EcoDrugPlus


Molecule Category	Free-form
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 ...

Molecule Category

Free-form

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	MWJZDLMYLURZEF-UHFFFAOYSA-N
Smiles	CCONCCCOc1ccc(CC(CC)CC)cc1
InChI	InChI=1S/C17H29NO2/c1-4-15(5-2)14-16-8-10-17(11-9-16)19-13-7-12-18-20-6-3/h8-11,15,18H,4-7,12-14H2,1-3H3

InChI Key

MWJZDLMYLURZEF-UHFFFAOYSA-N

Smiles

CCONCCCOc1ccc(CC(CC)CC)cc1

InChI

InChI=1S/C17H29NO2/c1-4-15(5-2)14-16-8-10-17(11-9-16)19-13-7-12-18-20-6-3/h8-11,15,18H,4-7,12-14H2,1-3H3

Property Name	Value
Molecular Formula	C17H29NO2
Molecular Weight	279.42
AlogP	4.16
Hydrogen Bond Acceptor	3.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	11.0
Polar Surface Area	30.49
Molecular species	NEUTRAL
Aromatic Rings	1.0
Heavy Atoms	20.0

Property Name

Value

Molecular Formula

C17H29NO2

Molecular Weight

279.42

AlogP

4.16

Hydrogen Bond Acceptor

3.0

Hydrogen Bond Donor

1.0

Number of Rotational Bond

11.0

Polar Surface Area

30.49

Molecular species

NEUTRAL

Aromatic Rings

1.0

Heavy Atoms

20.0

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Culex pipiens	-	3.72	-	-	-

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Culex pipiens

3.72

Resources	Reference
ChEMBL	CHEMBL2272189
PubChem	15676825
SureChEMBL	SCHEMBL9778406

Resources

Reference

ChEMBL

CHEMBL2272189

PubChem

15676825

SureChEMBL

SCHEMBL9778406

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

O-ETHYL-N-(3-(4-(2-ETHYLBUTYL)PHENOXY)PROPYL)HYDROXYLAMINE

Structure

Physicochemical Descriptors

Pharmacology

Cross References