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	DZGFIACXEOQLFQ-UHFFFAOYSA-N
Smiles	COC(=O)C1=CC2C(C=C1)N=C3N(C)c4ccccc4C(=C23)N5CCOCC5
InChI	InChI=1S/C22H23N3O3/c1-24-18-6-4-3-5-15(18)20(25-9-11-28-12-10-25)19-16-13-14(22(26)27-2)7-8-17(16)23-21(19)24/h3-8,13,16-17H,9-12H2,1-2H3

InChI Key

DZGFIACXEOQLFQ-UHFFFAOYSA-N

Smiles

COC(=O)C1=CC2C(C=C1)N=C3N(C)c4ccccc4C(=C23)N5CCOCC5

InChI

InChI=1S/C22H23N3O3/c1-24-18-6-4-3-5-15(18)20(25-9-11-28-12-10-25)19-16-13-14(22(26)27-2)7-8-17(16)23-21(19)24/h3-8,13,16-17H,9-12H2,1-2H3

Property Name	Value
Molecular Formula	C22H23N3O3
Molecular Weight	377.44
AlogP	1.58
Hydrogen Bond Acceptor	6.0
Number of Rotational Bond	3.0
Polar Surface Area	54.37
Molecular species	BASE
Aromatic Rings	1.0
Heavy Atoms	28.0

Property Name

Value

Molecular Formula

C22H23N3O3

Molecular Weight

377.44

AlogP

1.58

Hydrogen Bond Acceptor

6.0

Number of Rotational Bond

3.0

Polar Surface Area

54.37

Molecular species

BASE

Aromatic Rings

1.0

Heavy Atoms

28.0

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Homo sapiens	-	797-5090	-	-	-

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Homo sapiens

797-5090

Resources	Reference
ChEMBL	CHEMBL2297935
PubChem	76324160

Resources

Reference

ChEMBL

CHEMBL2297935

PubChem

76324160

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

METHYL 5-METHYL-11-MORPHOLINO-5H-INDOLO[2,3-B]QUINOLINE-9-CARBOXYLATE

Structure

Physicochemical Descriptors

Pharmacology

Cross References