(E,5S)-1,7-bis(4-hydroxyphenyl)-5-methoxyhept-1-en-3-one

Details

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Internal ID eea8a3fb-15bf-4750-a860-a06835a9e3f3
Taxonomy Phenylpropanoids and polyketides > Diarylheptanoids > Linear diarylheptanoids > Curcuminoids
IUPAC Name (E,5S)-1,7-bis(4-hydroxyphenyl)-5-methoxyhept-1-en-3-one
SMILES (Canonical) COC(CCC1=CC=C(C=C1)O)CC(=O)C=CC2=CC=C(C=C2)O
SMILES (Isomeric) CO[C@@H](CCC1=CC=C(C=C1)O)CC(=O)/C=C/C2=CC=C(C=C2)O
InChI InChI=1S/C20H22O4/c1-24-20(13-7-16-4-10-18(22)11-5-16)14-19(23)12-6-15-2-8-17(21)9-3-15/h2-6,8-12,20-22H,7,13-14H2,1H3/b12-6+/t20-/m0/s1
InChI Key ZTJBEIASUZSOPG-YLZBSDIZSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C20H22O4
Molecular Weight 326.40 g/mol
Exact Mass 326.15180918 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.72
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (E,5S)-1,7-bis(4-hydroxyphenyl)-5-methoxyhept-1-en-3-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9925 99.25%
Caco-2 - 0.5434 54.34%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.8168 81.68%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9102 91.02%
OATP1B3 inhibitior + 0.9315 93.15%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.7261 72.61%
P-glycoprotein inhibitior - 0.6034 60.34%
P-glycoprotein substrate - 0.6598 65.98%
CYP3A4 substrate + 0.5148 51.48%
CYP2C9 substrate - 0.6148 61.48%
CYP2D6 substrate - 0.7857 78.57%
CYP3A4 inhibition + 0.6516 65.16%
CYP2C9 inhibition - 0.5956 59.56%
CYP2C19 inhibition + 0.7695 76.95%
CYP2D6 inhibition - 0.8354 83.54%
CYP1A2 inhibition + 0.7601 76.01%
CYP2C8 inhibition + 0.5118 51.18%
CYP inhibitory promiscuity + 0.6670 66.70%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7236 72.36%
Carcinogenicity (trinary) Non-required 0.6070 60.70%
Eye corrosion - 0.9832 98.32%
Eye irritation - 0.6726 67.26%
Skin irritation - 0.7456 74.56%
Skin corrosion - 0.9686 96.86%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7839 78.39%
Micronuclear - 0.7800 78.00%
Hepatotoxicity - 0.7250 72.50%
skin sensitisation - 0.8909 89.09%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity - 0.6249 62.49%
Acute Oral Toxicity (c) III 0.5465 54.65%
Estrogen receptor binding + 0.9359 93.59%
Androgen receptor binding + 0.8548 85.48%
Thyroid receptor binding + 0.5778 57.78%
Glucocorticoid receptor binding + 0.6810 68.10%
Aromatase binding + 0.7348 73.48%
PPAR gamma + 0.5668 56.68%
Honey bee toxicity - 0.7317 73.17%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9769 97.69%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.08% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.61% 91.11%
CHEMBL2581 P07339 Cathepsin D 94.39% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.39% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.63% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.16% 94.45%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.29% 96.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 89.59% 95.50%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.35% 96.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.82% 95.56%
CHEMBL5939 Q9NZ08 Endoplasmic reticulum aminopeptidase 1 85.52% 100.00%
CHEMBL3401 O75469 Pregnane X receptor 83.39% 94.73%
CHEMBL3437 Q16853 Amine oxidase, copper containing 82.83% 94.00%
CHEMBL3194 P02766 Transthyretin 82.43% 90.71%
CHEMBL5852 Q96P65 Pyroglutamylated RFamide peptide receptor 81.37% 85.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.31% 95.89%

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.
Alpinia roxburghii

Cross-Links

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PubChem 11723901
NPASS NPC23402
ChEMBL CHEMBL502589
LOTUS LTS0194647
wikiData Q105278490