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	BKIDQCYOOHRQDR-UHFFFAOYSA-N
Smiles	CC1CC(Nc2ccc(C)cc2)c3cc(C)ccc3N1C(=O)c4ccc(cc4)C(C)(C)C
InChI	InChI=1S/C29H34N2O/c1-19-7-14-24(15-8-19)30-26-18-21(3)31(27-16-9-20(2)17-25(26)27)28(32)22-10-12-23(13-11-22)29(4,5)6/h7-17,21,26,30H,18H2,1-6H3

InChI Key

BKIDQCYOOHRQDR-UHFFFAOYSA-N

Smiles

CC1CC(Nc2ccc(C)cc2)c3cc(C)ccc3N1C(=O)c4ccc(cc4)C(C)(C)C

InChI

InChI=1S/C29H34N2O/c1-19-7-14-24(15-8-19)30-26-18-21(3)31(27-16-9-20(2)17-25(26)27)28(32)22-10-12-23(13-11-22)29(4,5)6/h7-17,21,26,30H,18H2,1-6H3

Property Name	Value
Molecular Formula	C29H34N2O
Molecular Weight	426.59
AlogP	6.87
Hydrogen Bond Acceptor	2.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	4.0
Polar Surface Area	32.34
Molecular species	NEUTRAL
Aromatic Rings	3.0
Heavy Atoms	32.0

Property Name

Value

Molecular Formula

C29H34N2O

Molecular Weight

426.59

AlogP

6.87

Hydrogen Bond Acceptor

2.0

Hydrogen Bond Donor

1.0

Number of Rotational Bond

4.0

Polar Surface Area

32.34

Molecular species

NEUTRAL

Aromatic Rings

3.0

Heavy Atoms

32.0

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Bombyx mori	-	23988.33	-	-	-

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Bombyx mori

23988.33

Resources	Reference
ChEMBL	CHEMBL2286414
PubChem	76323735

Resources

Reference

ChEMBL

CHEMBL2286414

PubChem

76323735

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

(4-TERT-BUTYLPHENYL)(2,6-DIMETHYL-4-(P-TOLYLAMINO)-3,4-DIHYDROQUINOLIN-1(2H)-YL)METHANONE

Structure

Physicochemical Descriptors

Pharmacology

Cross References