EcoDrugPlus


Synonyms	2,5-Bis(4-Fluorobenzylidene)Cyclopentanone
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 ...

Synonyms

2,5-Bis(4-Fluorobenzylidene)Cyclopentanone

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	CKZMWJORQGFJMR-JOBJLJCHSA-N
Smiles	Fc1ccc(\C=C\2/CC\C(=C/c3ccc(F)cc3)\C2=O)cc1
InChI	InChI=1S/C19H14F2O/c20-17-7-1-13(2-8-17)11-15-5-6-16(19(15)22)12-14-3-9-18(21)10-4-14/h1-4,7-12H,5-6H2/b15-11+,16-12+

InChI Key

CKZMWJORQGFJMR-JOBJLJCHSA-N

Smiles

Fc1ccc(\C=C\2/CC\C(=C/c3ccc(F)cc3)\C2=O)cc1

InChI

InChI=1S/C19H14F2O/c20-17-7-1-13(2-8-17)11-15-5-6-16(19(15)22)12-14-3-9-18(21)10-4-14/h1-4,7-12H,5-6H2/b15-11+,16-12+

Property Name	Value
Molecular Formula	C19H14F2O
Molecular Weight	296.31
AlogP	5.09
Hydrogen Bond Acceptor	1.0
Number of Rotational Bond	2.0
Polar Surface Area	17.07
Heavy Atoms	22.0

Property Name

Value

Molecular Formula

C19H14F2O

Molecular Weight

296.31

AlogP

5.09

Hydrogen Bond Acceptor

1.0

Number of Rotational Bond

2.0

Polar Surface Area

17.07

Heavy Atoms

22.0

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Buffalopox virus	-	-	-	-	73.69
Camelpox virus	-	-	-	-	54.29
Homo sapiens	-	39000-48000	-	-	-
Mus musculus	-	-	-	-	70

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Buffalopox virus

73.69

Camelpox virus

54.29

Homo sapiens

39000-48000

Mus musculus

Resources	Reference
ChEMBL	CHEMBL476846
PubChem	1551387
ZINC	ZINC04482199

Resources

Reference

ChEMBL

CHEMBL476846

PubChem

1551387

ZINC

ZINC04482199

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...

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Last update: Monday, 3 November 2025

(2E,5E)-2,5-BIS(4-FLUOROBENZYLIDENE)CYCLOPENTANONE

Structure

Physicochemical Descriptors

Pharmacology

Cross References