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	UNZUMKCIIIFEJI-UHFFFAOYSA-N
Smiles	CCOC(=O)C(C)(C)ON1C(=O)c2ccccc2C1=O
InChI	InChI=1S/C14H15NO5/c1-4-19-13(18)14(2,3)20-15-11(16)9-7-5-6-8-10(9)12(15)17/h5-8H,4H2,1-3H3

InChI Key

UNZUMKCIIIFEJI-UHFFFAOYSA-N

Smiles

CCOC(=O)C(C)(C)ON1C(=O)c2ccccc2C1=O

InChI

InChI=1S/C14H15NO5/c1-4-19-13(18)14(2,3)20-15-11(16)9-7-5-6-8-10(9)12(15)17/h5-8H,4H2,1-3H3

Property Name	Value
Molecular Formula	C14H15NO5
Molecular Weight	277.27
AlogP	1.56
Hydrogen Bond Acceptor	5.0
Number of Rotational Bond	5.0
Polar Surface Area	72.91
Heavy Atoms	20.0

Property Name

Value

Molecular Formula

C14H15NO5

Molecular Weight

277.27

AlogP

1.56

Hydrogen Bond Acceptor

5.0

Number of Rotational Bond

5.0

Polar Surface Area

72.91

Heavy Atoms

20.0

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Lepidium sativum	-	-	-	-	0-60

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Lepidium sativum

0-60

Resources	Reference
ChEMBL	CHEMBL2272247
PubChem	3016209
SureChEMBL	SCHEMBL14587496

Resources

Reference

ChEMBL

CHEMBL2272247

PubChem

3016209

SureChEMBL

SCHEMBL14587496

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

ETHYL 2-(1,3-DIOXOISOINDOLIN-2-YLOXY)-2-METHYLPROPANOATE

Structure

Physicochemical Descriptors

Pharmacology

Cross References