4-CHLORO-2-(3,4-DICHLOROPHENYLCARBAMOYL)PHENYL PROPYLCARBAMATE


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	NKPZBBDRVLRTLX-UHFFFAOYSA-N
Smiles	CCCNC(=O)Oc1ccc(Cl)cc1C(=O)Nc2ccc(Cl)c(Cl)c2
InChI	InChI=1S/C17H15Cl3N2O3/c1-2-7-21-17(24)25-15-6-3-10(18)8-12(15)16(23)22-11-4-5-13(19)14(20)9-11/h3-6,8-9H,2,7H2,1H3,(H,21,24)(H,22,23)

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C17H15Cl3N2O3
Molecular Weight	401.67
AlogP	5.24
Hydrogen Bond Acceptor	3.0
Hydrogen Bond Donor	2.0
Number of Rotational Bond	6.0
Polar Surface Area	67.43
Molecular species	NEUTRAL
Aromatic Rings	2.0
Heavy Atoms	25.0

Assay Description	Organism	Bioactivity
Half life in aqueous buffer solutions at pH 7.4 by HPLC analysis	None	43.0 hr
Half life in aqueous buffer solutions at pH 7 by HPLC analysis	None	64.0 hr
Chemical stability of the compound in aqueous buffer solutions at acidic pH by HPLC analysis	None	None
Lipophilicity, log K of the compound	None	1.05
Inhibition of photosystem II in Spinacia oleracea (spinach) chloroplasts assessed as reduction of photosynthetic electron transport	Spinacia oleracea	56400.0 nM

Cross References

Resources	Reference
ChEMBL	CHEMBL2287511
PubChem	76331057

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).