Meroindenon

Details

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Internal ID 0ef590de-f535-429f-b119-da2d08cd49f0
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (2S)-2-[(4E)-5,9-dimethyl-2-propan-2-ylidenedeca-4,8-dienyl]-4,6-dihydroxy-2-methylindene-1,3-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H32O4/c1-15(2)8-7-9-17(5)10-11-18(16(3)4)14-25(6)23(28)20-12-19(26)13-21(27)22(20)24(25)29/h8,10,12-13,26-27H,7,9,11,14H2,1-6H3/b17-10+/t25-/m0/s1
InChI Key MBRGORCSJIULPD-LWMHEAGWSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C25H32O4
Molecular Weight 396.50 g/mol
Exact Mass 396.23005950 g/mol
Topological Polar Surface Area (TPSA) 74.60 Ų
XlogP 7.60
Atomic LogP (AlogP) 6.29
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Meroindenon

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9933 99.33%
Caco-2 + 0.5092 50.92%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7936 79.36%
OATP2B1 inhibitior - 0.7161 71.61%
OATP1B1 inhibitior + 0.8314 83.14%
OATP1B3 inhibitior + 0.8899 88.99%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.7083 70.83%
P-glycoprotein inhibitior - 0.5414 54.14%
P-glycoprotein substrate - 0.7950 79.50%
CYP3A4 substrate + 0.5994 59.94%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8126 81.26%
CYP3A4 inhibition - 0.7479 74.79%
CYP2C9 inhibition + 0.5442 54.42%
CYP2C19 inhibition - 0.7197 71.97%
CYP2D6 inhibition - 0.9015 90.15%
CYP1A2 inhibition + 0.7293 72.93%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity - 0.5105 51.05%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.6802 68.02%
Eye corrosion - 0.9895 98.95%
Eye irritation - 0.7405 74.05%
Skin irritation - 0.5857 58.57%
Skin corrosion - 0.9488 94.88%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7080 70.80%
Micronuclear - 0.8100 81.00%
Hepatotoxicity - 0.6800 68.00%
skin sensitisation - 0.5961 59.61%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.7760 77.60%
Acute Oral Toxicity (c) III 0.4028 40.28%
Estrogen receptor binding + 0.7494 74.94%
Androgen receptor binding + 0.6908 69.08%
Thyroid receptor binding + 0.5964 59.64%
Glucocorticoid receptor binding + 0.7200 72.00%
Aromatase binding + 0.6575 65.75%
PPAR gamma + 0.8133 81.33%
Honey bee toxicity - 0.8392 83.92%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.13% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.24% 98.95%
CHEMBL4208 P20618 Proteasome component C5 93.09% 90.00%
CHEMBL1937 Q92769 Histone deacetylase 2 92.40% 94.75%
CHEMBL1929 P47989 Xanthine dehydrogenase 92.26% 96.12%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.53% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 89.80% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.49% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.38% 89.00%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 86.27% 92.08%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 84.95% 92.68%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 83.65% 93.10%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.50% 91.07%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.40% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.11% 94.45%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.01% 89.34%
CHEMBL3194 P02766 Transthyretin 81.35% 90.71%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.53% 90.71%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 80.12% 91.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.10% 99.23%

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.
There are no matching plants.

Cross-Links

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PubChem 146683230
LOTUS LTS0159578
wikiData Q105160929