cis-Parinaric acid

Details

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Internal ID 97c71631-ed3d-435f-aa2e-168caa0e1bb2
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Lineolic acids and derivatives
IUPAC Name (9Z,11E,13E,15Z)-octadeca-9,11,13,15-tetraenoic acid
SMILES (Canonical) CCC=CC=CC=CC=CCCCCCCCC(=O)O
SMILES (Isomeric) CC/C=C\C=C\C=C\C=C/CCCCCCCC(=O)O
InChI InChI=1S/C18H28O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h3-10H,2,11-17H2,1H3,(H,19,20)/b4-3-,6-5+,8-7+,10-9-
InChI Key IJTNSXPMYKJZPR-ZSCYQOFPSA-N
Popularity 230 references in papers

Physical and Chemical Properties

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Molecular Formula C18H28O2
Molecular Weight 276.40 g/mol
Exact Mass 276.208930132 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 5.90
Atomic LogP (AlogP) 5.44
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 12

Synonyms

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alpha-parinaric acid
593-38-4
9Z,11E,13E,15Z-octadecatetraenoic acid
(9Z,11E,13E,15Z)-octadeca-9,11,13,15-tetraenoic acid
KM4KXM284R
(9Z,11E,13E,15Z)-9,11,13,15-Octadecatetraenoic acid
C18:4n-3,5,7,9
cis-Parinaric acid [MI]
UNII-KM4KXM284R
alpha-Parinarinsaeure
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of cis-Parinaric acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9929 99.29%
Caco-2 + 0.5937 59.37%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Plasma membrane 0.5809 58.09%
OATP2B1 inhibitior - 0.8548 85.48%
OATP1B1 inhibitior + 0.8071 80.71%
OATP1B3 inhibitior - 0.2497 24.97%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.6536 65.36%
P-glycoprotein inhibitior - 0.8133 81.33%
P-glycoprotein substrate - 0.9508 95.08%
CYP3A4 substrate - 0.6492 64.92%
CYP2C9 substrate - 0.5827 58.27%
CYP2D6 substrate - 0.8834 88.34%
CYP3A4 inhibition - 0.9518 95.18%
CYP2C9 inhibition - 0.8463 84.63%
CYP2C19 inhibition - 0.9559 95.59%
CYP2D6 inhibition - 0.9619 96.19%
CYP1A2 inhibition + 0.6551 65.51%
CYP2C8 inhibition - 0.9335 93.35%
CYP inhibitory promiscuity - 0.9451 94.51%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6535 65.35%
Carcinogenicity (trinary) Non-required 0.6578 65.78%
Eye corrosion + 0.9561 95.61%
Eye irritation + 0.6729 67.29%
Skin irritation + 0.7684 76.84%
Skin corrosion - 0.5227 52.27%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4339 43.39%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation + 0.8241 82.41%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity - 0.7370 73.70%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.7484 74.84%
Acute Oral Toxicity (c) III 0.5396 53.96%
Estrogen receptor binding + 0.6883 68.83%
Androgen receptor binding - 0.7551 75.51%
Thyroid receptor binding + 0.5433 54.33%
Glucocorticoid receptor binding - 0.6398 63.98%
Aromatase binding + 0.5793 57.93%
PPAR gamma + 0.8280 82.80%
Honey bee toxicity - 0.9843 98.43%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.7871 78.71%

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 96.09% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.61% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.06% 98.95%
CHEMBL1781 P11387 DNA topoisomerase I 87.76% 97.00%
CHEMBL221 P23219 Cyclooxygenase-1 87.21% 90.17%
CHEMBL5285 Q99683 Mitogen-activated protein kinase kinase kinase 5 83.09% 92.26%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.69% 91.11%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.25% 96.95%

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.
Impatiens edgeworthii

Cross-Links

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PubChem 5460995
LOTUS LTS0145762
wikiData Q2823297