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	ASSMCDJDGFFFDY-UHFFFAOYSA-N
Smiles	COP(=O)(OC)C(OC(=O)COc1cccc(c1)C(F)(F)F)c2ccc(Cl)cc2
InChI	InChI=1S/C18H17ClF3O6P/c1-25-29(24,26-2)17(12-6-8-14(19)9-7-12)28-16(23)11-27-15-5-3-4-13(10-15)18(20,21)22/h3-10,17H,11H2,1-2H3

InChI Key

ASSMCDJDGFFFDY-UHFFFAOYSA-N

Smiles

COP(=O)(OC)C(OC(=O)COc1cccc(c1)C(F)(F)F)c2ccc(Cl)cc2

InChI

InChI=1S/C18H17ClF3O6P/c1-25-29(24,26-2)17(12-6-8-14(19)9-7-12)28-16(23)11-27-15-5-3-4-13(10-15)18(20,21)22/h3-10,17H,11H2,1-2H3

Property Name	Value
Molecular Formula	C18H17ClF3O6P
Molecular Weight	452.75
AlogP	4.22
Hydrogen Bond Acceptor	6.0
Number of Rotational Bond	10.0
Polar Surface Area	80.87
Heavy Atoms	29.0

Property Name

Value

Molecular Formula

C18H17ClF3O6P

Molecular Weight

452.75

AlogP

4.22

Hydrogen Bond Acceptor

6.0

Number of Rotational Bond

10.0

Polar Surface Area

80.87

Heavy Atoms

29.0

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Cucumis sativus	-	6918.31	-	-	-

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Cucumis sativus

6918.31

Resources	Reference
ChEMBL	CHEMBL2253443
PubChem	76330027

Resources

Reference

ChEMBL

CHEMBL2253443

PubChem

76330027

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

(4-CHLOROPHENYL)(DIMETHOXYPHOSPHORYL)METHYL 2-(3-(TRIFLUOROMETHYL)PHENOXY)ACETATE

Structure

Physicochemical Descriptors

Pharmacology

Cross References