[(1R,3S,13S)-3,13-dihydroxy-1-[(2R,5R)-5-[(1S)-1-hydroxytridecyl]oxolan-2-yl]-15-[(2S)-2-methyl-5-oxo-2H-furan-4-yl]pentadecyl] acetate

Details

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Internal ID b6aedfc8-b076-40a9-8256-d732a2b3d23f
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Annonaceous acetogenins
IUPAC Name [(1R,3S,13S)-3,13-dihydroxy-1-[(2R,5R)-5-[(1S)-1-hydroxytridecyl]oxolan-2-yl]-15-[(2S)-2-methyl-5-oxo-2H-furan-4-yl]pentadecyl] acetate
SMILES (Canonical) CCCCCCCCCCCCC(C1CCC(O1)C(CC(CCCCCCCCCC(CCC2=CC(OC2=O)C)O)O)OC(=O)C)O
SMILES (Isomeric) CCCCCCCCCCCC[C@@H]([C@H]1CC[C@@H](O1)[C@@H](C[C@H](CCCCCCCCC[C@@H](CCC2=C[C@@H](OC2=O)C)O)O)OC(=O)C)O
InChI InChI=1S/C39H70O8/c1-4-5-6-7-8-9-10-14-17-20-23-35(43)36-26-27-37(47-36)38(46-31(3)40)29-34(42)22-19-16-13-11-12-15-18-21-33(41)25-24-32-28-30(2)45-39(32)44/h28,30,33-38,41-43H,4-27,29H2,1-3H3/t30-,33-,34-,35-,36+,37+,38+/m0/s1
InChI Key BIODFBOSASJNMO-ZPIQHZIQSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C39H70O8
Molecular Weight 667.00 g/mol
Exact Mass 666.50706919 g/mol
Topological Polar Surface Area (TPSA) 123.00 Ų
XlogP 10.40
Atomic LogP (AlogP) 8.41
H-Bond Acceptor 8
H-Bond Donor 3
Rotatable Bonds 29

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1R,3S,13S)-3,13-dihydroxy-1-[(2R,5R)-5-[(1S)-1-hydroxytridecyl]oxolan-2-yl]-15-[(2S)-2-methyl-5-oxo-2H-furan-4-yl]pentadecyl] acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9557 95.57%
Caco-2 - 0.8255 82.55%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.8000 80.00%
Subcellular localzation Mitochondria 0.7347 73.47%
OATP2B1 inhibitior - 0.5649 56.49%
OATP1B1 inhibitior + 0.8607 86.07%
OATP1B3 inhibitior + 0.9084 90.84%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.8191 81.91%
P-glycoprotein inhibitior + 0.6964 69.64%
P-glycoprotein substrate + 0.5733 57.33%
CYP3A4 substrate + 0.6708 67.08%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8975 89.75%
CYP3A4 inhibition + 0.6768 67.68%
CYP2C9 inhibition - 0.7914 79.14%
CYP2C19 inhibition - 0.5000 50.00%
CYP2D6 inhibition - 0.9080 90.80%
CYP1A2 inhibition - 0.7474 74.74%
CYP2C8 inhibition - 0.5721 57.21%
CYP inhibitory promiscuity - 0.8825 88.25%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5960 59.60%
Eye corrosion - 0.9871 98.71%
Eye irritation - 0.8753 87.53%
Skin irritation - 0.5228 52.28%
Skin corrosion - 0.9396 93.96%
Ames mutagenesis - 0.6737 67.37%
Human Ether-a-go-go-Related Gene inhibition - 0.5198 51.98%
Micronuclear - 0.8500 85.00%
Hepatotoxicity - 0.5949 59.49%
skin sensitisation - 0.9049 90.49%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity + 0.7966 79.66%
Acute Oral Toxicity (c) II 0.3842 38.42%
Estrogen receptor binding + 0.7794 77.94%
Androgen receptor binding - 0.5052 50.52%
Thyroid receptor binding - 0.6402 64.02%
Glucocorticoid receptor binding + 0.6013 60.13%
Aromatase binding + 0.6052 60.52%
PPAR gamma + 0.5537 55.37%
Honey bee toxicity - 0.8743 87.43%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.6397 63.97%
Fish aquatic toxicity + 0.9800 98.00%

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
CHEMBL2581 P07339 Cathepsin D 98.84% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.06% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.28% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.41% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.80% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.77% 86.33%
CHEMBL3359 P21462 Formyl peptide receptor 1 89.98% 93.56%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 89.52% 100.00%
CHEMBL3401 O75469 Pregnane X receptor 88.39% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.84% 95.56%
CHEMBL240 Q12809 HERG 87.26% 89.76%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.36% 97.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.10% 96.95%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.39% 90.71%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 82.88% 94.80%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 82.31% 92.86%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.52% 99.23%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.38% 100.00%
CHEMBL5255 O00206 Toll-like receptor 4 81.23% 92.50%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.17% 95.89%

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.
Dasymaschalon sootepense

Cross-Links

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PubChem 10699606
LOTUS LTS0015015
wikiData Q104667984