EcoDrugPlus


Molecule Category	Salt-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

Salt-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	OYUYXHKLPGIKKY-UHFFFAOYSA-N
Smiles	CC(CN1CCN(C)CC1)Oc2c(Br)cccc2Br.OC(=O)C(=O)O
InChI	InChI=1S/C14H20Br2N2O.C2H2O4/c1-11(10-18-8-6-17(2)7-9-18)19-14-12(15)4-3-5-13(14)16;3-1(4)2(5)6/h3-5,11H,6-10H2,1-2H3;(H,3,4)(H,5,6)

InChI Key

OYUYXHKLPGIKKY-UHFFFAOYSA-N

Smiles

CC(CN1CCN(C)CC1)Oc2c(Br)cccc2Br.OC(=O)C(=O)O

InChI

InChI=1S/C14H20Br2N2O.C2H2O4/c1-11(10-18-8-6-17(2)7-9-18)19-14-12(15)4-3-5-13(14)16;3-1(4)2(5)6/h3-5,11H,6-10H2,1-2H3;(H,3,4)(H,5,6)

Property Name	Value
Molecular Formula	C16H22Br2N2O5
Molecular Weight	482.16
AlogP	3.78
Hydrogen Bond Acceptor	3.0
Number of Rotational Bond	4.0
Polar Surface Area	15.71
Molecular species	NEUTRAL
Aromatic Rings	1.0
Heavy Atoms	19.0

Property Name

Value

Molecular Formula

C16H22Br2N2O5

Molecular Weight

482.16

AlogP

3.78

Hydrogen Bond Acceptor

3.0

Number of Rotational Bond

4.0

Polar Surface Area

15.71

Molecular species

NEUTRAL

Aromatic Rings

1.0

Heavy Atoms

19.0

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Mus musculus	-	-	-	-	12.5-100

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Mus musculus

12.5-100

Resources	Reference
ChEMBL	CHEMBL2261776
PubChem	53233587

Resources

Reference

ChEMBL

CHEMBL2261776

PubChem

53233587

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

(+/-)1-(2-(2,6-DIBROMOPHENOXY)PROPYL)-4-METHYLPIPERAZINE DIOXALATE

Structure

Physicochemical Descriptors

Pharmacology

Cross References