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	CJZKUTNGRZKBRH-UHFFFAOYSA-N
Smiles	Cc1noc(n1)C2CN3CCC2CC3
InChI	InChI=1S/C10H15N3O/c1-7-11-10(14-12-7)9-6-13-4-2-8(9)3-5-13/h8-9H,2-6H2,1H3

InChI Key

CJZKUTNGRZKBRH-UHFFFAOYSA-N

Smiles

Cc1noc(n1)C2CN3CCC2CC3

InChI

InChI=1S/C10H15N3O/c1-7-11-10(14-12-7)9-6-13-4-2-8(9)3-5-13/h8-9H,2-6H2,1H3

Property Name	Value
Molecular Formula	C10H15N3O
Molecular Weight	193.25
AlogP	0.42
Hydrogen Bond Acceptor	3.0
Number of Rotational Bond	1.0
Polar Surface Area	42.16
Molecular species	BASE
Aromatic Rings	1.0
Heavy Atoms	14.0

Property Name

Value

Molecular Formula

C10H15N3O

Molecular Weight

193.25

AlogP

0.42

Hydrogen Bond Acceptor

3.0

Number of Rotational Bond

1.0

Polar Surface Area

42.16

Molecular species

BASE

Aromatic Rings

1.0

Heavy Atoms

14.0

Targets	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Membrane receptor Family A G protein-coupled receptor Small molecule receptor (family A GPCR) Monoamine receptor Acetylcholine receptor	-	-	-	1320-1330	-

Targets

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Membrane receptor Family A G protein-coupled receptor Small molecule receptor (family A GPCR) Monoamine receptor Acetylcholine receptor

1320-1330

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Drosophila melanogaster	-	-	-	1320-1330	-
Musca domestica	-	-	-	-	9-80

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Drosophila melanogaster

1320-1330

Musca domestica

9-80

Resources	Reference
ChEMBL	CHEMBL279356
PubChem	9794157
SureChEMBL	SCHEMBL661864

Resources

Reference

ChEMBL

CHEMBL279356

PubChem

9794157

SureChEMBL

SCHEMBL661864

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

1-METHYL-3-(3-METHYL-[1,2,4]OXADIAZOL-5-YL)-1-AZA-BICYCLO[2.2.2]OCTANE

Structure

Physicochemical Descriptors

Pharmacology

Cross References