EcoDrugPlus


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

Keyword(s):

Human Metabolites

Molecule Category

Free-form


InChI Key	AZFZQYUDLXNVMW-UHFFFAOYSA-N
Smiles	CCOc1ncc(C)c2NC(C)=C(C(c3ccc(cc3OC)C#N)c12)C(=O)OCCC#N
InChI	InChI=1S/C24H24N4O4/c1-5-31-23-21-20(17-8-7-16(12-26)11-18(17)30-4)19(24(29)32-10-6-9-25)15(3)28-22(21)14(2)13-27-23/h7-8,11,13,20,28H,5-6,10H2,1-4H3

InChI Key

AZFZQYUDLXNVMW-UHFFFAOYSA-N

Smiles

CCOc1ncc(C)c2NC(C)=C(C(c3ccc(cc3OC)C#N)c12)C(=O)OCCC#N

InChI

InChI=1S/C24H24N4O4/c1-5-31-23-21-20(17-8-7-16(12-26)11-18(17)30-4)19(24(29)32-10-6-9-25)15(3)28-22(21)14(2)13-27-23/h7-8,11,13,20,28H,5-6,10H2,1-4H3

Property Name	Value
Molecular Formula	C24H24N4O4
Molecular Weight	432.18
AlogP	3.96
Hydrogen Bond Acceptor	8.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	7.0
Polar Surface Area	117.26
Heavy Atoms	32.0

Property Name

Value

Molecular Formula

C24H24N4O4

Molecular Weight

432.18

AlogP

3.96

Hydrogen Bond Acceptor

8.0

Hydrogen Bond Donor

1.0

Number of Rotational Bond

7.0

Polar Surface Area

117.26

Heavy Atoms

32.0

Resources	Reference
CAS NUMBER	1050477-44-5
NORMAN SUSDAT
PubChem	68600597
ChemSpider	46095822.0

Resources

Reference

CAS NUMBER

1050477-44-5

NORMAN SUSDAT

PubChem

68600597

ChemSpider

46095822.0

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

2-CYANOETHYL 4-(4-CYANO-2-METHOXYPHENYL)-5-ETHOXY-2,8-DIMETHYL-1,4-DIHYDRO-1,6-NAPHTHYRIDINE-3-CARBOXYLATE

Structure

Physicochemical Descriptors

Cross References