Pentacosa-7,9-diene

Details

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Internal ID ce56854d-2ca0-470c-b0b4-420108b52aab
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Olefins > Acyclic olefins > Alkadienes
IUPAC Name pentacosa-7,9-diene
SMILES (Canonical)
SMILES (Isomeric)
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/h13,15,17,19H,3-12,14,16,18,20-25H2,1-2H3
InChI Key MOPZORIRSCDWHG-UHFFFAOYSA-N
Popularity 5 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 12.40
Atomic LogP (AlogP) 9.55
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 20

Synonyms

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7,9-Pentacosadiene
67169-11-3
DTXSID90791738

2D Structure

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2D Structure of Pentacosa-7,9-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 + 0.7076 70.76%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Lysosomes 0.4683 46.83%
OATP2B1 inhibitior - 0.8538 85.38%
OATP1B1 inhibitior + 0.8650 86.50%
OATP1B3 inhibitior + 0.9296 92.96%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.4655 46.55%
P-glycoprotein inhibitior - 0.6708 67.08%
P-glycoprotein substrate - 0.9446 94.46%
CYP3A4 substrate - 0.7065 70.65%
CYP2C9 substrate - 0.8164 81.64%
CYP2D6 substrate - 0.7603 76.03%
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 - 0.9285 92.85%
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 + 0.8713 87.13%
Skin irritation + 0.8759 87.59%
Skin corrosion - 0.9834 98.34%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4140 41.40%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6184 61.84%
skin sensitisation + 0.9753 97.53%
Respiratory toxicity - 0.9333 93.33%
Reproductive toxicity - 0.9970 99.70%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.5618 56.18%
Acute Oral Toxicity (c) III 0.8244 82.44%
Estrogen receptor binding + 0.6990 69.90%
Androgen receptor binding - 0.5912 59.12%
Thyroid receptor binding + 0.6986 69.86%
Glucocorticoid receptor binding - 0.6270 62.70%
Aromatase binding + 0.5439 54.39%
PPAR gamma + 0.7710 77.10%
Honey bee toxicity - 0.9863 98.63%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity + 0.9353 93.53%
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 96.10% 92.08%
CHEMBL230 P35354 Cyclooxygenase-2 95.93% 89.63%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 91.92% 92.86%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.16% 99.17%
CHEMBL2581 P07339 Cathepsin D 90.08% 98.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 89.29% 97.29%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 88.77% 91.81%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 86.15% 85.94%
CHEMBL2885 P07451 Carbonic anhydrase III 84.92% 87.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.71% 96.09%
CHEMBL1907 P15144 Aminopeptidase N 81.86% 93.31%
CHEMBL221 P23219 Cyclooxygenase-1 81.81% 90.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.08% 96.95%
CHEMBL1781 P11387 DNA topoisomerase I 80.49% 97.00%

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 71368684
LOTUS LTS0132694
wikiData Q82760354