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	UUCAJFDACITQCR-UHFFFAOYSA-N
Smiles	COc1cc2CC(Oc3ccc(cc3)C(C)N4CCCCC4)C(=O)c2cc1OC
InChI	InChI=1S/C24H29NO4/c1-16(25-11-5-4-6-12-25)17-7-9-19(10-8-17)29-23-14-18-13-21(27-2)22(28-3)15-20(18)24(23)26/h7-10,13,15-16,23H,4-6,11-12,14H2,1-3H3

InChI Key

UUCAJFDACITQCR-UHFFFAOYSA-N

Smiles

COc1cc2CC(Oc3ccc(cc3)C(C)N4CCCCC4)C(=O)c2cc1OC

InChI

InChI=1S/C24H29NO4/c1-16(25-11-5-4-6-12-25)17-7-9-19(10-8-17)29-23-14-18-13-21(27-2)22(28-3)15-20(18)24(23)26/h7-10,13,15-16,23H,4-6,11-12,14H2,1-3H3

Property Name	Value
Molecular Formula	C24H29NO4
Molecular Weight	395.49
AlogP	4.62
Hydrogen Bond Acceptor	5.0
Number of Rotational Bond	6.0
Polar Surface Area	48.0
Molecular species	BASE
Aromatic Rings	2.0
Heavy Atoms	29.0

Property Name

Value

Molecular Formula

C24H29NO4

Molecular Weight

395.49

AlogP

4.62

Hydrogen Bond Acceptor

5.0

Number of Rotational Bond

6.0

Polar Surface Area

48.0

Molecular species

BASE

Aromatic Rings

2.0

Heavy Atoms

29.0

Targets	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Enzyme Hydrolase	-	128.82-130	-	106.26	-

Targets

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Enzyme Hydrolase

128.82-130

106.26

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Homo sapiens	-	-	-	106.26	-
Rattus norvegicus	-	128.82-130	-	-	-

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Homo sapiens

106.26

Rattus norvegicus

128.82-130

Resources	Reference
ChEMBL	CHEMBL180413
PubChem	44390337
SureChEMBL	SCHEMBL8920169

Resources

Reference

ChEMBL

CHEMBL180413

PubChem

44390337

SureChEMBL

SCHEMBL8920169

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, 3 November 2025

5,6-DIMETHOXY-2-(4-(1-(PIPERIDIN-1-YL)ETHYL)PHENOXY)-2,3-DIHYDRO-1H-INDEN-1-ONE

Structure

Physicochemical Descriptors

Pharmacology

Cross References