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	GFZRAVDQCBNJMW-UHFFFAOYSA-N
Smiles	CCOP(=S)(OCC)SCc1ccc2ccccc2n1
InChI	InChI=1S/C14H18NO2PS2/c1-3-16-18(19,17-4-2)20-11-13-10-9-12-7-5-6-8-14(12)15-13/h5-10H,3-4,11H2,1-2H3

InChI Key

GFZRAVDQCBNJMW-UHFFFAOYSA-N

Smiles

CCOP(=S)(OCC)SCc1ccc2ccccc2n1

InChI

InChI=1S/C14H18NO2PS2/c1-3-16-18(19,17-4-2)20-11-13-10-9-12-7-5-6-8-14(12)15-13/h5-10H,3-4,11H2,1-2H3

Property Name	Value
Molecular Formula	C14H18NO2PS2
Molecular Weight	327.4
AlogP	3.98
Hydrogen Bond Acceptor	5.0
Number of Rotational Bond	7.0
Polar Surface Area	98.55
Molecular species	NEUTRAL
Aromatic Rings	2.0
Heavy Atoms	20.0

Property Name

Value

Molecular Formula

C14H18NO2PS2

Molecular Weight

327.4

AlogP

3.98

Hydrogen Bond Acceptor

5.0

Number of Rotational Bond

7.0

Polar Surface Area

98.55

Molecular species

NEUTRAL

Aromatic Rings

2.0

Heavy Atoms

20.0

Targets	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Enzyme Hydrolase	-	12010-15420	-	-	-

Targets

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Enzyme Hydrolase

12010-15420

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Electrophorus electricus	-	15420	-	-	-
Equus caballus	-	12010	-	-	-

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Electrophorus electricus

15420

Equus caballus

12010

Resources	Reference
ChEMBL	CHEMBL2268507
PubChem	76326881

Resources

Reference

ChEMBL

CHEMBL2268507

PubChem

76326881

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...

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Last update: Monday, 3 November 2025

S-QUINOLIN-2-YLMETHYL-O,O'-DIETHYL PHOSPHORODITHIOATE

Structure

Physicochemical Descriptors

Pharmacology

Cross References