1-Pyrrolidin-1-yloctadec-2-ene-1,12-dione

Details

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Internal ID eb68a599-2c1c-4411-9933-746b065c505c
Taxonomy Organoheterocyclic compounds > Pyrrolidines > N-acylpyrrolidines
IUPAC Name 1-pyrrolidin-1-yloctadec-2-ene-1,12-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H39NO2/c1-2-3-4-11-16-21(24)17-12-9-7-5-6-8-10-13-18-22(25)23-19-14-15-20-23/h13,18H,2-12,14-17,19-20H2,1H3
InChI Key PKNHPNCVMGDUJC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H39NO2
Molecular Weight 349.50 g/mol
Exact Mass 349.298079487 g/mol
Topological Polar Surface Area (TPSA) 37.40 Ų
XlogP 6.10
Atomic LogP (AlogP) 5.83
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 15

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Pyrrolidin-1-yloctadec-2-ene-1,12-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9877 98.77%
Caco-2 + 0.5572 55.72%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Plasma membrane 0.4864 48.64%
OATP2B1 inhibitior - 0.8550 85.50%
OATP1B1 inhibitior + 0.8865 88.65%
OATP1B3 inhibitior + 0.9425 94.25%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior + 0.7632 76.32%
P-glycoprotein inhibitior - 0.6240 62.40%
P-glycoprotein substrate - 0.7636 76.36%
CYP3A4 substrate - 0.5471 54.71%
CYP2C9 substrate - 0.8052 80.52%
CYP2D6 substrate - 0.8860 88.60%
CYP3A4 inhibition - 0.9250 92.50%
CYP2C9 inhibition - 0.7599 75.99%
CYP2C19 inhibition + 0.6071 60.71%
CYP2D6 inhibition - 0.8977 89.77%
CYP1A2 inhibition - 0.6358 63.58%
CYP2C8 inhibition - 0.8930 89.30%
CYP inhibitory promiscuity - 0.8211 82.11%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.5481 54.81%
Eye corrosion - 0.9107 91.07%
Eye irritation + 0.6639 66.39%
Skin irritation - 0.6451 64.51%
Skin corrosion - 0.5992 59.92%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4877 48.77%
Micronuclear - 0.8300 83.00%
Hepatotoxicity + 0.6234 62.34%
skin sensitisation - 0.9169 91.69%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity - 0.7776 77.76%
Acute Oral Toxicity (c) III 0.6803 68.03%
Estrogen receptor binding + 0.5866 58.66%
Androgen receptor binding - 0.5931 59.31%
Thyroid receptor binding + 0.5371 53.71%
Glucocorticoid receptor binding - 0.5911 59.11%
Aromatase binding - 0.7624 76.24%
PPAR gamma + 0.6567 65.67%
Honey bee toxicity - 0.9829 98.29%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity + 0.8578 85.78%
Fish aquatic toxicity - 0.5532 55.32%

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
CHEMBL230 P35354 Cyclooxygenase-2 98.43% 89.63%
CHEMBL2581 P07339 Cathepsin D 96.74% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.09% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.01% 99.17%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 93.05% 91.81%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 90.84% 92.86%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 90.41% 92.08%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 87.70% 100.00%
CHEMBL1781 P11387 DNA topoisomerase I 86.31% 97.00%
CHEMBL3105 P09874 Poly [ADP-ribose] polymerase-1 84.23% 93.90%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 84.10% 95.50%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 83.77% 94.33%
CHEMBL4588 P22894 Matrix metalloproteinase 8 83.13% 94.66%
CHEMBL1744525 P43490 Nicotinamide phosphoribosyltransferase 82.55% 96.25%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 82.47% 90.24%
CHEMBL5255 O00206 Toll-like receptor 4 82.36% 92.50%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 81.39% 97.50%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 81.31% 95.17%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 80.04% 82.38%

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.
Achillea lycaonica

Cross-Links

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PubChem 163023630
LOTUS LTS0084823
wikiData Q105210513