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Cat.No. Product name Product Description
R240411088 (2-(2-(2-羟基乙氧基)乙氧基)乙基)氨基甲酸叔丁酯 Boc-NH-PEG3 (PROTAC Linker 10) is a PEG-based PROTAC linker can be used in the s
R240411089 2-(2-(2-(2-羟基乙氧基)-乙氧基)乙氧基)氨基甲酸乙酯叔丁酯 Boc-NH-PEG4 (PROTAC Linker 12) is a PEG-based PROTAC linker can be used in the s
R240411090 N-Boc-PEG5-alcohol N-Boc-PEG5-alcohol is a PEG-based PROTAC linker that can be used in the synthesi
R240411091 (2-(2-(2-溴乙氧基)乙氧基)乙基)氨基甲酸叔丁酯 N-Boc-PEG3-bromide is a PEG/Alkyl/ether-based PROTAC linker can be used in the s
R240411092 N-Boc-PEG4-bromide N-Boc-PEG4-bromide is a PEG/Alkyl/ether-based PROTAC linker can be used in the s
R240411093 N-Boc-PEG5-bromide N-Boc-PEG5-bromide is a PEG/Alkyl/ether-based PROTAC linker can be used in the s
R240411094 Amino-PEG3-C2-sulfonic acid Amino-PEG3-C2-sulfonic acid is a PEG-based PROTAC linker that can be used in the
R240411095 Ald-Ph-amido-PEG4-C2-acid Ald-Ph-amido-PEG4-C2-acid is a noncleavable linker used for the antibody-drug co
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 Tersolisib  (STX-478) STX-478 (compound 80) is an oral CNS-penetrant allosteric mutant-selective PI3Kα
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-
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