EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Free-form
EPA CompTox	DTXSID20937541

Keyword(s):

Human Metabolites

Molecule Category

Free-form

EPA CompTox

DTXSID20937541


InChI Key	HUKWNEDRRBXWKG-UHFFFAOYSA-N
Smiles	O=C1OC(=O)C(N1)C(O)C
InChI	InChI=1/C5H7NO4/c1-2(7)3-4(8)10-5(9)6-3/h2-3,7H,1H3,(H,6,9)

InChI Key

HUKWNEDRRBXWKG-UHFFFAOYSA-N

Smiles

O=C1OC(=O)C(N1)C(O)C

InChI

InChI=1/C5H7NO4/c1-2(7)3-4(8)10-5(9)6-3/h2-3,7H,1H3,(H,6,9)

Property Name	Value
Molecular Formula	C5H7NO4
Molecular Weight	145.04
AlogP	-0.79
Hydrogen Bond Acceptor	4.0
Hydrogen Bond Donor	2.0
Number of Rotational Bond	1.0
Polar Surface Area	79.12
Heavy Atoms	10.0

Property Name

Value

Molecular Formula

C5H7NO4

Molecular Weight

145.04

AlogP

-0.79

Hydrogen Bond Acceptor

4.0

Hydrogen Bond Donor

2.0

Number of Rotational Bond

1.0

Polar Surface Area

79.12

Heavy Atoms

10.0

Resources	Reference
CAS NUMBER	16874-73-0
NORMAN SUSDAT
PubChem	86083

Resources

Reference

CAS NUMBER

16874-73-0

NORMAN SUSDAT

PubChem

86083

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,S)-4-(1-HYDROXYETHYL)OXAZOLIDINE-2,5-DIONE

Structure

Physicochemical Descriptors

Cross References

(R*,S*)-4-(1-HYDROXYETHYL)OXAZOLIDINE-2,5-DIONE

Structure

Physicochemical Descriptors

Cross References

(R,S)-4-(1-HYDROXYETHYL)OXAZOLIDINE-2,5-DIONE