4-(3',4'-Dimethoxyphenyl)but-3-en-1-ol

Details

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Internal ID f0032a6f-fd4b-45b1-80b6-23ba150d5aef
Taxonomy Benzenoids > Benzene and substituted derivatives > Methoxybenzenes > Dimethoxybenzenes
IUPAC Name 4-(3,4-dimethoxyphenyl)but-3-en-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H16O3/c1-14-11-7-6-10(5-3-4-8-13)9-12(11)15-2/h3,5-7,9,13H,4,8H2,1-2H3
InChI Key HJXARZMWFOEQTO-UHFFFAOYSA-N
Popularity 16 references in papers

Physical and Chemical Properties

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Molecular Formula C12H16O3
Molecular Weight 208.25 g/mol
Exact Mass 208.109944368 g/mol
Topological Polar Surface Area (TPSA) 38.70 Ų
XlogP 1.70
Atomic LogP (AlogP) 2.10
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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2-(3,4-dimethoxystyryl)ethanol
B0005-149110

2D Structure

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2D Structure of 4-(3',4'-Dimethoxyphenyl)but-3-en-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 + 0.9312 93.12%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.8917 89.17%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8762 87.62%
OATP1B3 inhibitior + 0.9643 96.43%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.6470 64.70%
P-glycoprotein inhibitior - 0.9747 97.47%
P-glycoprotein substrate - 0.8785 87.85%
CYP3A4 substrate - 0.6202 62.02%
CYP2C9 substrate - 0.6063 60.63%
CYP2D6 substrate + 0.3716 37.16%
CYP3A4 inhibition - 0.7831 78.31%
CYP2C9 inhibition - 0.9454 94.54%
CYP2C19 inhibition - 0.7291 72.91%
CYP2D6 inhibition - 0.9267 92.67%
CYP1A2 inhibition - 0.5515 55.15%
CYP2C8 inhibition - 0.7307 73.07%
CYP inhibitory promiscuity - 0.7529 75.29%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.8528 85.28%
Carcinogenicity (trinary) Non-required 0.7262 72.62%
Eye corrosion - 0.8723 87.23%
Eye irritation + 0.8564 85.64%
Skin irritation + 0.5256 52.56%
Skin corrosion - 0.9544 95.44%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6667 66.67%
Micronuclear - 0.9117 91.17%
Hepatotoxicity - 0.6267 62.67%
skin sensitisation + 0.7042 70.42%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.6222 62.22%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity - 0.7190 71.90%
Acute Oral Toxicity (c) III 0.8250 82.50%
Estrogen receptor binding - 0.6123 61.23%
Androgen receptor binding - 0.5670 56.70%
Thyroid receptor binding - 0.7430 74.30%
Glucocorticoid receptor binding - 0.7398 73.98%
Aromatase binding - 0.5419 54.19%
PPAR gamma - 0.8078 80.78%
Honey bee toxicity - 0.9484 94.84%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity - 0.6555 65.55%

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
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 95.09% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.95% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.58% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.05% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.54% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.50% 95.56%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 85.48% 89.62%
CHEMBL4208 P20618 Proteasome component C5 82.78% 90.00%

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 129668
LOTUS LTS0015943
wikiData Q105029499