2,3,5,8-Tetrahydroxy-6-methyl-1,4-naphthalenedione

Details

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Internal ID ff92c16e-e5ca-4976-8074-a3fc097d2841
Taxonomy Benzenoids > Naphthalenes > Naphthoquinones
IUPAC Name 5,6,7,8-tetrahydroxy-2-methylnaphthalene-1,4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H8O6/c1-3-2-4(12)5-6(7(3)13)9(15)11(17)10(16)8(5)14/h2,14-17H,1H3
InChI Key XATMXJYIXBGKBX-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C11H8O6
Molecular Weight 236.18 g/mol
Exact Mass 236.03208797 g/mol
Topological Polar Surface Area (TPSA) 115.00 Ų
XlogP 1.50
Atomic LogP (AlogP) 0.83
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,3,5,8-Tetrahydroxy-6-methyl-1,4-naphthalenedione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9836 98.36%
Caco-2 - 0.7671 76.71%
Blood Brain Barrier - 0.7879 78.79%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.6480 64.80%
OATP2B1 inhibitior - 0.8593 85.93%
OATP1B1 inhibitior + 0.8796 87.96%
OATP1B3 inhibitior + 0.9731 97.31%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9588 95.88%
BSEP inhibitior - 0.9381 93.81%
P-glycoprotein inhibitior - 0.9631 96.31%
P-glycoprotein substrate - 0.9783 97.83%
CYP3A4 substrate - 0.6307 63.07%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8666 86.66%
CYP3A4 inhibition - 0.7185 71.85%
CYP2C9 inhibition + 0.8567 85.67%
CYP2C19 inhibition - 0.7772 77.72%
CYP2D6 inhibition - 0.8220 82.20%
CYP1A2 inhibition + 0.8758 87.58%
CYP2C8 inhibition - 0.9787 97.87%
CYP inhibitory promiscuity + 0.6960 69.60%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9154 91.54%
Carcinogenicity (trinary) Non-required 0.5458 54.58%
Eye corrosion - 0.9866 98.66%
Eye irritation + 0.9278 92.78%
Skin irritation + 0.6002 60.02%
Skin corrosion - 0.7446 74.46%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7605 76.05%
Micronuclear + 0.7900 79.00%
Hepatotoxicity + 0.5713 57.13%
skin sensitisation + 0.6948 69.48%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity + 0.6281 62.81%
Acute Oral Toxicity (c) III 0.3985 39.85%
Estrogen receptor binding - 0.6833 68.33%
Androgen receptor binding + 0.5608 56.08%
Thyroid receptor binding - 0.8250 82.50%
Glucocorticoid receptor binding + 0.7584 75.84%
Aromatase binding - 0.7896 78.96%
PPAR gamma - 0.5627 56.27%
Honey bee toxicity - 0.9473 94.73%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9898 98.98%

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 93.46% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.63% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.27% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.17% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 83.57% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.22% 89.00%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 81.31% 96.67%
CHEMBL1937 Q92769 Histone deacetylase 2 80.16% 94.75%

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 39035
LOTUS LTS0013199
wikiData Q82943529