EcoDrugPlus


Molecule Category	Free-form
Source	Gaulton A, Kale N, van Westen GJ, Bellis LJ, Bento AP, Davies M, Hersey A, Papadatos G, Forster M, Wege P, Overington JP. A large-scale crop protection bioassay data set. Sci Data. 2015 Jul 7;2:150032. Read more ...

Molecule Category

Free-form

Source

Gaulton A, Kale N, van Westen GJ, Bellis LJ, Bento AP, Davies M, Hersey A, Papadatos G, Forster M, Wege P, Overington JP. A large-scale crop protection bioassay data set. Sci Data. 2015 Jul 7;2:150032. Read more ...


InChI Key	QOVQSZSXEGKYCD-UHFFFAOYSA-N
Smiles	CCOC(=O)C1C(N(N=O)C(C(C(=O)OCC)S1(=O)=O)c2ccc3OCOc3c2)c4ccc5OCOc5c4
InChI	InChI=1S/C24H24N2O11S/c1-3-32-23(27)21-19(13-5-7-15-17(9-13)36-11-34-15)26(25-29)20(22(38(21,30)31)24(28)33-4-2)14-6-8-16-18(10-14)37-12-35-16/h5-10,19-22H,3-4,11-12H2,1-2H3

InChI Key

QOVQSZSXEGKYCD-UHFFFAOYSA-N

Smiles

CCOC(=O)C1C(N(N=O)C(C(C(=O)OCC)S1(=O)=O)c2ccc3OCOc3c2)c4ccc5OCOc5c4

InChI

InChI=1S/C24H24N2O11S/c1-3-32-23(27)21-19(13-5-7-15-17(9-13)36-11-34-15)26(25-29)20(22(38(21,30)31)24(28)33-4-2)14-6-8-16-18(10-14)37-12-35-16/h5-10,19-22H,3-4,11-12H2,1-2H3

Property Name	Value
Molecular Formula	C24H24N2O11S
Molecular Weight	548.52
AlogP	2.65
Hydrogen Bond Acceptor	12.0
Number of Rotational Bond	9.0
Polar Surface Area	164.7
Molecular species	NEUTRAL
Aromatic Rings	2.0
Heavy Atoms	38.0

Property Name

Value

Molecular Formula

C24H24N2O11S

Molecular Weight

548.52

AlogP

2.65

Hydrogen Bond Acceptor

12.0

Number of Rotational Bond

9.0

Polar Surface Area

164.7

Molecular species

NEUTRAL

Aromatic Rings

2.0

Heavy Atoms

38.0

Resources	Reference
ChEMBL	CHEMBL2236184
PubChem	76322568

Resources

Reference

ChEMBL

CHEMBL2236184

PubChem

76322568

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, 2025, gkaf1251 Read...

This work is licensed under Creative Commons Attribution-ShareAlike 4.0 International License

Last update: Monday, 3 November 2025

N-NITROSO-2,6-DICARBETHOXY-3,5-BIS(1,3-BENZODIOXOL-6-YL)TETRAHYDRO-1,4-THIAZINE-1,1-DIOXIDE

Structure

Physicochemical Descriptors

Cross References