Feruloyl-caffeoyl spermidine

Details

Top
Internal ID f8bdb0b2-8420-44ad-9028-14686dea63fa
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Hydroxycinnamic acids and derivatives
IUPAC Name (E)-N-[4-(3-aminopropylamino)butyl]-3-(3,4-dihydroxyphenyl)-N-[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]prop-2-enamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C26H33N3O6/c1-35-24-18-20(6-10-22(24)31)8-12-26(34)29(16-3-2-14-28-15-4-13-27)25(33)11-7-19-5-9-21(30)23(32)17-19/h5-12,17-18,28,30-32H,2-4,13-16,27H2,1H3/b11-7+,12-8+
InChI Key BIMCZPOHHQBDAS-MKICQXMISA-N
Popularity 3 references in papers

Physical and Chemical Properties

Top
Molecular Formula C26H33N3O6
Molecular Weight 483.60 g/mol
Exact Mass 483.23693578 g/mol
Topological Polar Surface Area (TPSA) 145.00 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.61
H-Bond Acceptor 8
H-Bond Donor 5
Rotatable Bonds 13

Synonyms

Top
SCHEMBL32691836

2D Structure

Top
2D Structure of Feruloyl-caffeoyl spermidine

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7049 70.49%
Caco-2 - 0.8763 87.63%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.6462 64.62%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9220 92.20%
OATP1B3 inhibitior + 0.9420 94.20%
MATE1 inhibitior - 0.7000 70.00%
OCT2 inhibitior - 0.8838 88.38%
BSEP inhibitior + 0.9693 96.93%
P-glycoprotein inhibitior + 0.8531 85.31%
P-glycoprotein substrate + 0.6661 66.61%
CYP3A4 substrate + 0.5754 57.54%
CYP2C9 substrate - 0.8048 80.48%
CYP2D6 substrate - 0.7491 74.91%
CYP3A4 inhibition + 0.5714 57.14%
CYP2C9 inhibition - 0.8327 83.27%
CYP2C19 inhibition - 0.8580 85.80%
CYP2D6 inhibition - 0.6991 69.91%
CYP1A2 inhibition - 0.8705 87.05%
CYP2C8 inhibition + 0.5957 59.57%
CYP inhibitory promiscuity - 0.9677 96.77%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8043 80.43%
Carcinogenicity (trinary) Non-required 0.6787 67.87%
Eye corrosion - 0.9887 98.87%
Eye irritation - 0.9325 93.25%
Skin irritation - 0.7434 74.34%
Skin corrosion - 0.9280 92.80%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7178 71.78%
Micronuclear + 0.7600 76.00%
Hepatotoxicity - 0.8125 81.25%
skin sensitisation - 0.8815 88.15%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity - 0.9434 94.34%
Acute Oral Toxicity (c) III 0.6860 68.60%
Estrogen receptor binding + 0.7427 74.27%
Androgen receptor binding + 0.8864 88.64%
Thyroid receptor binding + 0.6441 64.41%
Glucocorticoid receptor binding + 0.7631 76.31%
Aromatase binding + 0.6541 65.41%
PPAR gamma + 0.7615 76.15%
Honey bee toxicity - 0.9139 91.39%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.8537 85.37%

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 99.55% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.52% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 96.81% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 96.41% 99.17%
CHEMBL3492 P49721 Proteasome Macropain subunit 95.74% 90.24%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.32% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.04% 86.33%
CHEMBL1255126 O15151 Protein Mdm4 91.75% 90.20%
CHEMBL3194 P02766 Transthyretin 88.06% 90.71%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 85.96% 89.62%
CHEMBL2581 P07339 Cathepsin D 85.49% 98.95%
CHEMBL4208 P20618 Proteasome component C5 85.12% 90.00%
CHEMBL3401 O75469 Pregnane X receptor 85.06% 94.73%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.54% 90.71%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 83.61% 98.11%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.36% 95.50%
CHEMBL4581 P52732 Kinesin-like protein 1 82.13% 93.18%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.07% 94.45%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 80.55% 80.78%

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.
Corylus avellana

Cross-Links

Top
PubChem 129821576
LOTUS LTS0098738
wikiData Q104936619