3,5-Dihydroxy-4-Methoxybenzaldehyde

Details

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Internal ID 7da6c835-bfc2-41e7-896b-2b5d3a8041d7
Taxonomy Benzenoids > Phenols > Methoxyphenols
IUPAC Name 3,5-dihydroxy-4-methoxybenzaldehyde
SMILES (Canonical) COC1=C(C=C(C=C1O)C=O)O
SMILES (Isomeric) COC1=C(C=C(C=C1O)C=O)O
InChI InChI=1S/C8H8O4/c1-12-8-6(10)2-5(4-9)3-7(8)11/h2-4,10-11H,1H3
InChI Key UAFQVVYJCLAIGY-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C8H8O4
Molecular Weight 168.15 g/mol
Exact Mass 168.04225873 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 0.60
Atomic LogP (AlogP) 0.92
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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29865-85-8
CHEMBL89737
SCHEMBL5155052
CS-0245708
EN300-309534
Z1511745745

2D Structure

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2D Structure of 3,5-Dihydroxy-4-Methoxybenzaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9588 95.88%
Caco-2 + 0.7034 70.34%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.7750 77.50%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8658 86.58%
OATP1B3 inhibitior + 0.9801 98.01%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9444 94.44%
P-glycoprotein inhibitior - 0.9660 96.60%
P-glycoprotein substrate - 0.9877 98.77%
CYP3A4 substrate - 0.6963 69.63%
CYP2C9 substrate - 0.6165 61.65%
CYP2D6 substrate - 0.6929 69.29%
CYP3A4 inhibition - 0.7778 77.78%
CYP2C9 inhibition - 0.6879 68.79%
CYP2C19 inhibition - 0.5388 53.88%
CYP2D6 inhibition - 0.9292 92.92%
CYP1A2 inhibition - 0.5248 52.48%
CYP2C8 inhibition - 0.9296 92.96%
CYP inhibitory promiscuity - 0.6503 65.03%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7974 79.74%
Carcinogenicity (trinary) Non-required 0.7021 70.21%
Eye corrosion + 0.6486 64.86%
Eye irritation + 0.9865 98.65%
Skin irritation + 0.7608 76.08%
Skin corrosion - 0.7443 74.43%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6615 66.15%
Micronuclear + 0.7000 70.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation + 0.5088 50.88%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity - 0.5696 56.96%
Acute Oral Toxicity (c) III 0.7501 75.01%
Estrogen receptor binding - 0.7833 78.33%
Androgen receptor binding - 0.7672 76.72%
Thyroid receptor binding - 0.8232 82.32%
Glucocorticoid receptor binding - 0.7871 78.71%
Aromatase binding - 0.8136 81.36%
PPAR gamma - 0.7197 71.97%
Honey bee toxicity - 0.9418 94.18%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.6455 64.55%
Fish aquatic toxicity + 0.7547 75.47%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.80% 91.11%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 94.64% 98.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.08% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.28% 96.09%
CHEMBL3194 P02766 Transthyretin 84.77% 90.71%
CHEMBL4208 P20618 Proteasome component C5 84.72% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.38% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.88% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.93% 96.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.72% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 80.39% 94.73%

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.
Cheniella glauca

Cross-Links

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PubChem 12928004
LOTUS LTS0073965
wikiData Q105268719