EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Free-form
EPA CompTox	DTXSID5067053

Keyword(s):

Human Metabolites

Molecule Category

Free-form

EPA CompTox

DTXSID5067053


InChI Key	JYAAXCNACZCCRH-UHFFFAOYSA-N
Smiles	COc1cc(N=Nc2c(Br)cc(cc2[N+](=O)[O-])[N+](=O)[O-])c(NC(=O)C)cc1N(Cc1ccccc1)Cc1ccccc1
InChI	InChI=1S/C29H25BrN6O6/c1-19(37)31-24-15-26(34(17-20-9-5-3-6-10-20)18-21-11-7-4-8-12-21)28(42-2)16-25(24)32-33-29-23(30)13-22(35(38)39)14-27(29)36(40)41/h3-16H,17-18H2,1-2H3,(H,31,37)/b33-32+

InChI Key

JYAAXCNACZCCRH-UHFFFAOYSA-N

Smiles

COc1cc(N=Nc2c(Br)cc(cc2[N+](=O)[O-])[N+](=O)[O-])c(NC(=O)C)cc1N(Cc1ccccc1)Cc1ccccc1

InChI

InChI=1S/C29H25BrN6O6/c1-19(37)31-24-15-26(34(17-20-9-5-3-6-10-20)18-21-11-7-4-8-12-21)28(42-2)16-25(24)32-33-29-23(30)13-22(35(38)39)14-27(29)36(40)41/h3-16H,17-18H2,1-2H3,(H,31,37)/b33-32+

Property Name	Value
Molecular Formula	C29H25Br1N6O6
Molecular Weight	632.1
AlogP	8.5
Hydrogen Bond Acceptor	9.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	11.0
Polar Surface Area	156.06
Heavy Atoms	42.0

Property Name

Value

Molecular Formula

C29H25Br1N6O6

Molecular Weight

632.1

AlogP

8.5

Hydrogen Bond Acceptor

9.0

Hydrogen Bond Donor

1.0

Number of Rotational Bond

11.0

Polar Surface Area

156.06

Heavy Atoms

42.0

Resources	Reference
CAS NUMBER	25080-15-3
NORMAN SUSDAT
PubChem	90709
ChemSpider	81897.0

Resources

Reference

CAS NUMBER

25080-15-3

NORMAN SUSDAT

PubChem

90709

ChemSpider

81897.0

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

ACETAMIDE, N-[5-[BIS(PHENYLMETHYL)AMINO]-2-[(2-BROMO-4,6-DINITROPHENYL)AZO]-4-METHOXYPHENYL]-

Structure

Physicochemical Descriptors

Cross References