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18 hours) and cell cycle arrest (20-50 μM
(S)-ML753286 is a breast cancer resistance protein (BCRP) inhibitor with an IC50 of 0
Cell penetrant Proteolysis Targeting Chimera (PROTAC®) compound based on (+)-JQ1 (Cat
The cellular wild-type FGFR1 activity is potently inhibited by low nanomolar concentrations of PP58
DD-03-156 ope muscari 18 hours) and cell cycleDD 03 156 is a potent and selective degrader of CDK17 and LIMK2. The selectivity and potency of DD 03 156 is exquisite and makes an advanced starting point for the development of a chemical probe for the degradation of CDK17. Product information Molecular Weight: 1106. 31 Formula: C53H62F3N9O8S3 Smiles:
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