1-(1-Hydroxy-6,8-dimethoxy-3-methylnaphthalen-2-yl)ethan-1-one

Details

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Internal ID 2c88ecfb-427a-4af4-b026-43e93484c1ef
Taxonomy Benzenoids > Naphthalenes > Naphthols and derivatives
IUPAC Name 1-(1-hydroxy-6,8-dimethoxy-3-methylnaphthalen-2-yl)ethanone
SMILES (Canonical) CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)OC)OC
SMILES (Isomeric) CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)OC)OC
InChI InChI=1S/C15H16O4/c1-8-5-10-6-11(18-3)7-12(19-4)14(10)15(17)13(8)9(2)16/h5-7,17H,1-4H3
InChI Key FHHUIFBQMMGHQW-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C15H16O4
Molecular Weight 260.28 g/mol
Exact Mass 260.10485899 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.07
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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CHEMBL3355661
DTXSID00499798
1-(1-Hydroxy-6,8-dimethoxy-3-methylnaphthalen-2-yl)ethan-1-one

2D Structure

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2D Structure of 1-(1-Hydroxy-6,8-dimethoxy-3-methylnaphthalen-2-yl)ethan-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9963 99.63%
Caco-2 + 0.8104 81.04%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.8271 82.71%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9127 91.27%
OATP1B3 inhibitior + 0.9721 97.21%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.5566 55.66%
P-glycoprotein inhibitior - 0.8159 81.59%
P-glycoprotein substrate - 0.8803 88.03%
CYP3A4 substrate - 0.5251 52.51%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8079 80.79%
CYP3A4 inhibition - 0.6680 66.80%
CYP2C9 inhibition - 0.9499 94.99%
CYP2C19 inhibition - 0.6484 64.84%
CYP2D6 inhibition - 0.9245 92.45%
CYP1A2 inhibition + 0.9570 95.70%
CYP2C8 inhibition + 0.5182 51.82%
CYP inhibitory promiscuity - 0.5494 54.94%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8055 80.55%
Carcinogenicity (trinary) Non-required 0.5617 56.17%
Eye corrosion - 0.9803 98.03%
Eye irritation + 0.8129 81.29%
Skin irritation - 0.6594 65.94%
Skin corrosion - 0.9917 99.17%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear + 0.7118 71.18%
Hepatotoxicity - 0.5094 50.94%
skin sensitisation - 0.9543 95.43%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.6507 65.07%
Acute Oral Toxicity (c) II 0.6011 60.11%
Estrogen receptor binding + 0.7577 75.77%
Androgen receptor binding - 0.5674 56.74%
Thyroid receptor binding - 0.5933 59.33%
Glucocorticoid receptor binding - 0.5000 50.00%
Aromatase binding + 0.7013 70.13%
PPAR gamma + 0.6185 61.85%
Honey bee toxicity - 0.9229 92.29%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9762 97.62%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.21% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.20% 85.14%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 91.10% 96.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.00% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.33% 99.15%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.64% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.53% 86.33%
CHEMBL4208 P20618 Proteasome component C5 86.52% 90.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.33% 95.50%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.31% 95.56%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 86.09% 97.21%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 85.34% 94.42%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.03% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 82.23% 94.73%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.54% 96.95%
CHEMBL2535 P11166 Glucose transporter 80.53% 98.75%

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.
Karwinskia humboldtiana
Karwinskia parvifolia
Morus mongolica
Senna alexandrina

Cross-Links

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PubChem 12478854
NPASS NPC84266
ChEMBL CHEMBL3355661
LOTUS LTS0122089
wikiData Q82350893