(2E,8E,10E)-16-hydroxyhexadeca-2,8,10-trien-4,6-diynal

Details

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Internal ID e3815d7f-5fa9-4cbb-88d1-403e50921146
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name (2E,8E,10E)-16-hydroxyhexadeca-2,8,10-trien-4,6-diynal
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H18O2/c17-15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-16-18/h1-3,5,12,14,16-17H,7,9,11,13,15H2/b2-1+,5-3+,14-12+
InChI Key RBBXQZDMGRGAFJ-ZRTWCMPSSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C16H18O2
Molecular Weight 242.31 g/mol
Exact Mass 242.130679813 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.41
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2E,8E,10E)-16-hydroxyhexadeca-2,8,10-trien-4,6-diynal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9860 98.60%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.8000 80.00%
Subcellular localzation Mitochondria 0.6461 64.61%
OATP2B1 inhibitior - 0.8608 86.08%
OATP1B1 inhibitior + 0.8623 86.23%
OATP1B3 inhibitior + 0.9212 92.12%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.8558 85.58%
P-glycoprotein inhibitior - 0.9272 92.72%
P-glycoprotein substrate - 0.9059 90.59%
CYP3A4 substrate - 0.5375 53.75%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8288 82.88%
CYP3A4 inhibition - 0.8959 89.59%
CYP2C9 inhibition - 0.7538 75.38%
CYP2C19 inhibition - 0.9173 91.73%
CYP2D6 inhibition - 0.9490 94.90%
CYP1A2 inhibition - 0.5409 54.09%
CYP2C8 inhibition - 0.8729 87.29%
CYP inhibitory promiscuity - 0.8891 88.91%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Non-required 0.6926 69.26%
Eye corrosion + 0.8982 89.82%
Eye irritation - 0.5314 53.14%
Skin irritation + 0.6280 62.80%
Skin corrosion - 0.7697 76.97%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4871 48.71%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.6122 61.22%
skin sensitisation + 0.6847 68.47%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.9333 93.33%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.6934 69.34%
Acute Oral Toxicity (c) III 0.4839 48.39%
Estrogen receptor binding + 0.5735 57.35%
Androgen receptor binding + 0.5405 54.05%
Thyroid receptor binding + 0.5747 57.47%
Glucocorticoid receptor binding - 0.5188 51.88%
Aromatase binding + 0.5573 55.73%
PPAR gamma + 0.5789 57.89%
Honey bee toxicity - 0.8825 88.25%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.5650 56.50%
Fish aquatic toxicity - 0.5795 57.95%

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 90.18% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.01% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.00% 97.29%
CHEMBL2885 P07451 Carbonic anhydrase III 80.65% 87.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.43% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.20% 95.56%

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.
Dahlia merckii

Cross-Links

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PubChem 101630350
LOTUS LTS0230918
wikiData Q105233030