EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Free-form
EPA CompTox	DTXSID5066031

Keyword(s):

Human Metabolites

Molecule Category

Free-form

EPA CompTox

DTXSID5066031


InChI Key	SXYCCJAPZKHOLS-UHFFFAOYSA-N
Smiles	[O-][N+](=O)c1cc2c(ccc(N/N=C/3C(=O)C=Cc4ccccc34)c2cc1)S(=O)(=O)[O-]
InChI	InChI=1S/C20H13N3O6S/c24-18-9-5-12-3-1-2-4-14(12)20(18)22-21-17-8-10-19(30(27,28)29)16-11-13(23(25)26)6-7-15(16)17/h1-11,21H,(H,27,28,29)/b22-20-

InChI Key

SXYCCJAPZKHOLS-UHFFFAOYSA-N

Smiles

[O-][N+](=O)c1cc2c(ccc(N/N=C/3C(=O)C=Cc4ccccc34)c2cc1)S(=O)(=O)[O-]

InChI

InChI=1S/C20H13N3O6S/c24-18-9-5-12-3-1-2-4-14(12)20(18)22-21-17-8-10-19(30(27,28)29)16-11-13(23(25)26)6-7-15(16)17/h1-11,21H,(H,27,28,29)/b22-20-

Property Name	Value
Molecular Formula	C20H13N3O6S1
Molecular Weight	423.05
AlogP	3.41
Hydrogen Bond Acceptor	7.0
Hydrogen Bond Donor	2.0
Number of Rotational Bond	4.0
Polar Surface Area	138.97
Heavy Atoms	30.0

Property Name

Value

Molecular Formula

C20H13N3O6S1

Molecular Weight

423.05

AlogP

3.41

Hydrogen Bond Acceptor

7.0

Hydrogen Bond Donor

2.0

Number of Rotational Bond

4.0

Polar Surface Area

138.97

Heavy Atoms

30.0

Resources	Reference
CAS NUMBER	16279-54-2
NORMAN SUSDAT
ChemSpider	4583604.0

Resources

Reference

CAS NUMBER

16279-54-2

NORMAN SUSDAT

ChemSpider

4583604.0

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, 2025, gkaf1251 Read...

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Last update: Monday, 3 November 2025

1-NAPHTHALENESULFONIC ACID, 3-HYDROXY-4-[(2-HYDROXY-1-NAPHTHALENYL)AZO]-7-NITRO-

Structure

Physicochemical Descriptors

Cross References