(E)-1,11-Tridecadiene-3,5,7,9-tetrayne

Details

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Internal ID 82ad9c95-a343-4c8b-9f1b-25782728dd93
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Enynes
IUPAC Name (11Z)-trideca-1,11-dien-3,5,7,9-tetrayne
SMILES (Canonical) CC=CC#CC#CC#CC#CC=C
SMILES (Isomeric) C/C=C\C#CC#CC#CC#CC=C
InChI InChI=1S/C13H8/c1-3-5-7-9-11-13-12-10-8-6-4-2/h3-4,6H,1H2,2H3/b6-4-
InChI Key KBEMPFYJJCTZIG-XQRVVYSFSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H8
Molecular Weight 164.20 g/mol
Exact Mass 164.062600255 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.70
Atomic LogP (AlogP) 1.76
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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(E)-1,11-Tridecadiene-3,5,7,9-tetrayne
(Z)-1,11-Tridecadiene-3,5,7,9-tetrayne
(11Z)-trideca-1,11-dien-3,5,7,9-tetrayne
KBEMPFYJJCTZIG-XQRVVYSFSA-N

2D Structure

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2D Structure of (E)-1,11-Tridecadiene-3,5,7,9-tetrayne

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9872 98.72%
Caco-2 + 0.5816 58.16%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Lysosomes 0.5631 56.31%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8554 85.54%
OATP1B3 inhibitior + 0.9599 95.99%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8766 87.66%
P-glycoprotein inhibitior - 0.9560 95.60%
P-glycoprotein substrate - 0.9660 96.60%
CYP3A4 substrate - 0.6471 64.71%
CYP2C9 substrate - 0.6027 60.27%
CYP2D6 substrate - 0.8194 81.94%
CYP3A4 inhibition - 0.9539 95.39%
CYP2C9 inhibition - 0.8695 86.95%
CYP2C19 inhibition - 0.9067 90.67%
CYP2D6 inhibition - 0.9671 96.71%
CYP1A2 inhibition - 0.7708 77.08%
CYP2C8 inhibition - 0.9479 94.79%
CYP inhibitory promiscuity - 0.7939 79.39%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.7483 74.83%
Carcinogenicity (trinary) Non-required 0.4259 42.59%
Eye corrosion + 0.9806 98.06%
Eye irritation + 0.7844 78.44%
Skin irritation + 0.8712 87.12%
Skin corrosion + 0.7907 79.07%
Ames mutagenesis - 0.5637 56.37%
Human Ether-a-go-go-Related Gene inhibition - 0.7485 74.85%
Micronuclear - 0.7900 79.00%
Hepatotoxicity + 0.6928 69.28%
skin sensitisation + 0.8377 83.77%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity + 0.7097 70.97%
Acute Oral Toxicity (c) III 0.4906 49.06%
Estrogen receptor binding - 0.8580 85.80%
Androgen receptor binding - 0.7707 77.07%
Thyroid receptor binding - 0.6325 63.25%
Glucocorticoid receptor binding - 0.7005 70.05%
Aromatase binding - 0.5208 52.08%
PPAR gamma - 0.6443 64.43%
Honey bee toxicity - 0.7033 70.33%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.8820 88.20%

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
CHEMBL1951 P21397 Monoamine oxidase A 82.39% 91.49%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 81.02% 96.42%

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.
Allium ampeloprasum
Bidens andicola
Carthamus tinctorius
Dahlia tubulata
Taxus baccata
Triticum aestivum

Cross-Links

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PubChem 5352703
NPASS NPC275823
LOTUS LTS0205597
wikiData Q76304609