6-Methoxy-7-methyl-8-oxoguanine

Details

Top
Internal ID d2006282-1288-41b9-ad69-763c4ddb1411
Taxonomy Organoheterocyclic compounds > Imidazopyrimidines > Purines and purine derivatives > Purinones > Hypoxanthines
IUPAC Name 2-amino-6-methoxy-7-methyl-9H-purin-8-one
SMILES (Canonical) CN1C2=C(NC1=O)N=C(N=C2OC)N
SMILES (Isomeric) CN1C2=C(NC1=O)N=C(N=C2OC)N
InChI InChI=1S/C7H9N5O2/c1-12-3-4(10-7(12)13)9-6(8)11-5(3)14-2/h1-2H3,(H3,8,9,10,11,13)
InChI Key DAHAOEBKKGDLMP-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C7H9N5O2
Molecular Weight 195.18 g/mol
Exact Mass 195.07562455 g/mol
Topological Polar Surface Area (TPSA) 93.40 Ų
XlogP -0.70
Atomic LogP (AlogP) -0.75
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

Top
2-amino-6-methoxy-7-methyl-9H-purin-8-one

2D Structure

Top
2D Structure of 6-Methoxy-7-methyl-8-oxoguanine

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9867 98.67%
Caco-2 - 0.6506 65.06%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Lysosomes 0.4626 46.26%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9677 96.77%
OATP1B3 inhibitior + 0.9488 94.88%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8997 89.97%
P-glycoprotein inhibitior - 0.9542 95.42%
P-glycoprotein substrate - 0.8122 81.22%
CYP3A4 substrate - 0.5677 56.77%
CYP2C9 substrate - 0.7953 79.53%
CYP2D6 substrate - 0.8530 85.30%
CYP3A4 inhibition - 0.9044 90.44%
CYP2C9 inhibition - 0.9864 98.64%
CYP2C19 inhibition - 0.9570 95.70%
CYP2D6 inhibition - 0.9529 95.29%
CYP1A2 inhibition + 0.5397 53.97%
CYP2C8 inhibition - 0.9665 96.65%
CYP inhibitory promiscuity - 0.9840 98.40%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6189 61.89%
Eye corrosion - 0.9894 98.94%
Eye irritation - 0.8290 82.90%
Skin irritation - 0.8069 80.69%
Skin corrosion - 0.9554 95.54%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5640 56.40%
Micronuclear + 0.9300 93.00%
Hepatotoxicity + 0.6790 67.90%
skin sensitisation - 0.9277 92.77%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity + 0.5639 56.39%
Acute Oral Toxicity (c) III 0.4586 45.86%
Estrogen receptor binding - 0.7908 79.08%
Androgen receptor binding - 0.7976 79.76%
Thyroid receptor binding - 0.5766 57.66%
Glucocorticoid receptor binding - 0.5313 53.13%
Aromatase binding + 0.5974 59.74%
PPAR gamma - 0.8043 80.43%
Honey bee toxicity - 0.9360 93.60%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity - 0.7374 73.74%

Targets

Top

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.89% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.83% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.93% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.28% 95.56%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 88.21% 94.42%
CHEMBL2581 P07339 Cathepsin D 87.16% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.96% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.40% 94.45%
CHEMBL1937 Q92769 Histone deacetylase 2 81.32% 94.75%
CHEMBL255 P29275 Adenosine A2b receptor 80.49% 98.59%

Plants that contains it

Top
Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Gentiana crassicaulis

Cross-Links

Top
PubChem 10584006
NPASS NPC17940
LOTUS LTS0208180
wikiData Q104973537