EcoDrugPlus


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 ...

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 ...


InChI Key	NUNGHCGIWAQKCC-ZHACJKMWSA-N
Smiles	FC(F)(F)c1ccccc1\C=C\C(=O)c2ccccc2
InChI	InChI=1S/C16H11F3O/c17-16(18,19)14-9-5-4-6-12(14)10-11-15(20)13-7-2-1-3-8-13/h1-11H/b11-10+

InChI Key

NUNGHCGIWAQKCC-ZHACJKMWSA-N

Smiles

FC(F)(F)c1ccccc1\C=C\C(=O)c2ccccc2

InChI

InChI=1S/C16H11F3O/c17-16(18,19)14-9-5-4-6-12(14)10-11-15(20)13-7-2-1-3-8-13/h1-11H/b11-10+

Property Name	Value
Molecular Formula	C16H11F3O
Molecular Weight	276.25
AlogP	4.64
Hydrogen Bond Acceptor	1.0
Number of Rotational Bond	4.0
Polar Surface Area	17.07
Heavy Atoms	20.0

Property Name

Value

Molecular Formula

C16H11F3O

Molecular Weight

276.25

AlogP

4.64

Hydrogen Bond Acceptor

1.0

Number of Rotational Bond

4.0

Polar Surface Area

17.07

Heavy Atoms

20.0

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Homo sapiens	-	40340-42860	-	-	-

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Homo sapiens

40340-42860

Resources	Reference
ChEMBL	CHEMBL1801961
PubChem	15722486
SureChEMBL	SCHEMBL785437

Resources

Reference

ChEMBL

CHEMBL1801961

PubChem

15722486

SureChEMBL

SCHEMBL785437

EcoDrug+ was developed under the PREMIER 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 EcoDrug+ contains.

Elements of EcoDrug+ were developed under the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT Center for Science Ltd is thanked for providing computational resources. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).

Content of EcoDrug+ is provided without guarantee for correctness.

Cite Us:

Ashenafi Legehar, Siobhán Monaghan, Mael Briand, Akseli Niemelä, Leo Ghemtio, Ziaurrehman Tanoli, A Ross Brown, Charles R Tyler, Henri Xhaard, EcoDrug PLUS: an advanced database for drug target conservation analysis and environmental risk assessment, Nucleic Acids Research, 2025, gkaf1251 Read...

This work is licensed under Creative Commons Attribution-ShareAlike 4.0 International License

Last update: Monday, 3 November 2025

(E)-1-PHENYL-3-(2-(TRIFLUOROMETHYL)PHENYL)PROP-2-EN-1-ONE

Structure

Physicochemical Descriptors

Pharmacology

Cross References