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| Cat.No. | Product name | Product Description |
| R0011145 | N-(3-methoxyphenyl)quinazolin-4-amine hydrochloride | N-(3-methoxyphenyl)quinazolin-4-amine hydrochloride |
| R0011146 | Orphenadrine | Orphenadrine is a noncompetitive N-methyl-D-aspartate (NMDA) receptor antagonist |
| R0011147 | U-14624 | U-14624 is a potent and orally active dopamine beta-hydroxylase inhibitor. U-146 |
| R0011148 | 4-(1H-吡咯并[2,3-b]吡啶-3-基)嘧啶-2-胺 | 4-(1H-pyrrolo[2,3-b]pyridin-3-yl)pyrimidin-2-amine |
| R0011149 | bradyzide | bradyzide; (C32H42N8O5S2‚2.5TFA‚0.5H2O) same to report. |
| R0011150 | ribosomal protein A0 | ribosomal protein A0 |
| R0011151 | WB 4101盐酸盐 | WB-4101 HCL |
| R0011152 | Dirlotapide | Dirlotapide (CP742033) is a gut-selective inhibitor of microsomal triglyceride t |
| R0011153 | LDN-211904 | LDN-211904 is an inhibitor of EphB3 receptor tyrosine kinase. LDN-211904 enhance |
| R0011154 | 盐酸丙卡巴肼 | Procarbazine Hydrochloride is an orally active alkylating agent, with anticancer |
| R0011155 | 枸酸芬那君 | Orphenadrine citrate is an orally active and non-competitive NMDA receptor antag |
| R0011156 | (±)-WB 4101 hydrochloride | (±)-WB 4101 is a potent antagonist of noradrenaline. (±)-WB 4101 interacts with |
| R0011157 | JNJ-31001074 | Bavisant (JNJ-31001074) is an orally active, potent, brain-penetrating and highl |
| R0011158 | GPBAR-A | GPBAR-A is a specific agonist of the bile acid receptor GPBAR1. GPBAR-A can be u |
| R0011159 | PHA-543613 | PHA-543613 is a potent, orally active, brain-penetrant and selective α7 nAChR ag |
| R0011160 | SB220025 | SB 220025 is a reversible, orally active, cell-permeable, ATP-competitive and se |
| R0011161 | Aerobactin | Aerobactin is a siderophore produced by bacteria. Aerobactin is a highly potent |
| R0011179 | PDD00017273 | PDD00017273 is a radiosensitizing PARG) inhibitor with antitumor or activity for |
| R0011180 | PF-05221304 | PF-05221304 (NSC-170984) is an orally active, liver-targeted inhibitor of acetyl |
| R0011181 | Butyzamide | Butyzamide is an effective and oral Mpl activator. It is a novel non-peptide-bas |
| R0011182 | Selatinib | Selatinib is an orally active and potent dual inhibitor of EGFR and ErbB2 with a |
| R0011183 | PI4KIIIbeta-IN-10 | PI4KIIIbeta-IN-10 is a potent inhibitor of PI4KIIIβ (IC50 of 3.6 nM). |
| R0011184 | ADT-OH | ADT-OH is a hydrogen sulfide-releasing donor. ADT-OH induces apoptosis and inhib |
| R0011185 | Ruboxistaurin hydrochloride | Ruboxistaurin (LY333531) hydrochloride is an orally active, selective PKC beta i |
| R0011186 | 浅蓝菌素 | Cerulenin, a potent, natural inhibitor of fatty acid synthase (FASN), is an epox |
