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

Details

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Internal ID 9473b2b9-4f12-48bd-9db3-bb5c4f435744
Taxonomy Benzenoids > Naphthalenes > Naphthoquinones
IUPAC Name 5-hydroxy-7-(4-hydroxy-7-methyl-5,8-dioxonaphthalen-2-yl)-2-methylnaphthalene-1,4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H14O6/c1-9-3-15(23)19-13(21(9)27)5-11(7-17(19)25)12-6-14-20(18(26)8-12)16(24)4-10(2)22(14)28/h3-8,25-26H,1-2H3
InChI Key TVNIEZKCCZXOBZ-UHFFFAOYSA-N
Popularity 2 references 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) 3.42
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-7-(4-hydroxy-7-methyl-5,8-dioxonaphthalen-2-yl)-2-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 + 0.5320 53.20%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Mitochondria 0.9018 90.18%
OATP2B1 inhibitior - 0.7020 70.20%
OATP1B1 inhibitior + 0.9310 93.10%
OATP1B3 inhibitior + 0.9148 91.48%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.8433 84.33%
P-glycoprotein inhibitior - 0.7956 79.56%
P-glycoprotein substrate - 0.9555 95.55%
CYP3A4 substrate - 0.5716 57.16%
CYP2C9 substrate - 0.8009 80.09%
CYP2D6 substrate - 0.8664 86.64%
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 - 0.8598 85.98%
CYP inhibitory promiscuity + 0.8403 84.03%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8088 80.88%
Carcinogenicity (trinary) Non-required 0.5102 51.02%
Eye corrosion - 0.9965 99.65%
Eye irritation + 0.7882 78.82%
Skin irritation - 0.5908 59.08%
Skin corrosion - 0.9423 94.23%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4535 45.35%
Micronuclear + 0.8400 84.00%
Hepatotoxicity + 0.7555 75.55%
skin sensitisation - 0.6582 65.82%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.6466 64.66%
Acute Oral Toxicity (c) III 0.4962 49.62%
Estrogen receptor binding + 0.8060 80.60%
Androgen receptor binding + 0.7457 74.57%
Thyroid receptor binding - 0.6459 64.59%
Glucocorticoid receptor binding + 0.6561 65.61%
Aromatase binding - 0.7359 73.59%
PPAR gamma + 0.7047 70.47%
Honey bee toxicity - 0.9240 92.40%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6800 68.00%
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 96.08% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.50% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.69% 89.00%
CHEMBL1951 P21397 Monoamine oxidase A 90.67% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.48% 91.11%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 87.17% 93.40%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.06% 99.15%
CHEMBL1937 Q92769 Histone deacetylase 2 84.74% 94.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.13% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.97% 85.14%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 83.88% 96.67%
CHEMBL3401 O75469 Pregnane X receptor 83.76% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.03% 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 wallichii

Cross-Links

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PubChem 49800114
LOTUS LTS0062719
wikiData Q105265429