yingweiwo
  1. Home
  2. Products
  3. Signaling Pathways
  4. New Products
  5. NEW1
  6. New1

New1

New1

New1 related products

Structure Cat No. Product Name CAS No. Product Description
PD-254552 V27191 PD-254552 284030-47-3 PD-254552 is a novel and potent bioactive compound
PD-298459 V27192 PD-298459 285127-00-6 PD-298459 is a novel and potent bioactive compound
PD-307243 V27193 PD-307243 313533-41-4 PD-307243 is an hERG channel activator.
PD-321852 V27194 PD-321852 622856-21-7 PD-321852 is a novel and potent Chk1 inhibitor
PD-34799-SA V27195 PD-34799-SA 860385-36-0 PD-34799-SA is a novel and potent inhibitor of vasoconstrictor
PD-404182 V16809 PD-404182 72596-74-8 PD-404182 (PD 404182;PD404182) is a novel and potent inhibitor of KDO 8-P synthase with antiangiogenic and antiviral activity (anti-HIV and anti-herpes simplex virus).
PD-85639 V27196 PD-85639 149838-21-1 PD-85639 is a novel and potent voltage-gated sodium (Na+) channel blocker
PD-89211 V27197 PD-89211 444725-49-9 PD-89211 is a novel and potent dopamine D4 receptor antagonist
PD089828 V27177 PD089828 179343-17-0 PD-089828 is an ATP-competitive inhibitor of FGFR-1, PDGFR-β and EGFR (IC50=0.15, 1.76, 5.47 µM, respectively) and a noncompetitive inhibitor of c-Src tyrosine kinase (IC50=0.18 µM).
PD159790 V27183 PD159790 179598-53-9 PD159790 is a novel and potent ECE-1 selective inhibitor.
PD164333 V22965 PD164333 PD164333 is a novel and potent endothelin ETA antagonist
PD166326 V27184 PD166326 185039-91-2 PD166326 is a pyridopyrimidine receptor tyrosine kinase inhibitor (TKI) (antagonist) with IC50s of 6 nM and 8 nM for Src and Abl inhibition, respectively.
PD168,077 V27185 PD168,077 190383-31-4 PD-168077 (PD168077) is a centrally active and selective dopamineD4receptor agonist with aKiof 9 nM.
PD180970 V22129 PD180970 287204-45-9 PD180970 (PD-180970) is a novel and potent Bcr-Abl inhbitor with anti-leukemia activity.
PD184161 V27187 PD184161 212631-67-9 PD184161 is an orally bioactive, time- and concentration-dependent MEK inhibitor (IC50=10-100 nM).
PDAT V13041 PDAT 1226213-83-7 PDAT is a noncompetitive indoleethylamine-N-methyltransferase (INMT) inhibitor (antagonist) with Ki of 84 μM for rabbit lung INMT (rabINMT).
PDD00017273 V40907 PDD00017273 1945950-21-9 PDD00017273 is a novel, potent and selective poly (ADP ribose) glycohydrolase (PARG) inhibitor with an IC50 of 26 nM.
PDD00017273 HCl V27198 PDD00017273 HCl 1945950-21-9 PDD00017273 is a novel, potent and selective poly (ADP ribose) glycohydrolase (PARG) inhibitor with an IC50 of 26 nM.
PDE10A-IN-8 V27200 PDE10A-IN-8 1354404-30-0 PDE10A-IN-8 is a novel and potent PDE10A inhibitor
PDE5-IN-6c V27202 PDE5-IN-6c 1448419-13-3 PDE5-IN-6c is a novel, potent and selective PDE5A1 inhibitor.
Contact Us
Tel: 1-708-310-1919 Fax: 1-708-557-7486 Email: sales@invivochem.com Frequently Asked Questions
Subscribe to our E-newsletter
Name
E-mail

Products are for research use only; We do not sell to patients
Copyright 2020 InvivoChem LLC | All Rights Reserved

linkedin facebook
Contact Us
Home Product Cart Member