Comparative Binding Analysis of Dipeptidyl Peptidase IV (DPP-4) with Antidiabetic Drugs - An Ab Initio Fragment Molecular Orbital Study

about

In silico analysis of interaction pattern switching in ligandreceptor binding in Golgi α-mannosidase II induced by the protonated states of inhibitors.

P2860

Q52661095-2258D96A-3D01-4297-B887-6913E03DCC11

P2860

Comparative Binding Analysis of Dipeptidyl Peptidase IV (DPP-4) with Antidiabetic Drugs - An Ab Initio Fragment Molecular Orbital Study

Item

http://www.wikidata.org/entity/Q36188856

description

2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

@zh-cn

name

Comparative Binding Analysis o ...... agment Molecular Orbital Study

@ast

Comparative Binding Analysis o ...... agment Molecular Orbital Study

@en

type

Item

label

Comparative Binding Analysis o ...... agment Molecular Orbital Study

@ast

Comparative Binding Analysis o ...... agment Molecular Orbital Study

@en

prefLabel

Comparative Binding Analysis o ...... agment Molecular Orbital Study

@ast

Comparative Binding Analysis o ...... agment Molecular Orbital Study

@en

P1476

Comparative Binding Analysis o ...... agment Molecular Orbital Study

@en

P2093

Erika Ishitsubo

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

Hitoshi Shimano

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

Naoya Matsuo

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

Seiji Okazaki

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

Sundaram Arulmozhiraja

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

P2860

New Biological Insights from Better Structure Models

Gaussian basis sets for use in correlated molecular calculations. I. The atoms boron through neon and hydrogen

8-(3-(R)-aminopiperidin-1-yl)-7-but-2-ynyl-3-methyl-1-(4-methyl-quinazolin-2-ylmethyl)-3,7-dihydropurine-2,6-dione (BI 1356), a highly potent, selective, long-acting, and orally bioavailable DPP-4 inhibitor for the treatment of type 2 diabetes

Involvement of DPP-IV catalytic residues in enzyme-saxagliptin complex formation

Design and synthesis of pyrimidinone and pyrimidinedione inhibitors of dipeptidyl peptidase IV

Discovery and preclinical profile of teneligliptin (3-[(2S,4S)-4-[4-(3-methyl-1-phenyl-1H-pyrazol-5-yl)piperazin-1-yl]pyrrolidin-2-ylcarbonyl]thiazolidine): a highly potent, selective, long-lasting and orally active dipeptidyl peptidase IV inhibitor

A comparative study of the binding modes of recently launched dipeptidyl peptidase IV inhibitors in the active site

Comparative Analysis of Binding Kinetics and Thermodynamics of Dipeptidyl Peptidase-4 Inhibitors and Their Relationship to Structure

Overview of the CCP4 suite and current developments

On the size of the active site in proteases. I. Papain

P304

e0166275

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

P31

scholarly article

P356

10.1371/JOURNAL.PONE.0166275

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

P50

Hiroaki Tokiwa

P577

2016-11-10T00:00:00Z

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

P698

27832184

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

P932

5104442

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

Comparative Binding Analysis of Dipeptidyl Peptidase IV (DPP-4) with Antidiabetic Drugs - An Ab Initio Fragment Molecular Orbital Study

about

P2860

P2860

Comparative Binding Analysis of Dipeptidyl Peptidase IV (DPP-4) with Antidiabetic Drugs - An Ab Initio Fragment Molecular Orbital Study

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932