3-(3,4-dimethoxyphenyl)-8-hydroxy-6,7-dimethoxy-4H-naphthalen-1-one

Details

Top
Internal ID 93892006-004f-4226-b003-42a31e52e783
Taxonomy Benzenoids > Naphthalenes > Phenylnaphthalenes
IUPAC Name 3-(3,4-dimethoxyphenyl)-8-hydroxy-6,7-dimethoxy-4H-naphthalen-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H20O6/c1-23-15-6-5-11(9-16(15)24-2)12-7-13-10-17(25-3)20(26-4)19(22)18(13)14(21)8-12/h5-6,8-10,22H,7H2,1-4H3
InChI Key YGJMHGKNTSIVBA-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C20H20O6
Molecular Weight 356.40 g/mol
Exact Mass 356.12598835 g/mol
Topological Polar Surface Area (TPSA) 74.20 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.25
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 3-(3,4-dimethoxyphenyl)-8-hydroxy-6,7-dimethoxy-4H-naphthalen-1-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9956 99.56%
Caco-2 + 0.9248 92.48%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.8032 80.32%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9211 92.11%
OATP1B3 inhibitior + 0.9566 95.66%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.6445 64.45%
P-glycoprotein inhibitior + 0.6287 62.87%
P-glycoprotein substrate - 0.7825 78.25%
CYP3A4 substrate + 0.6053 60.53%
CYP2C9 substrate - 0.8071 80.71%
CYP2D6 substrate - 0.8002 80.02%
CYP3A4 inhibition + 0.5648 56.48%
CYP2C9 inhibition - 0.5353 53.53%
CYP2C19 inhibition + 0.8173 81.73%
CYP2D6 inhibition - 0.8693 86.93%
CYP1A2 inhibition + 0.8129 81.29%
CYP2C8 inhibition + 0.7935 79.35%
CYP inhibitory promiscuity + 0.8562 85.62%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9263 92.63%
Carcinogenicity (trinary) Non-required 0.5197 51.97%
Eye corrosion - 0.9924 99.24%
Eye irritation - 0.6172 61.72%
Skin irritation - 0.6957 69.57%
Skin corrosion - 0.9795 97.95%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6602 66.02%
Micronuclear + 0.7359 73.59%
Hepatotoxicity + 0.5336 53.36%
skin sensitisation - 0.8563 85.63%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.7637 76.37%
Acute Oral Toxicity (c) II 0.4184 41.84%
Estrogen receptor binding + 0.9099 90.99%
Androgen receptor binding + 0.5671 56.71%
Thyroid receptor binding + 0.7340 73.40%
Glucocorticoid receptor binding + 0.7886 78.86%
Aromatase binding + 0.5553 55.53%
PPAR gamma + 0.6022 60.22%
Honey bee toxicity - 0.9003 90.03%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5049 50.49%
Fish aquatic toxicity + 0.9933 99.33%

Targets

Top

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 95.25% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.01% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.69% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.90% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.90% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.84% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.73% 94.00%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 89.39% 92.68%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.17% 92.94%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.80% 99.17%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.49% 93.99%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.12% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.73% 95.56%
CHEMBL4208 P20618 Proteasome component C5 84.39% 90.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.87% 99.15%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.37% 95.89%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.01% 90.71%
CHEMBL4302 P08183 P-glycoprotein 1 81.46% 92.98%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 81.21% 92.38%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 162943410
LOTUS LTS0273466
wikiData Q105348117