2,6,7-Trimethoxy-3-methylnaphthalene-1,4-dione

Details

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Internal ID df0d5272-a333-4c1d-9b5c-9b6008f1b38b
Taxonomy Benzenoids > Naphthalenes > Naphthoquinones
IUPAC Name 2,6,7-trimethoxy-3-methylnaphthalene-1,4-dione
SMILES (Canonical) CC1=C(C(=O)C2=CC(=C(C=C2C1=O)OC)OC)OC
SMILES (Isomeric) CC1=C(C(=O)C2=CC(=C(C=C2C1=O)OC)OC)OC
InChI InChI=1S/C14H14O5/c1-7-12(15)8-5-10(17-2)11(18-3)6-9(8)13(16)14(7)19-4/h5-6H,1-4H3
InChI Key HYDJFGIXYVSQGV-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H14O5
Molecular Weight 262.26 g/mol
Exact Mass 262.08412354 g/mol
Topological Polar Surface Area (TPSA) 61.80 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.00
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,6,7-Trimethoxy-3-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 + 1.0000 100.00%
Caco-2 + 0.7898 78.98%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.9714 97.14%
Subcellular localzation Mitochondria 0.7186 71.86%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9478 94.78%
OATP1B3 inhibitior + 0.9762 97.62%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7686 76.86%
P-glycoprotein inhibitior - 0.8078 80.78%
P-glycoprotein substrate - 0.9566 95.66%
CYP3A4 substrate - 0.5839 58.39%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8109 81.09%
CYP3A4 inhibition + 0.6821 68.21%
CYP2C9 inhibition - 0.7521 75.21%
CYP2C19 inhibition + 0.5669 56.69%
CYP2D6 inhibition - 0.8998 89.98%
CYP1A2 inhibition + 0.9361 93.61%
CYP2C8 inhibition - 0.9369 93.69%
CYP inhibitory promiscuity + 0.8338 83.38%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9235 92.35%
Carcinogenicity (trinary) Non-required 0.5554 55.54%
Eye corrosion - 0.9782 97.82%
Eye irritation + 0.9638 96.38%
Skin irritation - 0.7104 71.04%
Skin corrosion - 0.9769 97.69%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5259 52.59%
Micronuclear + 0.7059 70.59%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation - 0.7175 71.75%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity + 0.6344 63.44%
Acute Oral Toxicity (c) II 0.4619 46.19%
Estrogen receptor binding + 0.6970 69.70%
Androgen receptor binding - 0.6491 64.91%
Thyroid receptor binding - 0.7054 70.54%
Glucocorticoid receptor binding - 0.6841 68.41%
Aromatase binding + 0.5666 56.66%
PPAR gamma - 0.6231 62.31%
Honey bee toxicity - 0.8738 87.38%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9905 99.05%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.55% 95.56%
CHEMBL2581 P07339 Cathepsin D 90.84% 98.95%
CHEMBL2535 P11166 Glucose transporter 88.00% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.96% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.89% 94.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.10% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 80.91% 94.73%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.02% 97.14%

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.
Conospermum stoechadis

Cross-Links

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PubChem 162906499
LOTUS LTS0001931
wikiData Q105035256