EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Free-form
EPA CompTox	DTXSID10233706

Keyword(s):

Human Metabolites

Molecule Category

Free-form

EPA CompTox

DTXSID10233706


InChI Key	FIHSHUVRQWJTPB-NRFANRHFSA-N
Smiles	OC(=O)CNC(=O)CNC(=O)C(CCCCNC(=O)OCc1ccccc1)NC(=O)OCc1ccccc1
InChI	InChI=1S/C26H32N4O8/c31-22(28-16-23(32)33)15-29-24(34)21(30-26(36)38-18-20-11-5-2-6-12-20)13-7-8-14-27-25(35)37-17-19-9-3-1-4-10-19/h1-6,9-12,21H,7-8,13-18H2,(H,27,35)(H,28,31)(H,29,34)(H,30,36)(H,32,33)/t21-/m1/s1

InChI Key

FIHSHUVRQWJTPB-NRFANRHFSA-N

Smiles

OC(=O)CNC(=O)CNC(=O)C(CCCCNC(=O)OCc1ccccc1)NC(=O)OCc1ccccc1

InChI

InChI=1S/C26H32N4O8/c31-22(28-16-23(32)33)15-29-24(34)21(30-26(36)38-18-20-11-5-2-6-12-20)13-7-8-14-27-25(35)37-17-19-9-3-1-4-10-19/h1-6,9-12,21H,7-8,13-18H2,(H,27,35)(H,28,31)(H,29,34)(H,30,36)(H,32,33)/t21-/m1/s1

Property Name	Value
Molecular Formula	C26H32N4O8
Molecular Weight	528.22
AlogP	3.78
Hydrogen Bond Acceptor	7.0
Hydrogen Bond Donor	5.0
Number of Rotational Bond	15.0
Polar Surface Area	186.12
Heavy Atoms	38.0

Property Name

Value

Molecular Formula

C26H32N4O8

Molecular Weight

528.22

AlogP

3.78

Hydrogen Bond Acceptor

7.0

Hydrogen Bond Donor

5.0

Number of Rotational Bond

15.0

Polar Surface Area

186.12

Heavy Atoms

38.0

Resources	Reference
CAS NUMBER	84697-19-8
NORMAN SUSDAT
PubChem	44154308
ChemSpider	21164323.0

Resources

Reference

CAS NUMBER

84697-19-8

NORMAN SUSDAT

PubChem

44154308

ChemSpider

21164323.0

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

N-(N-(N2,N6-BIS((BENZYLOXY)CARBONYL)-L-LYSYL)GLYCYL)GLYCINE

Structure

Physicochemical Descriptors

Cross References