EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Salt-form
EPA CompTox	DTXSID3072878

Keyword(s):

Human Metabolites

Molecule Category

Salt-form

EPA CompTox

DTXSID3072878


InChI Key	IYSLRGNHTGJLSK-UHFFFAOYSA-J
Smiles	[Na+].[Na+].[Na+].[Na+].O=C(NC1=CC=C(C=2C=C(C(N=NC=3C=CC4=CC(=CC=C4C3S(=O)(=O)[O-])S(=O)(=O)CCOS(=O)(=O)[O-])=C(O)C12)S(=O)(=O)[O-])S(=O)(=O)[O-])C=5C=CC=CC5
InChI	InChI=1/C29H23N3O17S5.4Na/c33-27-25-20(23(51(37,38)39)11-10-21(25)30-29(34)16-4-2-1-3-5-16)15-24(52(40,41)42)26(27)32-31-22-9-6-17-14-18(7-8-19(17)28(22)53(43,44)45)50(35,36)13-12-49-54(46,47)48;;;;/h1-11,14-15,33H,12-13H2,(H,30,34)(H,37,38,39)(H,40,41,42)(H,43,44,45)(H,46,47,48);;;;/q;4*+1/p-4

InChI Key

IYSLRGNHTGJLSK-UHFFFAOYSA-J

Smiles

[Na+].[Na+].[Na+].[Na+].O=C(NC1=CC=C(C=2C=C(C(N=NC=3C=CC4=CC(=CC=C4C3S(=O)(=O)[O-])S(=O)(=O)CCOS(=O)(=O)[O-])=C(O)C12)S(=O)(=O)[O-])S(=O)(=O)[O-])C=5C=CC=CC5

InChI

InChI=1/C29H23N3O17S5.4Na/c33-27-25-20(23(51(37,38)39)11-10-21(25)30-29(34)16-4-2-1-3-5-16)15-24(52(40,41)42)26(27)32-31-22-9-6-17-14-18(7-8-19(17)28(22)53(43,44)45)50(35,36)13-12-49-54(46,47)48;;;;/h1-11,14-15,33H,12-13H2,(H,30,34)(H,37,38,39)(H,40,41,42)(H,43,44,45)(H,46,47,48);;;;/q;4*+1/p-4

Property Name	Value
Molecular Formula	C29H23N3O17S5
Molecular Weight	932.89
AlogP	-10.42
Hydrogen Bond Acceptor	18.0
Hydrogen Bond Donor	2.0
Number of Rotational Bond	12.0
Polar Surface Area	349.71
Heavy Atoms	58.0

Property Name

Value

Molecular Formula

C29H23N3O17S5

Molecular Weight

932.89

AlogP

-10.42

Hydrogen Bond Acceptor

18.0

Hydrogen Bond Donor

2.0

Number of Rotational Bond

12.0

Polar Surface Area

349.71

Heavy Atoms

58.0

Resources	Reference
CAS NUMBER	82199-13-1
NORMAN SUSDAT
PubChem	174267

Resources

Reference

CAS NUMBER

82199-13-1

NORMAN SUSDAT

PubChem

174267

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

TETRASODIUM 4-(BENZOYLAMINO)-5-HYDROXY-6-[[1-SULPHONATO-6-[[2-(SULPHONATOOXY)ETHYL]SULPHONYL]-2-NAPHTHYL]AZO]NAPHTHALENE-1,7-DISULPHONATE

Structure

Physicochemical Descriptors

Cross References