4-CHLORO-N-(4-CHLOROBENZYL)-N-ISOBUTYLPENT-2-ENAMIDE

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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	GGKDWEAIUIWIND-RUDMXATFSA-N
Smiles	CC(C)CN(Cc1ccc(Cl)cc1)C(=O)\C=C\C(C)Cl
InChI	InChI=1S/C16H21Cl2NO/c1-12(2)10-19(16(20)9-4-13(3)17)11-14-5-7-15(18)8-6-14/h4-9,12-13H,10-11H2,1-3H3/b9-4+

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C16H21Cl2NO
Molecular Weight	314.25
AlogP	4.61
Hydrogen Bond Acceptor	1.0
Hydrogen Bond Donor	0.0
Number of Rotational Bond	6.0
Polar Surface Area	20.31
Molecular species	NEUTRAL
Aromatic Rings	1.0
Heavy Atoms	20.0

Assay Description	Organism	Bioactivity	Reference
Herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as damage of seedlings	Echinochloa crus-galli	16.0 gAi/ha
Phytotoxic activity against Scenedesmus acutus assessed as growth inhibition measured after 20 hr	Scenedesmus acutus	724.44 nM
Phytotoxic activity against Scenedesmus acutus assessed as inhibition of carotenoid biosynthesis measured after 48 hr	Scenedesmus acutus	263.03 nM
Phytotoxic activity against Scenedesmus acutus assessed as ethane formation measured after 20 hr	Scenedesmus acutus	21877.62 nM
Phytotoxic activity against Scenedesmus acutus assessed as decrease in chlorophyll measured after 20 hr	Scenedesmus acutus	549.54 nM
Inhibition of Protoporphyrinogen IX oxidase in Zea mays (maize) seedlings assessed as proto-IX formation by fluorescence spectrophotometer	Zea mays	645.65 nM
Inhibition of Succinate-cytochrome c reductase in Pisum sativum (pea) mitochondrial respiratory-chain electron-transport system at 100 uM	Pisum sativum	0.0 %
Inhibition of chlorophyll biosynthesis of Chlorella salina	Chlorella salina	6309.57 nM
Inhibition of autotrophic growth of Chlorella salina	Chlorella salina	6309.57 nM
Inhibition of protoporphyrinogen oxidase in Gossypium hirsutum (cotton) seedlings assessed as inhibition of protox preparation in cotyledons	Gossypium hirsutum	2511.89 nM
Phytotoxicity against Gossypium hirsutum (cotton) seedlings assessed as inhibition of chlorophyll biosynthesis in cotyledons	Gossypium hirsutum	251.19 nM
Phytotoxicity against Gossypium hirsutum (cotton) seedlings assessed as moderate darkening measured under dark conditions at 100 uM	Gossypium hirsutum	None
Phytotoxicity against Gossypium hirsutum (cotton) seedlings assessed as cotyledons are killed but stems are not wilted measured under light conditions at 100 uM	Gossypium hirsutum	None
Potency index, ratio of ED90 for chlomethoxyfen to ED90 for test compound for herbicidal activity against Echinochloa oryzicola seedling	Echinochloa oryzicola	10.0
Light dependent herbicidal activity against Echinochloa oryzicola seedlings assessed as inhibition of seedlings growth at 10 ppm measured after 6 days post compound application under greenhouse conditions at 25 +/- 2 degC with day light	Echinochloa oryzicola	None
Herbicidal activity against Echinochloa oryzicola seedlings assessed as induction of seedlings damage measured after 3 weeks post compound application through paddy water	Echinochloa oryzicola	16.0 gAi/ha
Lipophilicity, log P of the compound	None	4.68
Herbicidal activity against Echinochloa oryzicola grown in greenhouse at 28 degC under sunshine in day time assessed as inhibition of shoot elongation measured after 7 days post compound application	Echinochloa oryzicola	234422.88 nM

Cross References

Resources	Reference
ChEMBL	CHEMBL2269208
PubChem	13101265

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).