Tricosanoic acid, 23-hydroxy-

Details

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Internal ID 5c58410c-15a9-4456-869f-f4abf32f482a
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Very long-chain fatty acids
IUPAC Name 23-hydroxytricosanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H46O3/c24-22-20-18-16-14-12-10-8-6-4-2-1-3-5-7-9-11-13-15-17-19-21-23(25)26/h24H,1-22H2,(H,25,26)
InChI Key HVWZNSXGOXRKIK-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C23H46O3
Molecular Weight 370.60 g/mol
Exact Mass 370.34469533 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 8.00
Atomic LogP (AlogP) 7.26
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 22

Synonyms

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61658-18-2
SCHEMBL737420
DTXSID20471955

2D Structure

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2D Structure of Tricosanoic acid, 23-hydroxy-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9461 94.61%
Caco-2 - 0.7972 79.72%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.8504 85.04%
OATP2B1 inhibitior - 0.8533 85.33%
OATP1B1 inhibitior + 0.9444 94.44%
OATP1B3 inhibitior + 0.9443 94.43%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8332 83.32%
P-glycoprotein inhibitior - 0.8130 81.30%
P-glycoprotein substrate - 0.9880 98.80%
CYP3A4 substrate - 0.7575 75.75%
CYP2C9 substrate - 0.5816 58.16%
CYP2D6 substrate - 0.8592 85.92%
CYP3A4 inhibition - 0.9543 95.43%
CYP2C9 inhibition - 0.9043 90.43%
CYP2C19 inhibition - 0.9622 96.22%
CYP2D6 inhibition - 0.9707 97.07%
CYP1A2 inhibition - 0.9088 90.88%
CYP2C8 inhibition - 0.9814 98.14%
CYP inhibitory promiscuity - 0.9759 97.59%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Non-required 0.7159 71.59%
Eye corrosion + 0.7655 76.55%
Eye irritation + 0.9699 96.99%
Skin irritation - 0.7750 77.50%
Skin corrosion - 0.8965 89.65%
Ames mutagenesis - 0.9900 99.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4728 47.28%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6708 67.08%
skin sensitisation - 0.9435 94.35%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity - 0.9320 93.20%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity - 0.5639 56.39%
Acute Oral Toxicity (c) III 0.5988 59.88%
Estrogen receptor binding - 0.7944 79.44%
Androgen receptor binding - 0.8774 87.74%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding - 0.6109 61.09%
Aromatase binding - 0.6355 63.55%
PPAR gamma + 0.6556 65.56%
Honey bee toxicity - 0.9845 98.45%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity - 0.8313 83.13%
Fish aquatic toxicity - 0.6286 62.86%

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 92.95% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.46% 99.17%
CHEMBL5285 Q99683 Mitogen-activated protein kinase kinase kinase 5 87.08% 92.26%
CHEMBL4040 P28482 MAP kinase ERK2 85.81% 83.82%
CHEMBL1781 P11387 DNA topoisomerase I 83.61% 97.00%
CHEMBL2581 P07339 Cathepsin D 83.26% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.22% 91.11%

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.
Arabidopsis thaliana

Cross-Links

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PubChem 11760442
LOTUS LTS0093966
wikiData Q82300664