1-Pyrrolidin-1-yloctadec-2-en-1-one

Details

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Internal ID 7dfee5f7-59b0-44fa-a4fd-b007c3e03a7a
Taxonomy Organoheterocyclic compounds > Pyrrolidines > N-acylpyrrolidines
IUPAC Name 1-pyrrolidin-1-yloctadec-2-en-1-one
SMILES (Canonical) CCCCCCCCCCCCCCCC=CC(=O)N1CCCC1
SMILES (Isomeric) CCCCCCCCCCCCCCCC=CC(=O)N1CCCC1
InChI InChI=1S/C22H41NO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-19-22(24)23-20-17-18-21-23/h16,19H,2-15,17-18,20-21H2,1H3
InChI Key VVCSLKWVXOOONE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H41NO
Molecular Weight 335.60 g/mol
Exact Mass 335.318814931 g/mol
Topological Polar Surface Area (TPSA) 20.30 Ų
XlogP 8.50
Atomic LogP (AlogP) 6.65
H-Bond Acceptor 1
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-en-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9876 98.76%
Caco-2 + 0.6157 61.57%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Plasma membrane 0.4463 44.63%
OATP2B1 inhibitior - 0.8532 85.32%
OATP1B1 inhibitior + 0.9030 90.30%
OATP1B3 inhibitior + 0.9444 94.44%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior + 0.5963 59.63%
P-glycoprotein inhibitior - 0.7423 74.23%
P-glycoprotein substrate - 0.8484 84.84%
CYP3A4 substrate - 0.5865 58.65%
CYP2C9 substrate + 0.5844 58.44%
CYP2D6 substrate - 0.8890 88.90%
CYP3A4 inhibition - 0.9797 97.97%
CYP2C9 inhibition - 0.8174 81.74%
CYP2C19 inhibition + 0.5075 50.75%
CYP2D6 inhibition - 0.8237 82.37%
CYP1A2 inhibition - 0.6111 61.11%
CYP2C8 inhibition - 0.9446 94.46%
CYP inhibitory promiscuity - 0.8349 83.49%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.5335 53.35%
Eye corrosion - 0.6626 66.26%
Eye irritation + 0.8124 81.24%
Skin irritation + 0.4917 49.17%
Skin corrosion - 0.5199 51.99%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4569 45.69%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.6110 61.10%
skin sensitisation - 0.9060 90.60%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.7279 72.79%
Acute Oral Toxicity (c) III 0.6425 64.25%
Estrogen receptor binding + 0.5886 58.86%
Androgen receptor binding - 0.5485 54.85%
Thyroid receptor binding + 0.5591 55.91%
Glucocorticoid receptor binding - 0.7057 70.57%
Aromatase binding - 0.7795 77.95%
PPAR gamma + 0.6459 64.59%
Honey bee toxicity - 0.9926 99.26%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity + 0.8124 81.24%
Fish aquatic toxicity + 0.6933 69.33%

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 97.09% 89.63%
CHEMBL2581 P07339 Cathepsin D 96.43% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.56% 96.09%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 93.40% 92.86%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 92.89% 91.81%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.31% 99.17%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 87.97% 100.00%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 86.42% 92.08%
CHEMBL1781 P11387 DNA topoisomerase I 84.15% 97.00%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 84.07% 94.33%
CHEMBL3105 P09874 Poly [ADP-ribose] polymerase-1 83.55% 93.90%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 83.29% 95.50%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 82.47% 90.24%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 80.39% 97.50%

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 amalago
Piper nigrum

Cross-Links

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PubChem 162986913
LOTUS LTS0086752
wikiData Q105297592