EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Free-form
EPA CompTox	DTXSID8071774

Keyword(s):

Human Metabolites

Molecule Category

Free-form

EPA CompTox

DTXSID8071774


InChI Key	FPYVZVAVJMWSOP-UHFFFAOYSA-N
Smiles	O=C(Nc1c2C(=O)c3c(cccc3)C(=O)c2c(Nc2cc3c(cc2)c2c4c(ccc5c6ccc(Nc7c8C(=O)c9c(cccc9)C(=O)c8c(NC(=O)c8ccccc8)cc7)cc6C(=O)c(cc2)c45)C3=O)cc1)c1ccccc1
InChI	InChI=1S/C66H36N4O8/c71-59-45-25-24-40-38-22-20-36(68-50-28-30-52(70-66(78)34-13-5-2-6-14-34)58-56(50)62(74)42-16-8-10-18-44(42)64(58)76)32-48(38)60(72)46-26-23-39(53(45)54(40)46)37-21-19-35(31-47(37)59)67-49-27-29-51(69-65(77)33-11-3-1-4-12-33)57-55(49)61(73)41-15-7-9-17-43(41)63(57)75/h1-32,67-68H,(H,69,77)(H,70,78)

InChI Key

FPYVZVAVJMWSOP-UHFFFAOYSA-N

Smiles

O=C(Nc1c2C(=O)c3c(cccc3)C(=O)c2c(Nc2cc3c(cc2)c2c4c(ccc5c6ccc(Nc7c8C(=O)c9c(cccc9)C(=O)c8c(NC(=O)c8ccccc8)cc7)cc6C(=O)c(cc2)c45)C3=O)cc1)c1ccccc1

InChI

InChI=1S/C66H36N4O8/c71-59-45-25-24-40-38-22-20-36(68-50-28-30-52(70-66(78)34-13-5-2-6-14-34)58-56(50)62(74)42-16-8-10-18-44(42)64(58)76)32-48(38)60(72)46-26-23-39(53(45)54(40)46)37-21-19-35(31-47(37)59)67-49-27-29-51(69-65(77)33-11-3-1-4-12-33)57-55(49)61(73)41-15-7-9-17-43(41)63(57)75/h1-32,67-68H,(H,69,77)(H,70,78)

Property Name	Value
Molecular Formula	C66H36N4O8
Molecular Weight	1012.25
AlogP	13.57
Hydrogen Bond Acceptor	10.0
Hydrogen Bond Donor	4.0
Number of Rotational Bond	8.0
Polar Surface Area	191.66
Heavy Atoms	78.0

Property Name

Value

Molecular Formula

C66H36N4O8

Molecular Weight

1012.25

AlogP

13.57

Hydrogen Bond Acceptor

10.0

Hydrogen Bond Donor

4.0

Number of Rotational Bond

8.0

Polar Surface Area

191.66

Heavy Atoms

78.0

Resources	Reference
CAS NUMBER	68834-03-7
NORMAN SUSDAT
PubChem	102060535
ChemSpider	17287974.0

Resources

Reference

CAS NUMBER

68834-03-7

NORMAN SUSDAT

PubChem

102060535

ChemSpider

17287974.0

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

BENZAMIDE, N,N'-[(7,14-DIHYDRO-7,14-DIOXODIBENZO[B,DEF]CHRYSENE-2,9-DIYL)BIS[IMINO(9,10-DIHYDRO-9,10-DIOXO-4,1-ANTHRACENEDIYL)]]BIS-

Structure

Physicochemical Descriptors

Cross References