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	VIFYCCSUPJQEBU-UHFFFAOYSA-N
Smiles	CC1(C)CNP(=O)(NC(=O)c2ccc(cc2)[N+](=O)[O-])NC1
InChI	InChI=1S/C12H17N4O4P/c1-12(2)7-13-21(20,14-8-12)15-11(17)9-3-5-10(6-4-9)16(18)19/h3-6H,7-8H2,1-2H3,(H3,13,14,15,17,20)

InChI Key

VIFYCCSUPJQEBU-UHFFFAOYSA-N

Smiles

CC1(C)CNP(=O)(NC(=O)c2ccc(cc2)[N+](=O)[O-])NC1

InChI

InChI=1S/C12H17N4O4P/c1-12(2)7-13-21(20,14-8-12)15-11(17)9-3-5-10(6-4-9)16(18)19/h3-6H,7-8H2,1-2H3,(H3,13,14,15,17,20)

Property Name	Value
Molecular Formula	C12H17N4O4P
Molecular Weight	312.26
AlogP	0.34
Hydrogen Bond Acceptor	4.0
Hydrogen Bond Donor	3.0
Number of Rotational Bond	3.0
Polar Surface Area	125.85
Molecular species	BASE
Aromatic Rings	1.0
Heavy Atoms	21.0

Property Name

Value

Molecular Formula

C12H17N4O4P

Molecular Weight

312.26

AlogP

0.34

Hydrogen Bond Acceptor

4.0

Hydrogen Bond Donor

3.0

Number of Rotational Bond

3.0

Polar Surface Area

125.85

Molecular species

BASE

Aromatic Rings

1.0

Heavy Atoms

21.0

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Homo sapiens	-	6492	-	-	-

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Homo sapiens

6492

Resources	Reference
ChEMBL	CHEMBL2234818
PubChem	76322451

Resources

Reference

ChEMBL

CHEMBL2234818

PubChem

76322451

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

N-(5,5-DIMETHYL-2-OXO-2LAMBDA5-[1,3,2]DIAZAPHOSPHINAN-2-YL)-4-NITRO-BENZAMIDE

Structure

Physicochemical Descriptors

Pharmacology

Cross References

N-(5,5-DIMETHYL-2-OXO-2LAMBDA*5*-[1,3,2]DIAZAPHOSPHINAN-2-YL)-4-NITRO-BENZAMIDE

Structure

Physicochemical Descriptors

Pharmacology

Cross References

N-(5,5-DIMETHYL-2-OXO-2LAMBDA5-[1,3,2]DIAZAPHOSPHINAN-2-YL)-4-NITRO-BENZAMIDE