Substructure-activity relationship studies on antibody recognition for phenylurea compounds using competitive immunoassay and computational chemistry.

about

Substructure-activity relationship studies on antibody recognition for phenylurea compounds using competitive immunoassay and computational chemistry.

Item

http://www.wikidata.org/entity/Q49958928

description

2018 nî lūn-bûn

@nan

2018年の論文

@ja

2018年学术文章

@wuu

2018年学术文章

@zh

2018年学术文章

@zh-cn

2018年学术文章

@zh-hans

2018年学术文章

@zh-my

2018年学术文章

@zh-sg

2018年學術文章

@yue

2018年學術文章

@zh-hant

name

Substructure-activity relation ...... y and computational chemistry.

@en

Substructure-activity relation ...... y and computational chemistry.

@nl

type

Item

label

Substructure-activity relation ...... y and computational chemistry.

@en

Substructure-activity relation ...... y and computational chemistry.

@nl

prefLabel

Substructure-activity relation ...... y and computational chemistry.

@en

Substructure-activity relation ...... y and computational chemistry.

@nl

P1476

Substructure-activity relation ...... y and computational chemistry.

@en

P2093

Bing Liu

http://www.w3.org/2001/XMLSchema#string

Fuyuan Zhang

http://www.w3.org/2001/XMLSchema#string

Guozhen Liu

http://www.w3.org/2001/XMLSchema#string

Junping Wang

http://www.w3.org/2001/XMLSchema#string

Shuo Wang

http://www.w3.org/2001/XMLSchema#string

Yan Zhang

http://www.w3.org/2001/XMLSchema#string

P2860

Crystal Structure of the Fab Fragment of an Anti-ofloxacin Antibody and Exploration of Its Specific Binding

Atrazine, triketone herbicides, and their degradation products in sediment, soil and surface water samples in Poland

Phenylurea herbicide sorption to biochars and agricultural soil

Pharmacophore modeling and virtual screening for designing potential 5-lipoxygenase inhibitors.

OptCDR: a general computational method for the design of antibody complementarity determining regions for targeted epitope binding.

A novel disposable electrochemical immunosensor for phenyl urea herbicide diuron.

Quantitative analysis of molecular surface based on improved Marching Tetrahedra algorithm.

Hapten-directed spontaneous disulfide shuffling: a universal technology for site-directed covalent coupling of payloads to antibodies.

Investigation of an Immunoassay with Broad Specificity to Quinolone Drugs by Genetic Algorithm with Linear Assignment of Hypermolecular Alignment of Data Sets and Advanced Quantitative Structure-Activity Relationship Analysis.

Investigation of antigen-antibody interactions of sulfonamides with a monoclonal antibody in a fluorescence polarization immunoassay using 3D-QSAR models.

P304

3131

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1038/S41598-018-21394-X

http://www.w3.org/2001/XMLSchema#string

P407

English

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2018-02-15T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

29449597

http://www.w3.org/2001/XMLSchema#string

P932

5814414

http://www.w3.org/2001/XMLSchema#string