(4E)-1,4-Icosadiene

Details

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Internal ID e6f5fb62-99aa-4918-86ce-fd48bd94c9f9
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Olefins > Acyclic olefins > Alkadienes
IUPAC Name (4E)-icosa-1,4-diene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H38/c1-3-5-7-9-11-13-15-17-19-20-18-16-14-12-10-8-6-4-2/h3,7,9H,1,4-6,8,10-20H2,2H3/b9-7+
InChI Key VMWPBZLUNCMQTJ-VQHVLOKHSA-N
Popularity 2 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 9.80
Atomic LogP (AlogP) 7.60
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 16

Synonyms

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(4E)-1,4-Icosadiene #
VMWPBZLUNCMQTJ-VQHVLOKHSA-N

2D Structure

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2D Structure of (4E)-1,4-Icosadiene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9906 99.06%
Caco-2 + 0.8246 82.46%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.4578 45.78%
OATP2B1 inhibitior - 0.8558 85.58%
OATP1B1 inhibitior + 0.7602 76.02%
OATP1B3 inhibitior + 0.9239 92.39%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.5830 58.30%
P-glycoprotein inhibitior - 0.8935 89.35%
P-glycoprotein substrate - 0.9388 93.88%
CYP3A4 substrate - 0.6421 64.21%
CYP2C9 substrate - 0.8202 82.02%
CYP2D6 substrate - 0.7454 74.54%
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 - 0.8734 87.34%
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 + 0.8807 88.07%
Skin irritation + 0.8622 86.22%
Skin corrosion - 0.9742 97.42%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7539 75.39%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5199 51.99%
skin sensitisation + 0.9605 96.05%
Respiratory toxicity - 0.9000 90.00%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.5093 50.93%
Acute Oral Toxicity (c) III 0.6572 65.72%
Estrogen receptor binding + 0.5379 53.79%
Androgen receptor binding - 0.7015 70.15%
Thyroid receptor binding + 0.6545 65.45%
Glucocorticoid receptor binding - 0.6032 60.32%
Aromatase binding - 0.6161 61.61%
PPAR gamma + 0.7229 72.29%
Honey bee toxicity - 0.9740 97.40%
Biodegradation + 0.8250 82.50%
Crustacea aquatic toxicity + 0.8800 88.00%
Fish aquatic toxicity + 0.9955 99.55%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 95.19% 92.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.71% 99.17%
CHEMBL2581 P07339 Cathepsin D 92.66% 98.95%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 89.50% 85.94%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 88.69% 91.81%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 88.00% 92.86%
CHEMBL230 P35354 Cyclooxygenase-2 87.29% 89.63%
CHEMBL2885 P07451 Carbonic anhydrase III 86.37% 87.45%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 86.23% 97.29%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.04% 96.09%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 84.55% 95.17%
CHEMBL221 P23219 Cyclooxygenase-1 83.39% 90.17%
CHEMBL239 Q07869 Peroxisome proliferator-activated receptor alpha 83.28% 90.75%
CHEMBL1781 P11387 DNA topoisomerase I 82.20% 97.00%
CHEMBL1907 P15144 Aminopeptidase N 81.46% 93.31%
CHEMBL3401 O75469 Pregnane X receptor 80.65% 94.73%

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.
Paronychia kapela

Cross-Links

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PubChem 5365774
LOTUS LTS0233855
wikiData Q105289351