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| Cat.No. | Product name | Product Description |
| R240411096 | MPEG2-Br | m-PEG2-Br is a PEG-based PROTAC linker that can be used in the synthesis of PROT |
| R240411097 | [2-[2-(2-叠氮基乙氧基)乙氧基]乙氧基]乙酸 | N3-PEG3-CH2COOH (PROTAC Linker 14) is a PEG-based PROTAC linker can be used in t |
| R240411098 | 叠氮-四聚乙二醇-乙酸 | N33-TEG-COOH (N3-TEG-COOH) is a PEG-based PROTAC linker can be used in the synth |
| R240411099 | 1-苯基-2,5,8,11-四氧杂十三烷-13-醇 | BnO-PEG4-OH is a PEG-based PROTAC linker can be used in the synthesis of PROTACs |
| R240411100 | 丙炔基-二聚乙二醇 | Propargyl-PEG2-OH is a PEG-based PROTAC linker can be used in the synthesis of T |
| R240411101 | 三乙二醇单(2-丙炔基)醚 | Propargyl-PEG3-alcohol is a PEG-based PROTAC linker can be used in the synthesis |
| R240411102 | 丙炔基-四聚乙二醇 | Propargyl-PEG5-OH |
| R240411103 | CFI-400945富马酸盐 | CFI-400945 fumarate is a potent, selective and orally bioavailable PLK4 inhibito |
| R240411104 | 1-(2-氨基嘧啶-5-基)-3-(1-(5,7-二氟-3-甲基苯并呋喃-2-基)-2,2,2-三氟乙基)脲 | 1-(2-aminopyrimidin-5-yl)-3-(1-(5,7-difluoro-3-methylbenzofuran-2-yl)-2,2,2-trif |
| R240411105 | STX-478 | STX-478 (compound 80) is an oral CNS-penetrant allosteric mutant-selective PI3Kα |
| R002739 | Danuglipron | PF-06882961 is a potent, orally bioavailable agonist of the glucagon-like peptid |
| R240411107 | JNJ-63576253 | JNJ-63576253 (TRC-253) is a potent and orally active full antagonist of androgen |
| R240411108 | YQ128 | YQ128 is a potent and selective second-generation NLRP3 (NOD-like receptor P3) i |
| R2000689 | Dot1L-IN-4 | Dot1L-IN-4 is a potent disruptor of telomeric silencing 1-like protein (DOT1L) i |
| R240411110 | AZD4747 | AZD4747 is a selective, blood-brain barrier-permeable mutant GTPase KRASG12C inh |
| R240411111 | L-168049 | L-168049 is a potent, selective, orally active and non-competitive glucagon rece |
| R240411112 | HG106 | HG106 is a potent SLC7A11 inhibitor. HG106 markedly decreased cystine uptake and |
| R240411113 | N-(4-氟-2-(三氟甲基)苄基)-5-甲氧基-2-(吡啶-2-基)嘧啶-4-胺 | 4-Pyrimidinamine, N-[[4-fluoro-2-(trifluoromethyl)phenyl]methyl]-5-methoxy-2-(2- |
| R000816 | LH846 | LH846 is a selective inhibitor of CKIδ, with an IC50 of 290 nM, and less potentl |
