4-(3,4-Dimethoxyphenyl)but-3-ene-1,2-diol

Details

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Internal ID 4a96cf88-fb10-4aa1-a105-e8d2acd14461
Taxonomy Benzenoids > Benzene and substituted derivatives > Methoxybenzenes > Dimethoxybenzenes
IUPAC Name 4-(3,4-dimethoxyphenyl)but-3-ene-1,2-diol
SMILES (Canonical) COC1=C(C=C(C=C1)C=CC(CO)O)OC
SMILES (Isomeric) COC1=C(C=C(C=C1)C=CC(CO)O)OC
InChI InChI=1S/C12H16O4/c1-15-11-6-4-9(7-12(11)16-2)3-5-10(14)8-13/h3-7,10,13-14H,8H2,1-2H3
InChI Key LFOKKKFXPSWWMO-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C12H16O4
Molecular Weight 224.25 g/mol
Exact Mass 224.10485899 g/mol
Topological Polar Surface Area (TPSA) 58.90 Ų
XlogP 0.60
Atomic LogP (AlogP) 1.07
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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DTXSID30702242

2D Structure

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2D Structure of 4-(3,4-Dimethoxyphenyl)but-3-ene-1,2-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9742 97.42%
Caco-2 + 0.6920 69.20%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.8112 81.12%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9031 90.31%
OATP1B3 inhibitior + 0.9678 96.78%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.6937 69.37%
P-glycoprotein inhibitior - 0.9711 97.11%
P-glycoprotein substrate - 0.8834 88.34%
CYP3A4 substrate - 0.6069 60.69%
CYP2C9 substrate - 0.5976 59.76%
CYP2D6 substrate - 0.7075 70.75%
CYP3A4 inhibition - 0.7017 70.17%
CYP2C9 inhibition - 0.9060 90.60%
CYP2C19 inhibition - 0.8043 80.43%
CYP2D6 inhibition - 0.8929 89.29%
CYP1A2 inhibition - 0.6892 68.92%
CYP2C8 inhibition + 0.5343 53.43%
CYP inhibitory promiscuity - 0.8341 83.41%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8415 84.15%
Carcinogenicity (trinary) Non-required 0.7333 73.33%
Eye corrosion - 0.9640 96.40%
Eye irritation - 0.6403 64.03%
Skin irritation - 0.6277 62.77%
Skin corrosion - 0.9287 92.87%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4238 42.38%
Micronuclear - 0.6201 62.01%
Hepatotoxicity - 0.7144 71.44%
skin sensitisation + 0.7254 72.54%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity - 0.8729 87.29%
Acute Oral Toxicity (c) III 0.7747 77.47%
Estrogen receptor binding - 0.6844 68.44%
Androgen receptor binding - 0.6129 61.29%
Thyroid receptor binding - 0.7334 73.34%
Glucocorticoid receptor binding - 0.6644 66.44%
Aromatase binding - 0.6355 63.55%
PPAR gamma - 0.7543 75.43%
Honey bee toxicity - 0.9363 93.63%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity - 0.3731 37.31%

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 96.08% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 95.82% 96.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 94.15% 89.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.17% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.21% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.21% 99.17%
CHEMBL2581 P07339 Cathepsin D 89.38% 98.95%
CHEMBL1255126 O15151 Protein Mdm4 88.94% 90.20%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.34% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.78% 95.56%
CHEMBL2535 P11166 Glucose transporter 83.86% 98.75%
CHEMBL3024 P53350 Serine/threonine-protein kinase PLK1 81.76% 97.43%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.40% 94.45%

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.
Zingiber montanum

Cross-Links

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PubChem 53439925
LOTUS LTS0091530
wikiData Q72468265