2-imino-1,3-dimethyl-7H-purin-6-one

Details

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Internal ID e93b4ca9-96cf-4aa2-b671-b615218e4c3c
Taxonomy Organoheterocyclic compounds > Imidazopyrimidines > Purines and purine derivatives > Purinones > 6-oxopurines
IUPAC Name 2-imino-1,3-dimethyl-7H-purin-6-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H9N5O/c1-11-5-4(9-3-10-5)6(13)12(2)7(11)8/h3,8H,1-2H3,(H,9,10)
InChI Key SUQCEMFRQRUHPN-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C7H9N5O
Molecular Weight 179.18 g/mol
Exact Mass 179.08070993 g/mol
Topological Polar Surface Area (TPSA) 76.10 Ų
XlogP 0.10
Atomic LogP (AlogP) -0.92
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-imino-1,3-dimethyl-7H-purin-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 + 0.9796 97.96%
Caco-2 - 0.6888 68.88%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Mitochondria 0.5411 54.11%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9461 94.61%
OATP1B3 inhibitior + 0.9464 94.64%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9491 94.91%
P-glycoprotein inhibitior - 0.9416 94.16%
P-glycoprotein substrate - 0.8567 85.67%
CYP3A4 substrate - 0.5822 58.22%
CYP2C9 substrate - 0.6066 60.66%
CYP2D6 substrate - 0.8742 87.42%
CYP3A4 inhibition - 0.9041 90.41%
CYP2C9 inhibition - 0.9702 97.02%
CYP2C19 inhibition - 0.9470 94.70%
CYP2D6 inhibition - 0.9664 96.64%
CYP1A2 inhibition + 0.5883 58.83%
CYP2C8 inhibition - 0.9653 96.53%
CYP inhibitory promiscuity - 0.9732 97.32%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.6582 65.82%
Eye corrosion - 0.9888 98.88%
Eye irritation - 0.8571 85.71%
Skin irritation - 0.7586 75.86%
Skin corrosion - 0.9518 95.18%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5287 52.87%
Micronuclear + 0.9100 91.00%
Hepatotoxicity - 0.6110 61.10%
skin sensitisation - 0.8953 89.53%
Respiratory toxicity + 0.8000 80.00%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity + 0.5115 51.15%
Acute Oral Toxicity (c) II 0.5815 58.15%
Estrogen receptor binding - 0.9280 92.80%
Androgen receptor binding - 0.7494 74.94%
Thyroid receptor binding - 0.5258 52.58%
Glucocorticoid receptor binding - 0.8492 84.92%
Aromatase binding - 0.6988 69.88%
PPAR gamma - 0.8971 89.71%
Honey bee toxicity - 0.9230 92.30%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity - 0.6112 61.12%

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
CHEMBL5697 Q9GZT9 Egl nine homolog 1 93.13% 93.40%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.87% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.43% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.76% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.15% 85.14%
CHEMBL2581 P07339 Cathepsin D 88.78% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.17% 99.23%
CHEMBL255 P29275 Adenosine A2b receptor 85.38% 98.59%
CHEMBL1937 Q92769 Histone deacetylase 2 81.16% 94.75%

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 10749841
LOTUS LTS0134278
wikiData Q105261282