Genomics of Drug Sensitivity in Cancer Daporinad
Synonyms APO866, FK866, FK866
Targets NAMPT
Target pathway Metabolism
PubCHEM ID 6914657
Jsmol
Download molecule 6914657
PUBCHEM IUPAC INCHI InChI=1S/C24H29N3O2/c28-23(12-11-21-8-6-15-25-19-21)26-16-5-4-7-20-13-17-27(18-14-20)24(29)22-9-2-1-3-10-22/h1-3,6,8-12,15,19-20H,4-5,7,13-14,16-18H2,(H,26,28)/b12-11+
Smiles O=C(N2(CCC(CCCCNC(=O)C=CC1(=CN=CC=C1))CC2))C3(=CC=CC=C3)
Cluster number 106
calculated LogS -3,697
Molecular weight 391,513
calculated LogP 3,9862
H-Acceptors 5
H-Donors 1
Ro5 violations 0
Druglikeness -1,0751
DrugScore 0,433709050448647
Mutagenic none
Tumorigenic none
Reproductive Effective none
Irritant none
Fish Toxicity Low FHMT
Fish Toxicity2 1,6805
Rat Acute Toxicity 2,5494
Acute Oral Toxicity III
Caco-2 Permeability Caco2-
Caco-2 Permeability2 0,9334
P-glycoprotein Substrate Substrate
P-glycoprotein Inhibitor Inhibitor
P-glycoprotein Inhibitor2 Non-inhibitor
Human Ether-a-go-go-Related Gene Inhibition Weak inhibitor
Human Ether-a-go-go-Related Gene Inhibition2 Inhibitor
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity2 0,3379
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 Non-inhibitor
CYP450 1A2 Inhibitor Non-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 Mitochondria
Human Intestinal Absorption HIA+
Aqueous solubility -2,5212
Information useful only for research purposes.