Genomics of Drug Sensitivity in Cancer Idelalisib
Synonyms CAL-101, Zydelig
Targets PI3Kdelta
Target pathway PI3K/MTOR signaling
PubCHEM ID 11625818
Jsmol
Download molecule 11625818
PUBCHEM IUPAC INCHI InChI=1S/C22H18FN7O/c1-2-15(28-20-18-19(25-11-24-18)26-12-27-20)21-29-16-10-6-9-14(23)17(16)22(31)30(21)13-7-4-3-5-8-13/h3-12,15H,2H2,1H3,(H2,24,25,26,27,28)/t15-/m0/s1
Smiles FC5(=C4(C(=O)N(C1(=CC=CC=C1))C(C(NC2(=NC=NC3(=C2NC=N3)))CC)=NC4=CC=C5))
Cluster number 67
calculated LogS -6,049
Molecular weight 415,431
calculated LogP 2,858
H-Acceptors 8
H-Donors 2
Ro5 violations 0
Druglikeness 1,6037
DrugScore 8,18985670843582E-02
Mutagenic high
Tumorigenic high
Reproductive Effective low
Irritant high
Fish Toxicity High FHMT
Fish Toxicity2 1,3224
Rat Acute Toxicity 2,7055
Acute Oral Toxicity III
Caco-2 Permeability Caco2-
Caco-2 Permeability2 0,5227
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 0,62
AMES Toxicity AMES toxic
CYP450 2C9 Substrate Non-substrate
CYP450 3A4 Substrate Substrate
CYP450 3A4 Inhibitor Non-inhibitor
CYP450 2C19 Inhibitor Non-inhibitor
CYP450 2C9 Inhibitor Non-inhibitor
CYP450 2D6 Inhibitor Non-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 High CYP Inhibitory Promiscuity
Honey Bee Toxicity Low HBT
Renal Organic Cation Transporter Non-inhibitor
Subcellular localization Mitochondria
Human Intestinal Absorption HIA+
Aqueous solubility -3,7103
Information useful only for research purposes.