AlCl₃·6H₂O-Catalyzed Friedel-Crafts Alkylation of Indoles by the para-Quinone Methide Moiety of Celastrol.

about

AlCl₃·6H₂O-Catalyzed Friedel-Crafts Alkylation of Indoles by the para-Quinone Methide Moiety of Celastrol.

Item

http://www.wikidata.org/entity/Q50643691

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

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-hant

name

AlCl₃·6H₂O-Catalyzed Friedel-C ...... e Methide Moiety of Celastrol.

@en

AlCl₃·6H₂O-Catalyzed Friedel-C ...... e Methide Moiety of Celastrol.

@nl

type

Item

label

AlCl₃·6H₂O-Catalyzed Friedel-C ...... e Methide Moiety of Celastrol.

@en

AlCl₃·6H₂O-Catalyzed Friedel-C ...... e Methide Moiety of Celastrol.

@nl

prefLabel

AlCl₃·6H₂O-Catalyzed Friedel-C ...... e Methide Moiety of Celastrol.

@en

AlCl₃·6H₂O-Catalyzed Friedel-C ...... e Methide Moiety of Celastrol.

@nl

P1476

AlCl₃·6H₂O-Catalyzed Friedel-C ...... ne Methide Moiety of Celastrol

@en

P2093

Hu Zhou

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

Siwei Yan

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

Xiaokun Zhang

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

Yi Zhu

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

Ying Su

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

Zhenfei Huang

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

Zhiping Zeng

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

Zhuoer Li

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

P2860

Preclinical studies of celastrol and acetyl isogambogic acid in melanoma.

Celastrol, a potent antioxidant and anti-inflammatory drug, as a possible treatment for Alzheimer's disease.

Formulation and evaluation of celastrol-loaded liposomes.

Celastrol analogues as inducers of the heat shock response. Design and synthesis of affinity probes for the identification of protein targets

Treatment of obesity with celastrol

Characterization of celastrol to inhibit hsp90 and cdc37 interaction.

A review of new developments in the Friedel-Crafts alkylation - From green chemistry to asymmetric catalysis

Novel celastrol derivatives inhibit the growth of hepatocellular carcinoma patient-derived xenografts.

Celastrol inhibits tumor cell proliferation and promotes apoptosis through the activation of c-Jun N-terminal kinase and suppression of PI3 K/Akt signaling pathways.

Reduction of beta-amyloid pathology by celastrol in a transgenic mouse model of Alzheimer's disease.

P31

scholarly article

P356

10.3390/MOLECULES22050742

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

Ziwen Chen

P577

2017-05-16T00:00:00Z

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

P698

28509859

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

P932

6154665

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