Dec-2-en-4,6-diyn-1-ol

Details

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Internal ID f21375b4-a3a8-4480-8cab-9c27d30c0c7c
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name dec-2-en-4,6-diyn-1-ol
SMILES (Canonical) CCCC#CC#CC=CCO
SMILES (Isomeric) CCCC#CC#CC=CCO
InChI InChI=1S/C10H12O/c1-2-3-4-5-6-7-8-9-10-11/h8-9,11H,2-3,10H2,1H3
InChI Key UVYOXYJPADNJRE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H12O
Molecular Weight 148.20 g/mol
Exact Mass 148.088815002 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.20
Atomic LogP (AlogP) 1.34
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Dec-2-en-4,6-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 + 0.9878 98.78%
Caco-2 + 0.6662 66.62%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Lysosomes 0.4340 43.40%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8742 87.42%
OATP1B3 inhibitior + 0.9391 93.91%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9178 91.78%
P-glycoprotein inhibitior - 0.9771 97.71%
P-glycoprotein substrate - 0.8946 89.46%
CYP3A4 substrate - 0.6125 61.25%
CYP2C9 substrate - 0.8016 80.16%
CYP2D6 substrate - 0.7877 78.77%
CYP3A4 inhibition - 0.9355 93.55%
CYP2C9 inhibition - 0.8810 88.10%
CYP2C19 inhibition - 0.8490 84.90%
CYP2D6 inhibition - 0.9491 94.91%
CYP1A2 inhibition - 0.5864 58.64%
CYP2C8 inhibition - 0.9375 93.75%
CYP inhibitory promiscuity - 0.7448 74.48%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.5400 54.00%
Carcinogenicity (trinary) Non-required 0.5282 52.82%
Eye corrosion + 0.9195 91.95%
Eye irritation + 0.7400 74.00%
Skin irritation + 0.7472 74.72%
Skin corrosion - 0.8736 87.36%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5621 56.21%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.5198 51.98%
skin sensitisation + 0.7468 74.68%
Respiratory toxicity - 0.8889 88.89%
Reproductive toxicity - 0.8556 85.56%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity + 0.5975 59.75%
Acute Oral Toxicity (c) I 0.5163 51.63%
Estrogen receptor binding - 0.8825 88.25%
Androgen receptor binding - 0.7501 75.01%
Thyroid receptor binding - 0.6967 69.67%
Glucocorticoid receptor binding - 0.8128 81.28%
Aromatase binding - 0.7655 76.55%
PPAR gamma - 0.6337 63.37%
Honey bee toxicity - 0.9339 93.39%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.8348 83.48%
Fish aquatic toxicity - 0.5250 52.50%

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 90.29% 96.09%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 87.10% 92.86%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.22% 99.17%
CHEMBL2581 P07339 Cathepsin D 82.02% 98.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.65% 89.34%

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.
Plagiocheilus bogotensis

Cross-Links

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PubChem 185531
LOTUS LTS0260782
wikiData Q105280185