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| Cat.No. | Product name | Product Description |
| R2304175 | dansylsarcosine | |
| R2304177 | Zanubrutinib | Zanubrutinib (BGB-3111) is a selective Bruton tyrosine kinase (Btk) in |
| R2304178 | Boc-Val-Cit-PAB | Boc-Val-Cit-PAB is a cleavable ADC linker used in the synthesis of&nbs |
| R2304179 | Gilteritinib(hemifumarate) | Gilteritinib (ASP2215) hemifumarate is a potent and ATP-competitive FLT3/AX |
| R2304180 | Emodepside | Emodepside (PF 1022-221) is a cyclooctadepsipeptide with broad-spectrum anthelmi |
| R2304181 | GANAXOLONE | Ganaxolone is a positive allosteric modulator of the action of the GABAA recepto |
| R2304182 | SB204741 | SB 204741 is a selective and high affinity 5-HT2B antagonist with a&nb |
| R2304183 | Lumigen APS 5 | Lumigen APS-5 is a substrate of alkaline phosphatase (ALP). Lumigen APS-5 can be |
| R2304184 | Selgantolimod (GS-9688) | Selgantolimod (GS-9688) is an orally active, potent and selective toll-like rece |
| R2304185 | Rotigotine Hydrochloride | Rotigotine Hydrochloride (N-0923 Hydrochloride) is a full agonist of dopamine re |
| R2304186 | LY78335 hydrochloride | 1-(2,3-Dichlorophenyl)ethanamine hydrochloride is a phenylethanolamine N-methylt |
| R2304187 | Bumetanide | Bumetanide (Ro 10-6338; PF 1593), a highly potent loop diuretic, is a Na+-K+-Cl+ |
| R2304188 | Pranoprofen | Pranoprofen is a non-steroidal anti-inflammatory agent (NSAID) for the research |
| R2304190 | F1063-0967 | F1063-0967 is a Dual-specificity phosphatase 26 (DUSP26) inhibitor with an IC50 |
| R2304191 | Lenacapavir;GS-6207 | Lenacapavir (GS-6207) is a HIV-1 capsid inhibitor. Lenacapavir shows anti-HIV ac |
| R2304192 | ASK1-IN-1 | ASK1-IN-1 is a CNS-penetrant ASK1 (apoptosis signal-regulating kinase 1) inhibit |
| R2304193 | JNJ-55308942 | JNJ-55308942 is a high-affinity, selective, brain-penetrant P2X7 functional anta |
| R2304196 | Azilsartan | Azilsartan (TAK-536) is an orally active, potent, selective and specific angiote |
| R2304197 | Ro5-3335;R287231 | Ro5-3335, a benzodiazepine, acts as an inhibitor of core binding factor (CBF) le |
| R2304198 | SM-102 | SM-102 is an ionizable amino lipid that can be used for the formation of lipid n |
| R2304199 | ALC-0315 | ALC-0315 is an ionisable aminolipid that is responsible for mRNA compaction and |
| R2304200 | Triprolidine hydrochloride | Triprolidine hydrochloride is an orally active histamine H1 antagonist. Triproli |
| R2304201 | PF-06260933 | PF-06260933 is an orally active and highly selective inhibitor of MAP4K4 with IC |
| R2304202 | Longdaysin | Longdaysin is a inhibitor of the Wnt/β-catenin signaling pathway, which exerts a |
| R2304203 | HA-100 hydrochloride | HA-100 hydrochloride is a potent protein kinase inhibitor, with IC50s of 4 μM, 8 |
