4-(4-TRIFLUOROMETHYL)PHENOXY-N-METHYL-PIPERIDINE


Molecule Category	Free-form
Source	Gaulton A, Kale N, van Westen GJ, Bellis LJ, Bento AP, Davies M, Hersey A, Papadatos G, Forster M, Wege P, Overington JP. A large-scale crop protection bioassay data set. Sci Data. 2015 Jul 7;2:150032. Read more ...


Active Pharmaceutical Ingredients Bioactive chemicals	Exact Similarity SubStructure	Threshold (%) >= 70

Structure


InChI Key	LYQFNMXUTCIRCY-UHFFFAOYSA-N
Smiles	CN1CCC(CC1)Oc2ccc(cc2)C(F)(F)F
InChI	InChI=1S/C13H16F3NO/c1-17-8-6-12(7-9-17)18-11-4-2-10(3-5-11)13(14,15)16/h2-5,12H,6-9H2,1H3

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C13H16F3NO
Molecular Weight	259.27
AlogP	2.87
Hydrogen Bond Acceptor	2.0
Hydrogen Bond Donor	0.0
Number of Rotational Bond	3.0
Polar Surface Area	12.47
Molecular species	NEUTRAL
Aromatic Rings	1.0
Heavy Atoms	18.0

Assay Description	Organism	Bioactivity
Anorexigenic activity in Mus musculus albino (mouse) assessed as anorexia at 75 umol/kg, ip relative to fluoxetine	Mus musculus	28.92 %
Anorexigenic activity in Mus musculus albino (mouse) assessed as anorexia at 75 umol/kg, ip	Mus musculus	23.6 %
Antidepressant activity in Mus musculus albino (mouse) assessed as reversal of reserpine-induced ptosis, sedation and crouching at 75 umol/kg, ip	Mus musculus	None
Toxicity in Mus musculus albino (mouse) assessed as effect on gross behavior activity at 75 umol/kg, ip	Mus musculus	None

Cross References

Resources	Reference
ChEMBL	CHEMBL2262190
PubChem	18722989
SureChEMBL	SCHEMBL5536145

CONTENTS


PREMIER has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 875508. The JU receives support from the EU’s Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations (EFPIA). The views reflect only the authors’ perspective and the JU is not responsible for any use that may be made of the information this manuscript contains. Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).

PREMIER has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 875508. The JU receives support from the EU’s Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations (EFPIA). The views reflect only the authors’ perspective and the JU is not responsible for any use that may be made of the information this manuscript contains.

Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).