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	TXLUVNBOLSPGOX-UHFFFAOYSA-N
Smiles	CONC(=O)OC(c1ccccc1)c2cccc(c2)C(C)C(=O)NOC
InChI	InChI=1S/C19H22N2O5/c1-13(18(22)20-24-2)15-10-7-11-16(12-15)17(26-19(23)21-25-3)14-8-5-4-6-9-14/h4-13,17H,1-3H3,(H,20,22)(H,21,23)

InChI Key

TXLUVNBOLSPGOX-UHFFFAOYSA-N

Smiles

CONC(=O)OC(c1ccccc1)c2cccc(c2)C(C)C(=O)NOC

InChI

InChI=1S/C19H22N2O5/c1-13(18(22)20-24-2)15-10-7-11-16(12-15)17(26-19(23)21-25-3)14-8-5-4-6-9-14/h4-13,17H,1-3H3,(H,20,22)(H,21,23)

Property Name	Value
Molecular Formula	C19H22N2O5
Molecular Weight	358.39
AlogP	2.61
Hydrogen Bond Acceptor	5.0
Hydrogen Bond Donor	2.0
Number of Rotational Bond	8.0
Polar Surface Area	85.89
Heavy Atoms	26.0

Property Name

Value

Molecular Formula

C19H22N2O5

Molecular Weight

358.39

AlogP

2.61

Hydrogen Bond Acceptor

5.0

Hydrogen Bond Donor

2.0

Number of Rotational Bond

8.0

Polar Surface Area

85.89

Heavy Atoms

26.0

Targets	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Enzyme Oxidoreductase	-	-	-	-	26.9

Targets

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Enzyme Oxidoreductase

26.9

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Glycine max	-	-	-	-	26.9
Homo sapiens	-	422000	-	-	-
Mus musculus	-	10000-334000	-	-	-

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Glycine max

26.9

Homo sapiens

422000

Mus musculus

10000-334000

Resources	Reference
ChEMBL	CHEMBL1170347
PubChem	46837462

Resources

Reference

ChEMBL

CHEMBL1170347

PubChem

46837462

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...

This work is licensed under Creative Commons Attribution-ShareAlike 4.0 International License

Last update: Monday, 3 November 2025

(3-(1-(METHOXYCARBAMOIL)ETHYL)PHENYL)(PHENYL)METHYLMETHOXYCARBAMATE

Structure

Physicochemical Descriptors

Pharmacology

Cross References