2-Hydroxy-3,4,6-trimethoxybenzaldehyde

Details

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Internal ID fd29e693-a523-4717-9456-eccfb7abeca0
Taxonomy Benzenoids > Phenols > Methoxyphenols
IUPAC Name 2-hydroxy-3,4,6-trimethoxybenzaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H12O5/c1-13-7-4-8(14-2)10(15-3)9(12)6(7)5-11/h4-5,12H,1-3H3
InChI Key LRGJWCQSWJHJKW-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C10H12O5
Molecular Weight 212.20 g/mol
Exact Mass 212.06847348 g/mol
Topological Polar Surface Area (TPSA) 65.00 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.23
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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65162-31-4
starbld0011705
3,4,6-trimethoxysalicylaldehyde
2-hydroxy-3,4,6-trimethoxy-benzaldehyde

2D Structure

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2D Structure of 2-Hydroxy-3,4,6-trimethoxybenzaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9881 98.81%
Caco-2 + 0.6743 67.43%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.8813 88.13%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7740 77.40%
OATP1B3 inhibitior + 0.9718 97.18%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8707 87.07%
P-glycoprotein inhibitior - 0.9293 92.93%
P-glycoprotein substrate - 0.9622 96.22%
CYP3A4 substrate - 0.6081 60.81%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7924 79.24%
CYP3A4 inhibition - 0.8467 84.67%
CYP2C9 inhibition - 0.9944 99.44%
CYP2C19 inhibition - 0.7886 78.86%
CYP2D6 inhibition - 0.9374 93.74%
CYP1A2 inhibition - 0.7261 72.61%
CYP2C8 inhibition - 0.6566 65.66%
CYP inhibitory promiscuity - 0.8362 83.62%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7554 75.54%
Carcinogenicity (trinary) Non-required 0.6658 66.58%
Eye corrosion + 0.6642 66.42%
Eye irritation + 0.9815 98.15%
Skin irritation + 0.5756 57.56%
Skin corrosion - 0.9609 96.09%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5881 58.81%
Micronuclear - 0.5067 50.67%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.8203 82.03%
Respiratory toxicity - 0.8667 86.67%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity - 0.6261 62.61%
Acute Oral Toxicity (c) III 0.6252 62.52%
Estrogen receptor binding + 0.5345 53.45%
Androgen receptor binding - 0.7190 71.90%
Thyroid receptor binding - 0.6710 67.10%
Glucocorticoid receptor binding - 0.7337 73.37%
Aromatase binding - 0.6783 67.83%
PPAR gamma - 0.5967 59.67%
Honey bee toxicity - 0.9226 92.26%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.8371 83.71%

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
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 98.91% 98.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.87% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.08% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.92% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.42% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.46% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.02% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.83% 94.00%
CHEMBL3194 P02766 Transthyretin 80.49% 90.71%

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.
Uvaria welwitschii

Cross-Links

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PubChem 12494693
LOTUS LTS0053201
wikiData Q105156119