(1R)-6,7,8-trimethoxy-1-(2,4,5-trimethoxyphenyl)-1,2-dihydronaphthalene

Details

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Internal ID 3bc01fa0-52ce-481e-8992-39a3e4133cd9
Taxonomy Benzenoids > Naphthalenes
IUPAC Name (1R)-6,7,8-trimethoxy-1-(2,4,5-trimethoxyphenyl)-1,2-dihydronaphthalene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H26O6/c1-23-16-12-18(25-3)17(24-2)11-15(16)14-9-7-8-13-10-19(26-4)21(27-5)22(28-6)20(13)14/h7-8,10-12,14H,9H2,1-6H3/t14-/m1/s1
InChI Key NNRIXDXVJQTLOC-CQSZACIVSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C22H26O6
Molecular Weight 386.40 g/mol
Exact Mass 386.17293854 g/mol
Topological Polar Surface Area (TPSA) 55.40 Ų
XlogP 4.30
Atomic LogP (AlogP) 4.29
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R)-6,7,8-trimethoxy-1-(2,4,5-trimethoxyphenyl)-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 + 0.9470 94.70%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.6724 67.24%
OATP2B1 inhibitior - 0.8754 87.54%
OATP1B1 inhibitior + 0.9109 91.09%
OATP1B3 inhibitior + 0.9793 97.93%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9126 91.26%
P-glycoprotein inhibitior + 0.7322 73.22%
P-glycoprotein substrate - 0.7057 70.57%
CYP3A4 substrate + 0.5454 54.54%
CYP2C9 substrate + 0.5617 56.17%
CYP2D6 substrate + 0.4412 44.12%
CYP3A4 inhibition + 0.7653 76.53%
CYP2C9 inhibition - 0.7771 77.71%
CYP2C19 inhibition + 0.5084 50.84%
CYP2D6 inhibition - 0.9443 94.43%
CYP1A2 inhibition + 0.9019 90.19%
CYP2C8 inhibition - 0.6152 61.52%
CYP inhibitory promiscuity + 0.8915 89.15%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8671 86.71%
Carcinogenicity (trinary) Non-required 0.4030 40.30%
Eye corrosion - 0.9867 98.67%
Eye irritation - 0.6287 62.87%
Skin irritation - 0.7844 78.44%
Skin corrosion - 0.9794 97.94%
Ames mutagenesis + 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7853 78.53%
Micronuclear + 0.5818 58.18%
Hepatotoxicity - 0.5301 53.01%
skin sensitisation - 0.8543 85.43%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.7790 77.90%
Acute Oral Toxicity (c) III 0.4313 43.13%
Estrogen receptor binding + 0.8738 87.38%
Androgen receptor binding + 0.6343 63.43%
Thyroid receptor binding + 0.8241 82.41%
Glucocorticoid receptor binding + 0.7925 79.25%
Aromatase binding - 0.5677 56.77%
PPAR gamma + 0.5684 56.84%
Honey bee toxicity - 0.8372 83.72%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.7800 78.00%
Fish aquatic toxicity + 0.9900 99.00%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.63% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.70% 91.11%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.20% 97.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.93% 99.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.37% 97.09%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 85.18% 89.62%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.75% 85.14%
CHEMBL2535 P11166 Glucose transporter 84.42% 98.75%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 84.22% 82.67%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.13% 92.94%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.19% 86.33%
CHEMBL4208 P20618 Proteasome component C5 82.81% 90.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.33% 92.62%

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.
Duguetia confinis

Cross-Links

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PubChem 162870528
LOTUS LTS0228486
wikiData Q105182276