(3S,8E,10R)-pentadeca-1,8-dien-4,6-diyne-3,10-diol

Details

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Internal ID 63bd2e3f-9ef5-4b38-a063-81cfbbbd47c3
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name (3S,8E,10R)-pentadeca-1,8-dien-4,6-diyne-3,10-diol
SMILES (Canonical) CCCCCC(C=CC#CC#CC(C=C)O)O
SMILES (Isomeric) CCCCC[C@H](/C=C/C#CC#C[C@H](C=C)O)O
InChI InChI=1S/C15H20O2/c1-3-5-8-12-15(17)13-10-7-6-9-11-14(16)4-2/h4,10,13-17H,2-3,5,8,12H2,1H3/b13-10+/t14-,15+/m0/s1
InChI Key DXXGLHOAKNZRRB-XEZFYOOLSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H20O2
Molecular Weight 232.32 g/mol
Exact Mass 232.146329876 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.04
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3S,8E,10R)-pentadeca-1,8-dien-4,6-diyne-3,10-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9831 98.31%
Caco-2 - 0.5667 56.67%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.4116 41.16%
OATP2B1 inhibitior - 0.8549 85.49%
OATP1B1 inhibitior + 0.8858 88.58%
OATP1B3 inhibitior + 0.8897 88.97%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9283 92.83%
P-glycoprotein inhibitior - 0.9505 95.05%
P-glycoprotein substrate - 0.7657 76.57%
CYP3A4 substrate - 0.5239 52.39%
CYP2C9 substrate - 0.7982 79.82%
CYP2D6 substrate - 0.7649 76.49%
CYP3A4 inhibition - 0.6454 64.54%
CYP2C9 inhibition - 0.8295 82.95%
CYP2C19 inhibition - 0.7710 77.10%
CYP2D6 inhibition - 0.9044 90.44%
CYP1A2 inhibition + 0.7554 75.54%
CYP2C8 inhibition - 0.8215 82.15%
CYP inhibitory promiscuity - 0.5778 57.78%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6100 61.00%
Carcinogenicity (trinary) Non-required 0.6178 61.78%
Eye corrosion + 0.4731 47.31%
Eye irritation - 0.9075 90.75%
Skin irritation + 0.6062 60.62%
Skin corrosion - 0.5327 53.27%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5261 52.61%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.5438 54.38%
skin sensitisation + 0.8801 88.01%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity - 0.9730 97.30%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity + 0.4934 49.34%
Acute Oral Toxicity (c) II 0.5564 55.64%
Estrogen receptor binding + 0.5353 53.53%
Androgen receptor binding - 0.8711 87.11%
Thyroid receptor binding + 0.6450 64.50%
Glucocorticoid receptor binding + 0.7499 74.99%
Aromatase binding + 0.5291 52.91%
PPAR gamma + 0.6116 61.16%
Honey bee toxicity - 0.8953 89.53%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5446 54.46%
Fish aquatic toxicity + 0.8951 89.51%

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 94.79% 98.95%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 93.42% 85.94%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 92.87% 92.86%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.41% 99.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 92.27% 97.29%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.74% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.63% 97.25%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 88.98% 92.08%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 88.82% 91.81%
CHEMBL2885 P07451 Carbonic anhydrase III 86.00% 87.45%
CHEMBL1907 P15144 Aminopeptidase N 85.42% 93.31%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 83.93% 96.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.79% 93.56%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 82.89% 100.00%
CHEMBL230 P35354 Cyclooxygenase-2 82.38% 89.63%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.94% 100.00%
CHEMBL256 P0DMS8 Adenosine A3 receptor 81.48% 95.93%
CHEMBL221 P23219 Cyclooxygenase-1 80.36% 90.17%
CHEMBL3401 O75469 Pregnane X receptor 80.18% 94.73%

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.
Centella asiatica

Cross-Links

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PubChem 162945435
LOTUS LTS0183330
wikiData Q104991249