4-Hydroxy-2-(2,4,5-trimethoxyphenyl)but-2-enal

Details

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Internal ID 9c38e487-2389-417e-a57f-c2ee324a1aca
Taxonomy Phenylpropanoids and polyketides > Cinnamyl alcohols
IUPAC Name 4-hydroxy-2-(2,4,5-trimethoxyphenyl)but-2-enal
SMILES (Canonical) COC1=CC(=C(C=C1C(=CCO)C=O)OC)OC
SMILES (Isomeric) COC1=CC(=C(C=C1C(=CCO)C=O)OC)OC
InChI InChI=1S/C13H16O5/c1-16-11-7-13(18-3)12(17-2)6-10(11)9(8-15)4-5-14/h4,6-8,14H,5H2,1-3H3
InChI Key VNJZIMNPESHAEJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H16O5
Molecular Weight 252.26 g/mol
Exact Mass 252.09977361 g/mol
Topological Polar Surface Area (TPSA) 65.00 Ų
XlogP 0.80
Atomic LogP (AlogP) 1.29
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-Hydroxy-2-(2,4,5-trimethoxyphenyl)but-2-enal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9926 99.26%
Caco-2 + 0.9024 90.24%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.8315 83.15%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8733 87.33%
OATP1B3 inhibitior + 0.9641 96.41%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.6286 62.86%
P-glycoprotein inhibitior - 0.9427 94.27%
P-glycoprotein substrate - 0.8859 88.59%
CYP3A4 substrate - 0.6446 64.46%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.7990 79.90%
CYP3A4 inhibition - 0.5976 59.76%
CYP2C9 inhibition - 0.8898 88.98%
CYP2C19 inhibition - 0.5317 53.17%
CYP2D6 inhibition - 0.9042 90.42%
CYP1A2 inhibition + 0.5448 54.48%
CYP2C8 inhibition - 0.8031 80.31%
CYP inhibitory promiscuity - 0.5291 52.91%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.7788 77.88%
Carcinogenicity (trinary) Non-required 0.7724 77.24%
Eye corrosion - 0.9390 93.90%
Eye irritation + 0.7191 71.91%
Skin irritation - 0.6695 66.95%
Skin corrosion - 0.9816 98.16%
Ames mutagenesis - 0.5770 57.70%
Human Ether-a-go-go-Related Gene inhibition - 0.4453 44.53%
Micronuclear - 0.5786 57.86%
Hepatotoxicity - 0.6591 65.91%
skin sensitisation + 0.4919 49.19%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity + 0.4604 46.04%
Acute Oral Toxicity (c) III 0.6202 62.02%
Estrogen receptor binding + 0.5505 55.05%
Androgen receptor binding - 0.7341 73.41%
Thyroid receptor binding + 0.5393 53.93%
Glucocorticoid receptor binding - 0.5961 59.61%
Aromatase binding + 0.5538 55.38%
PPAR gamma - 0.7070 70.70%
Honey bee toxicity - 0.9337 93.37%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.7855 78.55%
Fish aquatic toxicity + 0.8924 89.24%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.26% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.05% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.04% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.38% 99.17%
CHEMBL2535 P11166 Glucose transporter 86.78% 98.75%
CHEMBL4208 P20618 Proteasome component C5 86.45% 90.00%
CHEMBL3492 P49721 Proteasome Macropain subunit 85.04% 90.24%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.80% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.75% 91.11%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.69% 95.50%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 81.96% 86.92%
CHEMBL3401 O75469 Pregnane X receptor 81.96% 94.73%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 81.80% 92.38%

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.
Alpinia flabellata

Cross-Links

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PubChem 85280645
LOTUS LTS0257880
wikiData Q105289673