EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Free-form
EPA CompTox	DTXSID10432893

Keyword(s):

Human Metabolites

Molecule Category

Free-form

EPA CompTox

DTXSID10432893


InChI Key	GFZFELCFSBCPDB-AAEUAGOBSA-N
Smiles	CCOC(=O)[C@H](CCC1=CC=CC=C1)N1[C@@H](C)C(=O)OC1=O
InChI	InChI=1S/C16H19NO5/c1-3-21-15(19)13(10-9-12-7-5-4-6-8-12)17-11(2)14(18)22-16(17)20/h4-8,11,13H,3,9-10H2,1-2H3/t11-,13-/m0/s1

InChI Key

GFZFELCFSBCPDB-AAEUAGOBSA-N

Smiles

CCOC(=O)[C@H](CCC1=CC=CC=C1)N1[C@@H](C)C(=O)OC1=O

InChI

InChI=1S/C16H19NO5/c1-3-21-15(19)13(10-9-12-7-5-4-6-8-12)17-11(2)14(18)22-16(17)20/h4-8,11,13H,3,9-10H2,1-2H3/t11-,13-/m0/s1

Property Name	Value
Molecular Formula	C16H19N1O5
Molecular Weight	305.13
AlogP	1.92
Hydrogen Bond Acceptor	5.0
Number of Rotational Bond	6.0
Polar Surface Area	72.91
Heavy Atoms	22.0

Property Name

Value

Molecular Formula

C16H19N1O5

Molecular Weight

305.13

AlogP

1.92

Hydrogen Bond Acceptor

5.0

Number of Rotational Bond

6.0

Polar Surface Area

72.91

Heavy Atoms

22.0

Resources	Reference
CAS NUMBER	84793-24-8
NORMAN SUSDAT
PubChem	9922512
ChemSpider	3829422.0

Resources

Reference

CAS NUMBER

84793-24-8

NORMAN SUSDAT

PubChem

9922512

ChemSpider

3829422.0

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

ETHYL (2S)-2-[(4S)-4-METHYL-2,5-DIOXO-1,3-OXAZOLIDIN-3-YL]-4-PHENYLBUTANOATE

Structure

Physicochemical Descriptors

Cross References