(Z)-2-(acetyloxymethyl)but-2-enoic acid

Details

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Internal ID ab0d986b-f20d-474b-8f65-5c2146b9d851
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Branched fatty acids
IUPAC Name (Z)-2-(acetyloxymethyl)but-2-enoic acid
SMILES (Canonical) CC=C(COC(=O)C)C(=O)O
SMILES (Isomeric) C/C=C(/COC(=O)C)\C(=O)O
InChI InChI=1S/C7H10O4/c1-3-6(7(9)10)4-11-5(2)8/h3H,4H2,1-2H3,(H,9,10)/b6-3-
InChI Key XSYZFBODOKESPU-UTCJRWHESA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C7H10O4
Molecular Weight 158.15 g/mol
Exact Mass 158.05790880 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 0.30
Atomic LogP (AlogP) 0.58
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (Z)-2-(acetyloxymethyl)but-2-enoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9758 97.58%
Caco-2 - 0.6860 68.60%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.8157 81.57%
OATP2B1 inhibitior - 0.8595 85.95%
OATP1B1 inhibitior + 0.9273 92.73%
OATP1B3 inhibitior + 0.9509 95.09%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9204 92.04%
P-glycoprotein inhibitior - 0.9842 98.42%
P-glycoprotein substrate - 0.9853 98.53%
CYP3A4 substrate - 0.6872 68.72%
CYP2C9 substrate - 0.5592 55.92%
CYP2D6 substrate - 0.9214 92.14%
CYP3A4 inhibition - 0.9184 91.84%
CYP2C9 inhibition - 0.8482 84.82%
CYP2C19 inhibition - 0.8959 89.59%
CYP2D6 inhibition - 0.9051 90.51%
CYP1A2 inhibition - 0.9062 90.62%
CYP2C8 inhibition - 0.9765 97.65%
CYP inhibitory promiscuity - 0.9189 91.89%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5349 53.49%
Carcinogenicity (trinary) Non-required 0.7296 72.96%
Eye corrosion - 0.6293 62.93%
Eye irritation + 0.9923 99.23%
Skin irritation + 0.7382 73.82%
Skin corrosion - 0.6177 61.77%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8007 80.07%
Micronuclear - 0.8800 88.00%
Hepatotoxicity + 0.5651 56.51%
skin sensitisation + 0.4867 48.67%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.8137 81.37%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity + 0.6853 68.53%
Acute Oral Toxicity (c) II 0.5294 52.94%
Estrogen receptor binding - 0.8726 87.26%
Androgen receptor binding - 0.8284 82.84%
Thyroid receptor binding - 0.9405 94.05%
Glucocorticoid receptor binding - 0.9009 90.09%
Aromatase binding - 0.8363 83.63%
PPAR gamma - 0.9716 97.16%
Honey bee toxicity - 0.9257 92.57%
Biodegradation + 0.8000 80.00%
Crustacea aquatic toxicity - 0.8155 81.55%
Fish aquatic toxicity + 0.9553 95.53%

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 91.49% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.65% 96.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.43% 99.17%
CHEMBL2581 P07339 Cathepsin D 80.73% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.70% 86.33%
CHEMBL340 P08684 Cytochrome P450 3A4 80.13% 91.19%

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.
Calea cuneifolia

Cross-Links

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PubChem 133682229
LOTUS LTS0090258
wikiData Q105341374