Conjugation of Uridine with Oleanolic Acid Derivatives as Potential Antitumor Agents.

about

Improvement of uridine production of Bacillus subtilis by atmospheric and room temperature plasma mutagenesis and high-throughput screening Improvement of uridine production in Bacillus subtilis by metabolic engineering.

P2860

Q36363033-573E7A45-35AF-4A90-89E9-7DF40F225982 Q47438469-EB9C730C-CB33-45BC-BEB3-F35B40EC076E

P2860

Conjugation of Uridine with Oleanolic Acid Derivatives as Potential Antitumor Agents.

Item

http://www.wikidata.org/entity/Q35962166

description

2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年学术文章

@wuu

2016年学术文章

@zh-cn

2016年学术文章

@zh-hans

2016年学术文章

@zh-my

2016年学术文章

@zh-sg

2016年學術文章

@yue

2016年學術文章

@zh

2016年學術文章

@zh-hant

name

Conjugation of Uridine with Oleanolic Acid Derivatives as Potential Antitumor Agents.

@ast

Conjugation of Uridine with Oleanolic Acid Derivatives as Potential Antitumor Agents.

@en

type

Item

label

Conjugation of Uridine with Oleanolic Acid Derivatives as Potential Antitumor Agents.

@ast

Conjugation of Uridine with Oleanolic Acid Derivatives as Potential Antitumor Agents.

@en

prefLabel

Conjugation of Uridine with Oleanolic Acid Derivatives as Potential Antitumor Agents.

@ast

Conjugation of Uridine with Oleanolic Acid Derivatives as Potential Antitumor Agents.

@en

P1476

Conjugation of Uridine with Oleanolic Acid Derivatives as Potential Antitumor Agents.

@en

P2093

Chun-Hua Su

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

Jia-Yan Huang

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

Jun Liu

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

Ke-Guang Cheng

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

Yuan-Ting Zheng

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

Zhen-Feng Chen

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

P2860

Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays

Naturally occurring pentacyclic triterpenes as inhibitors of glycogen phosphorylase: synthesis, structure-activity relationships, and X-ray crystallographic studies

Pharmacology of oleanolic acid and ursolic acid

Enhancement of glucose uptake in mouse skeletal muscle cells and adipocytes by P2Y6 receptor agonists

Towards cytotoxic and selective derivatives of maslinic acid.

Visibly emissive and responsive extended 6-aza-uridines.

4-Alkyloxyimino derivatives of uridine-5'-triphosphate: distal modification of potent agonists as a strategy for molecular probes of P2Y2, P2Y4, and P2Y6 receptors

Oleanolic acid.

Cell death and cancer therapy.

Apoptotic pathways: the roads to ruin.

P304

329-340

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

P31

scholarly article

P356

10.1111/CBDD.12758

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

P433

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

P478

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

P577

2016-03-17T00:00:00Z

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

P698

26990000

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

Conjugation of Uridine with Oleanolic Acid Derivatives as Potential Antitumor Agents.

about

P2860

P2860

Conjugation of Uridine with Oleanolic Acid Derivatives as Potential Antitumor Agents.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698