(3E,5E)-1,3,5-Dodecatriene

Details

Top
Internal ID 5e9706e5-6e99-470f-bffc-2af704b891db
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Olefins > Acyclic olefins > Alkatrienes
IUPAC Name (3E,5E)-dodeca-1,3,5-triene
SMILES (Canonical) CCCCCCC=CC=CC=C
SMILES (Isomeric) CCCCCC/C=C/C=C/C=C
InChI InChI=1S/C12H20/c1-3-5-7-9-11-12-10-8-6-4-2/h3,5,7,9,11H,1,4,6,8,10,12H2,2H3/b7-5+,11-9+
InChI Key YTPLVOOAFADQJP-JEGFTUTRSA-N
Popularity 12 references in papers

Physical and Chemical Properties

Top
Molecular Formula C12H20
Molecular Weight 164.29 g/mol
Exact Mass 164.156500638 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.30
Atomic LogP (AlogP) 4.26
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

Top
(3E,5E)-1,3,5-Dodecatriene
(3E,5E)-dodeca-1,3,5-triene
YTPLVOOAFADQJP-JEGFTUTRSA-N
72084-21-0
(3E,5E)-1,3,5-Dodecatriene #

2D Structure

Top
2D Structure of (3E,5E)-1,3,5-Dodecatriene

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9906 99.06%
Caco-2 + 0.9822 98.22%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Lysosomes 0.4578 45.78%
OATP2B1 inhibitior - 0.8596 85.96%
OATP1B1 inhibitior + 0.8638 86.38%
OATP1B3 inhibitior + 0.9239 92.39%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8943 89.43%
P-glycoprotein inhibitior - 0.9770 97.70%
P-glycoprotein substrate - 0.9302 93.02%
CYP3A4 substrate - 0.6199 61.99%
CYP2C9 substrate - 0.8164 81.64%
CYP2D6 substrate - 0.7603 76.03%
CYP3A4 inhibition - 0.9832 98.32%
CYP2C9 inhibition - 0.9157 91.57%
CYP2C19 inhibition - 0.9190 91.90%
CYP2D6 inhibition - 0.9426 94.26%
CYP1A2 inhibition + 0.5418 54.18%
CYP2C8 inhibition - 0.8747 87.47%
CYP inhibitory promiscuity - 0.6838 68.38%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5800 58.00%
Carcinogenicity (trinary) Non-required 0.5494 54.94%
Eye corrosion + 0.9841 98.41%
Eye irritation + 0.9895 98.95%
Skin irritation + 0.8622 86.22%
Skin corrosion - 0.9742 97.42%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5204 52.04%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation + 0.9605 96.05%
Respiratory toxicity - 0.8889 88.89%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.6614 66.14%
Acute Oral Toxicity (c) III 0.6572 65.72%
Estrogen receptor binding - 0.7338 73.38%
Androgen receptor binding - 0.5747 57.47%
Thyroid receptor binding - 0.5764 57.64%
Glucocorticoid receptor binding - 0.6284 62.84%
Aromatase binding - 0.7856 78.56%
PPAR gamma + 0.5338 53.38%
Honey bee toxicity - 0.8937 89.37%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.9253 92.53%
Fish aquatic toxicity + 0.9955 99.55%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.93% 92.08%
CHEMBL230 P35354 Cyclooxygenase-2 94.09% 89.63%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 93.23% 92.86%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 92.65% 97.29%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.34% 99.17%
CHEMBL2581 P07339 Cathepsin D 89.88% 98.95%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 89.41% 91.81%
CHEMBL240 Q12809 HERG 89.14% 89.76%
CHEMBL2885 P07451 Carbonic anhydrase III 89.03% 87.45%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 88.16% 85.94%
CHEMBL1907 P15144 Aminopeptidase N 83.32% 93.31%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.59% 96.95%
CHEMBL221 P23219 Cyclooxygenase-1 81.63% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.87% 96.09%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.87% 100.00%

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.
Conioselinum anthriscoides
Ligusticum officinale

Cross-Links

Top
PubChem 5367416
NPASS NPC83184