A synthetic chalcone as a potent inducer of glutathione biosynthesis - Wikidata - awgldk - TriplyDB

A synthetic chalcone as a potent inducer of glutathione biosynthesis

A synthetic chalcone as a potent inducer of glutathione biosynthesis

http://www.wikidata.org/entity/Q33631139

about

4-methoxychalcone enhances cisplatin-induced oxidative stress and cytotoxicity by inhibiting the Nrf2/ARE-mediated defense mechanism in A549 lung cancer cells.Investigation of chalcones as selective inhibitors of the breast cancer resistance protein: critical role of methoxylation in both inhibition potency and cytotoxicity Post-translational Activation of Glutamate Cysteine Ligase with Dimercaprol: A NOVEL MECHANISM OF INHIBITING NEUROINFLAMMATION IN VITRO.Synthesis and cytotoxic evaluation of alkoxylated chalcones.Recent progress in the development of small molecule Nrf2 modulators: a patent review (2012-2016).1H and 13C NMR spectral assignments of 2'-hydroxychalcones.Impact of different resistance training protocols on muscular oxidative stress parameters.Design and development of Nrf2 modulators for cancer chemoprevention and therapy: a review

P2860

Q37462706-12B126BC-7D60-4AF6-AD34-D654079EDA8F Q37698421-F3657927-390E-4587-A3AB-A9E67E7CFE4A Q38716305-C95FFC64-71F5-4CEE-B1E4-8FF39D304BEC Q38944173-9634DB6F-C7B5-4E85-87EC-88CC5A5E704E Q39270529-765BE44C-B7BC-4E86-9DE6-4FEC7FC7F4BD Q45485001-BE9927C1-FDF8-4765-A301-5DE476ADFF40 Q50499983-5C0031F5-5F17-4098-8EC7-870DEEDBE63E Q57069735-22E7619F-CE1D-44BB-B8A5-AF5CC4506FCD

P2860

A synthetic chalcone as a potent inducer of glutathione biosynthesis

http://www.wikidata.org/entity/Q33631139

description

2012 nî lūn-bûn

@nan

2012 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի հունվարին հրատարակված գիտական հոդված

@hy

2012年の論文

@ja

2012年論文

@yue

2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

@zh-tw

2012年论文

@wuu

name

A synthetic chalcone as a potent inducer of glutathione biosynthesis

@ast

A synthetic chalcone as a potent inducer of glutathione biosynthesis

@en

type

label

A synthetic chalcone as a potent inducer of glutathione biosynthesis

@ast

A synthetic chalcone as a potent inducer of glutathione biosynthesis

@en

prefLabel

A synthetic chalcone as a potent inducer of glutathione biosynthesis

@ast

A synthetic chalcone as a potent inducer of glutathione biosynthesis

@en

P1433

Q33631139-7F44ED1B-30BF-4D26-B0E7-C3305181A139

P1476

Q33631139-8B59B799-740C-4F56-9579-97CC16B9B659

P2093

Q33631139-18971E1B-3A49-4B06-AE86-F9F6972CA13F

Q33631139-438A74B7-F40F-4DFB-B047-AEB5705E9723

Q33631139-49044398-611E-4972-A7FA-D0C29B316A9B

Q33631139-7CACECC4-5356-4C1F-94C6-E5560360F4DE

Q33631139-8431303C-219D-419F-A233-60FC4DFF4B89

Q33631139-B000EF1D-9F38-4504-997F-0FAF1589FF7B

Q33631139-CFCEB384-87A7-4CCB-93D5-97E24F075BD1

Q33631139-DE299E7D-C323-4154-9CE8-9F5FD30BAC22

Q33631139-FCC0E8CA-2255-40F1-947E-D0B3690C1046

P2860

Q33631139-08E27758-8CD9-4C2B-8B3B-66ECFAB2CF7F

Q33631139-10EA1898-377E-4E09-8DAC-E1D9BFA5874F

Q33631139-148E8920-5F4B-4CE7-8E77-D9A4BCF0D912

Q33631139-19580DB2-0EC2-442D-B1DD-BF92F4D55F69

Q33631139-29039F97-1FEC-4401-A46E-6785E8AB9D9A

Q33631139-2E843021-E89F-46CC-8632-27398978DCF7

Q33631139-38383917-7FB7-4633-96C3-571014BA0EFF

Q33631139-39A2E91B-FC7F-4C8C-895D-8A355F7C68F4

Q33631139-3E60F31E-2526-4F5E-A348-6176FB802816

Q33631139-44D193D6-CB44-4EA2-8A2E-BC22FC69F136

P304

Q33631139-F73D6738-C04E-4A7A-9C22-7B55F645621C

P31

Q33631139-0C8A075A-5399-4BFA-9BDB-22FB42303C07

P356

Q33631139-2F276545-5BE1-4CC7-A8E3-CBCB8337219B

P407

Q33631139-B13246AA-DBB1-4A0D-AE6E-89873F7F312D

P433

Q33631139-044138BD-908C-4691-8118-48E7BEE329B9

P478

Q33631139-886DE7CF-5A01-496F-A95F-AA70FD033245

P577

Q33631139-C67A8865-125E-4278-8F44-2BAD24AACC78

P5875

Q33631139-C30737B7-D26A-4C30-BB48-F14E242D8AEA

P698

Q33631139-1B9B7C71-C84E-451F-A29B-5287A907C154

P932

Q33631139-A0B92E94-4097-4592-AC89-4995DF67A189

P356

P1433

Journal of Medicinal Chemistry

P1476

A synthetic chalcone as a potent inducer of glutathione biosynthesis

@en

P2093

Ahcène Boumendjel

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

Attilio Di Pietro

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

Brian J Day

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

Charlotte Gauthier

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

Christopher C Franklin

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

Estelle Genoux-Bastide

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

Gregory Mahaffey

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

Remy Kachadourian

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

Subbiah Pugazhenti

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

P2860

Posttranslational modification and regulation of glutamate-cysteine ligase by the α,β-unsaturated aldehyde 4-hydroxy-2-nonenal

New synthetic triterpenoids: potent agents for prevention and treatment of tissue injury caused by inflammatory and oxidative stress

Structure, function, and post-translational regulation of the catalytic and modifier subunits of glutamate cysteine ligase

Regulation of glutathione synthesis

Flavonoids: antioxidants or signalling molecules?

SP600125, an anthrapyrazolone inhibitor of Jun N-terminal kinase

SB 203580 is a specific inhibitor of a MAP kinase homologue which is stimulated by cellular stresses and interleukin-1

Functionalized chalcones as selective inhibitors of P-glycoprotein and breast cancer resistance protein.

A novel chalcone derivative which acts as a microtubule depolymerising agent and an inhibitor of P-gp and BCRP in in-vitro and in-vivo glioblastoma models.

Antioxidant functions of sulforaphane: a potent inducer of Phase II detoxication enzymes.

P304

1382-1388

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

P31

scholarly article

P356

10.1021/JM2016073

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

P407

P433

3

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

P478

55

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

P577

2012-01-30T00:00:00Z

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

P5875

221742361

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

P698

22239485

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

P932

4026013

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