1,6,10-Dodecatriene

Details

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Internal ID 1ecf1693-d758-4496-a413-9a4474347a3d
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Olefins > Acyclic olefins > Alkatrienes
IUPAC Name (6E,10E)-dodeca-1,6,10-triene
SMILES (Canonical) CC=CCCC=CCCCC=C
SMILES (Isomeric) C/C=C/CC/C=C/CCCC=C
InChI InChI=1S/C12H20/c1-3-5-7-9-11-12-10-8-6-4-2/h3-4,6,11-12H,1,5,7-10H2,2H3/b6-4+,12-11+
InChI Key IASHBWQBTURGKJ-AISFQEEOSA-N
Popularity 11 references in papers

Physical and Chemical Properties

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Molecular Formula C12H20
Molecular Weight 164.29 g/mol
Exact Mass 164.156500638 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.40
Atomic LogP (AlogP) 4.26
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,6,10-Dodecatriene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9874 98.74%
Caco-2 + 0.8784 87.84%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Lysosomes 0.5400 54.00%
OATP2B1 inhibitior - 0.8604 86.04%
OATP1B1 inhibitior + 0.8065 80.65%
OATP1B3 inhibitior + 0.9386 93.86%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.7272 72.72%
P-glycoprotein inhibitior - 0.9784 97.84%
P-glycoprotein substrate - 0.9395 93.95%
CYP3A4 substrate - 0.6233 62.33%
CYP2C9 substrate - 0.8202 82.02%
CYP2D6 substrate - 0.7454 74.54%
CYP3A4 inhibition - 0.9835 98.35%
CYP2C9 inhibition - 0.9254 92.54%
CYP2C19 inhibition - 0.9205 92.05%
CYP2D6 inhibition - 0.9557 95.57%
CYP1A2 inhibition - 0.6388 63.88%
CYP2C8 inhibition - 0.9308 93.08%
CYP inhibitory promiscuity - 0.7707 77.07%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5500 55.00%
Carcinogenicity (trinary) Non-required 0.5241 52.41%
Eye corrosion + 0.9881 98.81%
Eye irritation + 0.9760 97.60%
Skin irritation + 0.8436 84.36%
Skin corrosion - 0.9607 96.07%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4574 45.74%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation + 0.9342 93.42%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity + 0.5377 53.77%
Acute Oral Toxicity (c) III 0.7056 70.56%
Estrogen receptor binding - 0.8354 83.54%
Androgen receptor binding - 0.9400 94.00%
Thyroid receptor binding - 0.7110 71.10%
Glucocorticoid receptor binding - 0.4700 47.00%
Aromatase binding - 0.8616 86.16%
PPAR gamma + 0.6211 62.11%
Honey bee toxicity - 0.8873 88.73%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9814 98.14%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 86.73% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.73% 91.11%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 82.53% 97.34%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.13% 96.09%
CHEMBL242 Q92731 Estrogen receptor beta 81.60% 98.35%

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.
Bupleurum chinense
Bupleurum falcatum
Bupleurum scorzonerifolium
Curcuma longa

Cross-Links

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PubChem 22508511
NPASS NPC283692