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	SRINGCYAKWTOIO-UHFFFAOYSA-N
Smiles	CC(=O)Oc1ccc(C2=NOC(C2)c3ccccc3)c(OC(=O)C)c1
InChI	InChI=1S/C19H17NO5/c1-12(21)23-15-8-9-16(19(10-15)24-13(2)22)17-11-18(25-20-17)14-6-4-3-5-7-14/h3-10,18H,11H2,1-2H3

InChI Key

SRINGCYAKWTOIO-UHFFFAOYSA-N

Smiles

CC(=O)Oc1ccc(C2=NOC(C2)c3ccccc3)c(OC(=O)C)c1

InChI

InChI=1S/C19H17NO5/c1-12(21)23-15-8-9-16(19(10-15)24-13(2)22)17-11-18(25-20-17)14-6-4-3-5-7-14/h3-10,18H,11H2,1-2H3

Property Name	Value
Molecular Formula	C19H17NO5
Molecular Weight	339.34
AlogP	2.76
Hydrogen Bond Acceptor	6.0
Number of Rotational Bond	6.0
Polar Surface Area	74.19
Heavy Atoms	25.0

Property Name

Value

Molecular Formula

C19H17NO5

Molecular Weight

339.34

AlogP

2.76

Hydrogen Bond Acceptor

6.0

Number of Rotational Bond

6.0

Polar Surface Area

74.19

Heavy Atoms

25.0

Targets	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Enzyme Phosphatase Protein Phosphatase Tyrosine protein phosphatase	-	62700	-	25000	91.6

Targets

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Enzyme Phosphatase Protein Phosphatase Tyrosine protein phosphatase

62700

25000

91.6

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Homo sapiens	-	62700	-	25000	91.6

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Homo sapiens

62700

25000

91.6

Resources	Reference
ChEMBL	CHEMBL2259735
PubChem	71463488

Resources

Reference

ChEMBL

CHEMBL2259735

PubChem

71463488

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

ACETIC ACID 3-ACETOXY-4-(5-PHENYL-4,5-DIHYDRO-ISOXAZOL-3-YL)-PHENYL ESTER

Structure

Physicochemical Descriptors

Pharmacology

Cross References