N-acylsulfonamides: Synthetic routes and biological potential in medicinal chemistry.

about

The Potential of a Novel Class of EPAC-Selective Agonists to Combat Cardiovascular Inflammation.

P2860

Q48172039-FEB71813-B631-408D-B931-A690F74C59CD

P2860

N-acylsulfonamides: Synthetic routes and biological potential in medicinal chemistry.

Item

http://www.wikidata.org/entity/Q39386218

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh

2017年學術文章

@zh-hant

name

N-acylsulfonamides: Synthetic routes and biological potential in medicinal chemistry.

@en

N-acylsulfonamides: Synthetic routes and biological potential in medicinal chemistry.

@nl

type

Item

label

N-acylsulfonamides: Synthetic routes and biological potential in medicinal chemistry.

@en

N-acylsulfonamides: Synthetic routes and biological potential in medicinal chemistry.

@nl

prefLabel

N-acylsulfonamides: Synthetic routes and biological potential in medicinal chemistry.

@en

N-acylsulfonamides: Synthetic routes and biological potential in medicinal chemistry.

@nl

P1476

N-acylsulfonamides: Synthetic routes and biological potential in medicinal chemistry.

@en

P2093

Barbara De Filippis

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

Rosa Amoroso

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

P2860

Discovery and early clinical evaluation of BMS-605339, a potent and orally efficacious tripeptidic acylsulfonamide NS3 protease inhibitor for the treatment of hepatitis C virus infection

ABT-199, a potent and selective BCL-2 inhibitor, achieves antitumor activity while sparing platelets

Discovery of danoprevir (ITMN-191/R7227), a highly selective and potent inhibitor of hepatitis C virus (HCV) NS3/4A protease

Discovery of 2-Indole-acylsulfonamide Myeloid Cell Leukemia 1 (Mcl-1) Inhibitors Using Fragment-Based Methods

An inhibitor of Bcl-2 family proteins induces regression of solid tumours

ABT-263: a potent and orally bioavailable Bcl-2 family inhibitor

Biochemical characterization of an inhibitor of Escherichia coli UDP-N-acetylmuramyl-l-alanine ligase.

Prostanoid receptor antagonists: development strategies and therapeutic applications

Synopsis of some recent tactical application of bioisosteres in drug design.

PPAR ligands for metabolic disorders.

P304

1094-1105

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

P31

scholarly article

P356

10.1111/CBDD.13043

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

P433

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

P478

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

P50

Alessandra Ammazzalorso

Letizia Giampietro

P577

2017-06-20T00:00:00Z

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

P698

28632928

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

N-acylsulfonamides: Synthetic routes and biological potential in medicinal chemistry.

about

P2860

P2860

N-acylsulfonamides: Synthetic routes and biological potential in medicinal chemistry.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698