4-(1,3-Benzodioxol-5-yl)-4-hydroxy-6,7-dimethoxy-2,3-dimethyl-2,3-dihydronaphthalen-1-one

Details

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Internal ID d05d9b82-99e2-4b21-865a-7787353f4fb6
Taxonomy Lignans, neolignans and related compounds > Aryltetralin lignans
IUPAC Name 4-(1,3-benzodioxol-5-yl)-4-hydroxy-6,7-dimethoxy-2,3-dimethyl-2,3-dihydronaphthalen-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H22O6/c1-11-12(2)21(23,13-5-6-16-19(7-13)27-10-26-16)15-9-18(25-4)17(24-3)8-14(15)20(11)22/h5-9,11-12,23H,10H2,1-4H3
InChI Key NDCKQHZMIZHJRH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H22O6
Molecular Weight 370.40 g/mol
Exact Mass 370.14163842 g/mol
Topological Polar Surface Area (TPSA) 74.20 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.14
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-(1,3-Benzodioxol-5-yl)-4-hydroxy-6,7-dimethoxy-2,3-dimethyl-2,3-dihydronaphthalen-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 + 0.9871 98.71%
Caco-2 + 0.8583 85.83%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.8142 81.42%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9039 90.39%
OATP1B3 inhibitior + 0.9112 91.12%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.7341 73.41%
P-glycoprotein inhibitior + 0.6818 68.18%
P-glycoprotein substrate - 0.7667 76.67%
CYP3A4 substrate + 0.5631 56.31%
CYP2C9 substrate - 0.8042 80.42%
CYP2D6 substrate - 0.8062 80.62%
CYP3A4 inhibition + 0.9296 92.96%
CYP2C9 inhibition + 0.8528 85.28%
CYP2C19 inhibition + 0.7421 74.21%
CYP2D6 inhibition - 0.7088 70.88%
CYP1A2 inhibition - 0.7885 78.85%
CYP2C8 inhibition - 0.8638 86.38%
CYP inhibitory promiscuity + 0.7649 76.49%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.3592 35.92%
Eye corrosion - 0.9906 99.06%
Eye irritation - 0.7160 71.60%
Skin irritation - 0.7960 79.60%
Skin corrosion - 0.9658 96.58%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4638 46.38%
Micronuclear + 0.7574 75.74%
Hepatotoxicity + 0.5824 58.24%
skin sensitisation - 0.8567 85.67%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.4736 47.36%
Acute Oral Toxicity (c) III 0.5913 59.13%
Estrogen receptor binding + 0.8620 86.20%
Androgen receptor binding + 0.6369 63.69%
Thyroid receptor binding + 0.6958 69.58%
Glucocorticoid receptor binding + 0.8582 85.82%
Aromatase binding + 0.6599 65.99%
PPAR gamma + 0.7888 78.88%
Honey bee toxicity - 0.8552 85.52%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.5451 54.51%
Fish aquatic toxicity + 0.9670 96.70%

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
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 98.09% 96.77%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.54% 91.11%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 93.27% 94.80%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.70% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.89% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.96% 95.56%
CHEMBL2581 P07339 Cathepsin D 90.22% 98.95%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 88.21% 92.62%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.47% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.17% 89.00%
CHEMBL4208 P20618 Proteasome component C5 86.81% 90.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.50% 97.14%
CHEMBL2535 P11166 Glucose transporter 86.16% 98.75%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 85.25% 82.67%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.23% 94.45%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.98% 92.94%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.76% 94.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.14% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.53% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.93% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.45% 99.23%

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.
Virola elongata
Virola sebifera

Cross-Links

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PubChem 14655052
LOTUS LTS0225319
wikiData Q104172333