EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Free-form
UNII	A6K16X67TA
EPA CompTox	DTXSID2067161

Keyword(s):

Human Metabolites

Molecule Category

Free-form

UNII

A6K16X67TA

EPA CompTox

DTXSID2067161


InChI Key	MIBWEBONCRNTAY-UHFFFAOYSA-N
Smiles	Cc1cc(cc(c1C)S(=O)(=O)NCCO)[N+](=O)[O-]
InChI	InChI=1S/C10H14N2O5S/c1-7-5-9(12(14)15)6-10(8(7)2)18(16,17)11-3-4-13/h5-6,11,13H,3-4H2,1-2H3

InChI Key

MIBWEBONCRNTAY-UHFFFAOYSA-N

Smiles

Cc1cc(cc(c1C)S(=O)(=O)NCCO)[N+](=O)[O-]

InChI

InChI=1S/C10H14N2O5S/c1-7-5-9(12(14)15)6-10(8(7)2)18(16,17)11-3-4-13/h5-6,11,13H,3-4H2,1-2H3

Property Name	Value
Molecular Formula	C10H14N2O5S1
Molecular Weight	274.06
AlogP	0.48
Hydrogen Bond Acceptor	5.0
Hydrogen Bond Donor	2.0
Number of Rotational Bond	5.0
Polar Surface Area	109.54
Heavy Atoms	18.0

Property Name

Value

Molecular Formula

C10H14N2O5S1

Molecular Weight

274.06

AlogP

0.48

Hydrogen Bond Acceptor

5.0

Hydrogen Bond Donor

2.0

Number of Rotational Bond

5.0

Polar Surface Area

109.54

Heavy Atoms

18.0

Resources	Reference
CAS NUMBER	25959-70-0
NORMAN SUSDAT
FDA SRS	A6K16X67TA
PubChem	117680
ChemSpider	105164.0

Resources

Reference

CAS NUMBER

25959-70-0

NORMAN SUSDAT

FDA SRS

A6K16X67TA

PubChem

117680

ChemSpider

105164.0

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

BENZENESULFONAMIDE, N-(2-HYDROXYETHYL)-2,3-DIMETHYL-5-NITRO-

Structure

Physicochemical Descriptors

Cross References