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	RDMYWZAKSDVRNT-ZZEZOPTASA-N
Smiles	CCOCCOC(=O)\C(=C(/NCc1onc(c1)c2ccccc2)\C(C)C)\C#N
InChI	InChI=1S/C21H25N3O4/c1-4-26-10-11-27-21(25)18(13-22)20(15(2)3)23-14-17-12-19(24-28-17)16-8-6-5-7-9-16/h5-9,12,15,23H,4,10-11,14H2,1-3H3/b20-18-

InChI Key

RDMYWZAKSDVRNT-ZZEZOPTASA-N

Smiles

CCOCCOC(=O)\C(=C(/NCc1onc(c1)c2ccccc2)\C(C)C)\C#N

InChI

InChI=1S/C21H25N3O4/c1-4-26-10-11-27-21(25)18(13-22)20(15(2)3)23-14-17-12-19(24-28-17)16-8-6-5-7-9-16/h5-9,12,15,23H,4,10-11,14H2,1-3H3/b20-18-

Property Name	Value
Molecular Formula	C21H25N3O4
Molecular Weight	383.44
AlogP	3.12
Hydrogen Bond Acceptor	6.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	11.0
Polar Surface Area	97.38
Molecular species	NEUTRAL
Aromatic Rings	2.0
Heavy Atoms	28.0

Property Name

Value

Molecular Formula

C21H25N3O4

Molecular Weight

383.44

AlogP

3.12

Hydrogen Bond Acceptor

6.0

Hydrogen Bond Donor

1.0

Number of Rotational Bond

11.0

Polar Surface Area

97.38

Molecular species

NEUTRAL

Aromatic Rings

2.0

Heavy Atoms

28.0

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Amaranthus retroflexus	-	-	-	-	17.4-100
Brassica napus	-	-	-	-	28.7-100
Digitaria sanguinalis	-	-	-	-	24.9-59.4
Echinochloa crus-galli	-	-	-	-	0-40

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Amaranthus retroflexus

17.4-100

Brassica napus

28.7-100

Digitaria sanguinalis

24.9-59.4

Echinochloa crus-galli

0-40

Resources	Reference
ChEMBL	CHEMBL2227890
PubChem	45277476

Resources

Reference

ChEMBL

CHEMBL2227890

PubChem

45277476

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, Volume 54, Issue D1, 6 January 2026, Pages D1397–D1404, https://doi.org/10.1093/nar/gkaf1251

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

Last update: Monday, 23^rd March 2026

2-ETHOXYETHYL 2-CYANO-4-METHYL-3-((3-PHENYLISOXAZOL-5-YL)METHYLAMINO)PENT-2-ENOATE

Structure

Physicochemical Descriptors

Pharmacology

Cross References