EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Free-form
EPA CompTox	DTXSID8066892

Keyword(s):

Human Metabolites

Molecule Category

Free-form

EPA CompTox

DTXSID8066892


InChI Key	CVESYTJURSOGNA-UHFFFAOYSA-N
Smiles	COC(=O)OCCN(CCOC(=O)OC)c1cc(NC(=O)C)c(cc1OC)N=Nc1c(Br)cc(cc1[N+](=O)[O-])[N+](=O)[O-]
InChI	InChI=1S/C23H25BrN6O12/c1-13(31)25-16-11-18(28(5-7-41-22(32)39-3)6-8-42-23(33)40-4)20(38-2)12-17(16)26-27-21-15(24)9-14(29(34)35)10-19(21)30(36)37/h9-12H,5-8H2,1-4H3,(H,25,31)/b27-26+

InChI Key

CVESYTJURSOGNA-UHFFFAOYSA-N

Smiles

COC(=O)OCCN(CCOC(=O)OC)c1cc(NC(=O)C)c(cc1OC)N=Nc1c(Br)cc(cc1[N+](=O)[O-])[N+](=O)[O-]

InChI

InChI=1S/C23H25BrN6O12/c1-13(31)25-16-11-18(28(5-7-41-22(32)39-3)6-8-42-23(33)40-4)20(38-2)12-17(16)26-27-21-15(24)9-14(29(34)35)10-19(21)30(36)37/h9-12H,5-8H2,1-4H3,(H,25,31)/b27-26+

Property Name	Value
Molecular Formula	C23H25Br1N6O12
Molecular Weight	656.07
AlogP	5.67
Hydrogen Bond Acceptor	15.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	13.0
Polar Surface Area	227.12
Heavy Atoms	42.0

Property Name

Value

Molecular Formula

C23H25Br1N6O12

Molecular Weight

656.07

AlogP

5.67

Hydrogen Bond Acceptor

15.0

Hydrogen Bond Donor

1.0

Number of Rotational Bond

13.0

Polar Surface Area

227.12

Heavy Atoms

42.0

Resources	Reference
CAS NUMBER	23422-33-5
NORMAN SUSDAT
PubChem	90096
ChemSpider	81335.0

Resources

Reference

CAS NUMBER

23422-33-5

NORMAN SUSDAT

PubChem

90096

ChemSpider

81335.0

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, 2025, gkaf1251 Read...

This work is licensed under Creative Commons Attribution-ShareAlike 4.0 International License

Last update: Monday, 3 November 2025

2,4,10-TRIOXA-7-AZAUNDECAN-11-OIC ACID, 7-[5-(ACETYLAMINO)-4-[(2-BROMO-4,6-DINITROPHENYL)AZO]-2-METHOXYPHENYL]-3-OXO-, METHYL ESTER

Structure

Physicochemical Descriptors

Cross References