EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Free-form
EPA CompTox	DTXSID401000297

Keyword(s):

Human Metabolites

Molecule Category

Free-form

EPA CompTox

DTXSID401000297


InChI Key	XCCIYECKBBTTIT-UHFFFAOYSA-N
Smiles	O=[N+]([O-])C1=CC(=CC=C1NC2=CC=C(OC3=CC=C(C=C3)C(C)(C)CC(C)(C)C)C=C2)S(=O)(=O)N(C=4C=CC=CC4)C
InChI	InChI=1/C33H37N3O5S/c1-32(2,3)23-33(4,5)24-12-16-27(17-13-24)41-28-18-14-25(15-19-28)34-30-21-20-29(22-31(30)36(37)38)42(39,40)35(6)26-10-8-7-9-11-26/h7-22,34H,23H2,1-6H3

InChI Key

XCCIYECKBBTTIT-UHFFFAOYSA-N

Smiles

O=[N+]([O-])C1=CC(=CC=C1NC2=CC=C(OC3=CC=C(C=C3)C(C)(C)CC(C)(C)C)C=C2)S(=O)(=O)N(C=4C=CC=CC4)C

InChI

InChI=1/C33H37N3O5S/c1-32(2,3)23-33(4,5)24-12-16-27(17-13-24)41-28-18-14-25(15-19-28)34-30-21-20-29(22-31(30)36(37)38)42(39,40)35(6)26-10-8-7-9-11-26/h7-22,34H,23H2,1-6H3

Property Name	Value
Molecular Formula	C33H38N3O5S
Molecular Weight	587.25
AlogP	8.67
Hydrogen Bond Acceptor	6.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	10.0
Polar Surface Area	101.78
Heavy Atoms	42.0

Property Name

Value

Molecular Formula

C33H38N3O5S

Molecular Weight

587.25

AlogP

8.67

Hydrogen Bond Acceptor

6.0

Hydrogen Bond Donor

1.0

Number of Rotational Bond

10.0

Polar Surface Area

101.78

Heavy Atoms

42.0

Resources	Reference
CAS NUMBER	79135-82-3
NORMAN SUSDAT
PubChem	3018809

Resources

Reference

CAS NUMBER

79135-82-3

NORMAN SUSDAT

PubChem

3018809

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

N-METHYL-3-NITRO-N-PHENYL-4-[[4-[4-(1,1,3,3-TETRAMETHYLBUTYL)PHENOXY]PHENYL]AMINO]BENZENESULPHONAMIDE

Structure

Physicochemical Descriptors

Cross References