(R)-1-(4-Methoxyphenyl)allylacetate

Details

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Internal ID 6af47d1f-93af-438a-8188-5457574ec3b9
Taxonomy Phenylpropanoids and polyketides > Phenylpropanoic acids
IUPAC Name (3R)-3-(4-methoxyphenyl)pent-4-enoate
SMILES (Canonical) COC1=CC=C(C=C1)C(CC(=O)[O-])C=C
SMILES (Isomeric) COC1=CC=C(C=C1)[C@H](CC(=O)[O-])C=C
InChI InChI=1S/C12H14O3/c1-3-9(8-12(13)14)10-4-6-11(15-2)7-5-10/h3-7,9H,1,8H2,2H3,(H,13,14)/p-1/t9-/m0/s1
InChI Key UDGQZNQOSUOHQP-VIFPVBQESA-M
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H13O3-
Molecular Weight 205.23 g/mol
Exact Mass 205.086469272 g/mol
Topological Polar Surface Area (TPSA) 49.40 Ų
XlogP 2.90
Atomic LogP (AlogP) 1.10
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (R)-1-(4-Methoxyphenyl)allylacetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9877 98.77%
Caco-2 + 0.9129 91.29%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.8324 83.24%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9135 91.35%
OATP1B3 inhibitior + 0.9670 96.70%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.7246 72.46%
P-glycoprotein inhibitior - 0.9848 98.48%
P-glycoprotein substrate - 0.9399 93.99%
CYP3A4 substrate - 0.6210 62.10%
CYP2C9 substrate + 0.5918 59.18%
CYP2D6 substrate - 0.8354 83.54%
CYP3A4 inhibition - 0.7915 79.15%
CYP2C9 inhibition - 0.9006 90.06%
CYP2C19 inhibition - 0.5800 58.00%
CYP2D6 inhibition - 0.9511 95.11%
CYP1A2 inhibition + 0.5448 54.48%
CYP2C8 inhibition - 0.9316 93.16%
CYP inhibitory promiscuity - 0.7595 75.95%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5953 59.53%
Carcinogenicity (trinary) Non-required 0.5858 58.58%
Eye corrosion + 0.5468 54.68%
Eye irritation + 0.8314 83.14%
Skin irritation - 0.6277 62.77%
Skin corrosion - 0.9566 95.66%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5568 55.68%
Micronuclear - 0.6183 61.83%
Hepatotoxicity - 0.5465 54.65%
skin sensitisation - 0.7358 73.58%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.6778 67.78%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity - 0.5774 57.74%
Acute Oral Toxicity (c) III 0.7034 70.34%
Estrogen receptor binding - 0.8532 85.32%
Androgen receptor binding - 0.5219 52.19%
Thyroid receptor binding - 0.8128 81.28%
Glucocorticoid receptor binding - 0.6339 63.39%
Aromatase binding - 0.5438 54.38%
PPAR gamma - 0.7560 75.60%
Honey bee toxicity - 0.8989 89.89%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.9350 93.50%

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 96.96% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.38% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.25% 95.56%
CHEMBL4208 P20618 Proteasome component C5 92.10% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.98% 99.17%
CHEMBL2581 P07339 Cathepsin D 90.28% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.07% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 88.46% 96.00%
CHEMBL1907 P15144 Aminopeptidase N 87.69% 93.31%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.40% 86.33%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.52% 91.07%

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.
Acorus calamus var. angustatus
Acorus gramineus

Cross-Links

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PubChem 101047096
NPASS NPC297225