EcoDrugPlus


Synonyms	1,4-Naphtho-Quinone 1,4-Naphthoquinone Naphthalene-1,4-Dione Naphthoquinone 1
Molecule Category	Free-form
UNII	RBF5ZU7R7K
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 ...

Synonyms

1,4-Naphtho-Quinone

1,4-Naphthoquinone

Naphthalene-1,4-Dione

Naphthoquinone 1

Molecule Category

Free-form

UNII

RBF5ZU7R7K

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	FRASJONUBLZVQX-UHFFFAOYSA-N
Smiles	O=C1C=CC(=O)c2ccccc12
InChI	InChI=1S/C10H6O2/c11-9-5-6-10(12)8-4-2-1-3-7(8)9/h1-6H

InChI Key

FRASJONUBLZVQX-UHFFFAOYSA-N

Smiles

O=C1C=CC(=O)c2ccccc12

InChI

InChI=1S/C10H6O2/c11-9-5-6-10(12)8-4-2-1-3-7(8)9/h1-6H

Property Name	Value
Molecular Formula	C10H6O2
Molecular Weight	158.15
AlogP	1.76
Hydrogen Bond Acceptor	2.0
Polar Surface Area	34.14
Heavy Atoms	12.0

Property Name

Value

Molecular Formula

C10H6O2

Molecular Weight

158.15

AlogP

1.76

Hydrogen Bond Acceptor

2.0

Polar Surface Area

34.14

Heavy Atoms

12.0

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Homo sapiens	-	15890-16920	-	-	-

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Homo sapiens

15890-16920

Resources	Reference
ChEMBL	CHEMBL55934
FDA SRS	RBF5ZU7R7K
PubChem	8530
SureChEMBL	SCHEMBL42139
ZINC	ZINC00901405

Resources

Reference

ChEMBL

FDA SRS

PubChem

SureChEMBL

ZINC

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

NAPHTHOQUINONE

Structure

Physicochemical Descriptors

Pharmacology

Cross References