EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Salt-form
EPA CompTox	DTXSID30220638

Keyword(s):

Human Metabolites

Molecule Category

Salt-form

EPA CompTox

DTXSID30220638


InChI Key	JYWCRDUTYUBXOL-FYZYNONXSA-N
Smiles	[Cl-].Cc1cc(=O)oc2c1ccc(NC(=O)C(CCCN=C(N)N)NC(=O)OCc1ccccc1)c2.[H+]
InChI	InChI=1S/C24H27N5O5/c1-15-12-21(30)34-20-13-17(9-10-18(15)20)28-22(31)19(8-5-11-27-23(25)26)29-24(32)33-14-16-6-3-2-4-7-16/h2-4,6-7,9-10,12-13,19H,5,8,11,14H2,1H3,(H,28,31)(H,29,32)(H4,25,26,27)/t19-/m1/s1

InChI Key

JYWCRDUTYUBXOL-FYZYNONXSA-N

Smiles

[Cl-].Cc1cc(=O)oc2c1ccc(NC(=O)C(CCCN=C(N)N)NC(=O)OCc1ccccc1)c2.[H+]

InChI

InChI=1S/C24H27N5O5/c1-15-12-21(30)34-20-13-17(9-10-18(15)20)28-22(31)19(8-5-11-27-23(25)26)29-24(32)33-14-16-6-3-2-4-7-16/h2-4,6-7,9-10,12-13,19H,5,8,11,14H2,1H3,(H,28,31)(H,29,32)(H4,25,26,27)/t19-/m1/s1

Property Name	Value
Molecular Formula	C24H27N5O5
Molecular Weight	465.2
AlogP	3.45
Hydrogen Bond Acceptor	6.0
Hydrogen Bond Donor	5.0
Number of Rotational Bond	9.0
Polar Surface Area	166.52
Heavy Atoms	34.0

Property Name

Value

Molecular Formula

C24H27N5O5

Molecular Weight

465.2

AlogP

3.45

Hydrogen Bond Acceptor

6.0

Hydrogen Bond Donor

5.0

Number of Rotational Bond

9.0

Polar Surface Area

166.52

Heavy Atoms

34.0

Resources	Reference
CAS NUMBER	70375-22-3
NORMAN SUSDAT
PubChem	16219161
ChemSpider	17333454.0

Resources

Reference

CAS NUMBER

70375-22-3

NORMAN SUSDAT

PubChem

16219161

ChemSpider

17333454.0

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

BENZYL (S)-(4-(AMIDINOAMINO)-1-(((4-METHYL-2-OXO-2H-1-BENZOPYRAN-7-YL)AMINO)CARBONYL)BUTYL)CARBAMATE MONOHYDROCHLORIDE

Structure

Physicochemical Descriptors

Cross References