20-Hydroxyicosanoic acid

Details

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Internal ID dd589150-e2cf-4c97-8976-18fcc0a16b92
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Long-chain fatty acids
IUPAC Name 20-hydroxyicosanoic acid
SMILES (Canonical) C(CCCCCCCCCC(=O)O)CCCCCCCCCO
SMILES (Isomeric) C(CCCCCCCCCC(=O)O)CCCCCCCCCO
InChI InChI=1S/C20H40O3/c21-19-17-15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-16-18-20(22)23/h21H,1-19H2,(H,22,23)
InChI Key JLDIWYKSFMPIDW-UHFFFAOYSA-N
Popularity 9 references in papers

Physical and Chemical Properties

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Molecular Formula C20H40O3
Molecular Weight 328.50 g/mol
Exact Mass 328.29774513 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 6.40
Atomic LogP (AlogP) 6.09
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 19

Synonyms

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62643-46-3
20-HYDROXYEICOSANOIC ACID
20-hydroxy-eicosanoicacid
20-hydroxy-eicosanoic acid
20-Hydroxy arachidic acid
LMFA01050075
20-hydroxyarachidic acid
omega-hydroxyarachidic acid
omega-hydroxyicosanoic acid
SCHEMBL401769
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 20-Hydroxyicosanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9461 94.61%
Caco-2 - 0.7576 75.76%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.8504 85.04%
OATP2B1 inhibitior - 0.8525 85.25%
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 - 0.8299 82.99%
P-glycoprotein inhibitior - 0.8626 86.26%
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 + 0.8000 80.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Non-required 0.7159 71.59%
Eye corrosion + 0.7655 76.55%
Eye irritation + 0.9787 97.87%
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 - 0.4394 43.94%
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 - 0.8039 80.39%
Androgen receptor binding - 0.8774 87.74%
Thyroid receptor binding - 0.5252 52.52%
Glucocorticoid receptor binding - 0.6914 69.14%
Aromatase binding - 0.6565 65.65%
PPAR gamma + 0.6408 64.08%
Honey bee toxicity - 0.9845 98.45%
Biodegradation + 0.8750 87.50%
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
Pinus radiata

Cross-Links

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PubChem 5282919
LOTUS LTS0009086
wikiData Q27148258