EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Free-form
EPA CompTox	DTXSID9072579

Keyword(s):

Human Metabolites

Molecule Category

Free-form

EPA CompTox

DTXSID9072579


InChI Key	QUTLRBYOTJDTQY-UHFFFAOYSA-N
Smiles	CCC(C)(C)c1ccc(Oc2cc(Nc3ccccc3)c3C(=O)c4ccccc4-c4c(C(=O)c5ccccc5)c(=O)[nH]c2c34)cc1
InChI	InChI=1S/C40H32N2O4/c1-4-40(2,3)25-19-21-27(22-20-25)46-31-23-30(41-26-15-9-6-10-16-26)33-34-32(28-17-11-12-18-29(28)38(33)44)35(39(45)42-36(31)34)37(43)24-13-7-5-8-14-24/h5-23,41H,4H2,1-3H3,(H,42,45)

InChI Key

QUTLRBYOTJDTQY-UHFFFAOYSA-N

Smiles

CCC(C)(C)c1ccc(Oc2cc(Nc3ccccc3)c3C(=O)c4ccccc4-c4c(C(=O)c5ccccc5)c(=O)[nH]c2c34)cc1

InChI

InChI=1S/C40H32N2O4/c1-4-40(2,3)25-19-21-27(22-20-25)46-31-23-30(41-26-15-9-6-10-16-26)33-34-32(28-17-11-12-18-29(28)38(33)44)35(39(45)42-36(31)34)37(43)24-13-7-5-8-14-24/h5-23,41H,4H2,1-3H3,(H,42,45)

Property Name	Value
Molecular Formula	C40H32N2O4
Molecular Weight	604.24
AlogP	9.61
Hydrogen Bond Acceptor	6.0
Hydrogen Bond Donor	2.0
Number of Rotational Bond	8.0
Polar Surface Area	88.52
Heavy Atoms	46.0

Property Name

Value

Molecular Formula

C40H32N2O4

Molecular Weight

604.24

AlogP

9.61

Hydrogen Bond Acceptor

6.0

Hydrogen Bond Donor

2.0

Number of Rotational Bond

8.0

Polar Surface Area

88.52

Heavy Atoms

46.0

Resources	Reference
CAS NUMBER	72453-58-8
NORMAN SUSDAT
PubChem	5748738
ChemSpider	4678113.0

Resources

Reference

CAS NUMBER

72453-58-8

NORMAN SUSDAT

PubChem

5748738

ChemSpider

4678113.0

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

3H-NAPHTHO[1,2,3-DE]QUINOLINE-2,7-DIONE, 1-BENZOYL-4-[4-(1,1-DIMETHYLPROPYL)PHENOXY]-6-(PHENYLAMINO)-

Structure

Physicochemical Descriptors

Cross References