EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Free-form
EPA CompTox	DTXSID00223176

Keyword(s):

Human Metabolites

Molecule Category

Free-form

EPA CompTox

DTXSID00223176


InChI Key	ZIDQIOZJEJFMOH-JKSUJKDBSA-N
Smiles	OC(CCN1C(CCCCCCC(=O)O)C(=O)NC1=O)C1CCCCC1
InChI	InChI=1S/C19H32N2O5/c22-16(14-8-4-3-5-9-14)12-13-21-15(18(25)20-19(21)26)10-6-1-2-7-11-17(23)24/h14-16,22H,1-13H2,(H,23,24)(H,20,25,26)/t15-,16-/m0/s1

InChI Key

ZIDQIOZJEJFMOH-JKSUJKDBSA-N

Smiles

OC(CCN1C(CCCCCCC(=O)O)C(=O)NC1=O)C1CCCCC1

InChI

InChI=1S/C19H32N2O5/c22-16(14-8-4-3-5-9-14)12-13-21-15(18(25)20-19(21)26)10-6-1-2-7-11-17(23)24/h14-16,22H,1-13H2,(H,23,24)(H,20,25,26)/t15-,16-/m0/s1

Property Name	Value
Molecular Formula	C19H32N2O5
Molecular Weight	368.23
AlogP	3.5
Hydrogen Bond Acceptor	3.0
Hydrogen Bond Donor	3.0
Number of Rotational Bond	11.0
Polar Surface Area	110.43
Heavy Atoms	26.0

Property Name

Value

Molecular Formula

C19H32N2O5

Molecular Weight

368.23

AlogP

3.5

Hydrogen Bond Acceptor

3.0

Hydrogen Bond Donor

3.0

Number of Rotational Bond

11.0

Polar Surface Area

110.43

Heavy Atoms

26.0

Resources	Reference
CAS NUMBER	72880-75-2
NORMAN SUSDAT
PubChem	3080928
ChemSpider	2338640.0

Resources

Reference

CAS NUMBER

72880-75-2

NORMAN SUSDAT

PubChem

3080928

ChemSpider

2338640.0

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, 2025, gkaf1251 Read...

This work is licensed under Creative Commons Attribution-ShareAlike 4.0 International License

Last update: Monday, 3 November 2025

(R-(R,S))-3-(3-CYCLOHEXYL-3-HYDROXYPROPYL)-2,5-DIOXOIMIDAZOLIDINE-4-HEPTANOIC ACID

Structure

Physicochemical Descriptors

Cross References

(R-(R*,S*))-3-(3-CYCLOHEXYL-3-HYDROXYPROPYL)-2,5-DIOXOIMIDAZOLIDINE-4-HEPTANOIC ACID

Structure

Physicochemical Descriptors

Cross References

(R-(R,S))-3-(3-CYCLOHEXYL-3-HYDROXYPROPYL)-2,5-DIOXOIMIDAZOLIDINE-4-HEPTANOIC ACID