(6Z,9Z,12Z,15Z)-6,9,12,15-Henicosatetrene

Details

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Internal ID e51341d3-6baa-44ab-8a67-2970eca9b496
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Olefins > Acyclic olefins > Alkatetraenes
IUPAC Name (6Z,9Z,12Z,15Z)-henicosa-6,9,12,15-tetraene
SMILES (Canonical) CCCCCC=CCC=CCC=CCC=CCCCCC
SMILES (Isomeric) CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCCC
InChI InChI=1S/C21H36/c1-3-5-7-9-11-13-15-17-19-21-20-18-16-14-12-10-8-6-4-2/h11-14,17-20H,3-10,15-16,21H2,1-2H3/b13-11-,14-12-,19-17-,20-18-
InChI Key CVBGPGIEPHKALM-MAZCIEHSSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H36
Molecular Weight 288.50 g/mol
Exact Mass 288.281701148 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 8.60
Atomic LogP (AlogP) 7.54
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 14

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (6Z,9Z,12Z,15Z)-6,9,12,15-Henicosatetrene

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 + 0.8131 81.31%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.4683 46.83%
OATP2B1 inhibitior - 0.8541 85.41%
OATP1B1 inhibitior - 0.3953 39.53%
OATP1B3 inhibitior + 0.9296 92.96%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.7069 70.69%
P-glycoprotein inhibitior - 0.5947 59.47%
P-glycoprotein substrate - 0.9512 95.12%
CYP3A4 substrate - 0.7195 71.95%
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 - 0.9244 92.44%
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 + 0.8287 82.87%
Skin irritation + 0.8759 87.59%
Skin corrosion - 0.9834 98.34%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7723 77.23%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5176 51.76%
skin sensitisation + 0.9753 97.53%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity - 0.9970 99.70%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity - 0.5729 57.29%
Acute Oral Toxicity (c) III 0.8244 82.44%
Estrogen receptor binding + 0.5433 54.33%
Androgen receptor binding - 0.7686 76.86%
Thyroid receptor binding + 0.6777 67.77%
Glucocorticoid receptor binding - 0.5648 56.48%
Aromatase binding - 0.5861 58.61%
PPAR gamma + 0.8421 84.21%
Honey bee toxicity - 0.9920 99.20%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.7053 70.53%
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
CHEMBL230 P35354 Cyclooxygenase-2 94.01% 89.63%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 93.10% 92.08%
CHEMBL2581 P07339 Cathepsin D 92.98% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.18% 99.17%
CHEMBL239 Q07869 Peroxisome proliferator-activated receptor alpha 89.42% 90.75%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 85.74% 85.94%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 85.13% 92.86%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 84.20% 91.81%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.88% 96.09%
CHEMBL1781 P11387 DNA topoisomerase I 82.20% 97.00%
CHEMBL221 P23219 Cyclooxygenase-1 82.07% 90.17%
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.
Adesmia boronioides
Croton ruizianus
Oxytropis muricata
Polytrichum commune

Cross-Links

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PubChem 21629433
NPASS NPC209676
LOTUS LTS0022468
wikiData Q104970644