6-(3-Methoxypropanoyl)-1,3-dimethylpteridine-2,4-dione

Details

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Internal ID 6bc464da-1021-485e-a9c0-cad5b3aba33f
Taxonomy Organoheterocyclic compounds > Pteridines and derivatives
IUPAC Name 6-(3-methoxypropanoyl)-1,3-dimethylpteridine-2,4-dione
SMILES (Canonical) CN1C2=NC=C(N=C2C(=O)N(C1=O)C)C(=O)CCOC
SMILES (Isomeric) CN1C2=NC=C(N=C2C(=O)N(C1=O)C)C(=O)CCOC
InChI InChI=1S/C12H14N4O4/c1-15-10-9(11(18)16(2)12(15)19)14-7(6-13-10)8(17)4-5-20-3/h6H,4-5H2,1-3H3
InChI Key HSJCSXIFBOYMQN-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C12H14N4O4
Molecular Weight 278.26 g/mol
Exact Mass 278.10150494 g/mol
Topological Polar Surface Area (TPSA) 92.70 Ų
XlogP -0.90
Atomic LogP (AlogP) -0.75
H-Bond Acceptor 8
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-(3-Methoxypropanoyl)-1,3-dimethylpteridine-2,4-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9896 98.96%
Caco-2 - 0.6637 66.37%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.6285 62.85%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9139 91.39%
OATP1B3 inhibitior + 0.9362 93.62%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.7749 77.49%
P-glycoprotein inhibitior - 0.9175 91.75%
P-glycoprotein substrate - 0.8345 83.45%
CYP3A4 substrate + 0.5897 58.97%
CYP2C9 substrate - 0.6511 65.11%
CYP2D6 substrate - 0.8668 86.68%
CYP3A4 inhibition - 0.7776 77.76%
CYP2C9 inhibition - 0.7768 77.68%
CYP2C19 inhibition - 0.7895 78.95%
CYP2D6 inhibition - 0.9686 96.86%
CYP1A2 inhibition + 0.6949 69.49%
CYP2C8 inhibition - 0.8487 84.87%
CYP inhibitory promiscuity - 0.6857 68.57%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.6608 66.08%
Eye corrosion - 0.9891 98.91%
Eye irritation - 0.9795 97.95%
Skin irritation - 0.8274 82.74%
Skin corrosion - 0.9542 95.42%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7036 70.36%
Micronuclear + 0.7700 77.00%
Hepatotoxicity - 0.5823 58.23%
skin sensitisation - 0.9124 91.24%
Respiratory toxicity + 0.8000 80.00%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity + 0.4900 49.00%
Acute Oral Toxicity (c) III 0.6758 67.58%
Estrogen receptor binding - 0.5831 58.31%
Androgen receptor binding - 0.7953 79.53%
Thyroid receptor binding - 0.5788 57.88%
Glucocorticoid receptor binding + 0.6795 67.95%
Aromatase binding + 0.5590 55.90%
PPAR gamma + 0.5783 57.83%
Honey bee toxicity - 0.9155 91.55%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity - 0.5055 50.55%

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 98.56% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 96.73% 83.82%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.62% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.50% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.79% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.06% 86.33%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 86.88% 94.42%
CHEMBL4208 P20618 Proteasome component C5 86.57% 90.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.43% 99.23%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 82.94% 93.10%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 82.20% 81.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.43% 97.25%
CHEMBL2039 P27338 Monoamine oxidase B 81.06% 92.51%

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 14825209
LOTUS LTS0035203
wikiData Q105033071