(6E,8E)-hexadeca-1,6,8-trien-10,12,14-triyne

Details

Top
Internal ID 277bad82-ff7f-46d7-80da-b29ec3c2e991
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Enynes
IUPAC Name (6E,8E)-hexadeca-1,6,8-trien-10,12,14-triyne
SMILES (Canonical) CC#CC#CC#CC=CC=CCCCC=C
SMILES (Isomeric) CC#CC#CC#C/C=C/C=C/CCCC=C
InChI InChI=1S/C16H16/c1-3-5-7-9-11-13-15-16-14-12-10-8-6-4-2/h3,11,13,15-16H,1,5,7,9H2,2H3/b13-11+,16-15+
InChI Key DAXAIPLUUQVVDQ-FYNKLQMPSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C16H16
Molecular Weight 208.30 g/mol
Exact Mass 208.125200510 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.00
Atomic LogP (AlogP) 3.49
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (6E,8E)-hexadeca-1,6,8-trien-10,12,14-triyne

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9805 98.05%
Caco-2 + 0.8277 82.77%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Lysosomes 0.4323 43.23%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8378 83.78%
OATP1B3 inhibitior + 0.9513 95.13%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8944 89.44%
P-glycoprotein inhibitior - 0.9441 94.41%
P-glycoprotein substrate - 0.8503 85.03%
CYP3A4 substrate + 0.5156 51.56%
CYP2C9 substrate - 0.6093 60.93%
CYP2D6 substrate - 0.7826 78.26%
CYP3A4 inhibition - 0.9392 93.92%
CYP2C9 inhibition - 0.8746 87.46%
CYP2C19 inhibition - 0.8838 88.38%
CYP2D6 inhibition - 0.9611 96.11%
CYP1A2 inhibition - 0.6916 69.16%
CYP2C8 inhibition - 0.8324 83.24%
CYP inhibitory promiscuity - 0.6479 64.79%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5900 59.00%
Carcinogenicity (trinary) Warning 0.3906 39.06%
Eye corrosion + 0.9827 98.27%
Eye irritation - 0.5669 56.69%
Skin irritation + 0.8108 81.08%
Skin corrosion - 0.7687 76.87%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4814 48.14%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation + 0.8326 83.26%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity - 0.9111 91.11%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity + 0.7842 78.42%
Acute Oral Toxicity (c) III 0.7675 76.75%
Estrogen receptor binding - 0.7410 74.10%
Androgen receptor binding - 0.5976 59.76%
Thyroid receptor binding + 0.5344 53.44%
Glucocorticoid receptor binding - 0.6100 61.00%
Aromatase binding - 0.5247 52.47%
PPAR gamma - 0.5427 54.27%
Honey bee toxicity - 0.7838 78.38%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.7986 79.86%

Targets

Top

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
CHEMBL242 Q92731 Estrogen receptor beta 89.77% 98.35%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 84.54% 96.42%
CHEMBL1951 P21397 Monoamine oxidase A 83.89% 91.49%
CHEMBL206 P03372 Estrogen receptor alpha 83.40% 97.64%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.83% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.36% 99.17%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 82.00% 97.34%
CHEMBL2581 P07339 Cathepsin D 80.29% 98.95%

Plants that contains it

Top
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.
Euthamia graminifolia
Leucanthemum maximum
Leucanthemum vulgare
Leucanthemum vulgare subsp. vulgare

Cross-Links

Top
PubChem 13964097
LOTUS LTS0248549
wikiData Q104974077