(3R,5S)-5-(methoxymethyl)-3-octadeca-9,11-diynyloxolan-2-one

Details

Top
Internal ID d08e2033-da0f-4bed-8b76-da30e8528792
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name (3R,5S)-5-(methoxymethyl)-3-octadeca-9,11-diynyloxolan-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H38O3/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/h22-23H,3-7,12-21H2,1-2H3/t22-,23+/m1/s1
InChI Key XLYZJZNKBWNURX-PKTZIBPZSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C24H38O3
Molecular Weight 374.60 g/mol
Exact Mass 374.28209507 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 7.80
Atomic LogP (AlogP) 5.66
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 14

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (3R,5S)-5-(methoxymethyl)-3-octadeca-9,11-diynyloxolan-2-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9875 98.75%
Caco-2 - 0.5369 53.69%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.6585 65.85%
OATP2B1 inhibitior - 0.8522 85.22%
OATP1B1 inhibitior + 0.9130 91.30%
OATP1B3 inhibitior + 0.9504 95.04%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.5970 59.70%
P-glycoprotein inhibitior - 0.5662 56.62%
P-glycoprotein substrate - 0.6300 63.00%
CYP3A4 substrate + 0.5716 57.16%
CYP2C9 substrate + 0.7980 79.80%
CYP2D6 substrate - 0.8613 86.13%
CYP3A4 inhibition - 0.6081 60.81%
CYP2C9 inhibition - 0.8736 87.36%
CYP2C19 inhibition - 0.7612 76.12%
CYP2D6 inhibition - 0.8974 89.74%
CYP1A2 inhibition - 0.6849 68.49%
CYP2C8 inhibition - 0.6874 68.74%
CYP inhibitory promiscuity - 0.8438 84.38%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.6850 68.50%
Eye corrosion - 0.9330 93.30%
Eye irritation - 0.4787 47.87%
Skin irritation - 0.7686 76.86%
Skin corrosion - 0.9545 95.45%
Ames mutagenesis - 0.8015 80.15%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.8800 88.00%
Hepatotoxicity + 0.6076 60.76%
skin sensitisation - 0.7571 75.71%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.7111 71.11%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity + 0.7922 79.22%
Acute Oral Toxicity (c) III 0.6646 66.46%
Estrogen receptor binding + 0.6309 63.09%
Androgen receptor binding + 0.6035 60.35%
Thyroid receptor binding + 0.5340 53.40%
Glucocorticoid receptor binding + 0.5393 53.93%
Aromatase binding - 0.5254 52.54%
PPAR gamma - 0.5574 55.74%
Honey bee toxicity - 0.8890 88.90%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.7253 72.53%
Fish aquatic toxicity + 0.8672 86.72%

Targets

Top

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
CHEMBL230 P35354 Cyclooxygenase-2 97.07% 89.63%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.26% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.40% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.78% 97.09%
CHEMBL2996 Q05655 Protein kinase C delta 90.61% 97.79%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.42% 91.11%
CHEMBL1871 P10275 Androgen Receptor 90.33% 96.43%
CHEMBL2581 P07339 Cathepsin D 90.32% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 88.52% 92.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.24% 99.17%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 86.83% 82.38%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.79% 97.25%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 85.43% 91.81%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 85.25% 100.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.18% 96.00%
CHEMBL1075162 Q13304 Uracil nucleotide/cysteinyl leukotriene receptor 85.13% 80.33%
CHEMBL5255 O00206 Toll-like receptor 4 84.59% 92.50%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 84.08% 94.80%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 81.47% 90.24%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.00% 99.23%

Plants that contains it

Top
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

Top
PubChem 54589745
LOTUS LTS0156355
wikiData Q105330568