Target
Cyclin-dependent kinase 9
Ligand
BDBM316268
Substrate
n/a
Meas. Tech.
Fluorescent Polarization Assay
IC50
>10000±n/a nM
Citation
 Lori, FChafouleas, JDe Forni, DSolinas, AVarga, ZGreff, ZÖrfi, LKéri, G 4,6-disubstituted aminopyrimidine derivatives have anti-HIV activity US Patent  US9617225 Publication Date 4/11/2017 
Target
Name:
Cyclin-dependent kinase 9
Synonyms:
C-2K | CDC2L4 | CDK9 | CDK9_HUMAN | Cell division cycle 2-like protein kinase 4 | Cell division protein kinase 9 | Cyclin-Dependent Kinase 9 (CDK9) | Cyclin-dependent kinase 9 (CDK9) | Serine/threonine-protein kinase PITALRE | TAK | Tat-associated kinase complex catalytic subunit
Type:
Enzyme Subunit
Mol. Mass.:
42789.13
Organism:
Homo sapiens (Human)
Description:
n/a
Residue:
372
Sequence:
MAKQYDSVECPFCDEVSKYEKLAKIGQGTFGEVFKARHRKTGQKVALKKVLMENEKEGFPITALREIKILQLLKHENVVNLIEICRTKASPYNRCKGSIYLVFDFCEHDLAGLLSNVLVKFTLSEIKRVMQMLLNGLYYIHRNKILHRDMKAANVLITRDGVLKLADFGLARAFSLAKNSQPNRYTNRVVTLWYRPPELLLGERDYGPPIDLWGAGCIMAEMWTRSPIMQGNTEQHQLALISQLCGSITPEVWPNVDNYELYEKLELVKGQKRKVKDRLKAYVRDPYALDLIDKLLVLDPAQRIDSDDALNHDFFWSDPMPSDLKGMLSTHLTSMFEYLAPPRRKGSQITQQSTNQSRNPATTNQTEFERVF
  
Inhibitor
Name:
BDBM316268
Synonyms:
US10294218, Example 96 | US9617225, Example 96 | [6-(2-Methoxy-phenyl)-pyrimidin-4-yl]-(3-nitro-4-phenoxy-phenyl)-amine
Type:
Small organic molecule
Emp. Form.:
C23H18N4O4
Mol. Mass.:
414.4134
SMILES:
COc1ccccc1-c1cc(Nc2ccc(Oc3ccccc3)c(c2)[N+]([O-])=O)ncn1
Structure:
Search PDB for entries with ligand similarity: