Genomics of Drug Sensitivity in Cancer AICA Ribonucleotide
Synonyms AICAR, N1-(b-D-Ribofuranosyl)-5-aminoimidazole-4-carboxamide
Targets AMPK agonist
Target pathway Metabolism
PubCHEM ID 65110
Jsmol
Download molecule 65110
PUBCHEM IUPAC INCHI InChI=1S/C9H15N4O8P/c10-7-4(8(11)16)12-2-13(7)9-6(15)5(14)3(21-9)1-20-22(17,18)19/h2-3,5-6,9,14-15H,1,10H2,(H2,11,16)(H2,17,18,19)/t3-,5-,6-,9-/m1/s1
Smiles P(=O)(OCC2(OC(N1(C(N)=C(C(=O)N)N=C1))C(C2O)O))(O)O
Cluster number 144
calculated LogS 0,379
Molecular weight 338,212
calculated LogP -6,1716
H-Acceptors 12
H-Donors 6
Ro5 violations 2
Druglikeness -18,802
DrugScore 0,46754892052748
Mutagenic none
Tumorigenic none
Reproductive Effective none
Irritant none
Fish Toxicity Low FHMT
Fish Toxicity2 1,603
Rat Acute Toxicity 2,4155
Acute Oral Toxicity III
Caco-2 Permeability Caco2-
Caco-2 Permeability2 -0,7722
P-glycoprotein Substrate Non-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 Non-inhibitor
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity2 0,3748
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 Non-inhibitor
Subcellular localization Mitochondria
Human Intestinal Absorption HIA-
Aqueous solubility -2,41
Information useful only for research purposes.