EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Free-form
EPA CompTox	DTXSID40239998

Keyword(s):

Human Metabolites

Molecule Category

Free-form

EPA CompTox

DTXSID40239998


InChI Key	AGSDLBDGIVXKLJ-UHFFFAOYSA-N
Smiles	OS(=O)(=O)c1cc(NC2=C(Cl)C(=O)C(Nc3ccc(Nc4ccccc4)c(S(O)(=O)=O)c3)=C(Cl)C2=O)ccc1Nc1ccccc1
InChI	InChI=1S/C30H22Cl2N4O8S2/c31-25-27(35-19-11-13-21(23(15-19)45(39,40)41)33-17-7-3-1-4-8-17)29(37)26(32)28(30(25)38)36-20-12-14-22(24(16-20)46(42,43)44)34-18-9-5-2-6-10-18/h1-16,33-36H,(H,39,40,41)(H,42,43,44)

InChI Key

AGSDLBDGIVXKLJ-UHFFFAOYSA-N

Smiles

OS(=O)(=O)c1cc(NC2=C(Cl)C(=O)C(Nc3ccc(Nc4ccccc4)c(S(O)(=O)=O)c3)=C(Cl)C2=O)ccc1Nc1ccccc1

InChI

InChI=1S/C30H22Cl2N4O8S2/c31-25-27(35-19-11-13-21(23(15-19)45(39,40)41)33-17-7-3-1-4-8-17)29(37)26(32)28(30(25)38)36-20-12-14-22(24(16-20)46(42,43)44)34-18-9-5-2-6-10-18/h1-16,33-36H,(H,39,40,41)(H,42,43,44)

Property Name	Value
Molecular Formula	C30H22Cl2N4O8S2
Molecular Weight	700.03
AlogP	6.24
Hydrogen Bond Acceptor	10.0
Hydrogen Bond Donor	6.0
Number of Rotational Bond	10.0
Polar Surface Area	191.0
Heavy Atoms	46.0

Property Name

Value

Molecular Formula

C30H22Cl2N4O8S2

Molecular Weight

700.03

AlogP

6.24

Hydrogen Bond Acceptor

10.0

Hydrogen Bond Donor

6.0

Number of Rotational Bond

10.0

Polar Surface Area

191.0

Heavy Atoms

46.0

Resources	Reference
CAS NUMBER	93964-65-9
NORMAN SUSDAT
PubChem	44153938
ChemSpider	21166319.0

Resources

Reference

CAS NUMBER

93964-65-9

NORMAN SUSDAT

PubChem

44153938

ChemSpider

21166319.0

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

3,3'-((2,5-DICHLORO-3,6-DIOXOCYCLOHEXA-1,4-DIENE-1,4-DIYL)DIIMINO)BIS(6-ANILINOBENZENESULPHONIC) ACID

Structure

Physicochemical Descriptors

Cross References