(3S,8E,10E)-pentadeca-8,10,14-trien-4,6-diyn-3-ol

Details

Top
Internal ID 66b20c0e-63bd-4a58-a0a2-9065129af7c7
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name (3S,8E,10E)-pentadeca-8,10,14-trien-4,6-diyn-3-ol
SMILES (Canonical) CCC(C#CC#CC=CC=CCCC=C)O
SMILES (Isomeric) CC[C@@H](C#CC#C/C=C/C=C/CCC=C)O
InChI InChI=1S/C15H18O/c1-3-5-6-7-8-9-10-11-12-13-14-15(16)4-2/h3,7-10,15-16H,1,4-6H2,2H3/b8-7+,10-9+/t15-/m0/s1
InChI Key PPECZXSSUPUVQR-IMVYBZFCSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H18O
Molecular Weight 214.30 g/mol
Exact Mass 214.135765193 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.80
Atomic LogP (AlogP) 2.84
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (3S,8E,10E)-pentadeca-8,10,14-trien-4,6-diyn-3-ol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9877 98.77%
Caco-2 + 0.7285 72.85%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.3204 32.04%
OATP2B1 inhibitior - 0.8618 86.18%
OATP1B1 inhibitior + 0.8612 86.12%
OATP1B3 inhibitior + 0.9426 94.26%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.7780 77.80%
P-glycoprotein inhibitior - 0.9628 96.28%
P-glycoprotein substrate - 0.8367 83.67%
CYP3A4 substrate - 0.5424 54.24%
CYP2C9 substrate - 0.7982 79.82%
CYP2D6 substrate - 0.7649 76.49%
CYP3A4 inhibition - 0.8726 87.26%
CYP2C9 inhibition - 0.8660 86.60%
CYP2C19 inhibition - 0.7754 77.54%
CYP2D6 inhibition - 0.9514 95.14%
CYP1A2 inhibition - 0.5000 50.00%
CYP2C8 inhibition - 0.8683 86.83%
CYP inhibitory promiscuity - 0.7450 74.50%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.5200 52.00%
Carcinogenicity (trinary) Non-required 0.6303 63.03%
Eye corrosion + 0.6431 64.31%
Eye irritation - 0.8120 81.20%
Skin irritation + 0.7373 73.73%
Skin corrosion - 0.6168 61.68%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5253 52.53%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.5338 53.38%
skin sensitisation + 0.8116 81.16%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity + 0.5470 54.70%
Acute Oral Toxicity (c) II 0.5576 55.76%
Estrogen receptor binding - 0.5289 52.89%
Androgen receptor binding - 0.6257 62.57%
Thyroid receptor binding + 0.6754 67.54%
Glucocorticoid receptor binding - 0.4706 47.06%
Aromatase binding + 0.5865 58.65%
PPAR gamma + 0.7024 70.24%
Honey bee toxicity - 0.7855 78.55%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity - 0.7521 75.21%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.19% 96.09%
CHEMBL2581 P07339 Cathepsin D 84.69% 98.95%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 83.86% 97.34%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.58% 97.25%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.45% 96.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.84% 99.17%

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.
Cotula coronopifolia

Cross-Links

Top
PubChem 163013140
LOTUS LTS0264207
wikiData Q105212844