Genomics of Drug Sensitivity in Cancer Rucaparib
Synonyms PF-01367338, AG-014699, AG-14447, AG-14699
Targets PARP1, PARP2
Target pathway Genome integrity
PubCHEM ID 9931953
Jsmol
Download molecule 9931953
PUBCHEM IUPAC INCHI InChI=1S/C19H18FN3O.H3O4P/c1-21-10-11-2-4-12(5-3-11)18-14-6-7-22-19(24)15-8-13(20)9-16(23-18)17(14)15;1-5(2,3)4/h2-5,8-9,21,23H,6-7,10H2,1H3,(H,22,24);(H3,1,2,3,4)
Smiles P(=O)(O)(O)O.FC2(=CC=1(C(=O)NCCC=4(C=1C(=C2)NC=4(C3(=CC=C(CNC)C=C3)))))
Cluster number 95
calculated LogS -4,463
Molecular weight 323,37
calculated LogP 2,5426
H-Acceptors 4
H-Donors 3
Ro5 violations 0
Druglikeness 1,6734
DrugScore 0,409698722612886
Mutagenic none
Tumorigenic none
Reproductive Effective high
Irritant none
Fish Toxicity High FHMT
Fish Toxicity2 1,4553
Rat Acute Toxicity 2,6348
Acute Oral Toxicity III
Caco-2 Permeability Caco2-
Caco-2 Permeability2 -0,45
P-glycoprotein Substrate Substrate
P-glycoprotein Inhibitor Non-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 0,5296
AMES Toxicity Non AMES toxic
CYP450 2C9 Substrate Non-substrate
CYP450 3A4 Substrate Substrate
CYP450 3A4 Inhibitor 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 Non-inhibitor
Subcellular localization Mitochondria
Human Intestinal Absorption HIA+
Aqueous solubility -3,3606
Information useful only for research purposes.