6-methoxy-N,N,7,9-tetramethylpurin-9-ium-2-amine

Details

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Internal ID cb98b360-b6cf-4897-92ec-0ddab09cf47c
Taxonomy Organoheterocyclic compounds > Imidazopyrimidines > Purines and purine derivatives > Purinones > Hypoxanthines
IUPAC Name 6-methoxy-N,N,7,9-tetramethylpurin-9-ium-2-amine
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H16N5O/c1-13(2)10-11-8-7(9(12-10)16-5)14(3)6-15(8)4/h6H,1-5H3/q+1
InChI Key IGSRXYBZHDPVJT-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16N5O+
Molecular Weight 222.27 g/mol
Exact Mass 222.13548515 g/mol
Topological Polar Surface Area (TPSA) 47.10 Ų
XlogP 0.90
Atomic LogP (AlogP) -0.13
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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CHEMBL1187533

2D Structure

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2D Structure of 6-methoxy-N,N,7,9-tetramethylpurin-9-ium-2-amine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9280 92.80%
Caco-2 - 0.7094 70.94%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.6533 65.33%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9489 94.89%
OATP1B3 inhibitior + 0.9433 94.33%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7819 78.19%
BSEP inhibitior - 0.8953 89.53%
P-glycoprotein inhibitior - 0.9376 93.76%
P-glycoprotein substrate - 0.7346 73.46%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8202 82.02%
CYP3A4 inhibition - 0.8746 87.46%
CYP2C9 inhibition - 0.9199 91.99%
CYP2C19 inhibition - 0.8861 88.61%
CYP2D6 inhibition - 0.8447 84.47%
CYP1A2 inhibition + 0.8851 88.51%
CYP2C8 inhibition - 0.9360 93.60%
CYP inhibitory promiscuity - 0.9470 94.70%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5887 58.87%
Eye corrosion - 0.9834 98.34%
Eye irritation - 0.9533 95.33%
Skin irritation - 0.7624 76.24%
Skin corrosion - 0.9347 93.47%
Ames mutagenesis + 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3626 36.26%
Micronuclear + 0.9100 91.00%
Hepatotoxicity + 0.5356 53.56%
skin sensitisation - 0.8965 89.65%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity - 0.7643 76.43%
Acute Oral Toxicity (c) III 0.4745 47.45%
Estrogen receptor binding - 0.8001 80.01%
Androgen receptor binding - 0.6543 65.43%
Thyroid receptor binding + 0.5383 53.83%
Glucocorticoid receptor binding - 0.6840 68.40%
Aromatase binding + 0.6149 61.49%
PPAR gamma - 0.9060 90.60%
Honey bee toxicity - 0.9287 92.87%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.7900 79.00%
Fish aquatic toxicity - 0.6833 68.33%

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 91.33% 96.09%
CHEMBL2581 P07339 Cathepsin D 88.97% 98.95%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 88.24% 93.65%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 86.22% 93.10%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.18% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.21% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.61% 95.56%

Plants that contains it

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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.
Heterostemma brownii

Cross-Links

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PubChem 391983
LOTUS LTS0181851
wikiData Q105112799