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| Cat.No. | Product name | Product Description |
| R10093 | VU0364439 | VU 0364439 is a mGlu4 positive allosteric modulator (PAM), with EC50 of 19.8 nM. |
| R10149 | Ticagrelor (AZD6140; AR-C 126532XX) | Ticagrelor is the first reversibly binding oral P2Y12 receptor antagonist with K |
| R10188 | ciproxifan; FUB359 | Ciproxifan is a highly potent and selective histamin H3-receptor antagonist with |
| R10211 | LY2886721 | LY2886721 is a BACE inhibitor used for the treatment of Alzheimer's Disease. Pha |
| R10357 | LY310762 | LY310762 is a 5-HT1D receptor antagonist with Ki of 249 nM, having a weaker affi |
| R10381 | Oxiracetam | Oxiracetam, a cyclic derivative of gamma-aminobutyric acid (GABA), is used as a |
| R10433 | Prasugrel | Prasugrel is a thienopyridine ADP receptor (P2Y12) antagonist, used for the redu |
| R10443 | Carvedilol; BM14190 | Carvedilol is a non-selective beta blocker/alpha-1 blocker, used to treat conges |
| R10451 | Ondansetron; GR38032 | Ondansetron is a serotonin 5-HT3 receptor antagonist used mainly as an antiemeti |
| R10452 | Tropisetron; Novaban; SDZ-ICS930 | Tropisetron HCl is a potent and selective 5-HT3 receptor antagonist and α7-nicot |
| R10455 | Granisetron | Granisetron is a serotonin 5-HT3 receptor antagonist used as an antiemetic to tr |
| R10466 | Mianserin hydrochloride | Mianserin is an potent antagonist of H1 histamine receptor and 5-HT serotonin re |
| R10522 | Blonanserin,AD5423 | Blonanserin is a relatively selective serotonin (5-HT)2A and dopamine D2 antagon |
| R10523 | Aripiprazole | Aripiprazole is a novel atypical antipsychotic drug that is reported to be a hig |
| R10533 | Agomelatine (S-20098) | Agomelatine is classified as a norepinephrine-dopamine disinhibitor (NDDI) due t |
| R10538 | Carteolol hydrochloride (OPC-1085 hydrochloride) | Carteolol HCl is a β-adrenoceptor antagonist, used for the treatment of glaucoma |
| R10551 | Escitalopram oxalate | Escitalopram Oxalate is a selective serotonin (5-HT) reuptake inhibitor (SSRI) w |
| R10604 | Clemizole | Clemizole is a H1 histamine receptor antagonist.Recently, researchers have ident |
| R10698 | J147 | J-147 is a broad spectrum neuroprotective phenyl hydrazide compound(EC50=60-115 |
| R10717 | NS11394 | NS11394 is a potent and subtype-selective GABA(A) receptor-positive modulator; p |
| R10767 | MPEP hydrochloride | MPEP is a potent, highly selective non-competitive antagonist at the mGlu5a rece |
| R10774 | TG6-10-1 | TG6-10-1 is an EP2 antagonist, shows low-nanomolar antagonist activity against o |
| R10805 | Elacridar HCl | Elacridar hydrochloride is a P-glycoprotein inhibitor, and has been used both in |
| R10814 | Muscimol HBr | Muscimol hydrobromide is a potent but toxic structural analog of g-aminobutyric |
| R10826 | Suvorexant; MK4305 | Suvorexant (MK-4305) is a potent dual OX receptor antagonist with Ki of 0.55 nM |
