2,8-Dihydroxy-4,7-dimethoxy-6-methyl-1-naphthalenecarboxaldehyde

Details

Top
Internal ID 563d7cfb-a860-4031-9a52-e04ea995061c
Taxonomy Benzenoids > Naphthalenes > Naphthols and derivatives
IUPAC Name 2,8-dihydroxy-4,7-dimethoxy-6-methylnaphthalene-1-carbaldehyde
SMILES (Canonical) CC1=CC2=C(C=C(C(=C2C(=C1OC)O)C=O)O)OC
SMILES (Isomeric) CC1=CC2=C(C=C(C(=C2C(=C1OC)O)C=O)O)OC
InChI InChI=1S/C14H14O5/c1-7-4-8-11(18-2)5-10(16)9(6-15)12(8)13(17)14(7)19-3/h4-6,16-17H,1-3H3
InChI Key GMVPDJNQIBINLE-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C14H14O5
Molecular Weight 262.26 g/mol
Exact Mass 262.08412354 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.39
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

Top
215050-63-8
2,8-Dihydroxy-4,7-dimethoxy-6-methyl-1-naphthalenecarboxaldehyde

2D Structure

Top
2D Structure of 2,8-Dihydroxy-4,7-dimethoxy-6-methyl-1-naphthalenecarboxaldehyde

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9916 99.16%
Caco-2 + 0.5573 55.73%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.8062 80.62%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8205 82.05%
OATP1B3 inhibitior + 0.8917 89.17%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6592 65.92%
P-glycoprotein inhibitior - 0.8671 86.71%
P-glycoprotein substrate - 0.9223 92.23%
CYP3A4 substrate - 0.5219 52.19%
CYP2C9 substrate - 0.8097 80.97%
CYP2D6 substrate - 0.7962 79.62%
CYP3A4 inhibition - 0.7190 71.90%
CYP2C9 inhibition - 0.8870 88.70%
CYP2C19 inhibition - 0.5981 59.81%
CYP2D6 inhibition - 0.8519 85.19%
CYP1A2 inhibition + 0.9289 92.89%
CYP2C8 inhibition + 0.4561 45.61%
CYP inhibitory promiscuity + 0.5000 50.00%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8920 89.20%
Carcinogenicity (trinary) Non-required 0.5386 53.86%
Eye corrosion - 0.9789 97.89%
Eye irritation + 0.7964 79.64%
Skin irritation - 0.6255 62.55%
Skin corrosion - 0.9777 97.77%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7763 77.63%
Micronuclear + 0.7600 76.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.9103 91.03%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.7022 70.22%
Acute Oral Toxicity (c) III 0.4586 45.86%
Estrogen receptor binding + 0.7942 79.42%
Androgen receptor binding - 0.6362 63.62%
Thyroid receptor binding - 0.5480 54.80%
Glucocorticoid receptor binding + 0.5649 56.49%
Aromatase binding + 0.6403 64.03%
PPAR gamma + 0.7132 71.32%
Honey bee toxicity - 0.8742 87.42%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9685 96.85%

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
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 99.41% 98.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.56% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.79% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.93% 94.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 86.18% 89.62%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.89% 89.00%
CHEMBL3194 P02766 Transthyretin 85.50% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.36% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.60% 96.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.08% 94.45%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.92% 99.15%
CHEMBL3401 O75469 Pregnane X receptor 82.64% 94.73%
CHEMBL2535 P11166 Glucose transporter 80.87% 98.75%
CHEMBL2581 P07339 Cathepsin D 80.72% 98.95%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.70% 95.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.10% 99.17%

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.
Hibiscus cannabinus

Cross-Links

Top
PubChem 10491696
LOTUS LTS0259133
wikiData Q105012189