26-Methyloctacosanoic acid

Details

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Internal ID 7c096456-90b0-411b-899e-386e5a0cd447
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Very long-chain fatty acids
IUPAC Name 26-methyloctacosanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C29H58O2/c1-3-28(2)26-24-22-20-18-16-14-12-10-8-6-4-5-7-9-11-13-15-17-19-21-23-25-27-29(30)31/h28H,3-27H2,1-2H3,(H,30,31)
InChI Key JZQNTAVPVKXDHG-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C29H58O2
Molecular Weight 438.80 g/mol
Exact Mass 438.44368109 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 13.90
Atomic LogP (AlogP) 10.48
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 26

Synonyms

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CHEBI:84885
26-Methyloctacosanoate
RefChem:89954
SCHEMBL1333549
Q27158150

2D Structure

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2D Structure of 26-Methyloctacosanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9938 99.38%
Caco-2 - 0.6866 68.66%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.5733 57.33%
OATP2B1 inhibitior - 0.8513 85.13%
OATP1B1 inhibitior + 0.9287 92.87%
OATP1B3 inhibitior - 0.2846 28.46%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.5429 54.29%
P-glycoprotein inhibitior - 0.6975 69.75%
P-glycoprotein substrate - 0.9196 91.96%
CYP3A4 substrate - 0.6819 68.19%
CYP2C9 substrate + 1.0000 100.00%
CYP2D6 substrate - 0.8908 89.08%
CYP3A4 inhibition - 0.9401 94.01%
CYP2C9 inhibition - 0.8701 87.01%
CYP2C19 inhibition - 0.9602 96.02%
CYP2D6 inhibition - 0.9509 95.09%
CYP1A2 inhibition + 0.7432 74.32%
CYP2C8 inhibition - 0.9872 98.72%
CYP inhibitory promiscuity - 0.9575 95.75%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6915 69.15%
Carcinogenicity (trinary) Non-required 0.7216 72.16%
Eye corrosion + 0.9723 97.23%
Eye irritation + 0.8528 85.28%
Skin irritation - 0.6026 60.26%
Skin corrosion - 0.7533 75.33%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6110 61.10%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5429 54.29%
skin sensitisation + 0.8864 88.64%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity - 0.6354 63.54%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.7005 70.05%
Acute Oral Toxicity (c) III 0.6572 65.72%
Estrogen receptor binding - 0.7262 72.62%
Androgen receptor binding - 0.8839 88.39%
Thyroid receptor binding + 0.6377 63.77%
Glucocorticoid receptor binding - 0.5965 59.65%
Aromatase binding - 0.6066 60.66%
PPAR gamma + 0.6510 65.10%
Honey bee toxicity - 0.9922 99.22%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9283 92.83%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.21% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.69% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.17% 99.17%
CHEMBL5285 Q99683 Mitogen-activated protein kinase kinase kinase 5 92.21% 92.26%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 87.86% 100.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 87.52% 93.56%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 83.88% 96.47%
CHEMBL221 P23219 Cyclooxygenase-1 82.86% 90.17%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.52% 90.71%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 81.32% 97.29%
CHEMBL1781 P11387 DNA topoisomerase I 80.73% 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 15047968
LOTUS LTS0050841
wikiData Q27158150