4-(3-Methylbut-2-enoyloxy)-3-(3-methylbut-2-enyl)benzoic acid

Details

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Internal ID 5ccbef5f-ef34-4f31-8637-866573c96ddc
Taxonomy Benzenoids > Phenol esters
IUPAC Name 4-(3-methylbut-2-enoyloxy)-3-(3-methylbut-2-enyl)benzoic acid
SMILES (Canonical) CC(=CCC1=C(C=CC(=C1)C(=O)O)OC(=O)C=C(C)C)C
SMILES (Isomeric) CC(=CCC1=C(C=CC(=C1)C(=O)O)OC(=O)C=C(C)C)C
InChI InChI=1S/C17H20O4/c1-11(2)5-6-13-10-14(17(19)20)7-8-15(13)21-16(18)9-12(3)4/h5,7-10H,6H2,1-4H3,(H,19,20)
InChI Key GZCRDEPNFSDVCM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H20O4
Molecular Weight 288.34 g/mol
Exact Mass 288.13615911 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 4.60
Atomic LogP (AlogP) 3.77
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-(3-Methylbut-2-enoyloxy)-3-(3-methylbut-2-enyl)benzoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9949 99.49%
Caco-2 + 0.7807 78.07%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.8990 89.90%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9465 94.65%
OATP1B3 inhibitior + 0.9117 91.17%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.5537 55.37%
P-glycoprotein inhibitior - 0.8375 83.75%
P-glycoprotein substrate - 0.8261 82.61%
CYP3A4 substrate - 0.6132 61.32%
CYP2C9 substrate + 0.6145 61.45%
CYP2D6 substrate - 0.9125 91.25%
CYP3A4 inhibition - 0.8242 82.42%
CYP2C9 inhibition + 0.5477 54.77%
CYP2C19 inhibition + 0.6676 66.76%
CYP2D6 inhibition - 0.7021 70.21%
CYP1A2 inhibition + 0.5683 56.83%
CYP2C8 inhibition + 0.4907 49.07%
CYP inhibitory promiscuity - 0.5793 57.93%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6042 60.42%
Carcinogenicity (trinary) Non-required 0.7183 71.83%
Eye corrosion - 0.9707 97.07%
Eye irritation + 0.7854 78.54%
Skin irritation - 0.6439 64.39%
Skin corrosion - 0.9525 95.25%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6945 69.45%
Micronuclear - 0.6100 61.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation + 0.5276 52.76%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity + 0.5584 55.84%
Acute Oral Toxicity (c) III 0.6811 68.11%
Estrogen receptor binding + 0.8503 85.03%
Androgen receptor binding - 0.5840 58.40%
Thyroid receptor binding - 0.5177 51.77%
Glucocorticoid receptor binding + 0.6406 64.06%
Aromatase binding + 0.7921 79.21%
PPAR gamma + 0.7346 73.46%
Honey bee toxicity - 0.8946 89.46%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.8452 84.52%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.75% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.06% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 91.09% 96.00%
CHEMBL3194 P02766 Transthyretin 90.77% 90.71%
CHEMBL2581 P07339 Cathepsin D 88.31% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 88.04% 94.73%
CHEMBL4208 P20618 Proteasome component C5 86.96% 90.00%
CHEMBL1255126 O15151 Protein Mdm4 85.99% 90.20%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.82% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.74% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 82.22% 97.21%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.80% 95.56%

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.
Anthemis aciphylla
Ozothamnus obcordatus

Cross-Links

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PubChem 101614957
LOTUS LTS0158604
wikiData Q105204972