6-(2,4-Dihydroxy-5-methylphenyl)-6-oxohex-2-enoic acid

Details

Top
Internal ID d2f5741f-f2ef-44b6-8be3-8313d3b60eab
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name 6-(2,4-dihydroxy-5-methylphenyl)-6-oxohex-2-enoic acid
SMILES (Canonical) CC1=CC(=C(C=C1O)O)C(=O)CCC=CC(=O)O
SMILES (Isomeric) CC1=CC(=C(C=C1O)O)C(=O)CCC=CC(=O)O
InChI InChI=1S/C13H14O5/c1-8-6-9(12(16)7-11(8)15)10(14)4-2-3-5-13(17)18/h3,5-7,15-16H,2,4H2,1H3,(H,17,18)
InChI Key GVLNMYQUWRBNBY-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C13H14O5
Molecular Weight 250.25 g/mol
Exact Mass 250.08412354 g/mol
Topological Polar Surface Area (TPSA) 94.80 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.01
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 5

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 6-(2,4-Dihydroxy-5-methylphenyl)-6-oxohex-2-enoic acid

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8473 84.73%
Caco-2 + 0.7866 78.66%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.8870 88.70%
OATP2B1 inhibitior - 0.5780 57.80%
OATP1B1 inhibitior + 0.8733 87.33%
OATP1B3 inhibitior + 0.9737 97.37%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9088 90.88%
BSEP inhibitior - 0.8597 85.97%
P-glycoprotein inhibitior - 0.9848 98.48%
P-glycoprotein substrate - 0.9419 94.19%
CYP3A4 substrate - 0.6351 63.51%
CYP2C9 substrate - 0.5795 57.95%
CYP2D6 substrate - 0.8858 88.58%
CYP3A4 inhibition + 0.5663 56.63%
CYP2C9 inhibition + 0.6460 64.60%
CYP2C19 inhibition - 0.5661 56.61%
CYP2D6 inhibition - 0.8550 85.50%
CYP1A2 inhibition - 0.7191 71.91%
CYP2C8 inhibition - 0.8137 81.37%
CYP inhibitory promiscuity - 0.8028 80.28%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.8026 80.26%
Carcinogenicity (trinary) Non-required 0.7708 77.08%
Eye corrosion - 0.9626 96.26%
Eye irritation + 0.8424 84.24%
Skin irritation - 0.5275 52.75%
Skin corrosion - 0.7519 75.19%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7316 73.16%
Micronuclear - 0.5582 55.82%
Hepatotoxicity - 0.6375 63.75%
skin sensitisation - 0.5396 53.96%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.7089 70.89%
Acute Oral Toxicity (c) III 0.5916 59.16%
Estrogen receptor binding - 0.5140 51.40%
Androgen receptor binding - 0.7571 75.71%
Thyroid receptor binding - 0.6998 69.98%
Glucocorticoid receptor binding + 0.5816 58.16%
Aromatase binding - 0.5234 52.34%
PPAR gamma + 0.5518 55.18%
Honey bee toxicity - 0.9507 95.07%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9451 94.51%

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 93.37% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.85% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.67% 99.17%
CHEMBL4208 P20618 Proteasome component C5 89.23% 90.00%
CHEMBL3401 O75469 Pregnane X receptor 87.96% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.68% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.66% 99.15%
CHEMBL3492 P49721 Proteasome Macropain subunit 80.95% 90.24%

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 76143755
LOTUS LTS0207771
wikiData Q104167518