EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Free-form
UNII	U3AM6X5NBZ
EPA CompTox	DTXSID9073547

Keyword(s):

Human Metabolites

Molecule Category

Free-form

UNII

U3AM6X5NBZ

EPA CompTox

DTXSID9073547


InChI Key	IUSYSZLVZMUVDO-UHFFFAOYSA-N
Smiles	OC(=O)c1cc(Oc2ccc(Cl)cc2Cl)ccc1[N+]([O-])=O
InChI	InChI=1S/C13H7Cl2NO5/c14-7-1-4-12(10(15)5-7)21-8-2-3-11(16(19)20)9(6-8)13(17)18/h1-6H,(H,17,18)

InChI Key

IUSYSZLVZMUVDO-UHFFFAOYSA-N

Smiles

OC(=O)c1cc(Oc2ccc(Cl)cc2Cl)ccc1[N+]([O-])=O

InChI

InChI=1S/C13H7Cl2NO5/c14-7-1-4-12(10(15)5-7)21-8-2-3-11(16(19)20)9(6-8)13(17)18/h1-6H,(H,17,18)

Property Name	Value
Molecular Formula	C13H7Cl2N1O5
Molecular Weight	326.97
AlogP	4.39
Hydrogen Bond Acceptor	4.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	4.0
Polar Surface Area	89.67
Heavy Atoms	21.0

Property Name

Value

Molecular Formula

C13H7Cl2N1O5

Molecular Weight

326.97

AlogP

4.39

Hydrogen Bond Acceptor

4.0

Hydrogen Bond Donor

1.0

Number of Rotational Bond

4.0

Polar Surface Area

89.67

Heavy Atoms

21.0

Resources	Reference
CAS NUMBER	53774-07-5
NORMAN SUSDAT
FDA SRS	U3AM6X5NBZ
PubChem	148653
ChemSpider	131044.0

Resources

Reference

CAS NUMBER

53774-07-5

NORMAN SUSDAT

FDA SRS

U3AM6X5NBZ

PubChem

148653

ChemSpider

131044.0

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, Volume 54, Issue D1, 6 January 2026, Pages D1397–D1404, https://doi.org/10.1093/nar/gkaf1251

This work is licensed under Creative Commons Attribution-ShareAlike 4.0 International License

Last update: Monday, 3 November 2025

BENZOIC ACID, 5-(2,4-DICHLOROPHENOXY)-2-NITRO-

Structure

Physicochemical Descriptors

Cross References