5-Hydroxy-6-(8-hydroxy-6-methyl-1,4-dioxonaphthalen-2-yl)-7-methylnaphthalene-1,4-dione

Details

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Internal ID 6166b878-e7e3-4648-89b0-63674dcda439
Taxonomy Benzenoids > Naphthalenes > Naphthoquinones
IUPAC Name 5-hydroxy-6-(8-hydroxy-6-methyl-1,4-dioxonaphthalen-2-yl)-7-methylnaphthalene-1,4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H14O6/c1-9-5-11-16(25)8-13(21(27)20(11)17(26)6-9)18-10(2)7-12-14(23)3-4-15(24)19(12)22(18)28/h3-8,26,28H,1-2H3
InChI Key DDCXOXHWSFIOKC-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C22H14O6
Molecular Weight 374.30 g/mol
Exact Mass 374.07903816 g/mol
Topological Polar Surface Area (TPSA) 109.00 Ų
XlogP 3.70
Atomic LogP (AlogP) 3.11
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Hydroxy-6-(8-hydroxy-6-methyl-1,4-dioxonaphthalen-2-yl)-7-methylnaphthalene-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 + 0.9968 99.68%
Caco-2 - 0.5839 58.39%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.9018 90.18%
OATP2B1 inhibitior - 0.5667 56.67%
OATP1B1 inhibitior + 0.8852 88.52%
OATP1B3 inhibitior + 0.9148 91.48%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.6195 61.95%
P-glycoprotein inhibitior - 0.8474 84.74%
P-glycoprotein substrate - 0.8838 88.38%
CYP3A4 substrate + 0.5346 53.46%
CYP2C9 substrate - 0.8042 80.42%
CYP2D6 substrate - 0.8665 86.65%
CYP3A4 inhibition - 0.7006 70.06%
CYP2C9 inhibition + 0.9592 95.92%
CYP2C19 inhibition + 0.7766 77.66%
CYP2D6 inhibition - 0.7041 70.41%
CYP1A2 inhibition + 0.9159 91.59%
CYP2C8 inhibition - 0.7967 79.67%
CYP inhibitory promiscuity + 0.8403 84.03%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8088 80.88%
Carcinogenicity (trinary) Non-required 0.5102 51.02%
Eye corrosion - 0.9965 99.65%
Eye irritation - 0.5716 57.16%
Skin irritation - 0.5908 59.08%
Skin corrosion - 0.9423 94.23%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5537 55.37%
Micronuclear + 0.8400 84.00%
Hepatotoxicity + 0.7607 76.07%
skin sensitisation - 0.6582 65.82%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.7158 71.58%
Acute Oral Toxicity (c) III 0.4962 49.62%
Estrogen receptor binding + 0.8123 81.23%
Androgen receptor binding + 0.6175 61.75%
Thyroid receptor binding - 0.7570 75.70%
Glucocorticoid receptor binding + 0.5867 58.67%
Aromatase binding - 0.6232 62.32%
PPAR gamma + 0.6986 69.86%
Honey bee toxicity - 0.9429 94.29%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 1.0000 100.00%

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 95.79% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.57% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.49% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.75% 99.15%
CHEMBL1951 P21397 Monoamine oxidase A 91.54% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.59% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.11% 99.23%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 89.00% 96.67%
CHEMBL4208 P20618 Proteasome component C5 84.54% 90.00%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 83.45% 93.03%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.66% 96.95%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 82.29% 96.21%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.65% 94.00%

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.
Diospyros chloroxylon

Cross-Links

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PubChem 15559060
LOTUS LTS0199761
wikiData Q104976234