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	JMYNPQVCVQVODQ-UPHRSURJSA-N
Smiles	Clc1ccc(\C=C/c2cc(Cl)cc(Cl)c2)cc1
InChI	InChI=1S/C14H9Cl3/c15-12-5-3-10(4-6-12)1-2-11-7-13(16)9-14(17)8-11/h1-9H/b2-1-

InChI Key

JMYNPQVCVQVODQ-UPHRSURJSA-N

Smiles

Clc1ccc(\C=C/c2cc(Cl)cc(Cl)c2)cc1

InChI

InChI=1S/C14H9Cl3/c15-12-5-3-10(4-6-12)1-2-11-7-13(16)9-14(17)8-11/h1-9H/b2-1-

Property Name	Value
Molecular Formula	C14H9Cl3
Molecular Weight	283.58
AlogP	5.81
Number of Rotational Bond	2.0
Heavy Atoms	17.0

Property Name

Value

Molecular Formula

C14H9Cl3

Molecular Weight

283.58

AlogP

5.81

Number of Rotational Bond

2.0

Heavy Atoms

17.0

Targets	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Transcription factor	-	-	-	12-13001695780.33	-

Targets

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Transcription factor

12-13001695780.33

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Homo sapiens	-	-	-	12-13001695780.33	-

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Homo sapiens

12-13001695780.33

Resources	Reference
ChEMBL	CHEMBL361413
PubChem	11266077
SureChEMBL	SCHEMBL6460048

Resources

Reference

ChEMBL

CHEMBL361413

PubChem

11266077

SureChEMBL

SCHEMBL6460048

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

(Z)-1,3-DICHLORO-5-(4-CHLOROSTYRYL)BENZENE

Structure

Physicochemical Descriptors

Pharmacology

Cross References