EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Free-form
EPA CompTox	DTXSID2071156

Keyword(s):

Human Metabolites

Molecule Category

Free-form

EPA CompTox

DTXSID2071156


InChI Key	QUCPKFUMCQOBHO-UHFFFAOYSA-N
Smiles	CC(=O)Nc1c2c(O)c(N=Nc3ccc(cc3)S(=O)(=O)CCOS(=O)(=O)O)c(cc2cc(c1)S(=O)(=O)O)S(=O)(=O)O
InChI	InChI=1S/C20H19N3O14S4/c1-11(24)21-16-10-15(39(28,29)30)8-12-9-17(40(31,32)33)19(20(25)18(12)16)23-22-13-2-4-14(5-3-13)38(26,27)7-6-37-41(34,35)36/h2-5,8-10,25H,6-7H2,1H3,(H,21,24)(H,28,29,30)(H,31,32,33)(H,34,35,36)/b23-22+

InChI Key

QUCPKFUMCQOBHO-UHFFFAOYSA-N

Smiles

CC(=O)Nc1c2c(O)c(N=Nc3ccc(cc3)S(=O)(=O)CCOS(=O)(=O)O)c(cc2cc(c1)S(=O)(=O)O)S(=O)(=O)O

InChI

InChI=1S/C20H19N3O14S4/c1-11(24)21-16-10-15(39(28,29)30)8-12-9-17(40(31,32)33)19(20(25)18(12)16)23-22-13-2-4-14(5-3-13)38(26,27)7-6-37-41(34,35)36/h2-5,8-10,25H,6-7H2,1H3,(H,21,24)(H,28,29,30)(H,31,32,33)(H,34,35,36)/b23-22+

Property Name	Value
Molecular Formula	C20H19N3O14S4
Molecular Weight	652.97
AlogP	2.66
Hydrogen Bond Acceptor	13.0
Hydrogen Bond Donor	5.0
Number of Rotational Bond	10.0
Polar Surface Area	284.02
Heavy Atoms	41.0

Property Name

Value

Molecular Formula

C20H19N3O14S4

Molecular Weight

652.97

AlogP

2.66

Hydrogen Bond Acceptor

13.0

Hydrogen Bond Donor

5.0

Number of Rotational Bond

10.0

Polar Surface Area

284.02

Heavy Atoms

41.0

Resources	Reference
CAS NUMBER	68134-16-7
NORMAN SUSDAT
ChemSpider	7850901.0

Resources

Reference

CAS NUMBER

68134-16-7

NORMAN SUSDAT

ChemSpider

7850901.0

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, 2025, gkaf1251 Read...

This work is licensed under Creative Commons Attribution-ShareAlike 4.0 International License

Last update: Monday, 3 November 2025

2,7-NAPHTHALENEDISULFONIC ACID, 4-(ACETYLAMINO)-5-HYDROXY-6-[[4-[[2-(SULFOOXY)ETHYL]SULFONYL]PHENYL]AZO]-

Structure

Physicochemical Descriptors

Cross References