EcoDrugPlus


Molecule Category	Free-form
UNII	WJ3768O35Z
EPA CompTox	DTXSID5058307
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

UNII

EPA CompTox

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	USSIUIGPBLPCDF-JMIUGGIZSA-N
Smiles	CO\N=C(\C)/c1cccc(Oc2nc(OC)cc(OC)n2)c1C(=O)OC
InChI	InChI=1S/C17H19N3O6/c1-10(20-25-5)11-7-6-8-12(15(11)16(21)24-4)26-17-18-13(22-2)9-14(19-17)23-3/h6-9H,1-5H3/b20-10-

InChI Key

USSIUIGPBLPCDF-JMIUGGIZSA-N

Smiles

CO\N=C(\C)/c1cccc(Oc2nc(OC)cc(OC)n2)c1C(=O)OC

InChI

InChI=1S/C17H19N3O6/c1-10(20-25-5)11-7-6-8-12(15(11)16(21)24-4)26-17-18-13(22-2)9-14(19-17)23-3/h6-9H,1-5H3/b20-10-

Property Name	Value
Molecular Formula	C17H19N3O6
Molecular Weight	361.35
AlogP	2.88
Hydrogen Bond Acceptor	9.0
Number of Rotational Bond	8.0
Polar Surface Area	101.36
Molecular species	NEUTRAL
Aromatic Rings	2.0
Heavy Atoms	26.0

Property Name

Value

Molecular Formula

C17H19N3O6

Molecular Weight

361.35

AlogP

2.88

Hydrogen Bond Acceptor

9.0

Number of Rotational Bond

8.0

Polar Surface Area

101.36

Molecular species

NEUTRAL

Aromatic Rings

2.0

Heavy Atoms

26.0

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Arabidopsis thaliana	-	-	-	49000	-

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Arabidopsis thaliana

49000

Resources	Reference
CAS NUMBER	147411-69-6
ChEMBL	CHEMBL2253237
FDA SRS	WJ3768O35Z
PubChem	6451138
SureChEMBL	SCHEMBL4451500

Resources

Reference

CAS NUMBER

ChEMBL

FDA SRS

PubChem

SureChEMBL

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

PYRIMINOBAC-METHYL

Structure

Physicochemical Descriptors

Pharmacology

Cross References