EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Salt-form
EPA CompTox	DTXSID40889497

Keyword(s):

Human Metabolites

Molecule Category

Salt-form

EPA CompTox

DTXSID40889497


InChI Key	MOGBMBYPOADVPS-UHFFFAOYSA-L
Smiles	[Na+].[Na+].O=C(NC1=CC=CC(=C1)C(=O)NC=2C=CC=3C(C2)=CC(=C(N=NC4=CC=C(N=NC5=CC=C(C=C5)S(=O)(=O)[O-])C=C4)C3O)S(=O)(=O)[O-])C6=CC=C(N)C=C6
InChI	InChI=1/C36H27N7O9S2.2Na/c37-24-6-4-21(5-7-24)35(45)38-28-3-1-2-22(18-28)36(46)39-29-14-17-31-23(19-29)20-32(54(50,51)52)33(34(31)44)43-42-26-10-8-25(9-11-26)40-41-27-12-15-30(16-13-27)53(47,48)49;;/h1-20,44H,37H2,(H,38,45)(H,39,46)(H,47,48,49)(H,50,51,52);;/q;2*+1/p-2

InChI Key

MOGBMBYPOADVPS-UHFFFAOYSA-L

Smiles

[Na+].[Na+].O=C(NC1=CC=CC(=C1)C(=O)NC=2C=CC=3C(C2)=CC(=C(N=NC4=CC=C(N=NC5=CC=C(C=C5)S(=O)(=O)[O-])C=C4)C3O)S(=O)(=O)[O-])C6=CC=C(N)C=C6

InChI

InChI=1/C36H27N7O9S2.2Na/c37-24-6-4-21(5-7-24)35(45)38-28-3-1-2-22(18-28)36(46)39-29-14-17-31-23(19-29)20-32(54(50,51)52)33(34(31)44)43-42-26-10-8-25(9-11-26)40-41-27-12-15-30(16-13-27)53(47,48)49;;/h1-20,44H,37H2,(H,38,45)(H,39,46)(H,47,48,49)(H,50,51,52);;/q;2*+1/p-2

Property Name	Value
Molecular Formula	C36H27N7O9S2
Molecular Weight	809.1
AlogP	0.99
Hydrogen Bond Acceptor	13.0
Hydrogen Bond Donor	4.0
Number of Rotational Bond	10.0
Polar Surface Area	268.29
Heavy Atoms	56.0

Property Name

Value

Molecular Formula

C36H27N7O9S2

Molecular Weight

809.1

AlogP

0.99

Hydrogen Bond Acceptor

13.0

Hydrogen Bond Donor

4.0

Number of Rotational Bond

10.0

Polar Surface Area

268.29

Heavy Atoms

56.0

Resources	Reference
CAS NUMBER	5905-22-6
NORMAN SUSDAT
PubChem	72698

Resources

Reference

CAS NUMBER

5905-22-6

NORMAN SUSDAT

PubChem

72698

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

DISODIUM 7-[[3-[(4-AMINOBENZOYL)AMINO]BENZOYL]AMINO]-4-HYDROXY-3-[[4-[(4-SULPHONATOPHENYL)AZO]PHENYL]AZO]NAPHTHALENE-2-SULPHONATE

Structure

Physicochemical Descriptors

Cross References