1-Pyrrolidin-1-yldeca-2,4-dien-1-one

Details

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Internal ID 167fa839-f2bc-47bc-b023-55f60df768d6
Taxonomy Organoheterocyclic compounds > Pyrrolidines > N-acylpyrrolidines
IUPAC Name 1-pyrrolidin-1-yldeca-2,4-dien-1-one
SMILES (Canonical) CCCCCC=CC=CC(=O)N1CCCC1
SMILES (Isomeric) CCCCCC=CC=CC(=O)N1CCCC1
InChI InChI=1S/C14H23NO/c1-2-3-4-5-6-7-8-11-14(16)15-12-9-10-13-15/h6-8,11H,2-5,9-10,12-13H2,1H3
InChI Key BFZBGTMIBOQWBA-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C14H23NO
Molecular Weight 221.34 g/mol
Exact Mass 221.177964357 g/mol
Topological Polar Surface Area (TPSA) 20.30 Ų
XlogP 3.70
Atomic LogP (AlogP) 3.30
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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FT-0674522

2D Structure

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2D Structure of 1-Pyrrolidin-1-yldeca-2,4-dien-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 + 0.9832 98.32%
Caco-2 + 0.9610 96.10%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Plasma membrane 0.4433 44.33%
OATP2B1 inhibitior - 0.8585 85.85%
OATP1B1 inhibitior + 0.8937 89.37%
OATP1B3 inhibitior + 0.9453 94.53%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6317 63.17%
BSEP inhibitior - 0.6977 69.77%
P-glycoprotein inhibitior - 0.9836 98.36%
P-glycoprotein substrate - 0.8067 80.67%
CYP3A4 substrate - 0.5780 57.80%
CYP2C9 substrate + 0.5844 58.44%
CYP2D6 substrate - 0.8890 88.90%
CYP3A4 inhibition - 0.9852 98.52%
CYP2C9 inhibition - 0.8030 80.30%
CYP2C19 inhibition - 0.5303 53.03%
CYP2D6 inhibition - 0.8571 85.71%
CYP1A2 inhibition - 0.5946 59.46%
CYP2C8 inhibition - 0.9376 93.76%
CYP inhibitory promiscuity - 0.8331 83.31%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.5241 52.41%
Eye corrosion - 0.6547 65.47%
Eye irritation + 0.8601 86.01%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.5231 52.31%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5157 51.57%
Micronuclear - 0.9000 90.00%
Hepatotoxicity + 0.6574 65.74%
skin sensitisation - 0.8857 88.57%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity - 0.6610 66.10%
Acute Oral Toxicity (c) III 0.6936 69.36%
Estrogen receptor binding - 0.6718 67.18%
Androgen receptor binding - 0.5696 56.96%
Thyroid receptor binding - 0.6867 68.67%
Glucocorticoid receptor binding + 0.5688 56.88%
Aromatase binding - 0.7468 74.68%
PPAR gamma + 0.6979 69.79%
Honey bee toxicity - 0.9905 99.05%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity + 0.6453 64.53%
Fish aquatic toxicity - 0.4883 48.83%

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 97.69% 89.63%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.50% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.45% 98.95%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 90.77% 91.81%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 89.96% 92.86%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.67% 99.17%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 85.59% 100.00%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 82.70% 94.33%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 82.13% 95.50%
CHEMBL3105 P09874 Poly [ADP-ribose] polymerase-1 82.08% 93.90%
CHEMBL1781 P11387 DNA topoisomerase I 81.20% 97.00%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 81.01% 90.24%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 80.52% 92.08%

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 longum
Piper nigrum
Piper sarmentosum
Piper sintenense

Cross-Links

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PubChem 157276
LOTUS LTS0131584
wikiData Q104935091