2,2-Dihydroxyhexadecanoic acid

Details

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Internal ID 22408046-93a8-4fe3-99d3-f91a4531bb8a
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Long-chain fatty acids
IUPAC Name 2,2-dihydroxyhexadecanoic acid
SMILES (Canonical) CCCCCCCCCCCCCCC(C(=O)O)(O)O
SMILES (Isomeric) CCCCCCCCCCCCCCC(C(=O)O)(O)O
InChI InChI=1S/C16H32O4/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-16(19,20)15(17)18/h19-20H,2-14H2,1H3,(H,17,18)
InChI Key HAFGDDFWCDLGEW-UHFFFAOYSA-N
Popularity 33 references in papers

Physical and Chemical Properties

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Molecular Formula C16H32O4
Molecular Weight 288.42 g/mol
Exact Mass 288.23005950 g/mol
Topological Polar Surface Area (TPSA) 77.80 Ų
XlogP 5.60
Atomic LogP (AlogP) 3.84
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 14

Synonyms

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35465-40-8
dihydroxyhexadecanoic acid
SCHEMBL1916481
DTXSID70707251

2D Structure

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2D Structure of 2,2-Dihydroxyhexadecanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8402 84.02%
Caco-2 - 0.5237 52.37%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.8072 80.72%
OATP2B1 inhibitior - 0.8496 84.96%
OATP1B1 inhibitior + 0.9118 91.18%
OATP1B3 inhibitior + 0.9327 93.27%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.6445 64.45%
P-glycoprotein inhibitior - 0.9396 93.96%
P-glycoprotein substrate - 0.9409 94.09%
CYP3A4 substrate - 0.6858 68.58%
CYP2C9 substrate + 0.6276 62.76%
CYP2D6 substrate - 0.8883 88.83%
CYP3A4 inhibition - 0.9119 91.19%
CYP2C9 inhibition - 0.8795 87.95%
CYP2C19 inhibition - 0.8892 88.92%
CYP2D6 inhibition - 0.9313 93.13%
CYP1A2 inhibition - 0.5066 50.66%
CYP2C8 inhibition - 0.9298 92.98%
CYP inhibitory promiscuity - 0.9775 97.75%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8220 82.20%
Carcinogenicity (trinary) Non-required 0.7585 75.85%
Eye corrosion - 0.8442 84.42%
Eye irritation + 0.8005 80.05%
Skin irritation - 0.6350 63.50%
Skin corrosion - 0.8372 83.72%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3973 39.73%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5321 53.21%
skin sensitisation - 0.6558 65.58%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity - 0.7705 77.05%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.4855 48.55%
Estrogen receptor binding - 0.7533 75.33%
Androgen receptor binding - 0.6341 63.41%
Thyroid receptor binding + 0.7112 71.12%
Glucocorticoid receptor binding - 0.4642 46.42%
Aromatase binding - 0.6694 66.94%
PPAR gamma + 0.7723 77.23%
Honey bee toxicity - 0.9961 99.61%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity + 0.6452 64.52%
Fish aquatic toxicity + 0.9084 90.84%

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
CHEMBL2581 P07339 Cathepsin D 94.06% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.57% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 91.13% 97.29%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.85% 99.17%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 90.73% 92.08%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 88.78% 85.94%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 85.42% 92.86%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 84.83% 100.00%
CHEMBL3401 O75469 Pregnane X receptor 82.33% 94.73%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.68% 93.56%

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.
Cynara cardunculus

Cross-Links

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PubChem 53866632
LOTUS LTS0096222
wikiData Q82640953