5-O-Methylsclerone

Details

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Internal ID 00e22270-ffa8-4aab-8f4b-d18c78bc474a
Taxonomy Benzenoids > Tetralins
IUPAC Name 4-hydroxy-5-methoxy-3,4-dihydro-2H-naphthalen-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H12O3/c1-14-10-4-2-3-7-8(12)5-6-9(13)11(7)10/h2-4,9,13H,5-6H2,1H3
InChI Key NMKVLUGRERNACB-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C11H12O3
Molecular Weight 192.21 g/mol
Exact Mass 192.078644241 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 0.90
Atomic LogP (AlogP) 1.71
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-O-Methylsclerone

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 + 0.8618 86.18%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.8689 86.89%
OATP2B1 inhibitior - 0.8622 86.22%
OATP1B1 inhibitior + 0.9704 97.04%
OATP1B3 inhibitior + 0.9797 97.97%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8958 89.58%
P-glycoprotein inhibitior - 0.9748 97.48%
P-glycoprotein substrate - 0.8135 81.35%
CYP3A4 substrate + 0.5540 55.40%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6657 66.57%
CYP3A4 inhibition - 0.8798 87.98%
CYP2C9 inhibition - 0.8852 88.52%
CYP2C19 inhibition + 0.6657 66.57%
CYP2D6 inhibition - 0.9253 92.53%
CYP1A2 inhibition + 0.9692 96.92%
CYP2C8 inhibition - 0.7623 76.23%
CYP inhibitory promiscuity - 0.8617 86.17%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8122 81.22%
Carcinogenicity (trinary) Non-required 0.4712 47.12%
Eye corrosion - 0.9265 92.65%
Eye irritation + 0.8524 85.24%
Skin irritation + 0.5312 53.12%
Skin corrosion - 0.9347 93.47%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4921 49.21%
Micronuclear - 0.6592 65.92%
Hepatotoxicity - 0.5574 55.74%
skin sensitisation - 0.8159 81.59%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity + 0.6421 64.21%
Acute Oral Toxicity (c) III 0.6506 65.06%
Estrogen receptor binding - 0.8077 80.77%
Androgen receptor binding - 0.6940 69.40%
Thyroid receptor binding - 0.6854 68.54%
Glucocorticoid receptor binding - 0.8784 87.84%
Aromatase binding - 0.9416 94.16%
PPAR gamma - 0.7034 70.34%
Honey bee toxicity - 0.9108 91.08%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity - 0.5000 50.00%

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 97.90% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.63% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.84% 95.56%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 90.64% 82.69%
CHEMBL2535 P11166 Glucose transporter 90.11% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.48% 86.33%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 88.95% 93.03%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.94% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.59% 99.23%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.65% 92.62%
CHEMBL2056 P21728 Dopamine D1 receptor 82.60% 91.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.30% 100.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.17% 97.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.42% 91.11%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 80.80% 96.00%

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 101257350
LOTUS LTS0268466
wikiData Q77493249