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In silico identification of 2-oxo-1,3-thiazolidine derivatives as novel inhibitor candidate of class II histone deacetylase (HDAC) in cervical cancer treatment

机译：在计算机上鉴定2-oxo-1,3-噻唑烷衍生物作为II类组蛋白脱乙酰基酶（HDAC）的新型抑制剂候选物在宫颈癌治疗中的作用

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Tambunan Usman S.F.; Parikesit Arli A.; Ghifari Abi S.; Satriyanto Cipta Prio;
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1. Identification of Novel, Selective, and Stable Inhibitors of Class II Histone Deacetylases. Validation Studies of the Inhibition of the Enzymatic Activity of HDAC4 by Small Molecules as a Novel Approach for Cancer Therapy [J] . Ontoria JM, Altamura S, Di Marco A, Journal of Medicinal Chemistry . 2009,第21期

机译：II类组蛋白去乙酰化酶的新型，选择性和稳定抑制剂的鉴定。小分子抑制HDAC4酶活性作为癌症治疗新方法的验证研究
2. In silico modification of suberoylanilide hydroxamic acid (SAHA) as potential inhibitor for class II histone deacetylase (HDAC) [J] . Usman SF Tambunan, N Bramantya, Arli A Parikesit BMC Bioinformatics . 2011,第SUPPLEMENTa13期

机译：在计算机上修饰辛二酰氨基苯胺异羟肟酸（SAHA）作为II类组蛋白脱乙酰基酶（HDAC）的潜在抑制剂
3. In silico modification of suberoylanilide hydroxamic acid (SAHA) as potential inhibitor for class II histone deacetylase (HDAC) [J] . Usman SF Tambunan, N Bramantya, Arli A Parikesit BMC Bioinformatics . 2011,第SUPPLEMENTa13期

机译：在计算机上修饰辛二酰氨基苯胺异羟肟酸（SAHA）作为II类组蛋白脱乙酰基酶（HDAC）的潜在抑制剂
4. In silico modification of Zn~(2+) binding group of suberoylanilide hydroxamic acid (SAHA) by organoselenium compounds as Homo sapiens class II HDAC inhibitor of cervical cancer [C] . Usman Sumo Friend Tambunan, Ridla Bakri, Arli Aditya Parikesit Joint Conference on Chemisty . 2016

机译：通过有机烯化合物作为Zn〜（2+）结合基团的Zn〜（2+）结合基团的Zn〜（2+）结合基团的组织化合物作为宫颈癌的HOMO SAPIENS II HDAC抑制剂
5. Regulation of NF-kappaB activity by the class I histone deacetylases, HDAC1, HDAC2, HDAC3 corepressors and the spermidine/spermine N1 acetyltransferase 2 (SSAT2) coactivator. [D] . Boeke, Marta. 2008

机译：I类组蛋白脱乙酰基酶，HDAC1，HDAC2，HDAC3核心加压因子和亚精胺/精胺N1乙酰转移酶2（SSAT2）共激活剂对NF-κB活性的调节。
6. Molecular dynamics simulation of complex Histones Deacetylase (HDAC) Class II Homo Sapiens with suberoylanilide hydroxamic acid (SAHA) and its derivatives as inhibitors of cervical cancer [O] . Usman Sumo Friend Tambunan, Ridla Bakri, Tirtana Prasetia, 2013

机译：辛二酰苯胺异羟肟酸（SAHA）及其衍生物作为宫颈癌抑制剂的复杂组蛋白脱乙酰基酶（HDAC）II类智人的分子动力学模拟
7. Molecular dynamics simulation of complex Histones Deacetylase (HDAC) Class II Homo Sapiens with suberoylanilide hydroxamic acid (SAHA) and its derivatives as inhibitors of cervical cancer [O] . Usman Tambunan, Ridla Bakri, Tirtana Prasetia, 2013

机译：复合团脱乙酰酶（HDAC）II型同性均同性Sapiens的分子动力学模拟与子酰胺羟肟酸（Saha）及其衍生物作为宫颈癌的抑制剂

In silico identification of 2-oxo-1,3-thiazolidine derivatives as novel inhibitor candidate of class II histone deacetylase (HDAC) in cervical cancer treatment

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