3,7,9-Trimethylpurine-6,8-dione

Details

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Internal ID 8fa05e0d-9be4-4928-9d78-8e4e96383fa9
Taxonomy Organoheterocyclic compounds > Imidazopyrimidines > Purines and purine derivatives > Purinones > Hypoxanthines
IUPAC Name 3,7,9-trimethylpurine-6,8-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H10N4O2/c1-10-4-9-6(13)5-7(10)12(3)8(14)11(5)2/h4H,1-3H3
InChI Key NWCPBHZYJHWSEL-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C8H10N4O2
Molecular Weight 194.19 g/mol
Exact Mass 194.08037557 g/mol
Topological Polar Surface Area (TPSA) 56.20 Ų
XlogP -1.10
Atomic LogP (AlogP) -1.03
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,7,9-Trimethylpurine-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 + 0.9921 99.21%
Caco-2 - 0.6714 67.14%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.8571 85.71%
Subcellular localzation Mitochondria 0.7353 73.53%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9656 96.56%
OATP1B3 inhibitior + 0.9510 95.10%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9569 95.69%
BSEP inhibitior - 0.9581 95.81%
P-glycoprotein inhibitior - 0.9399 93.99%
P-glycoprotein substrate - 0.9227 92.27%
CYP3A4 substrate - 0.6420 64.20%
CYP2C9 substrate + 0.5023 50.23%
CYP2D6 substrate - 0.8685 86.85%
CYP3A4 inhibition - 0.9605 96.05%
CYP2C9 inhibition - 0.9910 99.10%
CYP2C19 inhibition - 0.9925 99.25%
CYP2D6 inhibition - 0.9831 98.31%
CYP1A2 inhibition - 0.7999 79.99%
CYP2C8 inhibition - 0.9836 98.36%
CYP inhibitory promiscuity - 0.9868 98.68%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6930 69.30%
Eye corrosion - 0.9851 98.51%
Eye irritation - 0.9565 95.65%
Skin irritation - 0.8597 85.97%
Skin corrosion - 0.9636 96.36%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4079 40.79%
Micronuclear + 0.9200 92.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.9380 93.80%
Respiratory toxicity + 0.8444 84.44%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity + 0.4557 45.57%
Acute Oral Toxicity (c) II 0.7091 70.91%
Estrogen receptor binding - 0.9432 94.32%
Androgen receptor binding - 0.8076 80.76%
Thyroid receptor binding - 0.7454 74.54%
Glucocorticoid receptor binding - 0.7423 74.23%
Aromatase binding - 0.7355 73.55%
PPAR gamma - 0.9172 91.72%
Honey bee toxicity - 0.9564 95.64%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity - 0.7330 73.30%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.09% 95.56%
CHEMBL2581 P07339 Cathepsin D 91.25% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.36% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 86.96% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.38% 94.00%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 84.15% 94.42%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 83.38% 93.65%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 82.86% 93.40%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 80.56% 93.10%

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 163041436
LOTUS LTS0165081
wikiData Q105186535