(O-(1-O-Hexadecyl-2-O-((5Z,8Z,11Z,14Z)-1-oxo-5,8,11,14-icosatetrenyl)-L-glycero-3-phospho)choline)anion

Details

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Internal ID 8c3aa0c9-e33b-444b-8ca0-81ba59beb429
Taxonomy Lipids and lipid-like molecules > Glycerophospholipids > Glycerophosphocholines > 1-alkyl,2-acylglycero-3-phosphocholines
IUPAC Name 2-[[(2R)-3-hexadecoxy-2-[(5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraenoyl]oxypropoxy]-hydroxyphosphoryl]oxyethyl-trimethylazanium
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C44H82NO7P/c1-6-8-10-12-14-16-18-20-22-23-24-25-27-29-31-33-35-37-44(46)52-43(42-51-53(47,48)50-40-38-45(3,4)5)41-49-39-36-34-32-30-28-26-21-19-17-15-13-11-9-7-2/h14,16,20,22,24-25,29,31,43H,6-13,15,17-19,21,23,26-28,30,32-42H2,1-5H3/p+1/b16-14-,22-20-,25-24-,31-29-/t43-/m1/s1
InChI Key DUUSFCFZBREELS-WWBBCYQPSA-O
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C44H83NO7P+
Molecular Weight 769.10 g/mol
Exact Mass 768.59071598 g/mol
Topological Polar Surface Area (TPSA) 91.30 Ų
XlogP 13.10
Atomic LogP (AlogP) 12.38
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 39

Synonyms

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IDI1_034031
SR-01000947050
SR-01000947050-1

2D Structure

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2D Structure of (O-(1-O-Hexadecyl-2-O-((5Z,8Z,11Z,14Z)-1-oxo-5,8,11,14-icosatetrenyl)-L-glycero-3-phospho)choline)anion

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.9450 94.50%
Caco-2 - 0.8352 83.52%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.8000 80.00%
Subcellular localzation Plasma membrane 0.6306 63.06%
OATP2B1 inhibitior - 0.5681 56.81%
OATP1B1 inhibitior + 0.7781 77.81%
OATP1B3 inhibitior + 0.9365 93.65%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.9926 99.26%
P-glycoprotein inhibitior + 0.7419 74.19%
P-glycoprotein substrate - 0.6330 63.30%
CYP3A4 substrate + 0.6379 63.79%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8365 83.65%
CYP3A4 inhibition - 0.7849 78.49%
CYP2C9 inhibition - 0.8320 83.20%
CYP2C19 inhibition - 0.7545 75.45%
CYP2D6 inhibition - 0.8948 89.48%
CYP1A2 inhibition - 0.8388 83.88%
CYP2C8 inhibition + 0.6060 60.60%
CYP inhibitory promiscuity - 0.9665 96.65%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6500 65.00%
Carcinogenicity (trinary) Non-required 0.5510 55.10%
Eye corrosion - 0.9272 92.72%
Eye irritation - 0.8928 89.28%
Skin irritation - 0.7747 77.47%
Skin corrosion - 0.8988 89.88%
Ames mutagenesis - 0.6332 63.32%
Human Ether-a-go-go-Related Gene inhibition - 0.4417 44.17%
Micronuclear - 0.5800 58.00%
Hepatotoxicity - 0.7842 78.42%
skin sensitisation - 0.7984 79.84%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity - 0.7111 71.11%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.4336 43.36%
Estrogen receptor binding + 0.8005 80.05%
Androgen receptor binding - 0.5541 55.41%
Thyroid receptor binding - 0.5272 52.72%
Glucocorticoid receptor binding + 0.6472 64.72%
Aromatase binding + 0.5621 56.21%
PPAR gamma + 0.6336 63.36%
Honey bee toxicity - 0.8638 86.38%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.8124 81.24%
Fish aquatic toxicity + 0.8530 85.30%

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 98.63% 99.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 98.43% 97.29%
CHEMBL2581 P07339 Cathepsin D 97.18% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.42% 96.09%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 95.07% 92.86%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 95.04% 85.94%
CHEMBL239 Q07869 Peroxisome proliferator-activated receptor alpha 94.62% 90.75%
CHEMBL5255 O00206 Toll-like receptor 4 92.08% 92.50%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 90.66% 100.00%
CHEMBL3230 O95977 Sphingosine 1-phosphate receptor Edg-6 90.20% 94.01%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 90.08% 94.33%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 89.87% 95.17%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 89.34% 92.08%
CHEMBL1075162 Q13304 Uracil nucleotide/cysteinyl leukotriene receptor 89.24% 80.33%
CHEMBL221 P23219 Cyclooxygenase-1 88.96% 90.17%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 87.95% 93.03%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.39% 96.95%
CHEMBL3401 O75469 Pregnane X receptor 85.83% 94.73%
CHEMBL1907 P15144 Aminopeptidase N 84.79% 93.31%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.51% 93.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.18% 96.00%
CHEMBL1781 P11387 DNA topoisomerase I 83.78% 97.00%
CHEMBL230 P35354 Cyclooxygenase-2 83.62% 89.63%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 83.32% 91.71%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 81.72% 92.95%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.70% 100.00%

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 5313894
LOTUS LTS0231151
wikiData Q104989462