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	XFRURJLGPKRRIE-UHFFFAOYSA-N
Smiles	COC(=O)CCCN1N=C(OC1=O)c2cccc(c2)c3cc(F)ccc3OC
InChI	InChI=1S/C20H19FN2O5/c1-26-17-9-8-15(21)12-16(17)13-5-3-6-14(11-13)19-22-23(20(25)28-19)10-4-7-18(24)27-2/h3,5-6,8-9,11-12H,4,7,10H2,1-2H3

InChI Key

XFRURJLGPKRRIE-UHFFFAOYSA-N

Smiles

COC(=O)CCCN1N=C(OC1=O)c2cccc(c2)c3cc(F)ccc3OC

InChI

InChI=1S/C20H19FN2O5/c1-26-17-9-8-15(21)12-16(17)13-5-3-6-14(11-13)19-22-23(20(25)28-19)10-4-7-18(24)27-2/h3,5-6,8-9,11-12H,4,7,10H2,1-2H3

Property Name	Value
Molecular Formula	C20H19FN2O5
Molecular Weight	386.37
AlogP	3.71
Hydrogen Bond Acceptor	6.0
Number of Rotational Bond	8.0
Polar Surface Area	77.43
Molecular species	NEUTRAL
Aromatic Rings	2.0
Heavy Atoms	28.0

Property Name

Value

Molecular Formula

C20H19FN2O5

Molecular Weight

386.37

AlogP

3.71

Hydrogen Bond Acceptor

6.0

Number of Rotational Bond

8.0

Polar Surface Area

77.43

Molecular species

NEUTRAL

Aromatic Rings

2.0

Heavy Atoms

28.0

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Rattus norvegicus	-	-	-	-	31-87

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Rattus norvegicus

31-87

Resources	Reference
ChEMBL	CHEMBL2297646
PubChem	76313242

Resources

Reference

ChEMBL

CHEMBL2297646

PubChem

76313242

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

METHYL 4-[5-(5'-FLUORO-2'-METHOXYBIPHENYL-3-YL)-2-OXO-1,3,4-OXADIAZOL-3(2H)-YL]BUTANOATE

Structure

Physicochemical Descriptors

Pharmacology

Cross References