1,19-Eicosadiene

Details

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Internal ID 2fbc8df3-1826-4e02-8888-6e2631ac9dae
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Olefins > Acyclic olefins > Alkadienes
IUPAC Name icosa-1,19-diene
SMILES (Canonical) C=CCCCCCCCCCCCCCCCCC=C
SMILES (Isomeric) C=CCCCCCCCCCCCCCCCCC=C
InChI InChI=1S/C20H38/c1-3-5-7-9-11-13-15-17-19-20-18-16-14-12-10-8-6-4-2/h3-4H,1-2,5-20H2
InChI Key AWJFCAXSGQLCKK-UHFFFAOYSA-N
Popularity 11 references in papers

Physical and Chemical Properties

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Molecular Formula C20H38
Molecular Weight 278.50 g/mol
Exact Mass 278.297351212 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 10.00
Atomic LogP (AlogP) 7.60
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 17

Synonyms

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14811-95-1
icosa-1,19-diene
1,19-Icosadiene
1 19-EICOSADIENE
8MZ9N8W9QS
1,19-Icosadiene #
UNII-8MZ9N8W9QS
DTXSID70333872
AWJFCAXSGQLCKK-UHFFFAOYSA-N
BS-18921
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1,19-Eicosadiene

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 - 0.5319 53.19%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Plasma membrane 0.3808 38.08%
OATP2B1 inhibitior - 0.8581 85.81%
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 - 0.7729 77.29%
P-glycoprotein inhibitior - 0.8802 88.02%
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 + 0.9357 93.57%
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 + 0.7380 73.80%
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 - 0.6229 62.29%
Androgen receptor binding - 0.9102 91.02%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding - 0.4941 49.41%
Aromatase binding - 0.5974 59.74%
PPAR gamma + 0.6577 65.77%
Honey bee toxicity - 0.7552 75.52%
Biodegradation + 0.6000 60.00%
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.
Crocus sativus
Paronychia kapela
Terminalia chebula

Cross-Links

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PubChem 519006
NPASS NPC199137
LOTUS LTS0066140
wikiData Q82099431