3,5,7-Tridecatriene-9,11-diyne-1-ol

Details

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Internal ID f1a15e11-389c-4bfa-afe6-42acdca22b11
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name (3E,5E,7E)-trideca-3,5,7-trien-9,11-diyn-1-ol
SMILES (Canonical) CC#CC#CC=CC=CC=CCCO
SMILES (Isomeric) CC#CC#C/C=C/C=C/C=C/CCO
InChI InChI=1S/C13H14O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14/h6-11,14H,12-13H2,1H3/b7-6+,9-8+,11-10+
InChI Key CNMWTIVSNRLOLQ-OBWVEWQSSA-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 3.00
Atomic LogP (AlogP) 2.06
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,5,7-Tridecatriene-9,11-diyne-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 + 0.9853 98.53%
Caco-2 + 0.8609 86.09%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Lysosomes 0.5519 55.19%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8733 87.33%
OATP1B3 inhibitior + 0.9481 94.81%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8995 89.95%
P-glycoprotein inhibitior - 0.9703 97.03%
P-glycoprotein substrate - 0.9244 92.44%
CYP3A4 substrate - 0.5761 57.61%
CYP2C9 substrate - 0.8016 80.16%
CYP2D6 substrate - 0.7877 78.77%
CYP3A4 inhibition - 0.8734 87.34%
CYP2C9 inhibition - 0.9068 90.68%
CYP2C19 inhibition - 0.8984 89.84%
CYP2D6 inhibition - 0.9644 96.44%
CYP1A2 inhibition - 0.6419 64.19%
CYP2C8 inhibition - 0.9501 95.01%
CYP inhibitory promiscuity - 0.8422 84.22%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.5900 59.00%
Carcinogenicity (trinary) Non-required 0.6266 62.66%
Eye corrosion + 0.9457 94.57%
Eye irritation + 0.7418 74.18%
Skin irritation + 0.8771 87.71%
Skin corrosion + 0.6177 61.77%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5851 58.51%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.5483 54.83%
skin sensitisation + 0.5765 57.65%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.9222 92.22%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.7735 77.35%
Acute Oral Toxicity (c) III 0.4503 45.03%
Estrogen receptor binding - 0.7090 70.90%
Androgen receptor binding - 0.5683 56.83%
Thyroid receptor binding - 0.6226 62.26%
Glucocorticoid receptor binding - 0.5239 52.39%
Aromatase binding + 0.5296 52.96%
PPAR gamma - 0.5722 57.22%
Honey bee toxicity - 0.9076 90.76%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity - 0.9319 93.19%

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 85.68% 96.09%
CHEMBL226 P30542 Adenosine A1 receptor 85.38% 95.93%
CHEMBL2885 P07451 Carbonic anhydrase III 80.80% 87.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.61% 99.17%

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.
Ajuga reptans
Girgensohnia diptera
Smallanthus glabratus

Cross-Links

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PubChem 12302847
NPASS NPC264413