EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Free-form
EPA CompTox	DTXSID80915880

Keyword(s):

Human Metabolites

Molecule Category

Free-form

EPA CompTox

DTXSID80915880


InChI Key	XEXUZDAOYNFNDV-UHFFFAOYSA-N
Smiles	O=C(N(COCC(O)COCC(O)CO)COCC(O)COCC(O)CO)CCCCCCCCCCCCCCCCC
InChI	InChI=1/C32H65NO11/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-32(40)33(26-43-24-30(38)22-41-20-28(36)18-34)27-44-25-31(39)23-42-21-29(37)19-35/h28-31,34-39H,2-27H2,1H3

InChI Key

XEXUZDAOYNFNDV-UHFFFAOYSA-N

Smiles

O=C(N(COCC(O)COCC(O)CO)COCC(O)COCC(O)CO)CCCCCCCCCCCCCCCCC

InChI

InChI=1/C32H65NO11/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-32(40)33(26-43-24-30(38)22-41-20-28(36)18-34)27-44-25-31(39)23-42-21-29(37)19-35/h28-31,34-39H,2-27H2,1H3

Property Name	Value
Molecular Formula	C32H65NO11
Molecular Weight	639.46
AlogP	2.49
Hydrogen Bond Acceptor	11.0
Hydrogen Bond Donor	6.0
Number of Rotational Bond	34.0
Polar Surface Area	178.61
Heavy Atoms	44.0

Property Name

Value

Molecular Formula

C32H65NO11

Molecular Weight

639.46

AlogP

2.49

Hydrogen Bond Acceptor

11.0

Hydrogen Bond Donor

6.0

Number of Rotational Bond

34.0

Polar Surface Area

178.61

Heavy Atoms

44.0

Resources	Reference
CAS NUMBER	94248-87-0
NORMAN SUSDAT
PubChem	3024156

Resources

Reference

CAS NUMBER

94248-87-0

NORMAN SUSDAT

PubChem

3024156

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-BIS[[3-(2,3-DIHYDROXYPROPOXY)-2-HYDROXYPROPOXY]METHYL]STEARAMIDE

Structure

Physicochemical Descriptors

Cross References