Trideca-2,8,10-trien-4,6-diyn-1-ol

Details

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Internal ID 9c9214c0-b2d3-4663-a25e-769283dff9a6
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name trideca-2,8,10-trien-4,6-diyn-1-ol
SMILES (Canonical) CCC=CC=CC#CC#CC=CCO
SMILES (Isomeric) CCC=CC=CC#CC#CC=CCO
InChI InChI=1S/C13H14O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14/h3-6,11-12,14H,2,13H2,1H3
InChI Key YCXSBVALLBAGMY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H14O
Molecular Weight 186.25 g/mol
Exact Mass 186.104465066 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.06
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Trideca-2,8,10-trien-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 + 0.9902 99.02%
Caco-2 - 0.5457 54.57%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Lysosomes 0.5089 50.89%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8813 88.13%
OATP1B3 inhibitior + 0.9512 95.12%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8248 82.48%
P-glycoprotein inhibitior - 0.9607 96.07%
P-glycoprotein substrate - 0.9156 91.56%
CYP3A4 substrate - 0.6176 61.76%
CYP2C9 substrate - 0.8016 80.16%
CYP2D6 substrate - 0.7877 78.77%
CYP3A4 inhibition - 0.9471 94.71%
CYP2C9 inhibition - 0.8616 86.16%
CYP2C19 inhibition - 0.8658 86.58%
CYP2D6 inhibition - 0.9628 96.28%
CYP1A2 inhibition - 0.5789 57.89%
CYP2C8 inhibition - 0.9147 91.47%
CYP inhibitory promiscuity - 0.7655 76.55%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) + 0.5700 57.00%
Carcinogenicity (trinary) Non-required 0.5454 54.54%
Eye corrosion + 0.9106 91.06%
Eye irritation + 0.5408 54.08%
Skin irritation + 0.7619 76.19%
Skin corrosion + 0.5256 52.56%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6231 62.31%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.5178 51.78%
skin sensitisation + 0.5749 57.49%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity - 0.7333 73.33%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.6098 60.98%
Acute Oral Toxicity (c) I 0.5247 52.47%
Estrogen receptor binding - 0.6011 60.11%
Androgen receptor binding - 0.6314 63.14%
Thyroid receptor binding - 0.5808 58.08%
Glucocorticoid receptor binding - 0.6684 66.84%
Aromatase binding + 0.5760 57.60%
PPAR gamma - 0.5360 53.60%
Honey bee toxicity - 0.9131 91.31%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.7900 79.00%
Fish aquatic toxicity - 0.6168 61.68%

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 88.77% 96.09%
CHEMBL226 P30542 Adenosine A1 receptor 84.68% 95.93%
CHEMBL1977 P11473 Vitamin D receptor 82.75% 99.43%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.43% 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.
Aethusa cynapium

Cross-Links

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PubChem 162860632
LOTUS LTS0010887
wikiData Q105346578