5-(6,7-Dimethoxy-2,3-dimethyl-1,2-dihydronaphthalen-1-yl)-1,3-benzodioxole

Details

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Internal ID 5d0bbd27-4c29-48f7-8941-dd53853f1a64
Taxonomy Lignans, neolignans and related compounds > Aryltetralin lignans
IUPAC Name 5-(6,7-dimethoxy-2,3-dimethyl-1,2-dihydronaphthalen-1-yl)-1,3-benzodioxole
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H22O4/c1-12-7-15-9-18(22-3)19(23-4)10-16(15)21(13(12)2)14-5-6-17-20(8-14)25-11-24-17/h5-10,13,21H,11H2,1-4H3
InChI Key AXECTJWCJSQYPZ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H22O4
Molecular Weight 338.40 g/mol
Exact Mass 338.15180918 g/mol
Topological Polar Surface Area (TPSA) 36.90 Ų
XlogP 4.50
Atomic LogP (AlogP) 4.62
H-Bond Acceptor 4
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 5-(6,7-Dimethoxy-2,3-dimethyl-1,2-dihydronaphthalen-1-yl)-1,3-benzodioxole

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9951 99.51%
Caco-2 + 0.9265 92.65%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7035 70.35%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8962 89.62%
OATP1B3 inhibitior + 0.9556 95.56%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.8558 85.58%
P-glycoprotein inhibitior + 0.7121 71.21%
P-glycoprotein substrate - 0.8503 85.03%
CYP3A4 substrate + 0.5573 55.73%
CYP2C9 substrate - 0.8054 80.54%
CYP2D6 substrate - 0.7330 73.30%
CYP3A4 inhibition + 0.9658 96.58%
CYP2C9 inhibition + 0.9047 90.47%
CYP2C19 inhibition + 0.9568 95.68%
CYP2D6 inhibition + 0.5431 54.31%
CYP1A2 inhibition + 0.7543 75.43%
CYP2C8 inhibition - 0.6174 61.74%
CYP inhibitory promiscuity + 0.9852 98.52%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9408 94.08%
Carcinogenicity (trinary) Non-required 0.3852 38.52%
Eye corrosion - 0.9889 98.89%
Eye irritation - 0.7872 78.72%
Skin irritation - 0.7843 78.43%
Skin corrosion - 0.9675 96.75%
Ames mutagenesis + 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8698 86.98%
Micronuclear + 0.7000 70.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.7000 70.00%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity + 0.5625 56.25%
Acute Oral Toxicity (c) III 0.5935 59.35%
Estrogen receptor binding + 0.8084 80.84%
Androgen receptor binding + 0.6727 67.27%
Thyroid receptor binding + 0.7532 75.32%
Glucocorticoid receptor binding + 0.8000 80.00%
Aromatase binding + 0.5833 58.33%
PPAR gamma + 0.6471 64.71%
Honey bee toxicity - 0.8247 82.47%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity + 0.6600 66.00%
Fish aquatic toxicity + 0.9908 99.08%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.81% 85.14%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 94.04% 94.80%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.01% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.81% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.44% 97.09%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 91.43% 89.62%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 89.70% 82.67%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.72% 92.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.11% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.04% 95.56%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 86.61% 96.77%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 85.92% 86.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.78% 89.00%
CHEMBL2581 P07339 Cathepsin D 83.88% 98.95%
CHEMBL3438 Q05513 Protein kinase C zeta 83.87% 88.48%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.77% 94.45%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 81.99% 89.44%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.89% 94.00%
CHEMBL2535 P11166 Glucose transporter 81.04% 98.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.73% 96.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.73% 97.14%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.63% 95.89%
CHEMBL4247 Q9UM73 ALK tyrosine kinase receptor 80.38% 96.86%

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.
Pycnanthus angolensis

Cross-Links

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PubChem 75166459
LOTUS LTS0248570
wikiData Q104920483