2-Hydroxy-1,7,8-trimethoxypyrene

Details

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Internal ID 2ba40893-b666-4863-80a8-ebc6c11cb455
Taxonomy Benzenoids > Pyrenes
IUPAC Name 1,7,8-trimethoxypyren-2-ol
SMILES (Canonical) COC1=C(C2=C3C(=C1)C=CC4=CC(=C(C(=C43)C=C2)OC)O)OC
SMILES (Isomeric) COC1=C(C2=C3C(=C1)C=CC4=CC(=C(C(=C43)C=C2)OC)O)OC
InChI InChI=1S/C19H16O4/c1-21-15-9-11-5-4-10-8-14(20)18(22-2)12-6-7-13(19(15)23-3)17(11)16(10)12/h4-9,20H,1-3H3
InChI Key WDTIUHCVSBKXKZ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H16O4
Molecular Weight 308.30 g/mol
Exact Mass 308.10485899 g/mol
Topological Polar Surface Area (TPSA) 47.90 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.32
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Hydroxy-1,7,8-trimethoxypyrene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9928 99.28%
Caco-2 + 0.9299 92.99%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.7399 73.99%
OATP2B1 inhibitior - 0.8600 86.00%
OATP1B1 inhibitior + 0.9279 92.79%
OATP1B3 inhibitior + 0.9564 95.64%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.7703 77.03%
P-glycoprotein inhibitior - 0.7380 73.80%
P-glycoprotein substrate - 0.8593 85.93%
CYP3A4 substrate - 0.6005 60.05%
CYP2C9 substrate - 0.7933 79.33%
CYP2D6 substrate + 0.4916 49.16%
CYP3A4 inhibition - 0.5403 54.03%
CYP2C9 inhibition - 0.8815 88.15%
CYP2C19 inhibition - 0.5461 54.61%
CYP2D6 inhibition - 0.8484 84.84%
CYP1A2 inhibition + 0.9092 90.92%
CYP2C8 inhibition + 0.6742 67.42%
CYP inhibitory promiscuity - 0.5389 53.89%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8338 83.38%
Carcinogenicity (trinary) Non-required 0.4816 48.16%
Eye corrosion - 0.9803 98.03%
Eye irritation + 0.9214 92.14%
Skin irritation - 0.6717 67.17%
Skin corrosion - 0.9854 98.54%
Ames mutagenesis + 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4368 43.68%
Micronuclear + 0.5618 56.18%
Hepatotoxicity + 0.5197 51.97%
skin sensitisation - 0.8683 86.83%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.7104 71.04%
Acute Oral Toxicity (c) III 0.5550 55.50%
Estrogen receptor binding + 0.9161 91.61%
Androgen receptor binding + 0.5234 52.34%
Thyroid receptor binding + 0.7566 75.66%
Glucocorticoid receptor binding + 0.7437 74.37%
Aromatase binding + 0.8118 81.18%
PPAR gamma + 0.7695 76.95%
Honey bee toxicity - 0.9259 92.59%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.7051 70.51%
Fish aquatic toxicity + 0.9589 95.89%

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 97.27% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.45% 94.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 89.70% 89.62%
CHEMBL2535 P11166 Glucose transporter 86.70% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.50% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.73% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.13% 94.45%
CHEMBL1255126 O15151 Protein Mdm4 84.09% 90.20%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.15% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.60% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.39% 96.09%

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 10757180
NPASS NPC205293
LOTUS LTS0011785
wikiData Q105302683