2,7-Dihydroxy-1,8-dimethoxypyrene

Details

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Internal ID 55ed0b41-deef-48ec-a683-d3daf850896b
Taxonomy Benzenoids > Pyrenes
IUPAC Name 1,8-dimethoxypyrene-2,7-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H14O4/c1-21-17-11-5-6-12-16-10(8-14(20)18(12)22-2)4-3-9(15(11)16)7-13(17)19/h3-8,19-20H,1-2H3
InChI Key GCHNQYKYNHGZKM-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C18H14O4
Molecular Weight 294.30 g/mol
Exact Mass 294.08920892 g/mol
Topological Polar Surface Area (TPSA) 58.90 Ų
XlogP 4.30
Atomic LogP (AlogP) 4.01
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,7-Dihydroxy-1,8-dimethoxypyrene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9893 98.93%
Caco-2 + 0.8196 81.96%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.7802 78.02%
OATP2B1 inhibitior - 0.7147 71.47%
OATP1B1 inhibitior + 0.9224 92.24%
OATP1B3 inhibitior + 0.9570 95.70%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.7252 72.52%
P-glycoprotein inhibitior - 0.7855 78.55%
P-glycoprotein substrate - 0.9366 93.66%
CYP3A4 substrate - 0.6692 66.92%
CYP2C9 substrate - 0.7933 79.33%
CYP2D6 substrate + 0.4916 49.16%
CYP3A4 inhibition - 0.6758 67.58%
CYP2C9 inhibition + 0.5963 59.63%
CYP2C19 inhibition + 0.7208 72.08%
CYP2D6 inhibition - 0.7163 71.63%
CYP1A2 inhibition + 0.9360 93.60%
CYP2C8 inhibition - 0.6314 63.14%
CYP inhibitory promiscuity + 0.6483 64.83%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8138 81.38%
Carcinogenicity (trinary) Non-required 0.4682 46.82%
Eye corrosion - 0.9748 97.48%
Eye irritation + 0.9527 95.27%
Skin irritation - 0.5639 56.39%
Skin corrosion - 0.9615 96.15%
Ames mutagenesis + 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4746 47.46%
Micronuclear + 0.6700 67.00%
Hepatotoxicity + 0.6322 63.22%
skin sensitisation - 0.7913 79.13%
Respiratory toxicity - 0.8667 86.67%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.6346 63.46%
Acute Oral Toxicity (c) III 0.5993 59.93%
Estrogen receptor binding + 0.9110 91.10%
Androgen receptor binding + 0.6050 60.50%
Thyroid receptor binding + 0.7453 74.53%
Glucocorticoid receptor binding + 0.7147 71.47%
Aromatase binding + 0.7569 75.69%
PPAR gamma + 0.7524 75.24%
Honey bee toxicity - 0.9566 95.66%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.7000 70.00%
Fish aquatic toxicity + 0.9591 95.91%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.84% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.86% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.06% 94.45%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.86% 99.15%
CHEMBL1951 P21397 Monoamine oxidase A 84.32% 91.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.92% 96.09%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 82.65% 92.68%
CHEMBL2535 P11166 Glucose transporter 82.48% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.82% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.62% 99.17%

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.
Crotalaria pallida
Uvaria lucida

Cross-Links

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PubChem 10613704
NPASS NPC1320
LOTUS LTS0041354
wikiData Q105006292