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	DNFAPRJLWYGIBV-UHFFFAOYSA-N
Smiles	COc1ccc(CNCc2ccc(Oc3ccc(cc3)C(C)(C)C)cc2)cc1OC
InChI	InChI=1S/C26H31NO3/c1-26(2,3)21-9-13-23(14-10-21)30-22-11-6-19(7-12-22)17-27-18-20-8-15-24(28-4)25(16-20)29-5/h6-16,27H,17-18H2,1-5H3

InChI Key

DNFAPRJLWYGIBV-UHFFFAOYSA-N

Smiles

COc1ccc(CNCc2ccc(Oc3ccc(cc3)C(C)(C)C)cc2)cc1OC

InChI

InChI=1S/C26H31NO3/c1-26(2,3)21-9-13-23(14-10-21)30-22-11-6-19(7-12-22)17-27-18-20-8-15-24(28-4)25(16-20)29-5/h6-16,27H,17-18H2,1-5H3

Property Name	Value
Molecular Formula	C26H31NO3
Molecular Weight	405.53
AlogP	5.88
Hydrogen Bond Acceptor	4.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	9.0
Polar Surface Area	39.72
Molecular species	NEUTRAL
Aromatic Rings	3.0
Heavy Atoms	30.0

Property Name

Value

Molecular Formula

C26H31NO3

Molecular Weight

405.53

AlogP

5.88

Hydrogen Bond Acceptor

4.0

Hydrogen Bond Donor

1.0

Number of Rotational Bond

9.0

Polar Surface Area

39.72

Molecular species

NEUTRAL

Aromatic Rings

3.0

Heavy Atoms

30.0

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Bos taurus	-	120.23	-	-	-
Escherichia coli	-	2630.27	-	-	60
Solanum tuberosum	-	9772.37	-	-	-

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Bos taurus

120.23

Escherichia coli

2630.27

Solanum tuberosum

9772.37

Resources	Reference
ChEMBL	CHEMBL2268801
PubChem	76334014

Resources

Reference

ChEMBL

CHEMBL2268801

PubChem

76334014

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

N-(4-(4-TERT-BUTYLPHENOXY)BENZYL)-1-(3,4-DIMETHOXYPHENYL)METHANAMINE

Structure

Physicochemical Descriptors

Pharmacology

Cross References