Quantitative Structure-activity Relationships of Antifungal 1-(3,5-Dichlorophenyl)-2,5-pyrrolidinediones and 3-(3,5-Dichlorophenyl)-2,4-oxazolidinediones

Takayama, Chiyozo; Fujinami, Akira; Kirino, Osamu; Hisada, Yoshio

doi:10.1080/00021369.1982.10865517

Agricultural and Biological Chemistry

1982

DOI: 10.1080/00021369.1982.10865517

|View full text |Cite

Quantitative Structure-activity Relationships of Antifungal 1-(3,5-Dichlorophenyl)-2,5-pyrrolidinediones and 3-(3,5-Dichlorophenyl)-2,4-oxazolidinediones

Chiyozo Takayama¹,

Akira Fujinami²,

Osamu Kirino³

et al.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

Supporting

Mentioning

Contrasting

Year Published

1994

Publication Types

Select...

Article1

Relationship

Self Cite0

Independent1

Authors

Journals

Cited by 1 publication

(1 citation statement)

References 4 publications

(8 reference statements)

Supporting

Mentioning

Contrasting

Order By: Relevance

“…Plot of the antifungal activity of 12 l-(3,5-dichlorophenyl)-3-substituted-2,5-pyrrolidinediones against B.cinerea. Squares are proportional to ""7» values (mol Lr1) inducing 50 % inhibition of mycelial growth 46.…”

contrasting

confidence: 74%

A Nonlinear Map of Substituent Constants for Selecting Test Series and Deriving Structure-Activity Relationships. II. Aliphatic Series

Domine¹,

Devillers²,

Chastrette³

1994

J. Med. Chem.

View full text Add to dashboard Cite

A nonlinear mapping (NLM) analysis was performed on a set of 103 aliphatic substituents described by five variables encoding hydrophobic (Fr), steric (MR), and electronic effects (HBA, HBD, and F). NLM allowed to easily summarize the main information contained in the original data table. By means of collections of graphs, it was possible to relate the structure of the aliphatic substituents to their Fr, MR, HBA, HBD, and F values. The proposed approach provides a useful and easy tool for the selection of test series and for deriving structure-activity relationships.

show abstract

contrasting

confidence: 74%

A Nonlinear Map of Substituent Constants for Selecting Test Series and Deriving Structure-Activity Relationships. II. Aliphatic Series

Domine¹,

Devillers²,

Chastrette³

1994

J. Med. Chem.

View full text Add to dashboard Cite

show abstract

scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.

Contact Info

customersupport@researchsolutions.com

10624 S. Eastern Ave., Ste. A-614

Henderson, NV 89052, USA

Blog Terms and Conditions API Terms Privacy Policy Contact Cookie Preferences Do Not Sell or Share My Personal Information

Made with 💙 for researchers

Part of the Research Solutions Family.

Quantitative Structure-activity Relationships of Antifungal 1-(3,5-Dichlorophenyl)-2,5-pyrrolidinediones and 3-(3,5-Dichlorophenyl)-2,4-oxazolidinediones

Cited by 1 publication

References 4 publications

A Nonlinear Map of Substituent Constants for Selecting Test Series and Deriving Structure-Activity Relationships. II. Aliphatic Series

A Nonlinear Map of Substituent Constants for Selecting Test Series and Deriving Structure-Activity Relationships. II. Aliphatic Series

Contact Info

Product

Resources

About