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Structure Cat No. Product Name CAS No. Product Description
PD 142505-0028 V19159 PD 142505-0028 161774-09-0 PD 142505-0028 is a novel and potent M1-selective muscarinic agonist
PD 142893 V27171 PD 142893 143037-36-9 PD 142893 is a novel and potent antagonist of endothelin-stimulated vasoconstriction
PD 145065 V21584 PD 145065 153049-49-1 PD 145065 is a potent, non-selective endothelin receptor blocker (antagonist) with an ETA receptor IC50 of 4 nM on rabbit renal artery vascular smooth muscle cells.
PD 154740 V27172 PD 154740 159614-69-4 PD 154740 is a novel and potent tachykinin neurokinin3 (NK3) antagonist
PD 160336 V27173 PD 160336 149092-00-2 PD 160336 is a novel and potent bioactive compound
PD 161182 V27174 PD 161182 168570-35-2 PD 161182 is a novel and potent bioactive compound
PD 165929 V21420 PD 165929 185215-75-2 PD 165929 is a novel and potent Bombesin BB1 antagonist
PD 168368 V27175 PD 168368 204066-82-0 PD 168368 is a potent, competitive and selective neuregulin B receptor (NMB-R) antagonist (inhibitor) with Ki of 15-45 nM.
PD 174265 V27176 PD 174265 216163-53-0 PD 174265 is a potent, cell-penetrating/penetrable, reversible, and selective EGFR inhibitor (antagonist) with IC50 of 450 pM.
PD-135666 V27178 PD-135666 134557-41-8 PD-135666 is a novel and potent CCKA receptor antagonist
PD-140548 V27179 PD-140548 140677-01-6 PD-140548 is a novel and potent CCKA receptor antagonist
PD-144418 V27180 PD-144418 154130-99-1 PD 144418 is a novel, high affinity, highly potent and specific sigma 1 (σ1) receptor ligand with Ki values of 0.08 nM and 1377 nM for σ1 and σ2 respectively.
PD-149164 V27181 PD-149164 181941-32-2 PD-149164 is a novel and potent agonist for the CCK-A receptor
PD-151307 V17746 PD-151307 225925-12-2 PD-151307 is a novel and potent N-type CCB (calcium channel blocker).
PD-156707 V27182 PD-156707 162412-70-6 PD-156707 is an orally bioactive, non-peptide, selective endothelin A receptor blocker (antagonist).
PD-161570 V6478 PD-161570 192705-80-9 PD-161570 is a potent and ATP-competitive inhibitor of the human FGF-1 receptor with IC50 of 39.9 nM and Ki of 42 nM.
PD-166285 diHCl V6541 PD-166285 diHCl 212391-63-4 PD-166285 diHCl(PD0166285 dihydrochloride) is a novel Wee1 and Chk1 inhibitor with anticancer activity and enzymatic activity at nanomolar concentrations (IC50s of 24 and 72 nM for WEE1 and Myt1, respectively).
PD-173956 V21131 PD-173956 305820-76-2 PD-173956 is a novel and potent inhibitor of tyrosine kinases
PD-198306 V27188 PD-198306 212631-61-3 PD 198306 is a selective MAPK/ERK kinase (MEK) inhibitor.
PD-217014 HCl V27189 PD-217014 HCl 444088-20-4 PD-217014 HCl is a novel and potent GABA analogue
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