2-hydroxy-N-(1,3,4-trihydroxytetracosan-2-yl)octadec-4-enamide

Details

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Internal ID 4addddc8-7cab-4f36-a7dd-5e2b6ea37cff
Taxonomy Lipids and lipid-like molecules > Sphingolipids > Ceramides > Phytoceramides
IUPAC Name 2-hydroxy-N-(1,3,4-trihydroxytetracosan-2-yl)octadec-4-enamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C42H83NO5/c1-3-5-7-9-11-13-15-17-19-20-21-22-24-25-27-29-31-33-35-39(45)41(47)38(37-44)43-42(48)40(46)36-34-32-30-28-26-23-18-16-14-12-10-8-6-4-2/h32,34,38-41,44-47H,3-31,33,35-37H2,1-2H3,(H,43,48)
InChI Key XMDDGZCHKXAWPD-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C42H83NO5
Molecular Weight 682.10 g/mol
Exact Mass 681.62712475 g/mol
Topological Polar Surface Area (TPSA) 110.00 Ų
XlogP 15.30
Atomic LogP (AlogP) 10.63
H-Bond Acceptor 5
H-Bond Donor 5
Rotatable Bonds 38

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-hydroxy-N-(1,3,4-trihydroxytetracosan-2-yl)octadec-4-enamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8634 86.34%
Caco-2 - 0.8566 85.66%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.8131 81.31%
OATP2B1 inhibitior - 0.5646 56.46%
OATP1B1 inhibitior + 0.8727 87.27%
OATP1B3 inhibitior + 0.9104 91.04%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8879 88.79%
BSEP inhibitior + 0.5944 59.44%
P-glycoprotein inhibitior + 0.5780 57.80%
P-glycoprotein substrate - 0.6358 63.58%
CYP3A4 substrate + 0.5344 53.44%
CYP2C9 substrate - 0.6085 60.85%
CYP2D6 substrate - 0.8448 84.48%
CYP3A4 inhibition - 0.8064 80.64%
CYP2C9 inhibition - 0.6822 68.22%
CYP2C19 inhibition - 0.8802 88.02%
CYP2D6 inhibition + 0.5100 51.00%
CYP1A2 inhibition + 0.5962 59.62%
CYP2C8 inhibition - 0.8552 85.52%
CYP inhibitory promiscuity - 0.8268 82.68%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.7225 72.25%
Eye corrosion - 0.9822 98.22%
Eye irritation - 0.8826 88.26%
Skin irritation - 0.8722 87.22%
Skin corrosion - 0.9834 98.34%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3680 36.80%
Micronuclear + 0.5100 51.00%
Hepatotoxicity - 0.6529 65.29%
skin sensitisation - 0.9076 90.76%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.7243 72.43%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.5952 59.52%
Estrogen receptor binding + 0.7138 71.38%
Androgen receptor binding + 0.5215 52.15%
Thyroid receptor binding - 0.6172 61.72%
Glucocorticoid receptor binding + 0.5758 57.58%
Aromatase binding - 0.5177 51.77%
PPAR gamma + 0.5674 56.74%
Honey bee toxicity - 0.9755 97.55%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.6386 63.86%
Fish aquatic toxicity - 0.4884 48.84%

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
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 98.47% 97.29%
CHEMBL2581 P07339 Cathepsin D 98.30% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 97.14% 99.17%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 96.64% 92.86%
CHEMBL230 P35354 Cyclooxygenase-2 94.62% 89.63%
CHEMBL4040 P28482 MAP kinase ERK2 94.03% 83.82%
CHEMBL3359 P21462 Formyl peptide receptor 1 93.61% 93.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.76% 96.09%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 91.06% 96.47%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 89.28% 91.81%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 89.06% 100.00%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 88.77% 85.94%
CHEMBL4227 P25090 Lipoxin A4 receptor 88.65% 100.00%
CHEMBL3267 P48736 PI3-kinase p110-gamma subunit 87.27% 95.71%
CHEMBL299 P17252 Protein kinase C alpha 85.96% 98.03%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 85.86% 92.08%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 85.32% 98.75%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.12% 89.34%
CHEMBL1781 P11387 DNA topoisomerase I 83.87% 97.00%
CHEMBL4588 P22894 Matrix metalloproteinase 8 83.68% 94.66%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.43% 96.95%
CHEMBL2885 P07451 Carbonic anhydrase III 82.80% 87.45%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 82.75% 100.00%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 82.63% 91.24%
CHEMBL3401 O75469 Pregnane X receptor 81.92% 94.73%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.36% 94.33%
CHEMBL2664 P23526 Adenosylhomocysteinase 81.33% 86.67%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 81.21% 95.58%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.54% 96.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.20% 94.45%

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.
Pancovia laurentii

Cross-Links

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PubChem 75576403
LOTUS LTS0186085
wikiData Q105330655