2-amino-3,7-dihydropurin-6-one

Details

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Internal ID 12fdabbc-58b6-4687-9a00-8593b7eb1f54
Taxonomy Organoheterocyclic compounds > Imidazopyrimidines > Purines and purine derivatives
IUPAC Name 2-amino-3,7-dihydropurin-6-one
SMILES (Canonical) C1=NC2=C(N1)C(=O)N=C(N2)N
SMILES (Isomeric) C1=NC2=C(N1)C(=O)N=C(N2)N
InChI InChI=1S/C5H5N5O/c6-5-9-3-2(4(11)10-5)7-1-8-3/h1H,(H4,6,7,8,9,10,11)
InChI Key UYTPUPDQBNUYGX-UHFFFAOYSA-N
Popularity 71 references in papers

Physical and Chemical Properties

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Molecular Formula C5H5N5O
Molecular Weight 151.13 g/mol
Exact Mass 151.04940980 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP -1.00
Atomic LogP (AlogP) -0.77
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-amino-3,7-dihydropurin-6-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9899 98.99%
Caco-2 - 0.9011 90.11%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Lysosomes 0.3478 34.78%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9669 96.69%
OATP1B3 inhibitior + 0.9494 94.94%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9146 91.46%
P-glycoprotein inhibitior - 0.9866 98.66%
P-glycoprotein substrate - 0.8917 89.17%
CYP3A4 substrate - 0.6899 68.99%
CYP2C9 substrate - 0.6282 62.82%
CYP2D6 substrate - 0.8871 88.71%
CYP3A4 inhibition - 0.8874 88.74%
CYP2C9 inhibition - 0.9377 93.77%
CYP2C19 inhibition - 0.8102 81.02%
CYP2D6 inhibition - 0.8974 89.74%
CYP1A2 inhibition - 0.8290 82.90%
CYP2C8 inhibition - 0.9594 95.94%
CYP inhibitory promiscuity - 0.9798 97.98%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9423 94.23%
Carcinogenicity (trinary) Non-required 0.6511 65.11%
Eye corrosion - 0.9895 98.95%
Eye irritation + 0.5891 58.91%
Skin irritation - 0.5759 57.59%
Skin corrosion - 0.9699 96.99%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7389 73.89%
Micronuclear + 0.8500 85.00%
Hepatotoxicity + 0.7875 78.75%
skin sensitisation - 0.9280 92.80%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity + 0.4685 46.85%
Acute Oral Toxicity (c) III 0.7210 72.10%
Estrogen receptor binding - 0.8648 86.48%
Androgen receptor binding - 0.6608 66.08%
Thyroid receptor binding - 0.5388 53.88%
Glucocorticoid receptor binding - 0.8422 84.22%
Aromatase binding - 0.5134 51.34%
PPAR gamma - 0.7346 73.46%
Honey bee toxicity - 0.8946 89.46%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity - 0.8880 88.80%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL4338 P00491 Purine nucleoside phosphorylase 5000 nM
IC50
PMID: 3093681

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL4040 P28482 MAP kinase ERK2 93.26% 83.82%
CHEMBL1937 Q92769 Histone deacetylase 2 90.96% 94.75%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.64% 85.14%
CHEMBL4070 P19784 Casein kinase II alpha (prime) 89.24% 91.67%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.32% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.14% 95.56%
CHEMBL255 P29275 Adenosine A2b receptor 86.85% 98.59%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.48% 89.34%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 84.93% 85.30%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.62% 94.00%
CHEMBL1952 P04818 Thymidylate synthase 83.53% 93.53%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.09% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.10% 94.45%
CHEMBL2535 P11166 Glucose transporter 80.48% 98.75%

Plants that contains it

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Cross-Links

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PubChem 764
NPASS NPC59314
ChEMBL CHEMBL219568
LOTUS LTS0179440
wikiData Q169313