methyl (3R,11R)-3,11-dihydroxydodecanoate

Details

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Internal ID 2cb67c24-1895-4792-bf00-57e4c54ddfc7
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name methyl (3R,11R)-3,11-dihydroxydodecanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H26O4/c1-11(14)8-6-4-3-5-7-9-12(15)10-13(16)17-2/h11-12,14-15H,3-10H2,1-2H3/t11-,12-/m1/s1
InChI Key SEZWPDNGTCYOOK-VXGBXAGGSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C13H26O4
Molecular Weight 246.34 g/mol
Exact Mass 246.18310931 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.02
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of methyl (3R,11R)-3,11-dihydroxydodecanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9216 92.16%
Caco-2 + 0.6364 63.64%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.8381 83.81%
OATP2B1 inhibitior - 0.8517 85.17%
OATP1B1 inhibitior + 0.9640 96.40%
OATP1B3 inhibitior + 0.9144 91.44%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8613 86.13%
P-glycoprotein inhibitior - 0.9160 91.60%
P-glycoprotein substrate - 0.8242 82.42%
CYP3A4 substrate - 0.5248 52.48%
CYP2C9 substrate - 0.8037 80.37%
CYP2D6 substrate - 0.8433 84.33%
CYP3A4 inhibition - 0.9349 93.49%
CYP2C9 inhibition - 0.8633 86.33%
CYP2C19 inhibition - 0.9192 91.92%
CYP2D6 inhibition - 0.9491 94.91%
CYP1A2 inhibition - 0.7659 76.59%
CYP2C8 inhibition - 0.9845 98.45%
CYP inhibitory promiscuity - 0.9495 94.95%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7015 70.15%
Carcinogenicity (trinary) Non-required 0.7597 75.97%
Eye corrosion - 0.7860 78.60%
Eye irritation - 0.7154 71.54%
Skin irritation - 0.8741 87.41%
Skin corrosion - 0.9825 98.25%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6010 60.10%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5841 58.41%
skin sensitisation - 0.8079 80.79%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity - 0.8447 84.47%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.7376 73.76%
Acute Oral Toxicity (c) III 0.6074 60.74%
Estrogen receptor binding - 0.6704 67.04%
Androgen receptor binding - 0.7674 76.74%
Thyroid receptor binding - 0.5200 52.00%
Glucocorticoid receptor binding - 0.5205 52.05%
Aromatase binding - 0.7345 73.45%
PPAR gamma - 0.6204 62.04%
Honey bee toxicity - 0.9201 92.01%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity - 0.6938 69.38%
Fish aquatic toxicity + 0.8028 80.28%

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
CHEMBL4040 P28482 MAP kinase ERK2 97.96% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.14% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 92.76% 97.29%
CHEMBL2581 P07339 Cathepsin D 91.36% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.78% 99.17%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 88.59% 100.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.21% 85.14%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 86.98% 94.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.72% 91.11%
CHEMBL3437 Q16853 Amine oxidase, copper containing 83.16% 94.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.90% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 82.76% 97.21%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.29% 96.00%
CHEMBL3267 P48736 PI3-kinase p110-gamma subunit 82.24% 95.71%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 81.82% 98.75%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 81.16% 96.47%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.11% 93.56%
CHEMBL2885 P07451 Carbonic anhydrase III 81.06% 87.45%
CHEMBL3401 O75469 Pregnane X receptor 80.70% 94.73%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.04% 100.00%

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.
Blepharizonia plumosa

Cross-Links

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PubChem 14543660
LOTUS LTS0072968
wikiData Q105251636