EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Salt-form
EPA CompTox	DTXSID5064415

Keyword(s):

Human Metabolites

Molecule Category

Salt-form

EPA CompTox

DTXSID5064415


InChI Key	VIIUOXGZDWUVCX-UHFFFAOYSA-K
Smiles	[Na+].[Na+].[Na+].O=S(=O)([O-])C1=CC(N=NC=2C=C(C(=CC2C)C3=CC(=C(N=NC4=CC=C(OS(=O)(=O)C5=CC=C(C=C5)C)C=C4)C=C3S(=O)(=O)[O-])C)S(=O)(=O)[O-])=C(O)C=6C=CC=CC61
InChI	InChI=1/C37H30N4O13S4.3Na/c1-21-8-14-26(15-9-21)58(52,53)54-25-12-10-24(11-13-25)38-39-31-18-35(56(46,47)48)29(16-22(31)2)30-17-23(3)32(19-36(30)57(49,50)51)40-41-33-20-34(55(43,44)45)27-6-4-5-7-28(27)37(33)42;;;/h4-20,42H,1-3H3,(H,43,44,45)(H,46,47,48)(H,49,50,51);;;/q;3*+1/p-3

InChI Key

VIIUOXGZDWUVCX-UHFFFAOYSA-K

Smiles

[Na+].[Na+].[Na+].O=S(=O)([O-])C1=CC(N=NC=2C=C(C(=CC2C)C3=CC(=C(N=NC4=CC=C(OS(=O)(=O)C5=CC=C(C=C5)C)C=C4)C=C3S(=O)(=O)[O-])C)S(=O)(=O)[O-])=C(O)C=6C=CC=CC61

InChI

InChI=1/C37H30N4O13S4.3Na/c1-21-8-14-26(15-9-21)58(52,53)54-25-12-10-24(11-13-25)38-39-31-18-35(56(46,47)48)29(16-22(31)2)30-17-23(3)32(19-36(30)57(49,50)51)40-41-33-20-34(55(43,44)45)27-6-4-5-7-28(27)37(33)42;;;/h4-20,42H,1-3H3,(H,43,44,45)(H,46,47,48)(H,49,50,51);;;/q;3*+1/p-3

Property Name	Value
Molecular Formula	C37H30N4O13S4
Molecular Weight	932.02
AlogP	-1.83
Hydrogen Bond Acceptor	16.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	11.0
Polar Surface Area	284.64
Heavy Atoms	61.0

Property Name

Value

Molecular Formula

C37H30N4O13S4

Molecular Weight

932.02

AlogP

-1.83

Hydrogen Bond Acceptor

16.0

Hydrogen Bond Donor

1.0

Number of Rotational Bond

11.0

Polar Surface Area

284.64

Heavy Atoms

61.0

Resources	Reference
CAS NUMBER	6598-62-5
NORMAN SUSDAT
PubChem	81072

Resources

Reference

CAS NUMBER

6598-62-5

NORMAN SUSDAT

PubChem

81072

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...

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Last update: Monday, 3 November 2025

TRISODIUM 4-[(1-HYDROXY-4-SULPHONATO-2-NAPHTHYL)AZO]-5,5'-DIMETHYL-4'-[[4-[[(4-METHYLPHENYL)SULPHONYL]OXY]PHENYL]AZO][1,1'-BIPHENYL]-2,2'-DISULPHONATE

Structure

Physicochemical Descriptors

Cross References