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	AFNLNWQBAJKVAI-UHFFFAOYSA-N
Smiles	COc1ccc(CN(Cc2ccccc2)c3cccc(Cl)c3)cc1O
InChI	InChI=1S/C21H20ClNO2/c1-25-21-11-10-17(12-20(21)24)15-23(14-16-6-3-2-4-7-16)19-9-5-8-18(22)13-19/h2-13,24H,14-15H2,1H3

InChI Key

AFNLNWQBAJKVAI-UHFFFAOYSA-N

Smiles

COc1ccc(CN(Cc2ccccc2)c3cccc(Cl)c3)cc1O

InChI

InChI=1S/C21H20ClNO2/c1-25-21-11-10-17(12-20(21)24)15-23(14-16-6-3-2-4-7-16)19-9-5-8-18(22)13-19/h2-13,24H,14-15H2,1H3

Property Name	Value
Molecular Formula	C21H20ClNO2
Molecular Weight	353.84
AlogP	5.57
Hydrogen Bond Acceptor	3.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	6.0
Polar Surface Area	32.7
Molecular species	NEUTRAL
Aromatic Rings	3.0
Heavy Atoms	25.0

Property Name

Value

Molecular Formula

C21H20ClNO2

Molecular Weight

353.84

AlogP

5.57

Hydrogen Bond Acceptor

3.0

Hydrogen Bond Donor

1.0

Number of Rotational Bond

6.0

Polar Surface Area

32.7

Molecular species

NEUTRAL

Aromatic Rings

3.0

Heavy Atoms

25.0

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Leishmania donovani	39570	-	-	-	-
Plasmodium falciparum	13450	-	-	-	-
Plasmodium falciparum D6	13450	-	-	-	-

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Leishmania donovani

39570

Plasmodium falciparum

13450

Plasmodium falciparum D6

13450

Resources	Reference
ChEMBL	CHEMBL2262205
PubChem	76333894

Resources

Reference

ChEMBL

CHEMBL2262205

PubChem

76333894

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-((BENZYL(3-CHLOROPHENYL)AMINO)METHYL)-2-METHOXYPHENOL

Structure

Physicochemical Descriptors

Pharmacology

Cross References