EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Free-form
EPA CompTox	DTXSID60241437

Keyword(s):

Human Metabolites

Molecule Category

Free-form

EPA CompTox

DTXSID60241437


InChI Key	SSTSDBMLLNZAPW-UHFFFAOYSA-N
Smiles	CCCCCCCCCCCCCCCC(=O)NC1=NN(C(=O)C1)c1cc(c(Oc2ccccc2)cc1)S(=O)(=O)O
InChI	InChI=1S/C31H43N3O6S/c1-2-3-4-5-6-7-8-9-10-11-12-13-17-20-30(35)32-29-24-31(36)34(33-29)25-21-22-27(28(23-25)41(37,38)39)40-26-18-15-14-16-19-26/h14-16,18-19,21-23H,2-13,17,20,24H2,1H3,(H,32,33,35)(H,37,38,39)

InChI Key

SSTSDBMLLNZAPW-UHFFFAOYSA-N

Smiles

CCCCCCCCCCCCCCCC(=O)NC1=NN(C(=O)C1)c1cc(c(Oc2ccccc2)cc1)S(=O)(=O)O

InChI

InChI=1S/C31H43N3O6S/c1-2-3-4-5-6-7-8-9-10-11-12-13-17-20-30(35)32-29-24-31(36)34(33-29)25-21-22-27(28(23-25)41(37,38)39)40-26-18-15-14-16-19-26/h14-16,18-19,21-23H,2-13,17,20,24H2,1H3,(H,32,33,35)(H,37,38,39)

Property Name	Value
Molecular Formula	C31H43N3O6S1
Molecular Weight	585.29
AlogP	7.37
Hydrogen Bond Acceptor	5.0
Hydrogen Bond Donor	2.0
Number of Rotational Bond	18.0
Polar Surface Area	125.37
Heavy Atoms	41.0

Property Name

Value

Molecular Formula

C31H43N3O6S1

Molecular Weight

585.29

AlogP

7.37

Hydrogen Bond Acceptor

5.0

Hydrogen Bond Donor

2.0

Number of Rotational Bond

18.0

Polar Surface Area

125.37

Heavy Atoms

41.0

Resources	Reference
CAS NUMBER	94349-41-4
NORMAN SUSDAT
PubChem	3024337
ChemSpider	2290286.0

Resources

Reference

CAS NUMBER

94349-41-4

NORMAN SUSDAT

PubChem

3024337

ChemSpider

2290286.0

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

5-(4,5-DIHYDRO-5-OXO-3-((1-OXOHEXADECYL)AMINO)-1H-PYRAZOL-1-YL)-2-PHENOXYBENZENESULPHONIC ACID

Structure

Physicochemical Descriptors

Cross References