(16E)-pentacosa-1,16-diene

Details

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Internal ID d77222f3-2f4f-45f8-a76f-139284164b73
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Olefins > Acyclic olefins > Alkadienes
IUPAC Name (16E)-pentacosa-1,16-diene
SMILES (Canonical) CCCCCCCCC=CCCCCCCCCCCCCCC=C
SMILES (Isomeric) CCCCCCCC/C=C/CCCCCCCCCCCCCC=C
InChI InChI=1S/C25H48/c1-3-5-7-9-11-13-15-17-19-21-23-25-24-22-20-18-16-14-12-10-8-6-4-2/h3,18,20H,1,4-17,19,21-25H2,2H3/b20-18+
InChI Key NQZCMSLRHZPRMB-CZIZESTLSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C25H48
Molecular Weight 348.60 g/mol
Exact Mass 348.375601531 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 12.30
Atomic LogP (AlogP) 9.55
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 21

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (16E)-pentacosa-1,16-diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9906 99.06%
Caco-2 + 0.6452 64.52%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.4578 45.78%
OATP2B1 inhibitior - 0.8551 85.51%
OATP1B1 inhibitior + 0.8616 86.16%
OATP1B3 inhibitior + 0.9239 92.39%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.6860 68.60%
P-glycoprotein inhibitior - 0.7819 78.19%
P-glycoprotein substrate - 0.9402 94.02%
CYP3A4 substrate - 0.6513 65.13%
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 - 0.8742 87.42%
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 + 0.9291 92.91%
Skin irritation + 0.8622 86.22%
Skin corrosion - 0.9742 97.42%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6492 64.92%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5301 53.01%
skin sensitisation + 0.9605 96.05%
Respiratory toxicity - 0.9556 95.56%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.5786 57.86%
Acute Oral Toxicity (c) III 0.6572 65.72%
Estrogen receptor binding + 0.5611 56.11%
Androgen receptor binding - 0.7747 77.47%
Thyroid receptor binding + 0.6467 64.67%
Glucocorticoid receptor binding - 0.7183 71.83%
Aromatase binding - 0.7138 71.38%
PPAR gamma + 0.6571 65.71%
Honey bee toxicity - 0.9624 96.24%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity + 0.9000 90.00%
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 95.47% 92.08%
CHEMBL240 Q12809 HERG 93.74% 89.76%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.32% 99.17%
CHEMBL230 P35354 Cyclooxygenase-2 91.97% 89.63%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 90.10% 92.86%
CHEMBL2581 P07339 Cathepsin D 90.02% 98.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 90.00% 97.29%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 89.54% 85.94%
CHEMBL5979 P05186 Alkaline phosphatase, tissue-nonspecific isozyme 88.96% 85.40%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 88.77% 91.81%
CHEMBL2885 P07451 Carbonic anhydrase III 87.83% 87.45%
CHEMBL221 P23219 Cyclooxygenase-1 84.47% 90.17%
CHEMBL1781 P11387 DNA topoisomerase I 83.76% 97.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.65% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.18% 96.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.82% 89.34%
CHEMBL1907 P15144 Aminopeptidase N 80.71% 93.31%
CHEMBL242 Q92731 Estrogen receptor beta 80.62% 98.35%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 14841082
LOTUS LTS0171654
wikiData Q105184201