10-Methoxy-9,18-dihydroxyoctadecanoic acid

Details

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Internal ID b986a42d-5a43-412d-96bc-dbad0ceae595
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Long-chain fatty acids
IUPAC Name 9,18-dihydroxy-10-methoxyoctadecanoic acid
SMILES (Canonical) COC(CCCCCCCCO)C(CCCCCCCC(=O)O)O
SMILES (Isomeric) COC(CCCCCCCCO)C(CCCCCCCC(=O)O)O
InChI InChI=1S/C19H38O5/c1-24-18(14-10-6-2-3-8-12-16-20)17(21)13-9-5-4-7-11-15-19(22)23/h17-18,20-21H,2-16H2,1H3,(H,22,23)
InChI Key DRGAKKLILXXLIA-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H38O5
Molecular Weight 346.50 g/mol
Exact Mass 346.27192431 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.90
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 18

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 10-Methoxy-9,18-dihydroxyoctadecanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8780 87.80%
Caco-2 - 0.6361 63.61%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.8751 87.51%
OATP2B1 inhibitior - 0.8512 85.12%
OATP1B1 inhibitior + 0.9253 92.53%
OATP1B3 inhibitior + 0.9277 92.77%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.4579 45.79%
P-glycoprotein inhibitior - 0.7949 79.49%
P-glycoprotein substrate - 0.8888 88.88%
CYP3A4 substrate - 0.5512 55.12%
CYP2C9 substrate - 0.5981 59.81%
CYP2D6 substrate - 0.8433 84.33%
CYP3A4 inhibition - 0.9463 94.63%
CYP2C9 inhibition - 0.8895 88.95%
CYP2C19 inhibition - 0.9428 94.28%
CYP2D6 inhibition - 0.9530 95.30%
CYP1A2 inhibition - 0.8537 85.37%
CYP2C8 inhibition - 0.9542 95.42%
CYP inhibitory promiscuity - 0.9583 95.83%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7900 79.00%
Carcinogenicity (trinary) Non-required 0.8086 80.86%
Eye corrosion - 0.9316 93.16%
Eye irritation - 0.6494 64.94%
Skin irritation - 0.8554 85.54%
Skin corrosion - 0.9804 98.04%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4501 45.01%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.6885 68.85%
skin sensitisation - 0.8584 85.84%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.8497 84.97%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity - 0.5872 58.72%
Acute Oral Toxicity (c) IV 0.6961 69.61%
Estrogen receptor binding - 0.4858 48.58%
Androgen receptor binding - 0.7516 75.16%
Thyroid receptor binding + 0.6844 68.44%
Glucocorticoid receptor binding - 0.5992 59.92%
Aromatase binding - 0.7044 70.44%
PPAR gamma + 0.5318 53.18%
Honey bee toxicity - 0.9474 94.74%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.7469 74.69%
Fish aquatic toxicity - 0.6642 66.42%

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 98.55% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 96.45% 99.17%
CHEMBL4040 P28482 MAP kinase ERK2 95.86% 83.82%
CHEMBL2581 P07339 Cathepsin D 94.70% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.06% 91.11%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 89.57% 97.29%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.08% 95.50%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.15% 96.00%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 80.36% 100.00%
CHEMBL340 P08684 Cytochrome P450 3A4 80.13% 91.19%

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.
Pinus radiata

Cross-Links

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PubChem 129726042
LOTUS LTS0116601
wikiData Q104987387