Solaninaphthoquione

Details

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Internal ID 62e6bbd1-ffef-4fd4-8cbe-2713563e8d54
Taxonomy Benzenoids > Naphthalenes > Naphthoquinones
IUPAC Name 5-hydroxy-6-methoxy-2-methyl-3-(2-oxopropyl)naphthalene-1,4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H14O5/c1-7(16)6-10-8(2)13(17)9-4-5-11(20-3)15(19)12(9)14(10)18/h4-5,19H,6H2,1-3H3
InChI Key JINSRQVOJRVESY-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H14O5
Molecular Weight 274.27 g/mol
Exact Mass 274.08412354 g/mol
Topological Polar Surface Area (TPSA) 80.70 Ų
XlogP 1.60
Atomic LogP (AlogP) 2.08
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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RefChem:184212
CHEBI:198430
5-hydroxy-6-methoxy-2-methyl-3-(2-oxopropyl)naphthalene-1,4-dione

2D Structure

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2D Structure of Solaninaphthoquione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9973 99.73%
Caco-2 + 0.8016 80.16%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.6789 67.89%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9157 91.57%
OATP1B3 inhibitior + 0.9203 92.03%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7517 75.17%
P-glycoprotein inhibitior - 0.9087 90.87%
P-glycoprotein substrate - 0.7572 75.72%
CYP3A4 substrate + 0.5458 54.58%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8161 81.61%
CYP3A4 inhibition - 0.6822 68.22%
CYP2C9 inhibition - 0.7566 75.66%
CYP2C19 inhibition - 0.5275 52.75%
CYP2D6 inhibition - 0.6889 68.89%
CYP1A2 inhibition + 0.7973 79.73%
CYP2C8 inhibition - 0.6596 65.96%
CYP inhibitory promiscuity - 0.5232 52.32%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9292 92.92%
Carcinogenicity (trinary) Non-required 0.6587 65.87%
Eye corrosion - 0.9884 98.84%
Eye irritation + 0.7016 70.16%
Skin irritation - 0.7485 74.85%
Skin corrosion - 0.9701 97.01%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7780 77.80%
Micronuclear - 0.5341 53.41%
Hepatotoxicity + 0.6084 60.84%
skin sensitisation - 0.6790 67.90%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity + 0.5281 52.81%
Acute Oral Toxicity (c) III 0.4229 42.29%
Estrogen receptor binding + 0.7125 71.25%
Androgen receptor binding - 0.5583 55.83%
Thyroid receptor binding - 0.7796 77.96%
Glucocorticoid receptor binding - 0.5084 50.84%
Aromatase binding - 0.5762 57.62%
PPAR gamma + 0.6547 65.47%
Honey bee toxicity - 0.9349 93.49%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity + 0.9918 99.18%

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
CHEMBL2581 P07339 Cathepsin D 96.93% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.36% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.79% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.37% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.60% 96.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.80% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.72% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.89% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.80% 85.14%
CHEMBL2535 P11166 Glucose transporter 84.13% 98.75%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 83.76% 96.67%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.53% 99.17%
CHEMBL4208 P20618 Proteasome component C5 80.13% 90.00%

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 102531638
LOTUS LTS0152386
wikiData Q75059756