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	JOJHPMLIMNADIK-UHFFFAOYSA-N
Smiles	CCOC(=O)CSc1nc2cc(N3N=C(C)N(C(F)F)C3=O)c(Cl)cc2s1
InChI	InChI=1S/C15H13ClF2N4O3S2/c1-3-25-12(23)6-26-14-19-9-5-10(8(16)4-11(9)27-14)22-15(24)21(13(17)18)7(2)20-22/h4-5,13H,3,6H2,1-2H3

InChI Key

JOJHPMLIMNADIK-UHFFFAOYSA-N

Smiles

CCOC(=O)CSc1nc2cc(N3N=C(C)N(C(F)F)C3=O)c(Cl)cc2s1

InChI

InChI=1S/C15H13ClF2N4O3S2/c1-3-25-12(23)6-26-14-19-9-5-10(8(16)4-11(9)27-14)22-15(24)21(13(17)18)7(2)20-22/h4-5,13H,3,6H2,1-2H3

Property Name	Value
Molecular Formula	C15H13ClF2N4O3S2
Molecular Weight	434.87
AlogP	3.91
Hydrogen Bond Acceptor	6.0
Number of Rotational Bond	7.0
Polar Surface Area	128.63
Molecular species	NEUTRAL
Aromatic Rings	2.0
Heavy Atoms	27.0

Property Name

Value

Molecular Formula

C15H13ClF2N4O3S2

Molecular Weight

434.87

AlogP

3.91

Hydrogen Bond Acceptor

6.0

Number of Rotational Bond

7.0

Polar Surface Area

128.63

Molecular species

NEUTRAL

Aromatic Rings

2.0

Heavy Atoms

27.0

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Nicotiana tabacum	-	-	-	1370	-

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Nicotiana tabacum

1370

Resources	Reference
ChEMBL	CHEMBL2286228
PubChem	57731182
SureChEMBL	SCHEMBL13483225

Resources

Reference

ChEMBL

CHEMBL2286228

PubChem

57731182

SureChEMBL

SCHEMBL13483225

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

ETHYL 1-{6-CHLORO-5-[4-DIFLUOROMETHYL-3-METHYL-5-OXO-4,5-DIHYDRO-1,2,4-TRIAZOL-1-YL]BENZOTHIAZOL-2-YLTHIO}ACETATE

Structure

Physicochemical Descriptors

Pharmacology

Cross References