4-AMINO-5,6,7,8,9,10-HEXAHYDRO-5-(3,4-DIMETHOXYPHENYL)PYRIMIDO[4,5-B]QUINOLINE


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 ...


Active Pharmaceutical Ingredients Bioactive chemicals	Exact Similarity SubStructure	Threshold (%) >= 70

Structure


InChI Key	DITDFQJROAICDB-UHFFFAOYSA-N
Smiles	COc1ccc(cc1OC)C2C3=C(CCCC3)Nc4ncnc(N)c24
InChI	InChI=1S/C19H22N4O2/c1-24-14-8-7-11(9-15(14)25-2)16-12-5-3-4-6-13(12)23-19-17(16)18(20)21-10-22-19/h7-10,16H,3-6H2,1-2H3,(H3,20,21,22,23)

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C19H22N4O2
Molecular Weight	338.4
AlogP	3.16
Hydrogen Bond Acceptor	6.0
Hydrogen Bond Donor	2.0
Number of Rotational Bond	3.0
Polar Surface Area	82.29
Molecular species	NEUTRAL
Aromatic Rings	2.0
Heavy Atoms	25.0

Assay Description	Organism	Bioactivity
Displacement of methyl green from DNA after 24 hr by spectrophotometric analysis	None	12000.0 nM
Binding affinity to DNA at 5 mg/ml by TLC analysis	None	None
Cytotoxicity against Homo sapiens (human) MCF7 cells after 48 hr by SRB assay	Homo sapiens	3620.0 nM

Cross References

Resources	Reference
ChEMBL	CHEMBL2296388
PubChem	71730195

CONTENTS


PREMIER has received funding from the 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 this manuscript contains. Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).

PREMIER has received funding from the 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 this manuscript contains.

Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).