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	MMSNVYDJAORQJR-UHFFFAOYSA-N
Smiles	CN1CCN(CC1)C(=O)c2ccc(NC(=O)Nc3ccc4nc(NC(=O)C)sc4c3)cc2
InChI	InChI=1S/C22H24N6O3S/c1-14(29)23-22-26-18-8-7-17(13-19(18)32-22)25-21(31)24-16-5-3-15(4-6-16)20(30)28-11-9-27(2)10-12-28/h3-8,13H,9-12H2,1-2H3,(H,23,26,29)(H2,24,25,31)

InChI Key

MMSNVYDJAORQJR-UHFFFAOYSA-N

Smiles

CN1CCN(CC1)C(=O)c2ccc(NC(=O)Nc3ccc4nc(NC(=O)C)sc4c3)cc2

InChI

InChI=1S/C22H24N6O3S/c1-14(29)23-22-26-18-8-7-17(13-19(18)32-22)25-21(31)24-16-5-3-15(4-6-16)20(30)28-11-9-27(2)10-12-28/h3-8,13H,9-12H2,1-2H3,(H,23,26,29)(H2,24,25,31)

Property Name	Value
Molecular Formula	C22H24N6O3S
Molecular Weight	452.53
AlogP	1.64
Hydrogen Bond Acceptor	5.0
Hydrogen Bond Donor	3.0
Number of Rotational Bond	4.0
Polar Surface Area	134.91
Molecular species	NEUTRAL
Aromatic Rings	3.0
Heavy Atoms	32.0

Property Name

Value

Molecular Formula

C22H24N6O3S

Molecular Weight

452.53

AlogP

1.64

Hydrogen Bond Acceptor

5.0

Hydrogen Bond Donor

3.0

Number of Rotational Bond

4.0

Polar Surface Area

134.91

Molecular species

NEUTRAL

Aromatic Rings

3.0

Heavy Atoms

32.0

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Homo sapiens	-	570	-	-	-

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Homo sapiens

570

Resources	Reference
ChEMBL	CHEMBL2299132
PubChem	76324270

Resources

Reference

ChEMBL

CHEMBL2299132

PubChem

76324270

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-(6-(3-(4-(4-METHYLPIPERAZINE-1-CARBONYL)PHENYL)UREIDO)BENZO[D]THIAZOL-2-YL)ACETAMIDE

Structure

Physicochemical Descriptors

Pharmacology

Cross References