(E,Z)-1,3,5-Tridecatriene-7,9,11-triyne

Details

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Internal ID e56eea23-99fd-4709-bac5-f322e87479d4
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Enynes
IUPAC Name (3E,5Z)-trideca-1,3,5-trien-7,9,11-triyne
SMILES (Canonical) CC#CC#CC#CC=CC=CC=C
SMILES (Isomeric) CC#CC#CC#C/C=C\C=C\C=C
InChI InChI=1S/C13H10/c1-3-5-7-9-11-13-12-10-8-6-4-2/h3,5,7,9,11H,1H2,2H3/b7-5+,11-9-
InChI Key AJWRNFIZKHPOHC-STRRHFTISA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H10
Molecular Weight 166.22 g/mol
Exact Mass 166.078250319 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.90
Atomic LogP (AlogP) 2.31
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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AJWRNFIZKHPOHC-STRRHFTISA-N
DTXSID001272460
1,3,5-Tridecatriene-7,9,11-triyne, (Z,E)-
126381-91-7

2D Structure

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2D Structure of (E,Z)-1,3,5-Tridecatriene-7,9,11-triyne

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 + 0.8276 82.76%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Lysosomes 0.5631 56.31%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9100 91.00%
OATP1B3 inhibitior + 0.9599 95.99%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9183 91.83%
P-glycoprotein inhibitior - 0.9637 96.37%
P-glycoprotein substrate - 0.9582 95.82%
CYP3A4 substrate - 0.5728 57.28%
CYP2C9 substrate - 0.5942 59.42%
CYP2D6 substrate - 0.8080 80.80%
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 - 0.9470 94.70%
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 + 0.9148 91.48%
Skin irritation + 0.8712 87.12%
Skin corrosion + 0.7907 79.07%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7782 77.82%
Micronuclear - 0.7900 79.00%
Hepatotoxicity + 0.7625 76.25%
skin sensitisation + 0.8377 83.77%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity + 0.8494 84.94%
Acute Oral Toxicity (c) III 0.4906 49.06%
Estrogen receptor binding - 0.8261 82.61%
Androgen receptor binding - 0.6484 64.84%
Thyroid receptor binding - 0.5834 58.34%
Glucocorticoid receptor binding - 0.7354 73.54%
Aromatase binding - 0.5732 57.32%
PPAR gamma - 0.5386 53.86%
Honey bee toxicity + 0.6294 62.94%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.5900 59.00%
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
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 88.13% 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.
Achillea millefolium
Artemisia vulgaris subsp. vulgaris
Carthamus tinctorius

Cross-Links

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PubChem 5352700
NPASS NPC218610
LOTUS LTS0082958
wikiData Q104913444