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	XAGTWZKHFLBXSO-UHFFFAOYSA-N
Smiles	CCOC(=O)CSc1nnc(CCCCc2nnc(SCC(=O)OCC)n2c3ccc(OCC)cc3)n1c4ccc(OCC)cc4
InChI	InChI=1S/C32H40N6O6S2/c1-5-41-25-17-13-23(14-18-25)37-27(33-35-31(37)45-21-29(39)43-7-3)11-9-10-12-28-34-36-32(46-22-30(40)44-8-4)38(28)24-15-19-26(20-16-24)42-6-2/h13-20H,5-12,21-22H2,1-4H3

InChI Key

XAGTWZKHFLBXSO-UHFFFAOYSA-N

Smiles

CCOC(=O)CSc1nnc(CCCCc2nnc(SCC(=O)OCC)n2c3ccc(OCC)cc3)n1c4ccc(OCC)cc4

InChI

InChI=1S/C32H40N6O6S2/c1-5-41-25-17-13-23(14-18-25)37-27(33-35-31(37)45-21-29(39)43-7-3)11-9-10-12-28-34-36-32(46-22-30(40)44-8-4)38(28)24-15-19-26(20-16-24)42-6-2/h13-20H,5-12,21-22H2,1-4H3

Property Name	Value
Molecular Formula	C32H40N6O6S2
Molecular Weight	668.83
AlogP	6.38
Hydrogen Bond Acceptor	12.0
Number of Rotational Bond	21.0
Polar Surface Area	183.07
Molecular species	NEUTRAL
Aromatic Rings	4.0
Heavy Atoms	46.0

Property Name

Value

Molecular Formula

C32H40N6O6S2

Molecular Weight

668.83

AlogP

6.38

Hydrogen Bond Acceptor

12.0

Number of Rotational Bond

21.0

Polar Surface Area

183.07

Molecular species

NEUTRAL

Aromatic Rings

4.0

Heavy Atoms

46.0

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Homo sapiens	-	9300-15130	-	-	-

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Homo sapiens

9300-15130

Resources	Reference
ChEMBL	CHEMBL2234856
PubChem	56929213

Resources

Reference

ChEMBL

CHEMBL2234856

PubChem

56929213

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

1,4-BIS[5-(CARBETHOXY-METHYL)-THIO-4-(P-ETHOXYPHENYL)-1,2,4-TRIAZOL-3-YL]-BUTANE

Structure

Physicochemical Descriptors

Pharmacology

Cross References