CID 162876502

Details

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Internal ID 96ac870c-a571-441c-ba5c-bb2f654a8a9a
Taxonomy Benzenoids > Naphthalenes
IUPAC Name
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H12O5/c20-14-7-8-15(21)18(14)9-10-19(17(18)22)23-12-5-1-3-11-4-2-6-13(24-19)16(11)12/h1-10,17,22H/t17-/m1/s1
InChI Key GQHMDFLEHLUOBV-QGZVFWFLSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H12O5
Molecular Weight 320.30 g/mol
Exact Mass 320.06847348 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 2.20
Atomic LogP (AlogP) 1.93
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 162876502

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9760 97.60%
Caco-2 - 0.6193 61.93%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.6792 67.92%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9448 94.48%
OATP1B3 inhibitior + 0.9552 95.52%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.6031 60.31%
P-glycoprotein inhibitior - 0.6829 68.29%
P-glycoprotein substrate - 0.9316 93.16%
CYP3A4 substrate - 0.5215 52.15%
CYP2C9 substrate - 0.8134 81.34%
CYP2D6 substrate - 0.8114 81.14%
CYP3A4 inhibition + 0.5827 58.27%
CYP2C9 inhibition - 0.7597 75.97%
CYP2C19 inhibition - 0.8372 83.72%
CYP2D6 inhibition - 0.9041 90.41%
CYP1A2 inhibition - 0.8653 86.53%
CYP2C8 inhibition - 0.7841 78.41%
CYP inhibitory promiscuity - 0.8999 89.99%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.3604 36.04%
Eye corrosion - 0.9730 97.30%
Eye irritation + 0.7273 72.73%
Skin irritation + 0.5383 53.83%
Skin corrosion - 0.9510 95.10%
Ames mutagenesis + 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8437 84.37%
Micronuclear + 0.7600 76.00%
Hepatotoxicity + 0.5426 54.26%
skin sensitisation - 0.7159 71.59%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity + 0.7731 77.31%
Acute Oral Toxicity (c) II 0.4858 48.58%
Estrogen receptor binding + 0.8317 83.17%
Androgen receptor binding + 0.6957 69.57%
Thyroid receptor binding + 0.6053 60.53%
Glucocorticoid receptor binding - 0.5472 54.72%
Aromatase binding + 0.5748 57.48%
PPAR gamma + 0.8255 82.55%
Honey bee toxicity - 0.8920 89.20%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.9527 95.27%

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 96.20% 91.11%
CHEMBL230 P35354 Cyclooxygenase-2 92.96% 89.63%
CHEMBL1951 P21397 Monoamine oxidase A 90.60% 91.49%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.89% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.19% 95.56%
CHEMBL2581 P07339 Cathepsin D 87.12% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.20% 94.00%
CHEMBL240 Q12809 HERG 83.56% 89.76%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.24% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 80.99% 94.73%

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 162876502
LOTUS LTS0147873
wikiData Q105015384