(3R,5S)-5-(methoxymethyl)-3-octadec-13-en-9,11-diynyloxolan-2-one

Details

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Internal ID 9e277aee-f694-4ecb-b105-297a1aef673d
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name (3R,5S)-5-(methoxymethyl)-3-octadec-13-en-9,11-diynyloxolan-2-one
SMILES (Canonical) CCCCC=CC#CC#CCCCCCCCCC1CC(OC1=O)COC
SMILES (Isomeric) CCCCC=CC#CC#CCCCCCCCC[C@@H]1C[C@H](OC1=O)COC
InChI InChI=1S/C24H36O3/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-22-20-23(21-26-2)27-24(22)25/h6-7,22-23H,3-5,12-21H2,1-2H3/t22-,23+/m1/s1
InChI Key LDAWMCULWDOTLF-PKTZIBPZSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C24H36O3
Molecular Weight 372.50 g/mol
Exact Mass 372.26644501 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 7.40
Atomic LogP (AlogP) 5.44
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 13

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3R,5S)-5-(methoxymethyl)-3-octadec-13-en-9,11-diynyloxolan-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9905 99.05%
Caco-2 - 0.6355 63.55%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.6103 61.03%
OATP2B1 inhibitior - 0.8552 85.52%
OATP1B1 inhibitior + 0.8564 85.64%
OATP1B3 inhibitior + 0.9474 94.74%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.4778 47.78%
P-glycoprotein inhibitior - 0.4906 49.06%
P-glycoprotein substrate - 0.5477 54.77%
CYP3A4 substrate + 0.6362 63.62%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8769 87.69%
CYP3A4 inhibition - 0.5659 56.59%
CYP2C9 inhibition - 0.9055 90.55%
CYP2C19 inhibition - 0.7552 75.52%
CYP2D6 inhibition - 0.8977 89.77%
CYP1A2 inhibition - 0.6596 65.96%
CYP2C8 inhibition - 0.5692 56.92%
CYP inhibitory promiscuity - 0.7612 76.12%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.6845 68.45%
Eye corrosion - 0.9455 94.55%
Eye irritation - 0.8039 80.39%
Skin irritation - 0.7028 70.28%
Skin corrosion - 0.9510 95.10%
Ames mutagenesis - 0.7274 72.74%
Human Ether-a-go-go-Related Gene inhibition + 0.6905 69.05%
Micronuclear - 0.8700 87.00%
Hepatotoxicity + 0.5338 53.38%
skin sensitisation - 0.6947 69.47%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.7111 71.11%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity + 0.7899 78.99%
Acute Oral Toxicity (c) III 0.6037 60.37%
Estrogen receptor binding + 0.6843 68.43%
Androgen receptor binding + 0.6321 63.21%
Thyroid receptor binding + 0.6701 67.01%
Glucocorticoid receptor binding + 0.5962 59.62%
Aromatase binding - 0.4893 48.93%
PPAR gamma - 0.5432 54.32%
Honey bee toxicity - 0.8260 82.60%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.6800 68.00%
Fish aquatic toxicity + 0.9410 94.10%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.00% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.07% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.06% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.20% 91.11%
CHEMBL2996 Q05655 Protein kinase C delta 90.08% 97.79%
CHEMBL1871 P10275 Androgen Receptor 89.47% 96.43%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.32% 96.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.10% 97.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 88.47% 92.08%
CHEMBL2581 P07339 Cathepsin D 87.76% 98.95%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 86.96% 95.58%
CHEMBL230 P35354 Cyclooxygenase-2 86.20% 89.63%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 85.83% 82.38%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 85.71% 96.38%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 83.77% 91.81%
CHEMBL5255 O00206 Toll-like receptor 4 82.50% 92.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.46% 86.33%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 82.14% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.86% 95.56%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 80.42% 94.80%

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.
Cananga brandisiana

Cross-Links

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PubChem 162986171
LOTUS LTS0036552
wikiData Q105150129