2Z,4E-5-(4-Hydroxyphenyl)penta-2,4-dienoic acid

Details

Top
Internal ID 3ca549c6-1089-406f-8e0a-85c055749849
Taxonomy Benzenoids > Benzene and substituted derivatives > Styrenes
IUPAC Name (2Z,4E)-5-(4-hydroxyphenyl)penta-2,4-dienoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H10O3/c12-10-7-5-9(6-8-10)3-1-2-4-11(13)14/h1-8,12H,(H,13,14)/b3-1+,4-2-
InChI Key CYYTUYSFBHDJRH-TZFCGSKZSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C11H10O3
Molecular Weight 190.19 g/mol
Exact Mass 190.062994177 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.05
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

Top
CYYTUYSFBHDJRH-TZFCGSKZSA-N
(2Z,4E)-5-(4-Hydroxyphenyl)-2,4-pentadienoic acid #

2D Structure

Top
2D Structure of 2Z,4E-5-(4-Hydroxyphenyl)penta-2,4-dienoic acid

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9959 99.59%
Caco-2 + 0.7969 79.69%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.8227 82.27%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9301 93.01%
OATP1B3 inhibitior + 0.9445 94.45%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.7555 75.55%
P-glycoprotein inhibitior - 0.9868 98.68%
P-glycoprotein substrate - 0.9773 97.73%
CYP3A4 substrate - 0.6837 68.37%
CYP2C9 substrate - 0.7908 79.08%
CYP2D6 substrate - 0.8849 88.49%
CYP3A4 inhibition - 0.8693 86.93%
CYP2C9 inhibition - 0.9364 93.64%
CYP2C19 inhibition - 0.9116 91.16%
CYP2D6 inhibition - 0.9766 97.66%
CYP1A2 inhibition - 0.9458 94.58%
CYP2C8 inhibition - 0.6671 66.71%
CYP inhibitory promiscuity - 0.8913 89.13%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.6105 61.05%
Carcinogenicity (trinary) Non-required 0.6034 60.34%
Eye corrosion + 0.6040 60.40%
Eye irritation + 0.9924 99.24%
Skin irritation + 0.9245 92.45%
Skin corrosion - 0.8096 80.96%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.9116 91.16%
Micronuclear + 0.5900 59.00%
Hepatotoxicity - 0.5397 53.97%
skin sensitisation + 0.8695 86.95%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.5121 51.21%
Acute Oral Toxicity (c) III 0.4898 48.98%
Estrogen receptor binding + 0.7510 75.10%
Androgen receptor binding + 0.7504 75.04%
Thyroid receptor binding - 0.7318 73.18%
Glucocorticoid receptor binding + 0.6557 65.57%
Aromatase binding + 0.7513 75.13%
PPAR gamma + 0.5760 57.60%
Honey bee toxicity - 0.9530 95.30%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.9444 94.44%

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
CHEMBL3194 P02766 Transthyretin 89.75% 90.71%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.63% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.36% 95.56%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 86.18% 91.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.05% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.12% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.52% 96.00%
CHEMBL242 Q92731 Estrogen receptor beta 80.33% 98.35%

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.
There are no matching plants.

Cross-Links

Top
PubChem 5372825
LOTUS LTS0044964
wikiData Q104972609