PC(P-16:0/18:2(9Z,12Z))

Details

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Internal ID de8bcca8-6b44-4976-b68d-d916fe0349c1
Taxonomy Lipids and lipid-like molecules > Glycerophospholipids > Glycerophosphocholines > 1-(1Z-alkenyl),2-acyl-glycerophosphocholines
IUPAC Name [(2R)-3-[(Z)-hexadec-1-enoxy]-2-[(9Z,12Z)-octadeca-9,12-dienoyl]oxypropyl] 2-(trimethylazaniumyl)ethyl phosphate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C42H80NO7P/c1-6-8-10-12-14-16-18-20-22-23-25-27-29-31-33-35-42(44)50-41(40-49-51(45,46)48-38-36-43(3,4)5)39-47-37-34-32-30-28-26-24-21-19-17-15-13-11-9-7-2/h14,16,20,22,34,37,41H,6-13,15,17-19,21,23-33,35-36,38-40H2,1-5H3/b16-14-,22-20-,37-34-/t41-/m1/s1
InChI Key QLEHHUPUHJPURI-PWYDUFMYSA-N
Popularity 10 references in papers

Physical and Chemical Properties

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Molecular Formula C42H80NO7P
Molecular Weight 742.10 g/mol
Exact Mass 741.56724089 g/mol
Topological Polar Surface Area (TPSA) 94.10 Ų
XlogP 13.50
Atomic LogP (AlogP) 11.54
H-Bond Acceptor 7
H-Bond Donor 0
Rotatable Bonds 38

Synonyms

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PC(P-16:0/18:2)
1-(1Z-hexadecenyl)-2-(9Z,12Z-octadecadienoyl)-sn-glycero-3-phosphocholine
1-(1-enyl-palmitoyl)-2-linoleoyl-sn-glycero-3-phosphocholine
CHEBI:84557
LMGP01030008
phosphatidylcholine(P-16:0/18:2)
1-(1-enyl-palmitoyl)-2-linoleoyl-GPC
GPC(P-16:0/18:2)
phosphatidylcholine(P-16:0/18:2(9Z,12Z))
GPC(P-16:0/18:2(9Z,12Z))
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of PC(P-16:0/18:2(9Z,12Z))

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.8902 89.02%
Caco-2 - 0.8279 82.79%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Plasma membrane 0.7625 76.25%
OATP2B1 inhibitior - 0.7134 71.34%
OATP1B1 inhibitior + 0.8167 81.67%
OATP1B3 inhibitior + 0.9410 94.10%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9795 97.95%
P-glycoprotein inhibitior + 0.7294 72.94%
P-glycoprotein substrate + 0.5225 52.25%
CYP3A4 substrate + 0.6225 62.25%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8446 84.46%
CYP3A4 inhibition - 0.7487 74.87%
CYP2C9 inhibition - 0.8809 88.09%
CYP2C19 inhibition - 0.8148 81.48%
CYP2D6 inhibition - 0.8972 89.72%
CYP1A2 inhibition - 0.8590 85.90%
CYP2C8 inhibition + 0.5972 59.72%
CYP inhibitory promiscuity - 0.9548 95.48%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6100 61.00%
Carcinogenicity (trinary) Non-required 0.5439 54.39%
Eye corrosion - 0.9162 91.62%
Eye irritation - 0.8919 89.19%
Skin irritation - 0.7656 76.56%
Skin corrosion - 0.9334 93.34%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4628 46.28%
Micronuclear - 0.5400 54.00%
Hepatotoxicity - 0.7750 77.50%
skin sensitisation - 0.8111 81.11%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.7444 74.44%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity - 0.6560 65.60%
Acute Oral Toxicity (c) III 0.4787 47.87%
Estrogen receptor binding + 0.7886 78.86%
Androgen receptor binding - 0.5984 59.84%
Thyroid receptor binding - 0.5499 54.99%
Glucocorticoid receptor binding + 0.5865 58.65%
Aromatase binding - 0.5088 50.88%
PPAR gamma + 0.6021 60.21%
Honey bee toxicity - 0.8431 84.31%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.8224 82.24%
Fish aquatic toxicity + 0.8546 85.46%

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 98.88% 99.17%
CHEMBL2581 P07339 Cathepsin D 97.40% 98.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 96.75% 97.29%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.52% 96.09%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 94.75% 85.94%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 92.60% 92.86%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 92.33% 92.08%
CHEMBL3359 P21462 Formyl peptide receptor 1 88.07% 93.56%
CHEMBL5255 O00206 Toll-like receptor 4 86.04% 92.50%
CHEMBL1075162 Q13304 Uracil nucleotide/cysteinyl leukotriene receptor 85.82% 80.33%
CHEMBL1781 P11387 DNA topoisomerase I 85.68% 97.00%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 85.56% 94.33%
CHEMBL3401 O75469 Pregnane X receptor 85.46% 94.73%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 85.29% 91.81%
CHEMBL230 P35354 Cyclooxygenase-2 85.13% 89.63%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.54% 96.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.99% 96.00%
CHEMBL239 Q07869 Peroxisome proliferator-activated receptor alpha 83.61% 90.75%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 83.11% 100.00%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 82.78% 100.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.48% 100.00%
CHEMBL321 P14780 Matrix metalloproteinase 9 81.25% 92.12%

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.
There are no matching plants.

Cross-Links

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PubChem 24779386
LOTUS LTS0223319
wikiData Q27157861