Mer-A2026A

Details

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Internal ID 5d458f91-2cd1-49bf-8e05-4cb0c43b515b
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 2-[(2E,5E,7E,11E)-10-hydroxy-3,7,9,11,13-pentamethyltetradeca-2,5,7,11-tetraenyl]-6-methoxy-3-methyl-1H-pyridin-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C26H39NO3/c1-17(2)14-20(5)26(29)21(6)15-19(4)11-9-10-18(3)12-13-23-22(7)24(28)16-25(27-23)30-8/h9,11-12,14-17,21,26,29H,10,13H2,1-8H3,(H,27,28)/b11-9+,18-12+,19-15+,20-14+
InChI Key CHFFBNSQZJTFMA-HPVRZXAJSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C26H39NO3
Molecular Weight 413.60 g/mol
Exact Mass 413.29299411 g/mol
Topological Polar Surface Area (TPSA) 58.60 Ų
XlogP 6.70
Atomic LogP (AlogP) 5.67
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 10

Synonyms

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2-[(2E,5E,7E,11E)-10-Hydroxy-3,7,9,11,13-pentamethyltetradeca-2,5,7,11-tetraenyl]-6-methoxy-3-methyl-1H-pyridin-4-one

2D Structure

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2D Structure of Mer-A2026A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9967 99.67%
Caco-2 + 0.5744 57.44%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.7496 74.96%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8547 85.47%
OATP1B3 inhibitior + 0.9424 94.24%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.9301 93.01%
P-glycoprotein inhibitior + 0.8585 85.85%
P-glycoprotein substrate - 0.6273 62.73%
CYP3A4 substrate + 0.6160 61.60%
CYP2C9 substrate - 0.6047 60.47%
CYP2D6 substrate - 0.8073 80.73%
CYP3A4 inhibition - 0.7078 70.78%
CYP2C9 inhibition - 0.7082 70.82%
CYP2C19 inhibition - 0.5448 54.48%
CYP2D6 inhibition - 0.8080 80.80%
CYP1A2 inhibition + 0.5775 57.75%
CYP2C8 inhibition - 0.5590 55.90%
CYP inhibitory promiscuity - 0.7174 71.74%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8411 84.11%
Carcinogenicity (trinary) Non-required 0.6362 63.62%
Eye corrosion - 0.9890 98.90%
Eye irritation - 0.9690 96.90%
Skin irritation - 0.7837 78.37%
Skin corrosion - 0.9451 94.51%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8505 85.05%
Micronuclear - 0.5300 53.00%
Hepatotoxicity - 0.5002 50.02%
skin sensitisation - 0.8135 81.35%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.8390 83.90%
Acute Oral Toxicity (c) III 0.6037 60.37%
Estrogen receptor binding + 0.7627 76.27%
Androgen receptor binding - 0.5242 52.42%
Thyroid receptor binding + 0.7093 70.93%
Glucocorticoid receptor binding + 0.6750 67.50%
Aromatase binding + 0.5240 52.40%
PPAR gamma + 0.6945 69.45%
Honey bee toxicity - 0.8286 82.86%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.8306 83.06%

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 98.57% 85.14%
CHEMBL2581 P07339 Cathepsin D 97.04% 98.95%
CHEMBL2535 P11166 Glucose transporter 96.45% 98.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.07% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 94.40% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.36% 91.11%
CHEMBL1937 Q92769 Histone deacetylase 2 94.30% 94.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.09% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.02% 96.09%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 88.48% 91.07%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.68% 99.17%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 87.44% 97.21%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.22% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.01% 96.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.37% 99.23%

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 10319574
LOTUS LTS0022779
wikiData Q104958733