PG(18:2(9Z,12Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z))

Details

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Internal ID c60ba62d-07eb-42ff-8cc8-f2412f6e5ea7
Taxonomy Lipids and lipid-like molecules > Glycerophospholipids > Glycerophosphoglycerols > Phosphatidylglycerols
IUPAC Name [(2R)-1-[[(2S)-2,3-dihydroxypropoxy]-hydroxyphosphoryl]oxy-3-[(9Z,12Z)-octadeca-9,12-dienoyl]oxypropan-2-yl] (4Z,7Z,10Z,13Z,16Z,19Z)-docosa-4,7,10,13,16,19-hexaenoate
SMILES (Canonical) CCCCCC=CCC=CCCCCCCCC(=O)OCC(COP(=O)(O)OCC(CO)O)OC(=O)CCC=CCC=CCC=CCC=CCC=CCC=CCC
SMILES (Isomeric) CCCCC/C=C\C/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)(O)OC[C@H](CO)O)OC(=O)CC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CC
InChI InChI=1S/C46H75O10P/c1-3-5-7-9-11-13-15-17-19-20-21-22-24-26-28-30-32-34-36-38-46(50)56-44(42-55-57(51,52)54-40-43(48)39-47)41-53-45(49)37-35-33-31-29-27-25-23-18-16-14-12-10-8-6-4-2/h5,7,11-14,17-19,21-23,26,28,32,34,43-44,47-48H,3-4,6,8-10,15-16,20,24-25,27,29-31,33,35-42H2,1-2H3,(H,51,52)/b7-5-,13-11-,14-12-,19-17-,22-21-,23-18-,28-26-,34-32-/t43-,44+/m0/s1
InChI Key GMXYXYLCBAOPHA-KNVYJNGISA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C46H75O10P
Molecular Weight 819.10 g/mol
Exact Mass 818.50978558 g/mol
Topological Polar Surface Area (TPSA) 149.00 Ų
XlogP 10.70
Atomic LogP (AlogP) 11.22
H-Bond Acceptor 9
H-Bond Donor 3
Rotatable Bonds 38

Synonyms

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PG(18:2/22:6)
1-(9Z,12Z-octadecadienoyl)-2-(4Z,7Z,10Z,13Z,16Z,19Z-docosahexaenoyl)-glycero-3-phospho-(1'-sn-glycerol)
CHEBI:89365
Phosphatidylglycerol(18:2/22:6)
LMGP04010045
GPG(18:2n6/22:6n3)
GPG(18:2w6/22:6w3)
PG(18:2n6/22:6n3)
PG(18:2w6/22:6w3)
Phosphatidylglycerol(18:2n6/22:6n3)
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of PG(18:2(9Z,12Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z))

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6740 67.40%
Caco-2 - 0.8528 85.28%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.7756 77.56%
OATP2B1 inhibitior - 0.7161 71.61%
OATP1B1 inhibitior + 0.7466 74.66%
OATP1B3 inhibitior + 0.9371 93.71%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.9865 98.65%
P-glycoprotein inhibitior + 0.7544 75.44%
P-glycoprotein substrate - 0.5596 55.96%
CYP3A4 substrate + 0.6320 63.20%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8624 86.24%
CYP3A4 inhibition - 0.6986 69.86%
CYP2C9 inhibition - 0.8471 84.71%
CYP2C19 inhibition - 0.8047 80.47%
CYP2D6 inhibition - 0.8931 89.31%
CYP1A2 inhibition - 0.8116 81.16%
CYP2C8 inhibition - 0.5832 58.32%
CYP inhibitory promiscuity - 0.9696 96.96%
UGT catelyzed - 0.9000 90.00%
Carcinogenicity (binary) - 0.6500 65.00%
Carcinogenicity (trinary) Non-required 0.6596 65.96%
Eye corrosion - 0.7748 77.48%
Eye irritation - 0.9038 90.38%
Skin irritation - 0.7600 76.00%
Skin corrosion - 0.6601 66.01%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7659 76.59%
Micronuclear - 0.7900 79.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.8176 81.76%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity - 0.8778 87.78%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.7082 70.82%
Acute Oral Toxicity (c) III 0.5593 55.93%
Estrogen receptor binding + 0.8241 82.41%
Androgen receptor binding - 0.6297 62.97%
Thyroid receptor binding - 0.5182 51.82%
Glucocorticoid receptor binding + 0.5856 58.56%
Aromatase binding - 0.5000 50.00%
PPAR gamma + 0.6477 64.77%
Honey bee toxicity - 0.7948 79.48%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.6426 64.26%
Fish aquatic toxicity + 0.9637 96.37%

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 98.92% 99.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 98.87% 97.29%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 97.17% 85.94%
CHEMBL2581 P07339 Cathepsin D 96.63% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.07% 96.09%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 95.61% 92.86%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 91.73% 95.17%
CHEMBL5255 O00206 Toll-like receptor 4 91.25% 92.50%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 90.47% 100.00%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 88.96% 92.08%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 88.40% 96.00%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 86.12% 91.81%
CHEMBL230 P35354 Cyclooxygenase-2 86.07% 89.63%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.95% 93.56%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 84.86% 94.33%
CHEMBL2885 P07451 Carbonic anhydrase III 84.37% 87.45%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.58% 96.95%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.27% 100.00%
CHEMBL1781 P11387 DNA topoisomerase I 82.19% 97.00%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 81.91% 100.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.80% 89.34%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.74% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 80.32% 94.73%

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.
Datura innoxia
Datura stramonium

Cross-Links

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PubChem 52926310
LOTUS LTS0103146
wikiData Q105260183