EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Salt-form
EPA CompTox	DTXSID30889865

Keyword(s):

Human Metabolites

Molecule Category

Salt-form

EPA CompTox

DTXSID30889865


InChI Key	HOMNZOFYIUJVJO-MBCFVHIPSA-J
Smiles	[Na+].[Na+].[K+].[K+].O=S(=O)([O-])C1=CC=C(C=C1)NC=2N=C(N=C(N2)NCCO)NC3=CC=C(C=CC4=CC=C(C=C4S(=O)(=O)[O-])NC5=NC(=NC(=N5)NCCO)NC6=CC=C(C=C6)S(=O)(=O)[O-])C(=C3)S(=O)(=O)[O-]
InChI	InChI=1/C36H36N12O14S4.2K.2Na/c49-17-15-37-31-43-33(39-23-7-11-27(12-8-23)63(51,52)53)47-35(45-31)41-25-5-3-21(29(19-25)65(57,58)59)1-2-22-4-6-26(20-30(22)66(60,61)62)42-36-46-32(38-16-18-50)44-34(48-36)40-24-9-13-28(14-10-24)64(54,55)56;;;;/h1-14,19-20,49-50H,15-18H2,(H,51,52,53)(H,54,55,56)(H,57,58,59)(H,60,61,62)(H3,37,39,41,43,45,47)(H3,38,40,42,44,46,48);;;;/q;4*+1/p-4

InChI Key

HOMNZOFYIUJVJO-MBCFVHIPSA-J

Smiles

[Na+].[Na+].[K+].[K+].O=S(=O)([O-])C1=CC=C(C=C1)NC=2N=C(N=C(N2)NCCO)NC3=CC=C(C=CC4=CC=C(C=C4S(=O)(=O)[O-])NC5=NC(=NC(=N5)NCCO)NC6=CC=C(C=C6)S(=O)(=O)[O-])C(=C3)S(=O)(=O)[O-]

InChI

InChI=1/C36H36N12O14S4.2K.2Na/c49-17-15-37-31-43-33(39-23-7-11-27(12-8-23)63(51,52)53)47-35(45-31)41-25-5-3-21(29(19-25)65(57,58)59)1-2-22-4-6-26(20-30(22)66(60,61)62)42-36-46-32(38-16-18-50)44-34(48-36)40-24-9-13-28(14-10-24)64(54,55)56;;;;/h1-14,19-20,49-50H,15-18H2,(H,51,52,53)(H,54,55,56)(H,57,58,59)(H,60,61,62)(H3,37,39,41,43,45,47)(H3,38,40,42,44,46,48);;;;/q;4*+1/p-4

Property Name	Value
Molecular Formula	C36H36N12O14S4
Molecular Weight	1108.01
AlogP	-12.67
Hydrogen Bond Acceptor	22.0
Hydrogen Bond Donor	8.0
Number of Rotational Bond	16.0
Polar Surface Area	431.7
Heavy Atoms	70.0

Property Name

Value

Molecular Formula

C36H36N12O14S4

Molecular Weight

1108.01

AlogP

-12.67

Hydrogen Bond Acceptor

22.0

Hydrogen Bond Donor

8.0

Number of Rotational Bond

16.0

Polar Surface Area

431.7

Heavy Atoms

70.0

Resources	Reference
CAS NUMBER	67828-25-5
NORMAN SUSDAT
PubChem	6441722

Resources

Reference

CAS NUMBER

67828-25-5

NORMAN SUSDAT

PubChem

6441722

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

DIPOTASSIUM DISODIUM 4,4'-BIS[[4-[(2-HYDROXYETHYL)AMINO]-6-[(4-SULPHONATOPHENYL)AMINO]-1,3,5-TRIAZIN-2-YL]AMINO]STILBENE-2,2'-DISULPHONATE

Structure

Physicochemical Descriptors

Cross References