3-(8-Hydroxy-3,4-dimethyl-1-oxo-3,4-dihydroisochromen-7-yl)prop-2-enoic acid

Details

Top
Internal ID faf6ea58-dddb-4a0e-81e4-b880366ac927
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Hydroxycinnamic acids and derivatives > Coumaric acids and derivatives > Coumaric acids
IUPAC Name 3-(8-hydroxy-3,4-dimethyl-1-oxo-3,4-dihydroisochromen-7-yl)prop-2-enoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H14O5/c1-7-8(2)19-14(18)12-10(7)5-3-9(13(12)17)4-6-11(15)16/h3-8,17H,1-2H3,(H,15,16)
InChI Key XSYRDVCSKQJINC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C14H14O5
Molecular Weight 262.26 g/mol
Exact Mass 262.08412354 g/mol
Topological Polar Surface Area (TPSA) 83.80 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.15
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 3-(8-Hydroxy-3,4-dimethyl-1-oxo-3,4-dihydroisochromen-7-yl)prop-2-enoic acid

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9704 97.04%
Caco-2 + 0.5663 56.63%
Blood Brain Barrier - 0.8750 87.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.7734 77.34%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7231 72.31%
OATP1B3 inhibitior + 0.9765 97.65%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8910 89.10%
P-glycoprotein inhibitior - 0.9394 93.94%
P-glycoprotein substrate - 0.8396 83.96%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.6043 60.43%
CYP2D6 substrate - 0.9033 90.33%
CYP3A4 inhibition - 0.7533 75.33%
CYP2C9 inhibition + 0.7757 77.57%
CYP2C19 inhibition - 0.8410 84.10%
CYP2D6 inhibition - 0.9249 92.49%
CYP1A2 inhibition - 0.7866 78.66%
CYP2C8 inhibition - 0.5675 56.75%
CYP inhibitory promiscuity - 0.6894 68.94%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9513 95.13%
Carcinogenicity (trinary) Non-required 0.5310 53.10%
Eye corrosion - 0.9755 97.55%
Eye irritation - 0.4839 48.39%
Skin irritation + 0.5323 53.23%
Skin corrosion - 0.9267 92.67%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6791 67.91%
Micronuclear + 0.9300 93.00%
Hepatotoxicity + 0.5899 58.99%
skin sensitisation - 0.7805 78.05%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.6174 61.74%
Acute Oral Toxicity (c) II 0.5791 57.91%
Estrogen receptor binding + 0.6523 65.23%
Androgen receptor binding + 0.6632 66.32%
Thyroid receptor binding - 0.6788 67.88%
Glucocorticoid receptor binding - 0.7422 74.22%
Aromatase binding - 0.5759 57.59%
PPAR gamma - 0.6065 60.65%
Honey bee toxicity - 0.9633 96.33%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9790 97.90%

Targets

Top

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 97.22% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.95% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.15% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.43% 89.00%
CHEMBL2581 P07339 Cathepsin D 92.90% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 92.10% 91.49%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.57% 99.23%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.47% 93.56%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 83.45% 91.71%
CHEMBL3401 O75469 Pregnane X receptor 83.43% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.61% 99.17%

Plants that contains it

Top
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.
Rhizophora mucronata

Cross-Links

Top
PubChem 75954488
LOTUS LTS0252948
wikiData Q104201327