7-Hydroxy-3-methyl-5-propan-2-ylnaphthalene-1,2-dione

Details

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Internal ID 75994686-000c-43d6-a3cc-722cca73d7fa
Taxonomy Benzenoids > Naphthalenes > Naphthoquinones
IUPAC Name 7-hydroxy-3-methyl-5-propan-2-ylnaphthalene-1,2-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H14O3/c1-7(2)10-5-9(15)6-12-11(10)4-8(3)13(16)14(12)17/h4-7,15H,1-3H3
InChI Key QYFBOZGYYVUIEA-UHFFFAOYSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C14H14O3
Molecular Weight 230.26 g/mol
Exact Mass 230.094294304 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.68
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-Hydroxy-3-methyl-5-propan-2-ylnaphthalene-1,2-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8283 82.83%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.8718 87.18%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9227 92.27%
OATP1B3 inhibitior + 0.9212 92.12%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8865 88.65%
P-glycoprotein inhibitior - 0.9536 95.36%
P-glycoprotein substrate - 0.8909 89.09%
CYP3A4 substrate - 0.5603 56.03%
CYP2C9 substrate - 0.5905 59.05%
CYP2D6 substrate - 0.8279 82.79%
CYP3A4 inhibition - 0.6815 68.15%
CYP2C9 inhibition + 0.8582 85.82%
CYP2C19 inhibition + 0.6687 66.87%
CYP2D6 inhibition - 0.6507 65.07%
CYP1A2 inhibition + 0.9257 92.57%
CYP2C8 inhibition - 0.9382 93.82%
CYP inhibitory promiscuity + 0.7301 73.01%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9271 92.71%
Carcinogenicity (trinary) Non-required 0.5560 55.60%
Eye corrosion - 0.9828 98.28%
Eye irritation + 0.8384 83.84%
Skin irritation + 0.4928 49.28%
Skin corrosion - 0.9217 92.17%
Ames mutagenesis - 0.5054 50.54%
Human Ether-a-go-go-Related Gene inhibition - 0.7513 75.13%
Micronuclear + 0.6400 64.00%
Hepatotoxicity + 0.6482 64.82%
skin sensitisation + 0.6728 67.28%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity + 0.6997 69.97%
Acute Oral Toxicity (c) III 0.6836 68.36%
Estrogen receptor binding - 0.6004 60.04%
Androgen receptor binding - 0.5406 54.06%
Thyroid receptor binding - 0.5662 56.62%
Glucocorticoid receptor binding - 0.6275 62.75%
Aromatase binding - 0.5824 58.24%
PPAR gamma - 0.7617 76.17%
Honey bee toxicity - 0.8694 86.94%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9946 99.46%

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 96.83% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.71% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.36% 99.15%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 91.33% 90.71%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.49% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 87.30% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.82% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.76% 99.23%

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 10977282
LOTUS LTS0003826
wikiData Q105230083