EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Free-form
EPA CompTox	DTXSID7069734

Keyword(s):

Human Metabolites

Molecule Category

Free-form

EPA CompTox

DTXSID7069734


InChI Key	XAVDJYWQEBDPNQ-UHFFFAOYSA-N
Smiles	CCOC(=O)c1c2c3c(cccc3)c(=O)c3c(Nc4ccc(Cl)cc4S(=O)(=O)O)ccc(n(C)c1=O)c23
InChI	InChI=1S/C26H19ClN2O7S/c1-3-36-26(32)23-20-14-6-4-5-7-15(14)24(30)21-17(10-11-18(22(20)21)29(2)25(23)31)28-16-9-8-13(27)12-19(16)37(33,34)35/h4-12,28H,3H2,1-2H3,(H,33,34,35)

InChI Key

XAVDJYWQEBDPNQ-UHFFFAOYSA-N

Smiles

CCOC(=O)c1c2c3c(cccc3)c(=O)c3c(Nc4ccc(Cl)cc4S(=O)(=O)O)ccc(n(C)c1=O)c23

InChI

InChI=1S/C26H19ClN2O7S/c1-3-36-26(32)23-20-14-6-4-5-7-15(14)24(30)21-17(10-11-18(22(20)21)29(2)25(23)31)28-16-9-8-13(27)12-19(16)37(33,34)35/h4-12,28H,3H2,1-2H3,(H,33,34,35)

Property Name	Value
Molecular Formula	C26H19Cl1N2O7S1
Molecular Weight	538.06
AlogP	4.57
Hydrogen Bond Acceptor	8.0
Hydrogen Bond Donor	2.0
Number of Rotational Bond	5.0
Polar Surface Area	131.77
Heavy Atoms	37.0

Property Name

Value

Molecular Formula

C26H19Cl1N2O7S1

Molecular Weight

538.06

AlogP

4.57

Hydrogen Bond Acceptor

8.0

Hydrogen Bond Donor

2.0

Number of Rotational Bond

5.0

Polar Surface Area

131.77

Heavy Atoms

37.0

Resources	Reference
CAS NUMBER	63149-10-0
NORMAN SUSDAT
PubChem	113086
ChemSpider	101357.0

Resources

Reference

CAS NUMBER

63149-10-0

NORMAN SUSDAT

PubChem

113086

ChemSpider

101357.0

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

3H-DIBENZ[F,IJ]ISOQUINOLINE-1-CARBOXYLIC ACID, 6-[(4-CHLORO-2-SULFOPHENYL)AMINO]-2,7-DIHYDRO-3-METHYL-2,7-DIOXO-, 1-ETHYL ESTER

Structure

Physicochemical Descriptors

Cross References