EcoDrugPlus


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

Keyword(s):

Human Metabolites

Molecule Category

Salt-form


InChI Key	PCHTYMJTDHYWBP-HSEIHEFHSA-M
Smiles	[H+].[Na+].O=S(=O)([O-])C1=C(N=C2C=CC(C=C2)=C(C3=CC=C(C=C3)NC=4C=CC=5C=CC=CC5C4S(=O)(=O)[O-])C6=CC=C(N)C(=C6)C)C=CC=7C=CC=CC71
InChI	InChI=1/C40H31N3O6S2.Na.H2/c1-25-24-30(14-21-35(25)41)38(28-10-17-31(18-11-28)42-36-22-15-26-6-2-4-8-33(26)39(36)50(44,45)46)29-12-19-32(20-13-29)43-37-23-16-27-7-3-5-9-34(27)40(37)51(47,48)49;;/h2-24,42H,41H2,1H3,(H,44,45,46)(H,47,48,49);;1H/q;2*+1/p-2

InChI Key

PCHTYMJTDHYWBP-HSEIHEFHSA-M

Smiles

[H+].[Na+].O=S(=O)([O-])C1=C(N=C2C=CC(C=C2)=C(C3=CC=C(C=C3)NC=4C=CC=5C=CC=CC5C4S(=O)(=O)[O-])C6=CC=C(N)C(=C6)C)C=CC=7C=CC=CC71

InChI

InChI=1/C40H31N3O6S2.Na.H2/c1-25-24-30(14-21-35(25)41)38(28-10-17-31(18-11-28)42-36-22-15-26-6-2-4-8-33(26)39(36)50(44,45)46)29-12-19-32(20-13-29)43-37-23-16-27-7-3-5-9-34(27)40(37)51(47,48)49;;/h2-24,42H,41H2,1H3,(H,44,45,46)(H,47,48,49);;1H/q;2*+1/p-2

Property Name	Value
Molecular Formula	C40H31N3O6S2
Molecular Weight	736.16
AlogP	5.39
Hydrogen Bond Acceptor	9.0
Hydrogen Bond Donor	2.0
Number of Rotational Bond	7.0
Polar Surface Area	164.81
Heavy Atoms	52.0

Property Name

Value

Molecular Formula

C40H31N3O6S2

Molecular Weight

736.16

AlogP

5.39

Hydrogen Bond Acceptor

9.0

Hydrogen Bond Donor

2.0

Number of Rotational Bond

7.0

Polar Surface Area

164.81

Heavy Atoms

52.0

Resources	Reference
CAS NUMBER	1324-86-3
NORMAN SUSDAT
PubChem	164820

Resources

Reference

CAS NUMBER

1324-86-3

NORMAN SUSDAT

PubChem

164820

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

SODIUM HYDROGEN 2-[[4-[(4-AMINO-M-TOLYL)[4-[(SULPHONATO-2-NAPHTHYL)AMINO]PHENYL]METHYLENE]-2,5-CYCLOHEXADIEN-1-YLIDENE]AMINO]NAPHTHALENE-1-SULPHONATE

Structure

Physicochemical Descriptors

Cross References