3-Hydroxy-4,5-dimethoxycinnamyl alcohol

Details

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Internal ID ced7df12-80e8-48df-9f18-c82d13621679
Taxonomy Benzenoids > Phenols > Methoxyphenols
IUPAC Name 5-[(E)-3-hydroxyprop-1-enyl]-2,3-dimethoxyphenol
SMILES (Canonical) COC1=CC(=CC(=C1OC)O)C=CCO
SMILES (Isomeric) COC1=CC(=CC(=C1OC)O)/C=C/CO
InChI InChI=1S/C11H14O4/c1-14-10-7-8(4-3-5-12)6-9(13)11(10)15-2/h3-4,6-7,12-13H,5H2,1-2H3/b4-3+
InChI Key BKOHSGMZMRELEA-ONEGZZNKSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H14O4
Molecular Weight 210.23 g/mol
Exact Mass 210.08920892 g/mol
Topological Polar Surface Area (TPSA) 58.90 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.41
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-Hydroxy-4,5-dimethoxycinnamyl alcohol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9779 97.79%
Caco-2 + 0.8126 81.26%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.7812 78.12%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8663 86.63%
OATP1B3 inhibitior + 0.9726 97.26%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.5714 57.14%
P-glycoprotein inhibitior - 0.9687 96.87%
P-glycoprotein substrate - 0.9628 96.28%
CYP3A4 substrate - 0.6178 61.78%
CYP2C9 substrate - 0.5973 59.73%
CYP2D6 substrate - 0.6970 69.70%
CYP3A4 inhibition - 0.6052 60.52%
CYP2C9 inhibition - 0.8320 83.20%
CYP2C19 inhibition - 0.6156 61.56%
CYP2D6 inhibition - 0.8940 89.40%
CYP1A2 inhibition + 0.5341 53.41%
CYP2C8 inhibition - 0.5785 57.85%
CYP inhibitory promiscuity + 0.5000 50.00%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7918 79.18%
Carcinogenicity (trinary) Non-required 0.7441 74.41%
Eye corrosion - 0.8984 89.84%
Eye irritation + 0.9608 96.08%
Skin irritation - 0.5921 59.21%
Skin corrosion - 0.9183 91.83%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6631 66.31%
Micronuclear - 0.6819 68.19%
Hepatotoxicity - 0.5642 56.42%
skin sensitisation + 0.7338 73.38%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity - 0.5840 58.40%
Acute Oral Toxicity (c) III 0.7371 73.71%
Estrogen receptor binding + 0.5395 53.95%
Androgen receptor binding - 0.7379 73.79%
Thyroid receptor binding - 0.6537 65.37%
Glucocorticoid receptor binding - 0.7033 70.33%
Aromatase binding - 0.6551 65.51%
PPAR gamma - 0.6470 64.70%
Honey bee toxicity - 0.9327 93.27%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.7968 79.68%

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 96.71% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 93.74% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.61% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.95% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.50% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.30% 95.56%
CHEMBL3194 P02766 Transthyretin 86.31% 90.71%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 85.72% 92.68%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 83.96% 86.92%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 81.62% 89.62%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 81.05% 91.71%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 80.58% 80.78%

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.
Ferula sinaica

Cross-Links

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PubChem 14830746
LOTUS LTS0025296
wikiData Q104937708