EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Salt-form
EPA CompTox	DTXSID80889759

Keyword(s):

Human Metabolites

Molecule Category

Salt-form

EPA CompTox

DTXSID80889759


InChI Key	RZPXQVBZMHRBNY-UHFFFAOYSA-L
Smiles	[Na+].[Na+].O=S(=O)([O-])C1=CC(O)=C2C(C=CC(N)=C2N=NC=3C=CC=CC3S(=O)(=O)OC4=CC=C(C=C4)C(C5=CC=C(OS(=O)(=O)C=6C=CC=CC6N=NC7=C(N)C=CC8=CC(=CC(O)=C87)S(=O)(=O)[O-])C=C5)(C)C)=C1
InChI	InChI=1/C47H38N6O14S4.2Na/c1-47(2,29-13-17-31(18-14-29)66-70(62,63)41-9-5-3-7-37(41)50-52-45-35(48)21-11-27-23-33(68(56,57)58)25-39(54)43(27)45)30-15-19-32(20-16-30)67-71(64,65)42-10-6-4-8-38(42)51-53-46-36(49)22-12-28-24-34(69(59,60)61)26-40(55)44(28)46;;/h3-26,54-55H,48-49H2,1-2H3,(H,56,57,58)(H,59,60,61);;/q;2*+1/p-2

InChI Key

RZPXQVBZMHRBNY-UHFFFAOYSA-L

Smiles

[Na+].[Na+].O=S(=O)([O-])C1=CC(O)=C2C(C=CC(N)=C2N=NC=3C=CC=CC3S(=O)(=O)OC4=CC=C(C=C4)C(C5=CC=C(OS(=O)(=O)C=6C=CC=CC6N=NC7=C(N)C=CC8=CC(=CC(O)=C87)S(=O)(=O)[O-])C=C5)(C)C)=C1

InChI

InChI=1/C47H38N6O14S4.2Na/c1-47(2,29-13-17-31(18-14-29)66-70(62,63)41-9-5-3-7-37(41)50-52-45-35(48)21-11-27-23-33(68(56,57)58)25-39(54)43(27)45)30-15-19-32(20-16-30)67-71(64,65)42-10-6-4-8-38(42)51-53-46-36(49)22-12-28-24-34(69(59,60)61)26-40(55)44(28)46;;/h3-26,54-55H,48-49H2,1-2H3,(H,56,57,58)(H,59,60,61);;/q;2*+1/p-2

Property Name	Value
Molecular Formula	C47H38N6O14S4
Molecular Weight	1082.1
AlogP	2.5
Hydrogen Bond Acceptor	18.0
Hydrogen Bond Donor	4.0
Number of Rotational Bond	14.0
Polar Surface Area	343.08
Heavy Atoms	73.0

Property Name

Value

Molecular Formula

C47H38N6O14S4

Molecular Weight

1082.1

AlogP

2.5

Hydrogen Bond Acceptor

18.0

Hydrogen Bond Donor

4.0

Number of Rotational Bond

14.0

Polar Surface Area

343.08

Heavy Atoms

73.0

Resources	Reference
CAS NUMBER	52333-30-9
NORMAN SUSDAT
PubChem	135801436

Resources

Reference

CAS NUMBER

52333-30-9

NORMAN SUSDAT

PubChem

135801436

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 5,5'-[(1-METHYLETHYLIDENE)BIS(4,1-PHENYLENEOXYSULPHONYL-2,1-PHENYLENEAZO)]BIS[6-AMINO-4-HYDROXYNAPHTHALENE-2-SULPHONATE]

Structure

Physicochemical Descriptors

Cross References