Quinazoline-2,4(1H, 3H)-diones inhibit the growth of multiple human tumor cell lines.

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Quinazoline-2,4(1H, 3H)-diones inhibit the growth of multiple human tumor cell lines.

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2013 nî lūn-bûn

@nan

2013年の論文

@ja

2013年論文

@yue

2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

@zh-mo

2013年論文

@zh-tw

2013年论文

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2013年论文

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2013年论文

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Quinazoline-2,4(1H, 3H)-diones inhibit the growth of multiple human tumor cell lines.

@en

Quinazoline-2,4(1H, 3H)-diones inhibit the growth of multiple human tumor cell lines.

@nl

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Item

label

Quinazoline-2,4(1H, 3H)-diones inhibit the growth of multiple human tumor cell lines.

@en

Quinazoline-2,4(1H, 3H)-diones inhibit the growth of multiple human tumor cell lines.

@nl

prefLabel

Quinazoline-2,4(1H, 3H)-diones inhibit the growth of multiple human tumor cell lines.

@en

Quinazoline-2,4(1H, 3H)-diones inhibit the growth of multiple human tumor cell lines.

@nl

P1476

Quinazoline-2,4(1H, 3H)-diones inhibit the growth of multiple human tumor cell lines.

@en

P2093

Gang Liu

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

Xiaoli Zhou

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

Xilei Xie

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P2860

Discovery of novel benzimidazoles as potent inhibitors of TIE-2 and VEGFR-2 tyrosine kinase receptors

The NCI60 human tumour cell line anticancer drug screen

Microwave-assisted efficient and convenient synthesis of 2,4(1H,3H)-quinazolinediones and 2-thioxoquinazolines.

Dynamic covalent chemistry of disulfides offers a highly efficient synthesis of diverse benzofused nitrogen-sulfur heterocycles in one pot.

Pharmacological characterization of some selected 4,5-dihydro-4-oxo-1,2,4-triazolo[1,5-a]quinoxaline-2-carboxylates and 3-hydroxyquinazoline-2,4-diones as (S)-2-amino-3-(3-hydroxy-5-methylisoxazol-4-yl)-propionic acid receptor antagonists.

In vitro and in vivo activities of PD 0305970 and PD 0326448, new bacterial gyrase/topoisomerase inhibitors with potent antibacterial activities versus multidrug-resistant gram-positive and fastidious organism groups

Role of 1,4-benzothiazine derivatives in medicinal chemistry.

Parallel solution phase synthesis of 3,6,7-4(3H)-quinazolinones and evaluation of their antitumor activities against human cancer.

Synthesis, antiviral and antitumor activity of 2-substituted-5-amidino-benzimidazoles.

Novel inhibitors of the nuclear factor of activated T cells (NFAT)-mediated transcription of beta-galactosidase: potential immunosuppressive and antiinflammatory agents.

P2888

s11030-012-9421-y

P304

197-219

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P31

scholarly article

P356

10.1007/S11030-012-9421-Y

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P433

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

P478

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

P577

2013-01-26T00:00:00Z

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P698

23354539

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