9-(3,7-Dimethylocta-2,6-dienyl)-3,7-dimethylpurine-2,6,8-trione

Details

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Internal ID ec9dfab4-08f0-4f2c-a758-fae488359a7d
Taxonomy Organoheterocyclic compounds > Imidazopyrimidines > Purines and purine derivatives > Xanthines
IUPAC Name 9-(3,7-dimethylocta-2,6-dienyl)-3,7-dimethylpurine-2,6,8-trione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H24N4O3/c1-11(2)7-6-8-12(3)9-10-21-15-13(19(4)17(21)24)14(22)18-16(23)20(15)5/h7,9H,6,8,10H2,1-5H3,(H,18,22,23)
InChI Key RABARORWOHVBMF-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H24N4O3
Molecular Weight 332.40 g/mol
Exact Mass 332.18484064 g/mol
Topological Polar Surface Area (TPSA) 73.00 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.42
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 9-(3,7-Dimethylocta-2,6-dienyl)-3,7-dimethylpurine-2,6,8-trione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9948 99.48%
Caco-2 - 0.5390 53.90%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7582 75.82%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9220 92.20%
OATP1B3 inhibitior + 0.9386 93.86%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.5576 55.76%
P-glycoprotein inhibitior - 0.6298 62.98%
P-glycoprotein substrate - 0.7907 79.07%
CYP3A4 substrate - 0.5081 50.81%
CYP2C9 substrate - 0.7912 79.12%
CYP2D6 substrate - 0.8802 88.02%
CYP3A4 inhibition - 0.6585 65.85%
CYP2C9 inhibition - 0.7157 71.57%
CYP2C19 inhibition - 0.8281 82.81%
CYP2D6 inhibition - 0.9257 92.57%
CYP1A2 inhibition + 0.7517 75.17%
CYP2C8 inhibition - 0.9454 94.54%
CYP inhibitory promiscuity - 0.7917 79.17%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6914 69.14%
Eye corrosion - 0.9867 98.67%
Eye irritation - 0.9684 96.84%
Skin irritation - 0.7977 79.77%
Skin corrosion - 0.9296 92.96%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3644 36.44%
Micronuclear + 0.8200 82.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.8745 87.45%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity - 0.7309 73.09%
Acute Oral Toxicity (c) III 0.5147 51.47%
Estrogen receptor binding - 0.5955 59.55%
Androgen receptor binding - 0.6495 64.95%
Thyroid receptor binding - 0.4887 48.87%
Glucocorticoid receptor binding + 0.7030 70.30%
Aromatase binding - 0.5609 56.09%
PPAR gamma + 0.5424 54.24%
Honey bee toxicity - 0.8587 85.87%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9676 96.76%

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
CHEMBL255 P29275 Adenosine A2b receptor 95.60% 98.59%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.10% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.55% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.83% 94.45%
CHEMBL221 P23219 Cyclooxygenase-1 88.89% 90.17%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 88.45% 92.08%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.29% 95.56%
CHEMBL5103 Q969S8 Histone deacetylase 10 86.07% 90.08%
CHEMBL3401 O75469 Pregnane X receptor 85.14% 94.73%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 83.70% 93.10%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.56% 85.14%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 80.57% 86.92%

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 162843025
LOTUS LTS0016636
wikiData Q104196404