2-Tetradeca-5,12-dien-8,10-diynyloctadeca-2,9,16-trien-12,14-diyn-1-ol

Details

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Internal ID 8e0b3746-2c83-44c4-8340-f913794caa19
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name 2-tetradeca-5,12-dien-8,10-diynyloctadeca-2,9,16-trien-12,14-diyn-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C32H40O/c1-3-5-7-9-11-13-15-17-18-20-22-24-26-28-30-32(31-33)29-27-25-23-21-19-16-14-12-10-8-6-4-2/h3-6,17-19,21,30,33H,15-16,20,22-29,31H2,1-2H3
InChI Key HTKRPTVZCGJJIF-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C32H40O
Molecular Weight 440.70 g/mol
Exact Mass 440.307915895 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 9.70
Atomic LogP (AlogP) 7.47
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 14

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Tetradeca-5,12-dien-8,10-diynyloctadeca-2,9,16-trien-12,14-diyn-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9786 97.86%
Caco-2 - 0.7724 77.24%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Lysosomes 0.4978 49.78%
OATP2B1 inhibitior - 0.8580 85.80%
OATP1B1 inhibitior + 0.7987 79.87%
OATP1B3 inhibitior + 0.9571 95.71%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.8315 83.15%
P-glycoprotein inhibitior + 0.6760 67.60%
P-glycoprotein substrate - 0.7084 70.84%
CYP3A4 substrate + 0.5360 53.60%
CYP2C9 substrate - 0.8016 80.16%
CYP2D6 substrate - 0.7877 78.77%
CYP3A4 inhibition - 0.7839 78.39%
CYP2C9 inhibition - 0.7792 77.92%
CYP2C19 inhibition - 0.8380 83.80%
CYP2D6 inhibition - 0.9086 90.86%
CYP1A2 inhibition - 0.7283 72.83%
CYP2C8 inhibition - 0.6860 68.60%
CYP inhibitory promiscuity - 0.6614 66.14%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6500 65.00%
Carcinogenicity (trinary) Non-required 0.5867 58.67%
Eye corrosion + 0.6296 62.96%
Eye irritation - 0.8418 84.18%
Skin irritation - 0.6254 62.54%
Skin corrosion - 0.8809 88.09%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8000 80.00%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.6539 65.39%
skin sensitisation + 0.8153 81.53%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.9333 93.33%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity + 0.5080 50.80%
Acute Oral Toxicity (c) III 0.7734 77.34%
Estrogen receptor binding + 0.6718 67.18%
Androgen receptor binding - 0.6381 63.81%
Thyroid receptor binding + 0.5984 59.84%
Glucocorticoid receptor binding - 0.5609 56.09%
Aromatase binding - 0.5344 53.44%
PPAR gamma + 0.6695 66.95%
Honey bee toxicity - 0.8928 89.28%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5045 50.45%
Fish aquatic toxicity + 0.8101 81.01%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 94.87% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.79% 96.09%
CHEMBL2581 P07339 Cathepsin D 85.49% 98.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 81.88% 97.29%

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.
Centaurea macrocephala

Cross-Links

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PubChem 162975611
LOTUS LTS0017494
wikiData Q105033479