2,3-Dihydroxypropyl 28-hydroxyoctacosanoate

Details

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Internal ID 544f6178-3288-4eb4-a487-4d98a5105443
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name 2,3-dihydroxypropyl 28-hydroxyoctacosanoate
SMILES (Canonical) C(CCCCCCCCCCCCCC(=O)OCC(CO)O)CCCCCCCCCCCCCO
SMILES (Isomeric) C(CCCCCCCCCCCCCC(=O)OCC(CO)O)CCCCCCCCCCCCCO
InChI InChI=1S/C31H62O5/c32-27-25-23-21-19-17-15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-16-18-20-22-24-26-31(35)36-29-30(34)28-33/h30,32-34H,1-29H2
InChI Key KGRZWBVWLUKOGX-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C31H62O5
Molecular Weight 514.80 g/mol
Exact Mass 514.45972507 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 11.20
Atomic LogP (AlogP) 8.02
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 30

Synonyms

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162522-32-9
DTXSID50776304

2D Structure

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2D Structure of 2,3-Dihydroxypropyl 28-hydroxyoctacosanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5904 59.04%
Caco-2 - 0.8152 81.52%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.8849 88.49%
OATP2B1 inhibitior - 0.8517 85.17%
OATP1B1 inhibitior + 0.9503 95.03%
OATP1B3 inhibitior + 0.9448 94.48%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.5174 51.74%
P-glycoprotein inhibitior - 0.6123 61.23%
P-glycoprotein substrate - 0.9492 94.92%
CYP3A4 substrate - 0.5856 58.56%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8345 83.45%
CYP3A4 inhibition - 0.9428 94.28%
CYP2C9 inhibition - 0.8977 89.77%
CYP2C19 inhibition - 0.8716 87.16%
CYP2D6 inhibition - 0.9514 95.14%
CYP1A2 inhibition - 0.8261 82.61%
CYP2C8 inhibition - 0.9626 96.26%
CYP inhibitory promiscuity - 0.9721 97.21%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Non-required 0.7131 71.31%
Eye corrosion - 0.9192 91.92%
Eye irritation + 0.5512 55.12%
Skin irritation - 0.9190 91.90%
Skin corrosion - 0.9772 97.72%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3610 36.10%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6877 68.77%
skin sensitisation - 0.9126 91.26%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.9667 96.67%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.7247 72.47%
Acute Oral Toxicity (c) IV 0.5336 53.36%
Estrogen receptor binding - 0.5167 51.67%
Androgen receptor binding - 0.9299 92.99%
Thyroid receptor binding - 0.4883 48.83%
Glucocorticoid receptor binding - 0.5056 50.56%
Aromatase binding - 0.6706 67.06%
PPAR gamma - 0.5000 50.00%
Honey bee toxicity - 0.8813 88.13%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.7545 75.45%
Fish aquatic toxicity - 0.7624 76.24%

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 95.87% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.49% 99.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 91.02% 97.29%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 84.39% 86.92%
CHEMBL2581 P07339 Cathepsin D 83.58% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.90% 91.11%
CHEMBL340 P08684 Cytochrome P450 3A4 82.18% 91.19%
CHEMBL2885 P07451 Carbonic anhydrase III 81.34% 87.45%

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.
Cinnamomum camphora

Cross-Links

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PubChem 71350505
LOTUS LTS0004854
wikiData Q82738103