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	LARYSHBOMUVFBF-UHFFFAOYSA-N
Smiles	COc1ccc(CN(C)CCCCCCCOc2ccc3C(=O)c4ccccc4Oc3c2)cc1
InChI	InChI=1S/C29H33NO4/c1-30(21-22-12-14-23(32-2)15-13-22)18-8-4-3-5-9-19-33-24-16-17-26-28(20-24)34-27-11-7-6-10-25(27)29(26)31/h6-7,10-17,20H,3-5,8-9,18-19,21H2,1-2H3

InChI Key

LARYSHBOMUVFBF-UHFFFAOYSA-N

Smiles

COc1ccc(CN(C)CCCCCCCOc2ccc3C(=O)c4ccccc4Oc3c2)cc1

InChI

InChI=1S/C29H33NO4/c1-30(21-22-12-14-23(32-2)15-13-22)18-8-4-3-5-9-19-33-24-16-17-26-28(20-24)34-27-11-7-6-10-25(27)29(26)31/h6-7,10-17,20H,3-5,8-9,18-19,21H2,1-2H3

Property Name	Value
Molecular Formula	C29H33NO4
Molecular Weight	459.58
AlogP	6.66
Hydrogen Bond Acceptor	5.0
Number of Rotational Bond	12.0
Polar Surface Area	48.0
Molecular species	BASE
Aromatic Rings	3.0
Heavy Atoms	34.0

Property Name

Value

Molecular Formula

C29H33NO4

Molecular Weight

459.58

AlogP

6.66

Hydrogen Bond Acceptor

5.0

Number of Rotational Bond

12.0

Polar Surface Area

48.0

Molecular species

BASE

Aromatic Rings

3.0

Heavy Atoms

34.0

Targets	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Enzyme Hydrolase	-	360000	-	-	-

Targets

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Enzyme Hydrolase

360000

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Homo sapiens	-	360000	-	-	-

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Homo sapiens

360000

Resources	Reference
ChEMBL	CHEMBL225396
PubChem	44421986

Resources

Reference

ChEMBL

CHEMBL225396

PubChem

44421986

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

3-{7-[(4-METHOXYBENZYL)METHYLAMINO]HEPTYLOXY}XANTHEN-9-ONE

Structure

Physicochemical Descriptors

Pharmacology

Cross References