EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Free-form
EPA CompTox	DTXSID90182263

Keyword(s):

Human Metabolites

Molecule Category

Free-form

EPA CompTox

DTXSID90182263


InChI Key	WBRNAYOLDDFLPV-UHFFFAOYSA-N
Smiles	CCCCCCCCCCCCCCCCCC(=O)Nc1cccc(c1)C(=O)CC(=O)Nc1c(OC)ccc(c1)S(=O)(=O)O
InChI	InChI=1S/C34H50N2O7S/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-21-33(38)35-28-20-18-19-27(24-28)31(37)26-34(39)36-30-25-29(44(40,41)42)22-23-32(30)43-2/h18-20,22-25H,3-17,21,26H2,1-2H3,(H,35,38)(H,36,39)(H,40,41,42)

InChI Key

WBRNAYOLDDFLPV-UHFFFAOYSA-N

Smiles

CCCCCCCCCCCCCCCCCC(=O)Nc1cccc(c1)C(=O)CC(=O)Nc1c(OC)ccc(c1)S(=O)(=O)O

InChI

InChI=1S/C34H50N2O7S/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-21-33(38)35-28-20-18-19-27(24-28)31(37)26-34(39)36-30-25-29(44(40,41)42)22-23-32(30)43-2/h18-20,22-25H,3-17,21,26H2,1-2H3,(H,35,38)(H,36,39)(H,40,41,42)

Property Name	Value
Molecular Formula	C34H50N2O7S1
Molecular Weight	630.33
AlogP	9.65
Hydrogen Bond Acceptor	6.0
Hydrogen Bond Donor	3.0
Number of Rotational Bond	23.0
Polar Surface Area	145.85
Heavy Atoms	44.0

Property Name

Value

Molecular Formula

C34H50N2O7S1

Molecular Weight

630.33

AlogP

9.65

Hydrogen Bond Acceptor

6.0

Hydrogen Bond Donor

3.0

Number of Rotational Bond

23.0

Polar Surface Area

145.85

Heavy Atoms

44.0

Resources	Reference
CAS NUMBER	27982-29-2
NORMAN SUSDAT
PubChem	119779
ChemSpider	106948.0

Resources

Reference

CAS NUMBER

27982-29-2

NORMAN SUSDAT

PubChem

119779

ChemSpider

106948.0

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

3-((1,3-DIOXO-3-(3-((1-OXOOCTADECYL)AMINO)PHENYL)PROPYL)AMINO)-4-METHOXYBENZENESULPHONIC ACID

Structure

Physicochemical Descriptors

Cross References