2-amino-7-methyl-3,9-dihydropurine-6,8-dione

Details

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Internal ID 426283cf-3f40-453b-b82f-d28bf0560514
Taxonomy Organoheterocyclic compounds > Imidazopyrimidines > Purines and purine derivatives > Purinones > Hypoxanthines
IUPAC Name 2-amino-7-methyl-3,9-dihydropurine-6,8-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H7N5O2/c1-11-2-3(9-6(11)13)8-5(7)10-4(2)12/h1H3,(H4,7,8,9,10,12,13)
InChI Key VHPXSVXJBWZORQ-UHFFFAOYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C6H7N5O2
Molecular Weight 181.15 g/mol
Exact Mass 181.05997448 g/mol
Topological Polar Surface Area (TPSA) 99.80 Ų
XlogP -1.50
Atomic LogP (AlogP) -1.47
H-Bond Acceptor 5
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-7-methyl-3,9-dihydropurine-6,8-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9825 98.25%
Caco-2 - 0.7055 70.55%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.4480 44.80%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9617 96.17%
OATP1B3 inhibitior + 0.9486 94.86%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9435 94.35%
P-glycoprotein inhibitior - 0.9662 96.62%
P-glycoprotein substrate - 0.9027 90.27%
CYP3A4 substrate - 0.6399 63.99%
CYP2C9 substrate - 0.6066 60.66%
CYP2D6 substrate - 0.8838 88.38%
CYP3A4 inhibition - 0.9645 96.45%
CYP2C9 inhibition - 0.9755 97.55%
CYP2C19 inhibition - 0.9402 94.02%
CYP2D6 inhibition - 0.9580 95.80%
CYP1A2 inhibition - 0.8132 81.32%
CYP2C8 inhibition - 0.9848 98.48%
CYP inhibitory promiscuity - 0.9943 99.43%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6689 66.89%
Eye corrosion - 0.9885 98.85%
Eye irritation - 0.8822 88.22%
Skin irritation - 0.7914 79.14%
Skin corrosion - 0.9558 95.58%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6700 67.00%
Micronuclear + 0.9500 95.00%
Hepatotoxicity + 0.7500 75.00%
skin sensitisation - 0.9261 92.61%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity + 0.7099 70.99%
Acute Oral Toxicity (c) III 0.5058 50.58%
Estrogen receptor binding - 0.8869 88.69%
Androgen receptor binding - 0.8065 80.65%
Thyroid receptor binding - 0.5996 59.96%
Glucocorticoid receptor binding - 0.6116 61.16%
Aromatase binding + 0.5859 58.59%
PPAR gamma - 0.7733 77.33%
Honey bee toxicity - 0.9626 96.26%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity - 0.8222 82.22%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.18% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.79% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.70% 94.00%
CHEMBL2581 P07339 Cathepsin D 89.01% 98.95%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 88.99% 94.42%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.65% 99.23%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.98% 93.65%
CHEMBL255 P29275 Adenosine A2b receptor 80.83% 98.59%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 308075
LOTUS LTS0052443
wikiData Q27144377