2-Hydroxy-22-methyltricosanoic acid

Details

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Internal ID 297610d1-69dd-4748-ae58-5d56c616413d
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Very long-chain fatty acids
IUPAC Name 2-hydroxy-22-methyltricosanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H48O3/c1-22(2)20-18-16-14-12-10-8-6-4-3-5-7-9-11-13-15-17-19-21-23(25)24(26)27/h22-23,25H,3-21H2,1-2H3,(H,26,27)
InChI Key DVLZPXHAPNBGTD-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C24H48O3
Molecular Weight 384.60 g/mol
Exact Mass 384.36034539 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 10.40
Atomic LogP (AlogP) 7.50
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 21

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Hydroxy-22-methyltricosanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9553 95.53%
Caco-2 - 0.6542 65.42%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.8433 84.33%
OATP2B1 inhibitior - 0.8501 85.01%
OATP1B1 inhibitior + 0.9648 96.48%
OATP1B3 inhibitior + 0.9409 94.09%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.6671 66.71%
P-glycoprotein inhibitior - 0.7295 72.95%
P-glycoprotein substrate - 0.9396 93.96%
CYP3A4 substrate - 0.6545 65.45%
CYP2C9 substrate + 0.6012 60.12%
CYP2D6 substrate - 0.8609 86.09%
CYP3A4 inhibition - 0.9513 95.13%
CYP2C9 inhibition - 0.8387 83.87%
CYP2C19 inhibition - 0.9282 92.82%
CYP2D6 inhibition - 0.9527 95.27%
CYP1A2 inhibition - 0.6656 66.56%
CYP2C8 inhibition - 0.9934 99.34%
CYP inhibitory promiscuity - 0.9757 97.57%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Non-required 0.7675 76.75%
Eye corrosion + 0.4742 47.42%
Eye irritation + 0.8152 81.52%
Skin irritation - 0.7226 72.26%
Skin corrosion - 0.9702 97.02%
Ames mutagenesis - 0.9700 97.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7058 70.58%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation + 0.6357 63.57%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity - 0.6228 62.28%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity - 0.6858 68.58%
Acute Oral Toxicity (c) III 0.5860 58.60%
Estrogen receptor binding - 0.7676 76.76%
Androgen receptor binding - 0.7356 73.56%
Thyroid receptor binding - 0.4878 48.78%
Glucocorticoid receptor binding - 0.5858 58.58%
Aromatase binding - 0.7628 76.28%
PPAR gamma + 0.6304 63.04%
Honey bee toxicity - 0.9875 98.75%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.8076 80.76%
Fish aquatic toxicity + 0.8844 88.44%

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 95.17% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.40% 98.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 88.42% 97.29%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.68% 99.17%
CHEMBL3359 P21462 Formyl peptide receptor 1 87.38% 93.56%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 85.54% 100.00%
CHEMBL221 P23219 Cyclooxygenase-1 84.12% 90.17%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 83.28% 96.47%
CHEMBL2179 P04062 Beta-glucocerebrosidase 82.97% 85.31%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.40% 90.71%
CHEMBL1907 P15144 Aminopeptidase N 82.01% 93.31%

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 11036420
LOTUS LTS0220416
wikiData Q104254342