Pipnoohine

Details

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Internal ID 6213fedc-7c5c-4e20-bc67-c10088f97993
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty amides > N-acyl amines
IUPAC Name (2E,4E,12Z)-N-(4-methylpentyl)octadeca-2,4,12-trienamide
SMILES (Canonical) CCCCCC=CCCCCCCC=CC=CC(=O)NCCCC(C)C
SMILES (Isomeric) CCCCC/C=C\CCCCCC/C=C/C=C/C(=O)NCCCC(C)C
InChI InChI=1S/C24H43NO/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-21-24(26)25-22-19-20-23(2)3/h8-9,16-18,21,23H,4-7,10-15,19-20,22H2,1-3H3,(H,25,26)/b9-8-,17-16+,21-18+
InChI Key OQYWYNYZGPSILS-KVFRDMGPSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C24H43NO
Molecular Weight 361.60 g/mol
Exact Mass 361.334464995 g/mol
Topological Polar Surface Area (TPSA) 29.10 Ų
XlogP 8.50
Atomic LogP (AlogP) 7.13
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 17

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Pipnoohine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9970 99.70%
Caco-2 - 0.5809 58.09%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Lysosomes 0.5486 54.86%
OATP2B1 inhibitior - 0.8583 85.83%
OATP1B1 inhibitior + 0.8727 87.27%
OATP1B3 inhibitior + 0.9377 93.77%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior + 0.8005 80.05%
P-glycoprotein inhibitior - 0.5083 50.83%
P-glycoprotein substrate + 0.5000 50.00%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.6146 61.46%
CYP2D6 substrate - 0.8935 89.35%
CYP3A4 inhibition - 0.9478 94.78%
CYP2C9 inhibition - 0.7584 75.84%
CYP2C19 inhibition - 0.8770 87.70%
CYP2D6 inhibition - 0.8984 89.84%
CYP1A2 inhibition - 0.7081 70.81%
CYP2C8 inhibition - 0.8930 89.30%
CYP inhibitory promiscuity - 0.8101 81.01%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6500 65.00%
Carcinogenicity (trinary) Non-required 0.6485 64.85%
Eye corrosion - 0.5796 57.96%
Eye irritation - 0.7896 78.96%
Skin irritation - 0.7419 74.19%
Skin corrosion - 0.8471 84.71%
Ames mutagenesis - 0.8637 86.37%
Human Ether-a-go-go-Related Gene inhibition + 0.7695 76.95%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.6415 64.15%
skin sensitisation - 0.8036 80.36%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.7608 76.08%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.7997 79.97%
Acute Oral Toxicity (c) III 0.6780 67.80%
Estrogen receptor binding - 0.5921 59.21%
Androgen receptor binding + 0.6011 60.11%
Thyroid receptor binding + 0.6606 66.06%
Glucocorticoid receptor binding - 0.6401 64.01%
Aromatase binding - 0.6005 60.05%
PPAR gamma + 0.5750 57.50%
Honey bee toxicity - 0.9749 97.49%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.8187 81.87%
Fish aquatic toxicity + 0.8499 84.99%

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
CHEMBL2581 P07339 Cathepsin D 98.43% 98.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 98.02% 97.29%
CHEMBL3060 Q9Y345 Glycine transporter 2 96.89% 99.17%
CHEMBL230 P35354 Cyclooxygenase-2 96.54% 89.63%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 93.97% 92.86%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 93.41% 96.47%
CHEMBL221 P23219 Cyclooxygenase-1 92.79% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.56% 96.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 92.43% 93.56%
CHEMBL3267 P48736 PI3-kinase p110-gamma subunit 91.67% 95.71%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.32% 92.08%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 89.57% 89.34%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 89.57% 100.00%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 88.82% 96.38%
CHEMBL4227 P25090 Lipoxin A4 receptor 87.69% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.34% 91.11%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 87.28% 91.81%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.57% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 84.89% 94.73%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 84.55% 94.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.29% 96.00%
CHEMBL2514 O95665 Neurotensin receptor 2 83.75% 100.00%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 82.11% 96.00%
CHEMBL1781 P11387 DNA topoisomerase I 81.88% 97.00%
CHEMBL299 P17252 Protein kinase C alpha 81.75% 98.03%
CHEMBL2664 P23526 Adenosylhomocysteinase 81.65% 86.67%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.60% 94.45%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 81.57% 85.94%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 81.08% 96.90%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 81.07% 98.75%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.31% 96.95%
CHEMBL2179 P04062 Beta-glucocerebrosidase 80.23% 85.31%

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.
Piper nigrum

Cross-Links

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PubChem 11222182
NPASS NPC107657
LOTUS LTS0218287
wikiData Q105197319