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	SLKDNQRYGCKYDO-VXPUYCOJSA-N
Smiles	CCOCCOC(=O)\C(=C(/NCc1ccc(OCc2cnc(Cl)s2)cc1)\C(C)C)\C#N
InChI	InChI=1S/C22H26ClN3O4S/c1-4-28-9-10-29-21(27)19(11-24)20(15(2)3)25-12-16-5-7-17(8-6-16)30-14-18-13-26-22(23)31-18/h5-8,13,15,25H,4,9-10,12,14H2,1-3H3/b20-19-

InChI Key

SLKDNQRYGCKYDO-VXPUYCOJSA-N

Smiles

CCOCCOC(=O)\C(=C(/NCc1ccc(OCc2cnc(Cl)s2)cc1)\C(C)C)\C#N

InChI

InChI=1S/C22H26ClN3O4S/c1-4-28-9-10-29-21(27)19(11-24)20(15(2)3)25-12-16-5-7-17(8-6-16)30-14-18-13-26-22(23)31-18/h5-8,13,15,25H,4,9-10,12,14H2,1-3H3/b20-19-

Property Name	Value
Molecular Formula	C22H26ClN3O4S
Molecular Weight	463.98
AlogP	3.61
Hydrogen Bond Acceptor	7.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	13.0
Polar Surface Area	121.71
Molecular species	NEUTRAL
Aromatic Rings	2.0
Heavy Atoms	31.0

Property Name

Value

Molecular Formula

C22H26ClN3O4S

Molecular Weight

463.98

AlogP

3.61

Hydrogen Bond Acceptor

7.0

Hydrogen Bond Donor

1.0

Number of Rotational Bond

13.0

Polar Surface Area

121.71

Molecular species

NEUTRAL

Aromatic Rings

2.0

Heavy Atoms

31.0

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Spinacia oleracea	-	-	-	-	72.5

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Spinacia oleracea

72.5

Resources	Reference
ChEMBL	CHEMBL2271416
PubChem	76319740

Resources

Reference

ChEMBL

CHEMBL2271416

PubChem

76319740

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

(Z)-2-ETHOXYETHYL 3-(4-((2-CHLOROTHIAZOL-5-YL)METHOXY)BENZYLAMINO)-2-CYANO-4-METHYLPENT-2-ENOATE

Structure

Physicochemical Descriptors

Pharmacology

Cross References