1,11-Dodecadiene

Details

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Internal ID 3cf4abad-6579-488a-937d-049b2f3d58ef
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Olefins > Acyclic olefins > Alkadienes
IUPAC Name dodeca-1,11-diene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H22/c1-3-5-7-9-11-12-10-8-6-4-2/h3-4H,1-2,5-12H2
InChI Key IYPLTVKTLDQUGG-UHFFFAOYSA-N
Popularity 18 references in papers

Physical and Chemical Properties

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Molecular Formula C12H22
Molecular Weight 166.30 g/mol
Exact Mass 166.172150702 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 6.30
Atomic LogP (AlogP) 4.48
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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5876-87-9
Dodecadiene, 1,11-
DTXSID60207492
RefChem:71182
DTXCID60129983
IYPLTVKTLDQUGG-UHFFFAOYSA-N
dodeca-1,11-diene
MFCD00048156
SCHEMBL216225
SCHEMBL2036809
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1,11-Dodecadiene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9791 97.91%
Caco-2 + 0.8280 82.80%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Plasma membrane 0.3808 38.08%
OATP2B1 inhibitior - 0.8584 85.84%
OATP1B1 inhibitior + 0.9633 96.33%
OATP1B3 inhibitior + 0.9494 94.94%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8919 89.19%
P-glycoprotein inhibitior - 0.9759 97.59%
P-glycoprotein substrate - 0.9869 98.69%
CYP3A4 substrate - 0.7458 74.58%
CYP2C9 substrate - 0.8078 80.78%
CYP2D6 substrate - 0.6963 69.63%
CYP3A4 inhibition - 0.9753 97.53%
CYP2C9 inhibition - 0.8859 88.59%
CYP2C19 inhibition - 0.9008 90.08%
CYP2D6 inhibition - 0.9592 95.92%
CYP1A2 inhibition - 0.6904 69.04%
CYP2C8 inhibition - 0.9615 96.15%
CYP inhibitory promiscuity - 0.6610 66.10%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5400 54.00%
Carcinogenicity (trinary) Warning 0.4903 49.03%
Eye corrosion + 0.9925 99.25%
Eye irritation + 0.9844 98.44%
Skin irritation + 0.8242 82.42%
Skin corrosion - 0.9464 94.64%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6845 68.45%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation + 0.8535 85.35%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity - 0.9444 94.44%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.5921 59.21%
Acute Oral Toxicity (c) III 0.6047 60.47%
Estrogen receptor binding - 0.9406 94.06%
Androgen receptor binding - 0.9193 91.93%
Thyroid receptor binding - 0.7784 77.84%
Glucocorticoid receptor binding - 0.6909 69.09%
Aromatase binding - 0.7815 78.15%
PPAR gamma - 0.5091 50.91%
Honey bee toxicity - 0.7552 75.52%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.9419 94.19%

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
CHEMBL1829 O15379 Histone deacetylase 3 89.17% 95.00%
CHEMBL4070 P19784 Casein kinase II alpha (prime) 82.20% 91.67%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.08% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.54% 99.17%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 80.10% 92.95%

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.
Cephalotaxus fortunei

Cross-Links

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PubChem 22170
NPASS NPC151345