1-ETHYL-7-METHYL-4-OXO-1,4-DIHYDRO-[1,8]NAPHTHYRIDINE-3-CARBOXYLIC ACID(3-NITRO-BENZYLIDENE)-HYDRAZIDE

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Search structure


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	BXIRRJPRGYDSIJ-KEBDBYFISA-N
Smiles	CCN1C=C(C(=O)N\N=C\c2cccc(c2)[N+](=O)[O-])C(=O)c3ccc(C)nc13
InChI	InChI=1S/C19H17N5O4/c1-3-23-11-16(17(25)15-8-7-12(2)21-18(15)23)19(26)22-20-10-13-5-4-6-14(9-13)24(27)28/h4-11H,3H2,1-2H3,(H,22,26)/b20-10+

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C19H17N5O4
Molecular Weight	379.37
AlogP	2.29
Hydrogen Bond Acceptor	7.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	5.0
Polar Surface Area	120.47
Molecular species	NEUTRAL
Aromatic Rings	2.0
Heavy Atoms	28.0

Assay Description	Organism	Bioactivity	Reference
Insecticidal activity against adult Callosobruchus maculatus assessed as mortality at 0.1% at 27 +/-1 degC after 24 hr by contact based film residue method	Callosobruchus maculatus	10.0 %
Insecticidal activity against third-instar larval stage of prestarved Spodoptera litura in castor leaf assessed as mortality at 0.1% treated for 2 secs before larval infestation measured after 24 hr by feeding method	Spodoptera litura	80.0 %
Fungicidal activity against Fusarium oxysporum by poisoned food technique	Fusarium oxysporum	212.2 ug ml-1
Fungicidal activity against Alternaria porri by poisoned food technique	Alternaria porri	89.0 ug ml-1
Fungicidal activity against Rhizoctonia solani by poisoned food technique	Rhizoctonia solani	244.7 ug ml-1
Fungicidal activity against Rhizoctonia bataticola by poisoned food technique	Rhizoctonia bataticola	271.5 ug ml-1
Fungicidal activity against Athelia rolfsii by poisoned food technique	Athelia rolfsii	286.9 ug ml-1

Cross References

Resources	Reference
ChEMBL	CHEMBL2228729
PubChem	45277965

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).