Icosa-6,9-diene

Details

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Internal ID 647dafdb-20f2-464c-b5fe-805beeda1e02
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Olefins > Acyclic olefins > Alkadienes
IUPAC Name icosa-6,9-diene
SMILES (Canonical) CCCCCCCCCCC=CCC=CCCCCC
SMILES (Isomeric) CCCCCCCCCCC=CCC=CCCCCC
InChI InChI=1S/C20H38/c1-3-5-7-9-11-13-15-17-19-20-18-16-14-12-10-8-6-4-2/h11,13,17,19H,3-10,12,14-16,18,20H2,1-2H3
InChI Key ZXRQQYKZWAJTJO-UHFFFAOYSA-N
Popularity 3 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 9.40
Atomic LogP (AlogP) 7.60
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 15

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Icosa-6,9-diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9924 99.24%
Caco-2 + 0.9217 92.17%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.4683 46.83%
OATP2B1 inhibitior - 0.8530 85.30%
OATP1B1 inhibitior - 0.3332 33.32%
OATP1B3 inhibitior + 0.9296 92.96%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.4535 45.35%
P-glycoprotein inhibitior - 0.8202 82.02%
P-glycoprotein substrate - 0.9456 94.56%
CYP3A4 substrate - 0.7011 70.11%
CYP2C9 substrate - 0.8202 82.02%
CYP2D6 substrate - 0.7454 74.54%
CYP3A4 inhibition - 0.9849 98.49%
CYP2C9 inhibition - 0.9314 93.14%
CYP2C19 inhibition - 0.9425 94.25%
CYP2D6 inhibition - 0.9380 93.80%
CYP1A2 inhibition + 0.5051 50.51%
CYP2C8 inhibition - 0.9072 90.72%
CYP inhibitory promiscuity - 0.6865 68.65%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5900 59.00%
Carcinogenicity (trinary) Non-required 0.5827 58.27%
Eye corrosion + 0.9822 98.22%
Eye irritation + 0.9797 97.97%
Skin irritation + 0.8759 87.59%
Skin corrosion - 0.9834 98.34%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4795 47.95%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5434 54.34%
skin sensitisation + 0.9753 97.53%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.9970 99.70%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity - 0.5717 57.17%
Acute Oral Toxicity (c) III 0.8244 82.44%
Estrogen receptor binding - 0.5169 51.69%
Androgen receptor binding - 0.7836 78.36%
Thyroid receptor binding + 0.7504 75.04%
Glucocorticoid receptor binding - 0.7228 72.28%
Aromatase binding - 0.6416 64.16%
PPAR gamma + 0.7182 71.82%
Honey bee toxicity - 0.9920 99.20%
Biodegradation + 0.8000 80.00%
Crustacea aquatic toxicity + 0.9053 90.53%
Fish aquatic toxicity + 0.9908 99.08%

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 96.01% 92.08%
CHEMBL230 P35354 Cyclooxygenase-2 95.44% 89.63%
CHEMBL2581 P07339 Cathepsin D 93.03% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.49% 99.17%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 90.68% 92.86%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 89.47% 85.94%
CHEMBL239 Q07869 Peroxisome proliferator-activated receptor alpha 88.34% 90.75%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 87.96% 91.81%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.03% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 84.77% 90.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.42% 97.29%
CHEMBL1781 P11387 DNA topoisomerase I 83.56% 97.00%
CHEMBL2885 P07451 Carbonic anhydrase III 82.33% 87.45%
CHEMBL1907 P15144 Aminopeptidase N 80.34% 93.31%

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.
Baccharoides anthelmintica

Cross-Links

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PubChem 53686554
LOTUS LTS0158148
wikiData Q105385738