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	PZPWBGMCUWMVOI-UHFFFAOYSA-N
Smiles	COc1cccc(C(N)P(=O)(O)O)c1OC
InChI	InChI=1S/C9H14NO5P/c1-14-7-5-3-4-6(8(7)15-2)9(10)16(11,12)13/h3-5,9H,10H2,1-2H3,(H2,11,12,13)

InChI Key

PZPWBGMCUWMVOI-UHFFFAOYSA-N

Smiles

COc1cccc(C(N)P(=O)(O)O)c1OC

InChI

InChI=1S/C9H14NO5P/c1-14-7-5-3-4-6(8(7)15-2)9(10)16(11,12)13/h3-5,9H,10H2,1-2H3,(H2,11,12,13)

Property Name	Value
Molecular Formula	C9H14NO5P
Molecular Weight	247.18
AlogP	0.34
Hydrogen Bond Acceptor	6.0
Hydrogen Bond Donor	3.0
Number of Rotational Bond	4.0
Polar Surface Area	111.82
Molecular species	ZWITTERION
Aromatic Rings	1.0
Heavy Atoms	16.0

Property Name

Value

Molecular Formula

C9H14NO5P

Molecular Weight

247.18

AlogP

0.34

Hydrogen Bond Acceptor

6.0

Hydrogen Bond Donor

3.0

Number of Rotational Bond

4.0

Polar Surface Area

111.82

Molecular species

ZWITTERION

Aromatic Rings

1.0

Heavy Atoms

16.0

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Arabidopsis thaliana	-	15995580.29-16000000	-	-	-
Zea mays	-	-	-	-

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Arabidopsis thaliana

15995580.29-16000000

Zea mays

Resources	Reference
ChEMBL	CHEMBL2252825
PubChem	24866950

Resources

Reference

ChEMBL

CHEMBL2252825

PubChem

24866950

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

AMINO(2,3-DIMETHOXYPHENYL)METHYLPHOSPHONIC ACID

Structure

Physicochemical Descriptors

Pharmacology

Cross References