Genomics of Drug Sensitivity in Cancer CGP-082996
Synonyms CINK4, KIN001-021
Targets CDK4
Target pathway Cell cycle
PubCHEM ID 24825971
Jsmol
Download molecule 24825971
PUBCHEM IUPAC INCHI InChI=1S/C27H32N6O/c1-2-28-25-17-26(29-21-8-11-23(34)12-9-21)32-27(31-25)30-22-10-13-24-20(16-22)14-15-33(24)18-19-6-4-3-5-7-19/h3-7,10,13-17,21,23,34H,2,8-9,11-12,18H2,1H3,(H3,28,29,30,31,32)
Smiles OC5(CCC(NC1(=NC(=NC(=C1)NCC)NC4(=CC3(=C(N(CC2(=CC=CC=C2))C=C3)C=C4))))CC5)
Cluster number 48
calculated LogS -6,084
Molecular weight 456,592
calculated LogP 4,6327
H-Acceptors 7
H-Donors 4
Ro5 violations 0
Druglikeness 2,3047
DrugScore 0,386999955359863
Mutagenic none
Tumorigenic none
Reproductive Effective none
Irritant none
Fish Toxicity Low FHMT
Fish Toxicity2 1,7616
Rat Acute Toxicity 2,4834
Acute Oral Toxicity III
Caco-2 Permeability Caco2-
Caco-2 Permeability2 0,6024
P-glycoprotein Substrate Substrate
P-glycoprotein Inhibitor Inhibitor
P-glycoprotein Inhibitor2 Inhibitor
Human Ether-a-go-go-Related Gene Inhibition Strong inhibitor
Human Ether-a-go-go-Related Gene Inhibition2 Inhibitor
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity2 0,2969
AMES Toxicity Non AMES toxic
CYP450 2C9 Substrate Non-substrate
CYP450 3A4 Substrate Non-substrate
CYP450 3A4 Inhibitor Non-inhibitor
CYP450 2C19 Inhibitor Non-inhibitor
CYP450 2C9 Inhibitor Non-inhibitor
CYP450 2D6 Inhibitor Inhibitor
CYP450 1A2 Inhibitor Inhibitor
CYP450 2D6 Substrate Non-substrate
Biodegradation Not ready biodegradable
Carcinogenicity (Three-class) Non-carcinogens
Carcinogens Non-required
Blood-Brain Barrier BBB+
CYP Inhibitory Promiscuity Low CYP Inhibitory Promiscuity
Honey Bee Toxicity Low HBT
Renal Organic Cation Transporter Inhibitor
Subcellular localization Lysosome
Human Intestinal Absorption HIA+
Aqueous solubility -3,213
Information useful only for research purposes.