5-Hydroxy-2-(2-hydroxypropyl)naphthalene-1,4-dione

Details

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Internal ID babae9b1-1d24-4e01-9caf-3136258b859b
Taxonomy Benzenoids > Naphthalenes > Naphthoquinones
IUPAC Name 5-hydroxy-2-[(2S)-2-hydroxypropyl]naphthalene-1,4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H12O4/c1-7(14)5-8-6-11(16)12-9(13(8)17)3-2-4-10(12)15/h2-4,6-7,14-15H,5H2,1H3/t7-/m0/s1
InChI Key DCDLYEHUMFWYSD-ZETCQYMHSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C13H12O4
Molecular Weight 232.23 g/mol
Exact Mass 232.07355886 g/mol
Topological Polar Surface Area (TPSA) 74.60 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.47
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 5-Hydroxy-2-(2-hydroxypropyl)naphthalene-1,4-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9969 99.69%
Caco-2 + 0.6606 66.06%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.7880 78.80%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9213 92.13%
OATP1B3 inhibitior + 0.9675 96.75%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9210 92.10%
P-glycoprotein inhibitior - 0.9776 97.76%
P-glycoprotein substrate - 0.8131 81.31%
CYP3A4 substrate - 0.5352 53.52%
CYP2C9 substrate - 0.6023 60.23%
CYP2D6 substrate - 0.8340 83.40%
CYP3A4 inhibition - 0.6798 67.98%
CYP2C9 inhibition + 0.7876 78.76%
CYP2C19 inhibition + 0.5103 51.03%
CYP2D6 inhibition - 0.6711 67.11%
CYP1A2 inhibition + 0.8023 80.23%
CYP2C8 inhibition - 0.9479 94.79%
CYP inhibitory promiscuity + 0.6309 63.09%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8163 81.63%
Carcinogenicity (trinary) Non-required 0.5374 53.74%
Eye corrosion - 0.9894 98.94%
Eye irritation + 0.5846 58.46%
Skin irritation - 0.5909 59.09%
Skin corrosion - 0.9250 92.50%
Ames mutagenesis + 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8427 84.27%
Micronuclear + 0.6300 63.00%
Hepatotoxicity + 0.5984 59.84%
skin sensitisation + 0.6167 61.67%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.6496 64.96%
Acute Oral Toxicity (c) III 0.4984 49.84%
Estrogen receptor binding + 0.6403 64.03%
Androgen receptor binding + 0.5560 55.60%
Thyroid receptor binding - 0.6395 63.95%
Glucocorticoid receptor binding - 0.5000 50.00%
Aromatase binding - 0.6254 62.54%
PPAR gamma - 0.5297 52.97%
Honey bee toxicity - 0.9442 94.42%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.8200 82.00%
Fish aquatic toxicity + 0.9900 99.00%

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 99.53% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.70% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.86% 85.14%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.50% 99.15%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.45% 96.09%
CHEMBL1951 P21397 Monoamine oxidase A 88.94% 91.49%
CHEMBL3401 O75469 Pregnane X receptor 88.74% 94.73%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 88.06% 96.67%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 85.57% 93.03%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.71% 99.23%
CHEMBL2535 P11166 Glucose transporter 83.97% 98.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.75% 89.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.51% 91.11%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.12% 82.69%

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 146682565
LOTUS LTS0160286
wikiData Q104975215