Piericidin E1

Details

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Internal ID 1ccf4be8-0ddd-494e-af78-5fb6817a3689
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 2-[[3-[(2E,4E,6R,7R,8E)-7-hydroxy-4,6,8-trimethyldeca-2,4,8-trienyl]-3-methyloxiran-2-yl]methyl]-6-methoxy-3-methyl-1H-pyridin-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H35NO4/c1-8-16(3)23(27)17(4)12-15(2)10-9-11-24(6)21(29-24)13-19-18(5)20(26)14-22(25-19)28-7/h8-10,12,14,17,21,23,27H,11,13H2,1-7H3,(H,25,26)/b10-9+,15-12+,16-8+/t17-,21?,23+,24?/m1/s1
InChI Key VQCXUYLCVXHMED-ORTKWPHJSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C24H35NO4
Molecular Weight 401.50 g/mol
Exact Mass 401.25660860 g/mol
Topological Polar Surface Area (TPSA) 71.10 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.25
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Piericidin E1

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9855 98.55%
Caco-2 + 0.4897 48.97%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.5928 59.28%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8441 84.41%
OATP1B3 inhibitior + 0.9361 93.61%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.8545 85.45%
P-glycoprotein inhibitior + 0.6834 68.34%
P-glycoprotein substrate + 0.5000 50.00%
CYP3A4 substrate + 0.6630 66.30%
CYP2C9 substrate - 0.7986 79.86%
CYP2D6 substrate - 0.8170 81.70%
CYP3A4 inhibition - 0.7776 77.76%
CYP2C9 inhibition - 0.8000 80.00%
CYP2C19 inhibition - 0.7093 70.93%
CYP2D6 inhibition - 0.8890 88.90%
CYP1A2 inhibition - 0.6222 62.22%
CYP2C8 inhibition + 0.4856 48.56%
CYP inhibitory promiscuity - 0.8406 84.06%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8711 87.11%
Carcinogenicity (trinary) Non-required 0.5823 58.23%
Eye corrosion - 0.9859 98.59%
Eye irritation - 0.9570 95.70%
Skin irritation - 0.7635 76.35%
Skin corrosion - 0.9368 93.68%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8173 81.73%
Micronuclear + 0.6500 65.00%
Hepatotoxicity + 0.5175 51.75%
skin sensitisation - 0.7969 79.69%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.7598 75.98%
Acute Oral Toxicity (c) III 0.4890 48.90%
Estrogen receptor binding + 0.6647 66.47%
Androgen receptor binding + 0.5951 59.51%
Thyroid receptor binding + 0.7702 77.02%
Glucocorticoid receptor binding + 0.6315 63.15%
Aromatase binding + 0.5182 51.82%
PPAR gamma + 0.8019 80.19%
Honey bee toxicity - 0.8005 80.05%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.7837 78.37%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 99.14% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.63% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.60% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.40% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.87% 96.09%
CHEMBL1937 Q92769 Histone deacetylase 2 95.69% 94.75%
CHEMBL3401 O75469 Pregnane X receptor 92.63% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.91% 95.56%
CHEMBL2535 P11166 Glucose transporter 91.34% 98.75%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 91.28% 91.07%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.73% 93.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.72% 86.33%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 87.60% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.08% 92.62%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.71% 89.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.12% 97.14%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.98% 96.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.95% 97.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.53% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.49% 99.23%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.57% 97.25%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.42% 94.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.97% 95.89%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 102223691
LOTUS LTS0274864
wikiData Q105291184