1-(3,4-Dimethoxyphenyl)-6,7-dimethoxy-2,3-dimethyl-1,2-dihydronaphthalene

Details

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Internal ID 9c88de5c-e8c4-42c8-809e-0e97c8f9a213
Taxonomy Lignans, neolignans and related compounds > Aryltetralin lignans
IUPAC Name 1-(3,4-dimethoxyphenyl)-6,7-dimethoxy-2,3-dimethyl-1,2-dihydronaphthalene
SMILES (Canonical) CC1C(C2=CC(=C(C=C2C=C1C)OC)OC)C3=CC(=C(C=C3)OC)OC
SMILES (Isomeric) CC1C(C2=CC(=C(C=C2C=C1C)OC)OC)C3=CC(=C(C=C3)OC)OC
InChI InChI=1S/C22H26O4/c1-13-9-16-11-20(25-5)21(26-6)12-17(16)22(14(13)2)15-7-8-18(23-3)19(10-15)24-4/h7-12,14,22H,1-6H3
InChI Key GRJMIMFTPGNXIC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H26O4
Molecular Weight 354.40 g/mol
Exact Mass 354.18310931 g/mol
Topological Polar Surface Area (TPSA) 36.90 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.91
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-(3,4-Dimethoxyphenyl)-6,7-dimethoxy-2,3-dimethyl-1,2-dihydronaphthalene

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 + 0.9390 93.90%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.7065 70.65%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9105 91.05%
OATP1B3 inhibitior + 0.9708 97.08%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.8492 84.92%
P-glycoprotein inhibitior + 0.7222 72.22%
P-glycoprotein substrate - 0.7375 73.75%
CYP3A4 substrate + 0.5193 51.93%
CYP2C9 substrate + 0.6036 60.36%
CYP2D6 substrate + 0.3505 35.05%
CYP3A4 inhibition + 0.8969 89.69%
CYP2C9 inhibition + 0.5550 55.50%
CYP2C19 inhibition + 0.8534 85.34%
CYP2D6 inhibition - 0.8843 88.43%
CYP1A2 inhibition + 0.8521 85.21%
CYP2C8 inhibition + 0.5657 56.57%
CYP inhibitory promiscuity + 0.9432 94.32%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8581 85.81%
Carcinogenicity (trinary) Non-required 0.4689 46.89%
Eye corrosion - 0.9926 99.26%
Eye irritation - 0.5392 53.92%
Skin irritation - 0.7970 79.70%
Skin corrosion - 0.9862 98.62%
Ames mutagenesis - 0.5478 54.78%
Human Ether-a-go-go-Related Gene inhibition + 0.7928 79.28%
Micronuclear + 0.5818 58.18%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.8008 80.08%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.6108 61.08%
Acute Oral Toxicity (c) III 0.5378 53.78%
Estrogen receptor binding + 0.8824 88.24%
Androgen receptor binding + 0.5699 56.99%
Thyroid receptor binding + 0.8415 84.15%
Glucocorticoid receptor binding + 0.7110 71.10%
Aromatase binding + 0.6269 62.69%
PPAR gamma + 0.6723 67.23%
Honey bee toxicity - 0.8594 85.94%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.9942 99.42%

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 97.10% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.69% 96.09%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 92.62% 89.62%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.23% 92.94%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.64% 86.33%
CHEMBL2581 P07339 Cathepsin D 84.95% 98.95%
CHEMBL2535 P11166 Glucose transporter 83.16% 98.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.76% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.35% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.21% 96.00%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 80.97% 94.03%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.66% 95.89%

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.
Allium schoenoprasum
Aristolochia holostylis

Cross-Links

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PubChem 12305410
LOTUS LTS0007471
wikiData Q105350838