1,7-Bis(3,4-dihydroxyphenyl)hept-1-ene-3,5-dione

Details

Top
Internal ID be10cada-aeb4-4a4c-bced-0f44f1f08143
Taxonomy Phenylpropanoids and polyketides > Diarylheptanoids > Linear diarylheptanoids
IUPAC Name 1,7-bis(3,4-dihydroxyphenyl)hept-1-ene-3,5-dione
SMILES (Canonical) C1=CC(=C(C=C1CCC(=O)CC(=O)C=CC2=CC(=C(C=C2)O)O)O)O
SMILES (Isomeric) C1=CC(=C(C=C1CCC(=O)CC(=O)C=CC2=CC(=C(C=C2)O)O)O)O
InChI InChI=1S/C19H18O6/c20-14(5-1-12-3-7-16(22)18(24)9-12)11-15(21)6-2-13-4-8-17(23)19(25)10-13/h1,3-5,7-10,22-25H,2,6,11H2
InChI Key CURCUCRHDWZQLO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C19H18O6
Molecular Weight 342.30 g/mol
Exact Mass 342.11033829 g/mol
Topological Polar Surface Area (TPSA) 115.00 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.68
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 7

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 1,7-Bis(3,4-dihydroxyphenyl)hept-1-ene-3,5-dione

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8746 87.46%
Caco-2 - 0.8518 85.18%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.8719 87.19%
OATP2B1 inhibitior - 0.5715 57.15%
OATP1B1 inhibitior + 0.9509 95.09%
OATP1B3 inhibitior + 0.9685 96.85%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.8058 80.58%
P-glycoprotein inhibitior - 0.6764 67.64%
P-glycoprotein substrate - 0.8687 86.87%
CYP3A4 substrate - 0.5752 57.52%
CYP2C9 substrate + 0.5841 58.41%
CYP2D6 substrate - 0.7984 79.84%
CYP3A4 inhibition + 0.5209 52.09%
CYP2C9 inhibition + 0.6439 64.39%
CYP2C19 inhibition - 0.6231 62.31%
CYP2D6 inhibition - 0.8300 83.00%
CYP1A2 inhibition + 0.7352 73.52%
CYP2C8 inhibition + 0.5962 59.62%
CYP inhibitory promiscuity - 0.7527 75.27%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7676 76.76%
Carcinogenicity (trinary) Non-required 0.6213 62.13%
Eye corrosion - 0.9857 98.57%
Eye irritation + 0.6309 63.09%
Skin irritation - 0.6607 66.07%
Skin corrosion - 0.8855 88.55%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4716 47.16%
Micronuclear - 0.5382 53.82%
Hepatotoxicity - 0.7375 73.75%
skin sensitisation - 0.5485 54.85%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.8202 82.02%
Acute Oral Toxicity (c) III 0.7583 75.83%
Estrogen receptor binding + 0.8692 86.92%
Androgen receptor binding + 0.7957 79.57%
Thyroid receptor binding + 0.6162 61.62%
Glucocorticoid receptor binding + 0.7331 73.31%
Aromatase binding + 0.6632 66.32%
PPAR gamma + 0.8328 83.28%
Honey bee toxicity - 0.8467 84.67%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9904 99.04%

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 99.14% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 95.25% 91.49%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.38% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.45% 94.45%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 88.03% 96.00%
CHEMBL3194 P02766 Transthyretin 87.34% 90.71%
CHEMBL2581 P07339 Cathepsin D 86.96% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.12% 86.33%
CHEMBL4208 P20618 Proteasome component C5 85.88% 90.00%
CHEMBL5261 Q7L7X3 Serine/threonine-protein kinase TAO1 85.80% 89.33%
CHEMBL3492 P49721 Proteasome Macropain subunit 85.27% 90.24%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.78% 90.71%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.64% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.63% 95.56%
CHEMBL2535 P11166 Glucose transporter 82.98% 98.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.38% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 82.04% 94.73%
CHEMBL3437 Q16853 Amine oxidase, copper containing 81.44% 94.00%

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.
Alpinia roxburghii

Cross-Links

Top
PubChem 123535663
LOTUS LTS0163560
wikiData Q104970432