ZNL 02-096 is a potent and selective Wee1 Degrader (PROTAC®) that comprises the Wee1 inhibitor AZD 1775 joined by a linker to the cereblon-binding ligand Pomalidomide (Cat
Azilsartan blocks the vasoconstrictor and aldosteronesecreting effects of angiotensin II by selectively blocking the binding of angiotensin II to the AT1 receptor in many tissues
Smiles: CC(=O)N1CCN(CCOC2=CC3=NC=NC(NC4=C(Cl)C=NC5OCOC=54)=C3C(=C2)OC(C)C)CC1
InChi: InChI=1S/C20H24O7/c1-12(15(21)22)4-3-8-18(2)14-7-10-19(17(25)27-18)9-5-13(16(23)24)6-11-20(14
FKBP12 PROTAC dTAG-13 (dTAG-13) also is a selective degrader of BET bromodomain transcriptional co-activator BRD4 by bridging BET bromodomains to an E3 ubiquitin ligase CRBN
Azido-PEG8-CH2COO-PFP Size:Contact [email protected] for quotation ZNL 02-096 is a potentAzido PEG8 CH2COO PFP is a PEG based PROTAC linker that can be used in the synthesis of PROTACs. Product information CAS Number: 2182601 80 3 Molecular Weight: 619. 53 Formula: C24H34F5N3O10 Chemical Name: 2,3,4,5,6 pentafluorophenyl 26 azido 3,6,9,12,15,18,21,24 octaoxahexacosanoate Smiles: [N ]=[N+]=NCCOCCOCCOCCOCCOCCOCCOCCOCC(=O)OC1C(F)=C(F)C(F)=C(F)C=1F InChiKey: JAGMBOXHJXUFJS UHFFFAOYSA N InChi: InChI=1S C24H34F5N3O10 c25 19