Oploxyne A

Details

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Internal ID e082ffab-3b7b-4640-99bc-532436b13bea
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (1R,6S)-1-[(2R,3S)-3-heptyloxiran-2-yl]octa-2,4-diyne-1,6-diol
SMILES (Canonical) CCCCCCCC1C(O1)C(C#CC#CC(CC)O)O
SMILES (Isomeric) CCCCCCC[C@H]1[C@H](O1)[C@@H](C#CC#C[C@H](CC)O)O
InChI InChI=1S/C17H26O3/c1-3-5-6-7-8-13-16-17(20-16)15(19)12-10-9-11-14(18)4-2/h14-19H,3-8,13H2,1-2H3/t14-,15+,16-,17+/m0/s1
InChI Key SNQQXKPWASLFFZ-VVLHAWIVSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C17H26O3
Molecular Weight 278.40 g/mol
Exact Mass 278.18819469 g/mol
Topological Polar Surface Area (TPSA) 53.00 Ų
XlogP 3.50
Atomic LogP (AlogP) 2.25
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 8

Synonyms

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CHEMBL1098421

2D Structure

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2D Structure of Oploxyne A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9350 93.50%
Caco-2 + 0.5644 56.44%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.5277 52.77%
OATP2B1 inhibitior - 0.8524 85.24%
OATP1B1 inhibitior + 0.8857 88.57%
OATP1B3 inhibitior + 0.9462 94.62%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9290 92.90%
P-glycoprotein inhibitior - 0.9075 90.75%
P-glycoprotein substrate - 0.7684 76.84%
CYP3A4 substrate - 0.5362 53.62%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7408 74.08%
CYP3A4 inhibition + 0.5122 51.22%
CYP2C9 inhibition - 0.7128 71.28%
CYP2C19 inhibition - 0.5998 59.98%
CYP2D6 inhibition - 0.8956 89.56%
CYP1A2 inhibition - 0.6539 65.39%
CYP2C8 inhibition - 0.8264 82.64%
CYP inhibitory promiscuity - 0.8171 81.71%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.6521 65.21%
Eye corrosion - 0.9115 91.15%
Eye irritation - 0.7210 72.10%
Skin irritation - 0.5248 52.48%
Skin corrosion - 0.8764 87.64%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3720 37.20%
Micronuclear - 0.7400 74.00%
Hepatotoxicity - 0.5139 51.39%
skin sensitisation - 0.5555 55.55%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.6079 60.79%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity + 0.4859 48.59%
Acute Oral Toxicity (c) III 0.5015 50.15%
Estrogen receptor binding + 0.6644 66.44%
Androgen receptor binding - 0.5729 57.29%
Thyroid receptor binding + 0.7491 74.91%
Glucocorticoid receptor binding + 0.6204 62.04%
Aromatase binding - 0.5055 50.55%
PPAR gamma - 0.6481 64.81%
Honey bee toxicity - 0.9387 93.87%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.5882 58.82%
Fish aquatic toxicity + 0.7775 77.75%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.80% 96.09%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 95.36% 92.86%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.72% 97.25%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 93.15% 96.95%
CHEMBL2581 P07339 Cathepsin D 91.60% 98.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 91.48% 97.29%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 90.30% 90.24%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.53% 99.17%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 88.44% 95.58%
CHEMBL1914 P06276 Butyrylcholinesterase 88.19% 95.00%
CHEMBL2996 Q05655 Protein kinase C delta 88.08% 97.79%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 87.70% 97.21%
CHEMBL3401 O75469 Pregnane X receptor 87.26% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.48% 91.11%
CHEMBL218 P21554 Cannabinoid CB1 receptor 86.37% 96.61%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 85.43% 100.00%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 83.00% 92.08%
CHEMBL1075162 Q13304 Uracil nucleotide/cysteinyl leukotriene receptor 82.47% 80.33%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 82.06% 91.81%
CHEMBL256 P0DMS8 Adenosine A3 receptor 81.95% 95.93%
CHEMBL1907 P15144 Aminopeptidase N 81.78% 93.31%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 80.98% 85.94%
CHEMBL226 P30542 Adenosine A1 receptor 80.85% 95.93%

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.
Oplopanax elatus

Cross-Links

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PubChem 46832812
NPASS NPC8597
ChEMBL CHEMBL1098421