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

Details

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Internal ID 3c046a85-e5b1-4348-8c8f-8ab49203d39c
Taxonomy Benzenoids > Naphthalenes > Naphthoquinones
IUPAC Name 8-hydroxy-5-(5-hydroxy-7-methyl-1,4-dioxonaphthalen-2-yl)-6-methylnaphthalene-1,4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H14O6/c1-9-5-11-19(15(25)6-9)17(27)8-12(22(11)28)18-10(2)7-16(26)20-13(23)3-4-14(24)21(18)20/h3-8,25-26H,1-2H3
InChI Key VAXTVWFPVRQSJK-UHFFFAOYSA-N
Popularity 4 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) 3.11
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 8-Hydroxy-5-(5-hydroxy-7-methyl-1,4-dioxonaphthalen-2-yl)-6-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 + 0.6026 60.26%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Mitochondria 0.9018 90.18%
OATP2B1 inhibitior - 0.5641 56.41%
OATP1B1 inhibitior + 0.9301 93.01%
OATP1B3 inhibitior + 0.9148 91.48%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.5822 58.22%
P-glycoprotein inhibitior - 0.8421 84.21%
P-glycoprotein substrate - 0.8807 88.07%
CYP3A4 substrate + 0.5231 52.31%
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 - 0.8381 83.81%
CYP inhibitory promiscuity + 0.8403 84.03%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8088 80.88%
Carcinogenicity (trinary) Non-required 0.5102 51.02%
Eye corrosion - 0.9965 99.65%
Eye irritation + 0.5258 52.58%
Skin irritation - 0.5908 59.08%
Skin corrosion - 0.9423 94.23%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5476 54.76%
Micronuclear + 0.8400 84.00%
Hepatotoxicity + 0.7482 74.82%
skin sensitisation - 0.6582 65.82%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.4962 49.62%
Estrogen receptor binding + 0.8555 85.55%
Androgen receptor binding + 0.6477 64.77%
Thyroid receptor binding - 0.7307 73.07%
Glucocorticoid receptor binding + 0.6380 63.80%
Aromatase binding - 0.6499 64.99%
PPAR gamma + 0.6470 64.70%
Honey bee toxicity - 0.9402 94.02%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5700 57.00%
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
CHEMBL1951 P21397 Monoamine oxidase A 98.21% 91.49%
CHEMBL2581 P07339 Cathepsin D 96.19% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.30% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.63% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.45% 89.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.63% 99.15%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 87.48% 96.67%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.43% 99.23%
CHEMBL279 P35968 Vascular endothelial growth factor receptor 2 84.78% 95.52%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 84.21% 93.40%
CHEMBL4208 P20618 Proteasome component C5 83.88% 90.00%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.16% 93.03%

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 5320076
NPASS NPC235707