EcoDrugPlus


Synonyms	N-(2-Hydroxyethyl)Stearamide N-Stearoylethanolamide
Molecule Category	Free-form
UNII	03XV449Q24
Source	Gaulton A, Kale N, van Westen GJ, Bellis LJ, Bento AP, Davies M, Hersey A, Papadatos G, Forster M, Wege P, Overington JP. A large-scale crop protection bioassay data set. Sci Data. 2015 Jul 7;2:150032. Read more ...

Synonyms

N-(2-Hydroxyethyl)Stearamide

N-Stearoylethanolamide

Molecule Category

Free-form

UNII

Source

Gaulton A, Kale N, van Westen GJ, Bellis LJ, Bento AP, Davies M, Hersey A, Papadatos G, Forster M, Wege P, Overington JP. A large-scale crop protection bioassay data set. Sci Data. 2015 Jul 7;2:150032. Read more ...


InChI Key	OTGQIQQTPXJQRG-UHFFFAOYSA-N
Smiles	CCCCCCCCCCCCCCCCCC(=O)NCCO
InChI	InChI=1S/C20H41NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-20(23)21-18-19-22/h22H,2-19H2,1H3,(H,21,23)

InChI Key

OTGQIQQTPXJQRG-UHFFFAOYSA-N

Smiles

CCCCCCCCCCCCCCCCCC(=O)NCCO

InChI

InChI=1S/C20H41NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-20(23)21-18-19-22/h22H,2-19H2,1H3,(H,21,23)

Property Name	Value
Molecular Formula	C20H41NO2
Molecular Weight	327.55
AlogP	6.34
Hydrogen Bond Acceptor	2.0
Hydrogen Bond Donor	2.0
Number of Rotational Bond	18.0
Polar Surface Area	49.33
Molecular species	NEUTRAL
Aromatic Rings	0.0
Heavy Atoms	23.0

Property Name

Value

Molecular Formula

C20H41NO2

Molecular Weight

327.55

AlogP

6.34

Hydrogen Bond Acceptor

2.0

Hydrogen Bond Donor

2.0

Number of Rotational Bond

18.0

Polar Surface Area

49.33

Molecular species

NEUTRAL

Aromatic Rings

0.0

Heavy Atoms

23.0

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Mus musculus	-	-	-	-	5.65

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Mus musculus

5.65

Resources	Reference
ChEMBL	CHEMBL171447
FDA SRS	03XV449Q24
PubChem	27902
SureChEMBL	SCHEMBL50178
ZINC	ZINC36294576

Resources

Reference

ChEMBL

FDA SRS

PubChem

SureChEMBL

ZINC

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...

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Last update: Monday, 3 November 2025

N-(2-HYDROXYETHYL)STEARAMIDE

Structure

Physicochemical Descriptors

Pharmacology

Cross References