4,5,6-Trimethoxy-2-naphthaldehyde

Details

Top
Internal ID 936d4bfd-b253-4754-a98c-c6a92118b1c6
Taxonomy Benzenoids > Naphthalenes
IUPAC Name 4,5,6-trimethoxynaphthalene-2-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H14O4/c1-16-11-5-4-10-6-9(8-15)7-12(17-2)13(10)14(11)18-3/h4-8H,1-3H3
InChI Key DWBLTAMFRSBZJC-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

Top
Molecular Formula C14H14O4
Molecular Weight 246.26 g/mol
Exact Mass 246.08920892 g/mol
Topological Polar Surface Area (TPSA) 44.80 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.68
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 4,5,6-Trimethoxy-2-naphthaldehyde

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9971 99.71%
Caco-2 + 0.8040 80.40%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.7400 74.00%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9115 91.15%
OATP1B3 inhibitior + 0.9825 98.25%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6029 60.29%
P-glycoprotein inhibitior - 0.9264 92.64%
P-glycoprotein substrate - 0.9222 92.22%
CYP3A4 substrate - 0.6072 60.72%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3525 35.25%
CYP3A4 inhibition + 0.5564 55.64%
CYP2C9 inhibition - 0.9317 93.17%
CYP2C19 inhibition - 0.5493 54.93%
CYP2D6 inhibition - 0.9534 95.34%
CYP1A2 inhibition + 0.9787 97.87%
CYP2C8 inhibition - 0.5844 58.44%
CYP inhibitory promiscuity + 0.6505 65.05%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9020 90.20%
Carcinogenicity (trinary) Non-required 0.4921 49.21%
Eye corrosion - 0.9595 95.95%
Eye irritation + 0.8940 89.40%
Skin irritation - 0.7168 71.68%
Skin corrosion - 0.9890 98.90%
Ames mutagenesis + 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6761 67.61%
Micronuclear + 0.6718 67.18%
Hepatotoxicity + 0.6909 69.09%
skin sensitisation - 0.9123 91.23%
Respiratory toxicity - 0.8667 86.67%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) II 0.5116 51.16%
Estrogen receptor binding + 0.8319 83.19%
Androgen receptor binding - 0.5131 51.31%
Thyroid receptor binding - 0.5360 53.60%
Glucocorticoid receptor binding + 0.5644 56.44%
Aromatase binding + 0.5896 58.96%
PPAR gamma - 0.7602 76.02%
Honey bee toxicity - 0.8974 89.74%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.9761 97.61%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.83% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 92.75% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.63% 86.33%
CHEMBL1255126 O15151 Protein Mdm4 90.51% 90.20%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.66% 96.09%
CHEMBL4208 P20618 Proteasome component C5 84.29% 90.00%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 84.21% 98.11%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 83.47% 89.62%
CHEMBL2535 P11166 Glucose transporter 81.87% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.80% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.24% 94.45%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 80.92% 80.78%

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.
Diospyros ebenum
Diospyros paniculata

Cross-Links

Top
PubChem 129711718
LOTUS LTS0148081
wikiData Q104990466