15-Oxoicosyl 14-oxoheptadecanoate

Details

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Internal ID 18937d90-7421-4527-a27e-8530f2407c01
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters > Wax esters > Wax monoesters
IUPAC Name 15-oxoicosyl 14-oxoheptadecanoate
SMILES (Canonical) CCCCCC(=O)CCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCC(=O)CCC
SMILES (Isomeric) CCCCCC(=O)CCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCC(=O)CCC
InChI InChI=1S/C37H70O4/c1-3-5-24-30-36(39)32-26-21-17-12-8-6-7-11-15-19-23-28-34-41-37(40)33-27-22-18-14-10-9-13-16-20-25-31-35(38)29-4-2/h3-34H2,1-2H3
InChI Key YJHTUUPWFIQWNY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C37H70O4
Molecular Weight 578.90 g/mol
Exact Mass 578.52741071 g/mol
Topological Polar Surface Area (TPSA) 60.40 Ų
XlogP 13.10
Atomic LogP (AlogP) 11.80
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 34

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 15-Oxoicosyl 14-oxoheptadecanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9846 98.46%
Caco-2 - 0.6975 69.75%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.8780 87.80%
OATP2B1 inhibitior - 0.8529 85.29%
OATP1B1 inhibitior + 0.9229 92.29%
OATP1B3 inhibitior + 0.9593 95.93%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.8028 80.28%
P-glycoprotein inhibitior + 0.6059 60.59%
P-glycoprotein substrate - 0.8914 89.14%
CYP3A4 substrate - 0.5361 53.61%
CYP2C9 substrate - 0.6285 62.85%
CYP2D6 substrate - 0.8613 86.13%
CYP3A4 inhibition - 0.8807 88.07%
CYP2C9 inhibition - 0.9019 90.19%
CYP2C19 inhibition - 0.9330 93.30%
CYP2D6 inhibition - 0.9076 90.76%
CYP1A2 inhibition - 0.7946 79.46%
CYP2C8 inhibition - 0.7654 76.54%
CYP inhibitory promiscuity - 0.8407 84.07%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6723 67.23%
Carcinogenicity (trinary) Non-required 0.6938 69.38%
Eye corrosion + 0.6109 61.09%
Eye irritation + 0.7142 71.42%
Skin irritation - 0.8659 86.59%
Skin corrosion - 0.9920 99.20%
Ames mutagenesis - 0.9900 99.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4684 46.84%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5039 50.39%
skin sensitisation - 0.8869 88.69%
Respiratory toxicity - 0.9556 95.56%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.7678 76.78%
Estrogen receptor binding + 0.6386 63.86%
Androgen receptor binding - 0.8181 81.81%
Thyroid receptor binding - 0.5560 55.60%
Glucocorticoid receptor binding - 0.5164 51.64%
Aromatase binding - 0.6461 64.61%
PPAR gamma + 0.5910 59.10%
Honey bee toxicity - 0.9737 97.37%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity + 0.7818 78.18%
Fish aquatic toxicity + 0.9692 96.92%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 96.91% 99.17%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.37% 92.08%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 93.99% 97.29%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 93.83% 85.94%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.60% 96.09%
CHEMBL230 P35354 Cyclooxygenase-2 90.45% 89.63%
CHEMBL2581 P07339 Cathepsin D 88.95% 98.95%
CHEMBL202 P00374 Dihydrofolate reductase 88.06% 89.92%
CHEMBL299 P17252 Protein kinase C alpha 86.72% 98.03%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 85.89% 96.00%
CHEMBL2885 P07451 Carbonic anhydrase III 85.51% 87.45%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 84.84% 91.81%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.66% 91.11%
CHEMBL5255 O00206 Toll-like receptor 4 83.35% 92.50%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 82.62% 95.17%
CHEMBL2996 Q05655 Protein kinase C delta 82.39% 97.79%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 82.21% 94.33%

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.
Cryptocoryne spiralis

Cross-Links

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PubChem 86243284
LOTUS LTS0186843
wikiData Q105349265