Ornithine-containing lipid

Details

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Internal ID b3c61b33-f456-44c4-886b-a76842de22af
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > N-acyl-alpha amino acids
IUPAC Name 5-amino-2-[[15-methyl-3-(13-methyltetradecanoyloxy)hexadecanoyl]amino]pentanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C37H72N2O5/c1-31(2)24-19-15-11-7-5-9-13-17-21-26-33(30-35(40)39-34(37(42)43)27-23-29-38)44-36(41)28-22-18-14-10-6-8-12-16-20-25-32(3)4/h31-34H,5-30,38H2,1-4H3,(H,39,40)(H,42,43)
InChI Key PUZMSNPCMYUOTE-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C37H72N2O5
Molecular Weight 625.00 g/mol
Exact Mass 624.54412340 g/mol
Topological Polar Surface Area (TPSA) 119.00 Ų
XlogP 10.00
Atomic LogP (AlogP) 9.49
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 32

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Ornithine-containing lipid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6787 67.87%
Caco-2 - 0.8311 83.11%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.8217 82.17%
OATP2B1 inhibitior - 0.5604 56.04%
OATP1B1 inhibitior + 0.9212 92.12%
OATP1B3 inhibitior + 0.9321 93.21%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.6004 60.04%
P-glycoprotein inhibitior + 0.6319 63.19%
P-glycoprotein substrate - 0.5299 52.99%
CYP3A4 substrate + 0.5432 54.32%
CYP2C9 substrate - 0.5963 59.63%
CYP2D6 substrate - 0.8270 82.70%
CYP3A4 inhibition - 0.7938 79.38%
CYP2C9 inhibition - 0.8922 89.22%
CYP2C19 inhibition - 0.8837 88.37%
CYP2D6 inhibition - 0.8889 88.89%
CYP1A2 inhibition - 0.9111 91.11%
CYP2C8 inhibition - 0.8415 84.15%
CYP inhibitory promiscuity - 0.9632 96.32%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.6491 64.91%
Eye corrosion - 0.9827 98.27%
Eye irritation - 0.8219 82.19%
Skin irritation - 0.8801 88.01%
Skin corrosion - 0.9685 96.85%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7258 72.58%
Micronuclear + 0.5400 54.00%
Hepatotoxicity - 0.5948 59.48%
skin sensitisation - 0.8952 89.52%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity - 0.8556 85.56%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.4777 47.77%
Acute Oral Toxicity (c) III 0.6383 63.83%
Estrogen receptor binding + 0.6554 65.54%
Androgen receptor binding - 0.6143 61.43%
Thyroid receptor binding - 0.5740 57.40%
Glucocorticoid receptor binding + 0.5438 54.38%
Aromatase binding + 0.5849 58.49%
PPAR gamma + 0.6091 60.91%
Honey bee toxicity - 0.9097 90.97%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5424 54.24%
Fish aquatic toxicity - 0.3962 39.62%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 98.48% 99.17%
CHEMBL4040 P28482 MAP kinase ERK2 96.62% 83.82%
CHEMBL2581 P07339 Cathepsin D 95.95% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.09% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.81% 96.09%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 93.60% 97.21%
CHEMBL1255126 O15151 Protein Mdm4 91.97% 90.20%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 90.58% 95.17%
CHEMBL3359 P21462 Formyl peptide receptor 1 90.44% 93.56%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 90.01% 100.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.01% 96.00%
CHEMBL2973 O75116 Rho-associated protein kinase 2 89.75% 96.73%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 88.94% 97.29%
CHEMBL221 P23219 Cyclooxygenase-1 88.23% 90.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 87.41% 96.95%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 87.38% 96.47%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 87.11% 90.71%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 85.52% 97.23%
CHEMBL5255 O00206 Toll-like receptor 4 85.30% 92.50%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.93% 94.45%
CHEMBL3231 Q13464 Rho-associated protein kinase 1 84.66% 95.55%
CHEMBL4581 P52732 Kinesin-like protein 1 84.56% 93.18%
CHEMBL3776 Q14790 Caspase-8 82.74% 97.06%
CHEMBL2885 P07451 Carbonic anhydrase III 82.73% 87.45%
CHEMBL2514 O95665 Neurotensin receptor 2 82.58% 100.00%
CHEMBL236 P41143 Delta opioid receptor 82.06% 99.35%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 81.96% 92.29%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.94% 100.00%
CHEMBL340 P08684 Cytochrome P450 3A4 81.58% 91.19%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 81.47% 82.69%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.33% 93.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.24% 95.50%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 21778445
LOTUS LTS0136417
wikiData Q77375926