EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Free-form
EPA CompTox	DTXSID9067932

Keyword(s):

Human Metabolites

Molecule Category

Free-form

EPA CompTox

DTXSID9067932


InChI Key	VSNAWXHIKBJFHM-UHFFFAOYSA-N
Smiles	CNc1nc(Nc2ccccc2)nc(Nc2ccc(/C=C/c3c(cc(Nc4nc(Nc5ccccc5)nc(NC)n4)cc3)S(=O)(=O)O)c(c2)S(=O)(=O)O)n1
InChI	InChI=1S/C34H32N12O6S2/c1-35-29-41-31(37-23-9-5-3-6-10-23)45-33(43-29)39-25-17-15-21(27(19-25)53(47,48)49)13-14-22-16-18-26(20-28(22)54(50,51)52)40-34-44-30(36-2)42-32(46-34)38-24-11-7-4-8-12-24/h3-20H,1-2H3,(H,47,48,49)(H,50,51,52)(H3,35,37,39,41,43,45)(H3,36,38,40,42,44,46)/b14-13+

InChI Key

VSNAWXHIKBJFHM-UHFFFAOYSA-N

Smiles

CNc1nc(Nc2ccccc2)nc(Nc2ccc(/C=C/c3c(cc(Nc4nc(Nc5ccccc5)nc(NC)n4)cc3)S(=O)(=O)O)c(c2)S(=O)(=O)O)n1

InChI

InChI=1S/C34H32N12O6S2/c1-35-29-41-31(37-23-9-5-3-6-10-23)45-33(43-29)39-25-17-15-21(27(19-25)53(47,48)49)13-14-22-16-18-26(20-28(22)54(50,51)52)40-34-44-30(36-2)42-32(46-34)38-24-11-7-4-8-12-24/h3-20H,1-2H3,(H,47,48,49)(H,50,51,52)(H3,35,37,39,41,43,45)(H3,36,38,40,42,44,46)/b14-13+

Property Name	Value
Molecular Formula	C34H32N12O6S2
Molecular Weight	768.2
AlogP	2.31
Hydrogen Bond Acceptor	10.0
Hydrogen Bond Donor	8.0
Number of Rotational Bond	8.0
Polar Surface Area	277.64
Heavy Atoms	54.0

Property Name

Value

Molecular Formula

C34H32N12O6S2

Molecular Weight

768.2

AlogP

2.31

Hydrogen Bond Acceptor

10.0

Hydrogen Bond Donor

8.0

Number of Rotational Bond

8.0

Polar Surface Area

277.64

Heavy Atoms

54.0

Resources	Reference
CAS NUMBER	35632-99-6
NORMAN SUSDAT
PubChem	147401
ChemSpider	4944326.0

Resources

Reference

CAS NUMBER

35632-99-6

NORMAN SUSDAT

PubChem

147401

ChemSpider

4944326.0

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

4,4'-BIS[(4-ANILINO-6-METHYLAMINO-S-TRIAZIN-2-YL)AMINO]-2,2'-STILBENEDISULFONIC ACID

Structure

Physicochemical Descriptors

Cross References