(2S)-2-methyl-4-[(2R,10R,11R)-2,10,11-trihydroxy-14-[(2S,5R)-5-[(E,1S)-1-hydroxytetradec-9-enyl]oxolan-2-yl]tetradecyl]-2H-furan-5-one

Details

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Internal ID ff42e2e8-1008-4580-88a5-e9c0432bc169
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Annonaceous acetogenins
IUPAC Name (2S)-2-methyl-4-[(2R,10R,11R)-2,10,11-trihydroxy-14-[(2S,5R)-5-[(E,1S)-1-hydroxytetradec-9-enyl]oxolan-2-yl]tetradecyl]-2H-furan-5-one
SMILES (Canonical) CCCCC=CCCCCCCCC(C1CCC(O1)CCCC(C(CCCCCCCC(CC2=CC(OC2=O)C)O)O)O)O
SMILES (Isomeric) CCCC/C=C/CCCCCCC[C@@H]([C@H]1CC[C@@H](O1)CCC[C@H]([C@@H](CCCCCCC[C@H](CC2=C[C@@H](OC2=O)C)O)O)O)O
InChI InChI=1S/C37H66O7/c1-3-4-5-6-7-8-9-10-11-14-18-23-35(41)36-26-25-32(44-36)21-19-24-34(40)33(39)22-17-15-12-13-16-20-31(38)28-30-27-29(2)43-37(30)42/h6-7,27,29,31-36,38-41H,3-5,8-26,28H2,1-2H3/b7-6+/t29-,31+,32-,33+,34+,35-,36+/m0/s1
InChI Key LENXDXYFHDZCNH-UPZGFMGYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C37H66O7
Molecular Weight 622.90 g/mol
Exact Mass 622.48085444 g/mol
Topological Polar Surface Area (TPSA) 116.00 Ų
XlogP 8.80
Atomic LogP (AlogP) 7.62
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 27

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2S)-2-methyl-4-[(2R,10R,11R)-2,10,11-trihydroxy-14-[(2S,5R)-5-[(E,1S)-1-hydroxytetradec-9-enyl]oxolan-2-yl]tetradecyl]-2H-furan-5-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9439 94.39%
Caco-2 - 0.8246 82.46%
Blood Brain Barrier + 0.5605 56.05%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.7441 74.41%
OATP2B1 inhibitior - 0.5668 56.68%
OATP1B1 inhibitior + 0.8332 83.32%
OATP1B3 inhibitior + 0.9382 93.82%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.8755 87.55%
P-glycoprotein inhibitior + 0.6349 63.49%
P-glycoprotein substrate - 0.5227 52.27%
CYP3A4 substrate + 0.6488 64.88%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8672 86.72%
CYP3A4 inhibition - 0.6259 62.59%
CYP2C9 inhibition - 0.8552 85.52%
CYP2C19 inhibition - 0.6226 62.26%
CYP2D6 inhibition - 0.8935 89.35%
CYP1A2 inhibition - 0.7599 75.99%
CYP2C8 inhibition - 0.6176 61.76%
CYP inhibitory promiscuity - 0.9099 90.99%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6215 62.15%
Eye corrosion - 0.9876 98.76%
Eye irritation - 0.8930 89.30%
Skin irritation - 0.5565 55.65%
Skin corrosion - 0.9247 92.47%
Ames mutagenesis - 0.7583 75.83%
Human Ether-a-go-go-Related Gene inhibition - 0.4576 45.76%
Micronuclear - 0.9200 92.00%
Hepatotoxicity - 0.5823 58.23%
skin sensitisation - 0.8075 80.75%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.6572 65.72%
Acute Oral Toxicity (c) III 0.4523 45.23%
Estrogen receptor binding + 0.7353 73.53%
Androgen receptor binding + 0.5646 56.46%
Thyroid receptor binding - 0.6364 63.64%
Glucocorticoid receptor binding - 0.5665 56.65%
Aromatase binding + 0.5496 54.96%
PPAR gamma - 0.5000 50.00%
Honey bee toxicity - 0.9026 90.26%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.5162 51.62%
Fish aquatic toxicity + 0.9751 97.51%

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
CHEMBL2581 P07339 Cathepsin D 98.56% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.41% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.04% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.52% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 91.97% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.12% 95.56%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 89.46% 95.58%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.72% 97.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 87.25% 93.56%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 86.71% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.50% 97.25%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 84.87% 92.88%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.82% 97.29%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.57% 86.33%
CHEMBL4227 P25090 Lipoxin A4 receptor 83.62% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.24% 89.00%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 81.47% 96.47%
CHEMBL221 P23219 Cyclooxygenase-1 81.21% 90.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.72% 99.23%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.07% 90.71%

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.
Annona senegalensis

Cross-Links

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PubChem 162877125
LOTUS LTS0246085
wikiData Q105150672