Substituted N-aminothioglycolurils containing thiosemicarbazone moiety and their cytotoxic activity in vitro.

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Substituted N-aminothioglycolurils containing thiosemicarbazone moiety and their cytotoxic activity in vitro.

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2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

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name

Substituted N-aminothioglycolu ...... r cytotoxic activity in vitro.

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Item

label

Substituted N-aminothioglycolu ...... r cytotoxic activity in vitro.

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prefLabel

Substituted N-aminothioglycolu ...... r cytotoxic activity in vitro.

@en

P1476

Substituted N-aminothioglycolu ...... ir cytotoxic activity in vitro

@en

P2093

Angelina N Kravchenko

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Galina A Gazieva

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Lada V Anikina

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Sergei A Pukhov

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Tatyana B Karpova

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

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Thiosemicarbazones from the old to new: iron chelators that are more than just ribonucleotide reductase inhibitors.

Synthesis of thiophene-thiosemicarbazone derivatives and evaluation of their in vitro and in vivo antitumor activities.

Novel R-(+)-limonene-based thiosemicarbazones and their antitumor activity against human tumor cell lines.

Role of metalation in the topoisomerase IIα inhibition and antiproliferation activity of a series of α-heterocyclic-N4-substituted thiosemicarbazones and their Cu(II) complexes.

Synthesis and cytotoxic potency of novel tris(1-alkylindol-3-yl)methylium salts: role of N-alkyl substituents.

Synthesis and antitumor activity of liquiritigenin thiosemicarbazone derivatives.

A series of alpha-heterocyclic carboxaldehyde thiosemicarbazones inhibit topoisomerase IIalpha catalytic activity.

P2888

s11030-016-9671-1

P304

837-846

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P31

scholarly article

P356

10.1007/S11030-016-9671-1

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P433

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

P478

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P50

Yulia V. Nelyubina

P577

2016-05-23T00:00:00Z

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P698

27216444

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