EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Free-form
EPA CompTox	DTXSID70240138

Keyword(s):

Human Metabolites

Molecule Category

Free-form

EPA CompTox

DTXSID70240138


InChI Key	GTBGZMMEAUYMQS-UHFFFAOYSA-N
Smiles	OS(=O)(=O)c1cc(c(cc1)C(c1ccc(cc1)N(Cc1ccccc1)Cc1ccccc1)c1ccc(cc1)N(Cc1ccccc1)Cc1ccccc1)S(=O)(=O)O
InChI	InChI=1S/C47H42N2O6S2/c50-56(51,52)44-29-30-45(46(31-44)57(53,54)55)47(40-21-25-42(26-22-40)48(32-36-13-5-1-6-14-36)33-37-15-7-2-8-16-37)41-23-27-43(28-24-41)49(34-38-17-9-3-10-18-38)35-39-19-11-4-12-20-39/h1-31,47H,32-35H2,(H,50,51,52)(H,53,54,55)

InChI Key

GTBGZMMEAUYMQS-UHFFFAOYSA-N

Smiles

OS(=O)(=O)c1cc(c(cc1)C(c1ccc(cc1)N(Cc1ccccc1)Cc1ccccc1)c1ccc(cc1)N(Cc1ccccc1)Cc1ccccc1)S(=O)(=O)O

InChI

InChI=1S/C47H42N2O6S2/c50-56(51,52)44-29-30-45(46(31-44)57(53,54)55)47(40-21-25-42(26-22-40)48(32-36-13-5-1-6-14-36)33-37-15-7-2-8-16-37)41-23-27-43(28-24-41)49(34-38-17-9-3-10-18-38)35-39-19-11-4-12-20-39/h1-31,47H,32-35H2,(H,50,51,52)(H,53,54,55)

Property Name	Value
Molecular Formula	C47H42N2O6S2
Molecular Weight	794.25
AlogP	9.77
Hydrogen Bond Acceptor	6.0
Hydrogen Bond Donor	2.0
Number of Rotational Bond	15.0
Polar Surface Area	115.22
Heavy Atoms	57.0

Property Name

Value

Molecular Formula

C47H42N2O6S2

Molecular Weight

794.25

AlogP

9.77

Hydrogen Bond Acceptor

6.0

Hydrogen Bond Donor

2.0

Number of Rotational Bond

15.0

Polar Surface Area

115.22

Heavy Atoms

57.0

Resources	Reference
CAS NUMBER	93982-50-4
NORMAN SUSDAT
PubChem	3023209
ChemSpider	2289484.0

Resources

Reference

CAS NUMBER

93982-50-4

NORMAN SUSDAT

PubChem

3023209

ChemSpider

2289484.0

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

4-(BIS(4-(BIS(PHENYLMETHYL)AMINO)PHENYL)METHYL)BENZENE-1,3-DISULPHONIC ACID

Structure

Physicochemical Descriptors

Cross References