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	XVKBQTSYYKTSTH-UHFFFAOYSA-N
Smiles	CCN(CC)CCOC(=O)Cc1c(C)n(C(=O)c2ccc(Cl)cc2)c3ccc(OC)cc13
InChI	InChI=1S/C25H29ClN2O4/c1-5-27(6-2)13-14-32-24(29)16-21-17(3)28(23-12-11-20(31-4)15-22(21)23)25(30)18-7-9-19(26)10-8-18/h7-12,15H,5-6,13-14,16H2,1-4H3

InChI Key

XVKBQTSYYKTSTH-UHFFFAOYSA-N

Smiles

CCN(CC)CCOC(=O)Cc1c(C)n(C(=O)c2ccc(Cl)cc2)c3ccc(OC)cc13

InChI

InChI=1S/C25H29ClN2O4/c1-5-27(6-2)13-14-32-24(29)16-21-17(3)28(23-12-11-20(31-4)15-22(21)23)25(30)18-7-9-19(26)10-8-18/h7-12,15H,5-6,13-14,16H2,1-4H3

Property Name	Value
Molecular Formula	C25H29ClN2O4
Molecular Weight	456.96
AlogP	5.3
Hydrogen Bond Acceptor	5.0
Number of Rotational Bond	10.0
Polar Surface Area	60.77
Molecular species	BASE
Aromatic Rings	3.0
Heavy Atoms	32.0

Property Name

Value

Molecular Formula

C25H29ClN2O4

Molecular Weight

456.96

AlogP

5.3

Hydrogen Bond Acceptor

5.0

Number of Rotational Bond

10.0

Polar Surface Area

60.77

Molecular species

BASE

Aromatic Rings

3.0

Heavy Atoms

32.0

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Mus musculus	-	-	-	-	23.04
Rattus norvegicus	-	-	32359.37	-	34.56

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Mus musculus

23.04

Rattus norvegicus

32359.37

34.56

Resources	Reference
ChEMBL	CHEMBL2262719
PubChem	3061101
SureChEMBL	SCHEMBL3810907

Resources

Reference

ChEMBL

CHEMBL2262719

PubChem

3061101

SureChEMBL

SCHEMBL3810907

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-DIETHYLAMINOETHYL 1-(4-CHLOROBENZOYL)-5-METHOXY-2-METHYL-1H-INDOLE-3-ACETATE

Structure

Physicochemical Descriptors

Pharmacology

Cross References