EcoDrugPlus


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

Keyword(s):

Human Metabolites

Molecule Category

Salt-form


InChI Key	FTLCGVVRFDRTGD-UHFFFAOYSA-H
Smiles	[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].O=S(=O)([O-])C=1C=CC=C2C3=NN(N=C3C=CC21)C4=CC=5C(=CC(N=NC=6C=C7C(C=C(C=C7S(=O)(=O)[O-])N8N=C9C=CC=%10C(=CC=CC%10S(=O)(=O)[O-])C9=N8)=C(C6)S(=O)(=O)[O-])=CC5S(=O)(=O)[O-])C(=C4)S(=O)(=O)[O-]
InChI	InChI=1/C40H24N8O18S6.6Na/c49-67(50,51)33-5-1-3-25-23(33)7-9-31-39(25)45-47(43-31)21-15-29-27(37(17-21)71(61,62)63)11-19(13-35(29)69(55,56)57)41-42-20-12-28-30(36(14-20)70(58,59)60)16-22(18-38(28)72(64,65)66)48-44-32-10-8-24-26(40(32)46-48)4-2-6-34(24)68(52,53)54;;;;;;/h1-18H,(H,49,50,51)(H,52,53,54)(H,55,56,57)(H,58,59,60)(H,61,62,63)(H,64,65,66);;;;;;/q;6*+1/p-6

InChI Key

FTLCGVVRFDRTGD-UHFFFAOYSA-H

Smiles

[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].O=S(=O)([O-])C=1C=CC=C2C3=NN(N=C3C=CC21)C4=CC=5C(=CC(N=NC=6C=C7C(C=C(C=C7S(=O)(=O)[O-])N8N=C9C=CC=%10C(=CC=CC%10S(=O)(=O)[O-])C9=N8)=C(C6)S(=O)(=O)[O-])=CC5S(=O)(=O)[O-])C(=C4)S(=O)(=O)[O-]

InChI

InChI=1/C40H24N8O18S6.6Na/c49-67(50,51)33-5-1-3-25-23(33)7-9-31-39(25)45-47(43-31)21-15-29-27(37(17-21)71(61,62)63)11-19(13-35(29)69(55,56)57)41-42-20-12-28-30(36(14-20)70(58,59)60)16-22(18-38(28)72(64,65)66)48-44-32-10-8-24-26(40(32)46-48)4-2-6-34(24)68(52,53)54;;;;;;/h1-18H,(H,49,50,51)(H,52,53,54)(H,55,56,57)(H,58,59,60)(H,61,62,63)(H,64,65,66);;;;;;/q;6*+1/p-6

Property Name	Value
Molecular Formula	C40H24N8O18S6
Molecular Weight	1227.84
AlogP	-14.37
Hydrogen Bond Acceptor	26.0
Number of Rotational Bond	10.0
Polar Surface Area	429.34
Heavy Atoms	78.0

Property Name

Value

Molecular Formula

C40H24N8O18S6

Molecular Weight

1227.84

AlogP

-14.37

Hydrogen Bond Acceptor

26.0

Number of Rotational Bond

10.0

Polar Surface Area

429.34

Heavy Atoms

78.0

Resources	Reference
CAS NUMBER	6508-68-5
NORMAN SUSDAT
PubChem	6455025

Resources

Reference

CAS NUMBER

6508-68-5

NORMAN SUSDAT

PubChem

6455025

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

HEXASODIUM 3,3'-AZOBIS[7-(6-SULPHONATO-2H-NAPHTHO[1,2-D]TRIAZOL-2-YL)NAPHTHALENE-1,5-DISULPHONATE]

Structure

Physicochemical Descriptors

Cross References