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 ...


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


InChI Key	ZEDIHMXSKFVJJF-UHFFFAOYSA-N
Smiles	CC(=O)Nc1ccc(cc1)C(=O)NC2=CC(=O)C(=O)c3ccccc23
InChI	InChI=1S/C19H14N2O4/c1-11(22)20-13-8-6-12(7-9-13)19(25)21-16-10-17(23)18(24)15-5-3-2-4-14(15)16/h2-10H,1H3,(H,20,22)(H,21,25)

InChI Key

ZEDIHMXSKFVJJF-UHFFFAOYSA-N

Smiles

CC(=O)Nc1ccc(cc1)C(=O)NC2=CC(=O)C(=O)c3ccccc23

InChI

InChI=1S/C19H14N2O4/c1-11(22)20-13-8-6-12(7-9-13)19(25)21-16-10-17(23)18(24)15-5-3-2-4-14(15)16/h2-10H,1H3,(H,20,22)(H,21,25)

Property Name	Value
Molecular Formula	C19H14N2O4
Molecular Weight	334.33
AlogP	1.36
Hydrogen Bond Acceptor	4.0
Hydrogen Bond Donor	2.0
Number of Rotational Bond	3.0
Polar Surface Area	92.34
Molecular species	NEUTRAL
Aromatic Rings	2.0
Heavy Atoms	25.0

Property Name

Value

Molecular Formula

C19H14N2O4

Molecular Weight

334.33

AlogP

1.36

Hydrogen Bond Acceptor

4.0

Hydrogen Bond Donor

2.0

Number of Rotational Bond

3.0

Polar Surface Area

92.34

Molecular species

NEUTRAL

Aromatic Rings

2.0

Heavy Atoms

25.0

Resources	Reference
ChEMBL	CHEMBL2296230
PubChem	76309428

Resources

Reference

ChEMBL

CHEMBL2296230

PubChem

76309428


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).

4-ACETAMIDO-N-(1,2-DIHYDRO-1,2-DIOXONAPHTHALEN-4-YL)BENZAMIDE

Structure

Physicochemical Descriptors

Cross References