EcoDrugPlus


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

Keyword(s):

Human Metabolites

Molecule Category

Salt-form


InChI Key	RBDJQFKUZPMOFH-UHFFFAOYSA-I
Smiles	[Na+].[Na+].[Na+].[Na+].[Na+].O=S(=O)([O-])C=1C=CC=2C(C1)=CC(=C(N)C2N=NC3=CC=C(C=C3)C4=CC=C(N=NC=5C(N)=C(C=C6C=C(C=CC65)S(=O)(=O)[O-])S(=O)(=O)[O-])C(=C4)S(=O)(=O)[O-])S(=O)(=O)[O-]
InChI	InChI=1/C32H24N6O15S5.5Na/c33-29-27(57(48,49)50)14-18-11-21(54(39,40)41)6-8-23(18)31(29)37-35-20-4-1-16(2-5-20)17-3-10-25(26(13-17)56(45,46)47)36-38-32-24-9-7-22(55(42,43)44)12-19(24)15-28(30(32)34)58(51,52)53;;;;;/h1-15H,33-34H2,(H,39,40,41)(H,42,43,44)(H,45,46,47)(H,48,49,50)(H,51,52,53);;;;;/q;5*+1/p-5

InChI Key

RBDJQFKUZPMOFH-UHFFFAOYSA-I

Smiles

[Na+].[Na+].[Na+].[Na+].[Na+].O=S(=O)([O-])C=1C=CC=2C(C1)=CC(=C(N)C2N=NC3=CC=C(C=C3)C4=CC=C(N=NC=5C(N)=C(C=C6C=C(C=CC65)S(=O)(=O)[O-])S(=O)(=O)[O-])C(=C4)S(=O)(=O)[O-])S(=O)(=O)[O-]

InChI

InChI=1/C32H24N6O15S5.5Na/c33-29-27(57(48,49)50)14-18-11-21(54(39,40)41)6-8-23(18)31(29)37-35-20-4-1-16(2-5-20)17-3-10-25(26(13-17)56(45,46)47)36-38-32-24-9-7-22(55(42,43)44)12-19(24)15-28(30(32)34)58(51,52)53;;;;;/h1-15H,33-34H2,(H,39,40,41)(H,42,43,44)(H,45,46,47)(H,48,49,50)(H,51,52,53);;;;;/q;5*+1/p-5

Property Name	Value
Molecular Formula	C32H24N6O15S5
Molecular Weight	1001.9
AlogP	-10.8
Hydrogen Bond Acceptor	21.0
Hydrogen Bond Donor	2.0
Number of Rotational Bond	10.0
Polar Surface Area	387.48
Heavy Atoms	63.0

Property Name

Value

Molecular Formula

C32H24N6O15S5

Molecular Weight

1001.9

AlogP

-10.8

Hydrogen Bond Acceptor

21.0

Hydrogen Bond Donor

2.0

Number of Rotational Bond

10.0

Polar Surface Area

387.48

Heavy Atoms

63.0

Resources	Reference
CAS NUMBER	574-64-1
NORMAN SUSDAT
PubChem	73031

Resources

Reference

CAS NUMBER

574-64-1

NORMAN SUSDAT

PubChem

73031

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

PENTASODIUM 4,4'-[(3-SULPHONATO[1,1'-BIPHENYL]-4,4'-DIYL)BIS(AZO)]BIS[3-AMINONAPHTHALENE-2,7-DISULPHONATE]

Structure

Physicochemical Descriptors

Cross References