EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Free-form
EPA CompTox	DTXSID80887497

Keyword(s):

Human Metabolites

Molecule Category

Free-form

EPA CompTox

DTXSID80887497


InChI Key	WGWPYVUPZBSOPX-UHFFFAOYSA-N
Smiles	O=C(O)CN1C(=S)N(C(=O)C1=C2SC(=CC=C3C=CC=4C=C(OCC)C=CC4N3CC)C(=O)N2CC)C=5C=CC=CC5
InChI	InChI=1/C31H30N4O5S2/c1-4-32-21(13-12-20-18-23(40-6-3)15-16-24(20)32)14-17-25-28(38)33(5-2)30(42-25)27-29(39)35(22-10-8-7-9-11-22)31(41)34(27)19-26(36)37/h7-18H,4-6,19H2,1-3H3,(H,36,37)

InChI Key

WGWPYVUPZBSOPX-UHFFFAOYSA-N

Smiles

O=C(O)CN1C(=S)N(C(=O)C1=C2SC(=CC=C3C=CC=4C=C(OCC)C=CC4N3CC)C(=O)N2CC)C=5C=CC=CC5

InChI

InChI=1/C31H30N4O5S2/c1-4-32-21(13-12-20-18-23(40-6-3)15-16-24(20)32)14-17-25-28(38)33(5-2)30(42-25)27-29(39)35(22-10-8-7-9-11-22)31(41)34(27)19-26(36)37/h7-18H,4-6,19H2,1-3H3,(H,36,37)

Property Name	Value
Molecular Formula	C31H30N4O5S2
Molecular Weight	602.17
AlogP	3.37
Hydrogen Bond Acceptor	8.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	8.0
Polar Surface Area	95.32
Heavy Atoms	42.0

Property Name

Value

Molecular Formula

C31H30N4O5S2

Molecular Weight

602.17

AlogP

3.37

Hydrogen Bond Acceptor

8.0

Hydrogen Bond Donor

1.0

Number of Rotational Bond

8.0

Polar Surface Area

95.32

Heavy Atoms

42.0

Resources	Reference
CAS NUMBER	68758-87-2
NORMAN SUSDAT
PubChem	71439850

Resources

Reference

CAS NUMBER

68758-87-2

NORMAN SUSDAT

PubChem

71439850

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-[5-[(6-ETHOXY-1-ETHYL-1H-QUINOLIN-2-YLIDENE)ETHYLIDENE]-3-ETHYL-4-OXOTHIAZOLIDIN-2-YLIDENE]-4-OXO-3-PHENYL-2-THIOXOIMIDAZOLIDINE-1-ACETIC ACID

Structure

Physicochemical Descriptors

Cross References