an orally active and selective vasopressin receptor V2 antagonist,with IC50 values of 1.2 and 2.3 nM for human and rat V2,respectively. | price> |
| R-R-3305 | Quetiapine hemifumarate (Standard) CAS No.111974-72-2 | Quetiapine (hemifumarate) (Standard)/CAS No.111974-72-2 is the analytical standard of Quetiapine (hemifumarate). This product is intended for research and analytical applications. Quetiapine hemifumarate is a 5-HT receptors agonist with a pEC50 of 4.77 for human 5-HT1A receptor. Quetiapine hemifumarate is a dopamine receptor antagonist with a pIC50 of 6.33 for human D2 receptor. Quetiapine hemifumarate has moderate to high affinity for the human D2, HT1A, 5-HT2A, 5-HT2C receptor with pKis of 7.25, 5.74, 7.54, 5.55. Antidepressant and anxiolytic effects. | price> |
| R-C-1606 | Entacapone CAS:130929-57-6 | Entacapone(OR-611)inhibits catechol-O-methyltransferase(COMT)with IC50 of 151 nM.Entacapone can be used for the research of Parkinson is disease.Entacapone serves as a inhibitor of FTO demethylation with an IC50 of 3.5 μM, can be used for the research of metabolic disorders. | price> |
| R-R-3306 | Eltoprazine hydrochloride CAS No.98206-09-8 | Eltoprazine (DU 28853) hydrochloride/CAS No.98206-09-8 is a 5-HT1A/5-HT1B receptors agonist and a 5-HT2C receptor antagonist. Eltoprazine hydrochloride shows antiaggressive and anxiogenic effects. | price> |
| R-C-1607 | FGFR4-IN-1 CAS:1708971-72-5 | FGFR4-IN-1 is a potent and selective FGFR4 inhibitor.FGFR4 may be a novel therapeutic target for gastric cancer. | price> |
| R-R-3307 | Eplivanserin hemifumarate CAS No.130580-02-8 | Eplivanserin (SR-46349) hemifumarate/CAS No.130580-02-8 is a potent, selective and orally active 5-HT2A receptor antagonist, with an IC50 of 5.8 nM in rat cortical membrane, and a Kd of 1.14 nM. Eplivanserin hemifumarate displays >20-fold selectivity more selective for 5-HT2A than 5-HT2B and 5-HT2C. | price> |

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