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	HBJXIOLROYQESO-UHFFFAOYSA-N
Smiles	CN1C2=NC3C=CC=CC3C2=C(NCCCN)c4ccccc14
InChI	InChI=1S/C19H22N4/c1-23-16-10-5-3-8-14(16)18(21-12-6-11-20)17-13-7-2-4-9-15(13)22-19(17)23/h2-5,7-10,13,15,21H,6,11-12,20H2,1H3

InChI Key

HBJXIOLROYQESO-UHFFFAOYSA-N

Smiles

CN1C2=NC3C=CC=CC3C2=C(NCCCN)c4ccccc14

InChI

InChI=1S/C19H22N4/c1-23-16-10-5-3-8-14(16)18(21-12-6-11-20)17-13-7-2-4-9-15(13)22-19(17)23/h2-5,7-10,13,15,21H,6,11-12,20H2,1H3

Property Name	Value
Molecular Formula	C19H22N4
Molecular Weight	306.4
AlogP	0.77
Hydrogen Bond Acceptor	4.0
Hydrogen Bond Donor	2.0
Number of Rotational Bond	4.0
Polar Surface Area	53.65
Molecular species	BASE
Aromatic Rings	1.0
Heavy Atoms	23.0

Property Name

Value

Molecular Formula

C19H22N4

Molecular Weight

306.4

AlogP

0.77

Hydrogen Bond Acceptor

4.0

Hydrogen Bond Donor

2.0

Number of Rotational Bond

4.0

Polar Surface Area

53.65

Molecular species

BASE

Aromatic Rings

1.0

Heavy Atoms

23.0

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Homo sapiens	-	66	-	-	-

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Homo sapiens

Resources	Reference
ChEMBL	CHEMBL2297941
PubChem	76327717

Resources

Reference

ChEMBL

CHEMBL2297941

PubChem

76327717

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

N1-(5-METHYL-6A,10A-DIHYDRO-5H-INDOLO[2,3-B]QUINOLIN-11-YL)PROPANE-1,3-DIAMINE

Structure

Physicochemical Descriptors

Pharmacology

Cross References