(+)-Monocycloalternarene A

Details

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Internal ID 53a7e822-33c8-472e-b818-613522750788
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 2-[(2E,6E,10R)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dienyl]-4-methoxybenzene-1,3-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H34O5/c1-15(7-6-8-16(2)10-14-20(24)22(3,4)26)9-11-17-18(23)12-13-19(27-5)21(17)25/h8-9,12-13,20,23-26H,6-7,10-11,14H2,1-5H3/b15-9+,16-8+/t20-/m1/s1
InChI Key NSCCERMMAMCXJP-ZIJICOGKSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C22H34O5
Molecular Weight 378.50 g/mol
Exact Mass 378.24062418 g/mol
Topological Polar Surface Area (TPSA) 90.20 Ų
XlogP 4.50
Atomic LogP (AlogP) 4.23
H-Bond Acceptor 5
H-Bond Donor 4
Rotatable Bonds 10

Synonyms

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(+)-MONOCYCLOALTERNARENE A

2D Structure

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2D Structure of (+)-Monocycloalternarene A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9708 97.08%
Caco-2 + 0.4893 48.93%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7696 76.96%
OATP2B1 inhibitior - 0.8586 85.86%
OATP1B1 inhibitior + 0.8911 89.11%
OATP1B3 inhibitior + 0.9141 91.41%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.7867 78.67%
P-glycoprotein inhibitior - 0.6117 61.17%
P-glycoprotein substrate - 0.6928 69.28%
CYP3A4 substrate + 0.5633 56.33%
CYP2C9 substrate - 0.8086 80.86%
CYP2D6 substrate + 0.3479 34.79%
CYP3A4 inhibition - 0.6851 68.51%
CYP2C9 inhibition + 0.5425 54.25%
CYP2C19 inhibition + 0.6252 62.52%
CYP2D6 inhibition - 0.8869 88.69%
CYP1A2 inhibition + 0.5522 55.22%
CYP2C8 inhibition - 0.5624 56.24%
CYP inhibitory promiscuity - 0.8445 84.45%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8943 89.43%
Carcinogenicity (trinary) Non-required 0.6984 69.84%
Eye corrosion - 0.9875 98.75%
Eye irritation - 0.8639 86.39%
Skin irritation - 0.6513 65.13%
Skin corrosion - 0.9404 94.04%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8115 81.15%
Micronuclear - 0.8800 88.00%
Hepatotoxicity - 0.5676 56.76%
skin sensitisation - 0.6084 60.84%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.7764 77.64%
Acute Oral Toxicity (c) III 0.4887 48.87%
Estrogen receptor binding + 0.6446 64.46%
Androgen receptor binding + 0.5690 56.90%
Thyroid receptor binding + 0.7929 79.29%
Glucocorticoid receptor binding + 0.7592 75.92%
Aromatase binding + 0.6726 67.26%
PPAR gamma + 0.7826 78.26%
Honey bee toxicity - 0.8339 83.39%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9882 98.82%

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 97.84% 91.11%
CHEMBL2581 P07339 Cathepsin D 92.99% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.71% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.89% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 90.64% 94.73%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 86.46% 89.62%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 86.41% 92.68%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.88% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.91% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.84% 94.45%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 84.63% 97.21%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.38% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.31% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.22% 96.00%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 80.40% 98.11%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 80.30% 92.08%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 80.02% 96.90%

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 72704674
LOTUS LTS0107729
wikiData Q105184956