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Kesadaran Wajib Pajak, Sanksi Perpajakan dan Kualitas Pelayanan Perpajakan terhadap Kepatuhan Wajib Pajak dalam Membayar Pajak Bumi dan Bangunan

Manazhim (Lombok Timur), 2022-01, Vol.4 (1), p.110-132

2022

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Bifunctional building blocks in the Ugi-azide condensation reaction: a general strategy toward exploration of new molecular diversity

Organic & biomolecular chemistry, 2013-09, Vol.11 (36), p.6036-6046

2013

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Construction of functionalized tricyclic dihydropyrazino-quinazolinedione chemotypes via an Ugi/N-acyliminium ion cyclization cascade

Tetrahedron letters, 2013-08, Vol.54 (33), p.4467-4470

2013

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Oxidations of pyrrolidines and piperidines to afford CH-functionalized isopropyl-1-carboxylate congeners

Tetrahedron letters, 2021-04, Vol.69, p.152978, Article 152978

2021

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Parsonage-turner syndrome after COVID-19 vaccination in a 25-year-old woman: A case report

Journal of the neurological sciences, 2023-12, Vol.455, p.122549, Article 122549

2023

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Bifunctional building blocks in the Ugi-azide condensation reaction: a general strategy toward exploration of new molecular diversityElectronic supplementary information (ESI) available: General procedure, 1H and 13C NMR spectra for aldo/keto-esters (8b, 19b, 19 and 30). 1H and 13C NMR spectra for all new synthesized compounds (10, 10b-j, 20a-e, 22a-f, 24a-e, 29a-e and 31a-f). CCDC 936637. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c3ob40900g

2013-09

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Structural Insights into JAK2 Inhibition by Ruxolitinib, Fedratinib, and Derivatives Thereof

Journal of medicinal chemistry, 2021-02, Vol.64 (4), p.2228-2241

2021

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Spontaneous intracerebral hemorrhage after anticoagulation therapy in a 57-year-old man with SARS-COV-2 infection: A case report

Journal of the neurological sciences, 2021-10, Vol.429, p.119785-119785, Article 119785

2021

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Concise One-Pot Preparation of Unique Bis-Pyrrolidinone Tetrazoles

ACS combinatorial science, 2012-03, Vol.14 (3), p.160-163

2012

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Concise route to a series of novel 3-(tetrazol-5-yl)quinoxalin-2(1H)-ones

Tetrahedron letters, 2012-03, Vol.53 (13), p.1664-1667

2012

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Differential BET Bromodomain Inhibition by Dihydropteridinone and Pyrimidodiazepinone Kinase Inhibitors

Journal of medicinal chemistry, 2021-11, Vol.64 (21), p.15772-15786

2021

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2-Butyl-11-phenyl-5,10-dihydro-1H-benzo[e]imidazo[1,5-a][1,4]diazepine-1,3(2H)-dione

Acta crystallographica. Section E, Structure reports online, 2010-02, Vol.66 (Pt 3), p.o625-o625

2010

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Abstract 4879: Mutation selectivity of the allosteric SHP2 inhibitor SHP099

Cancer research (Chicago, Ill.), 2018-07, Vol.78 (13_Supplement), p.4879-4879

2018

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2-Propyl 3,3-dibromo-2-hydroxypyrrolidine-1-carboxylate

Acta crystallographica. Section E, Structure reports online, 2010-03, Vol.66 (3), p.o597-o597

2010

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Targeting Aurora kinase A and JAK2 prevents GVHD while maintaining T reg and antitumor CTL function

Science translational medicine, 2017-01, Vol.9 (372)

2017

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Ligand-mediated protein degradation reveals functional conservation among sequence variants of the CUL4-type E3 ligase substrate receptor cereblon

The Journal of biological chemistry, 2018-04, Vol.293 (16), p.6187-6200

2018

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Potent Dual BET Bromodomain-Kinase Inhibitors as Value-Added Multitargeted Chemical Probes and Cancer Therapeutics

Molecular cancer therapeutics, 2017-06, Vol.16 (6), p.1054-1067

2017

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Synthesis of tetrazolo-fused benzodiazepines and benzodiazepinones by a two-step protocol using an Ugi-azide reaction for initial diversity generation

Tetrahedron, 2012-07, Vol.68 (27-28), p.5606-5611

2012

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Targeting the BRD4-HOXB13 Coregulated Transcriptional Networks with Bromodomain-Kinase Inhibitors to Suppress Metastatic Castration-Resistant Prostate Cancer

Molecular cancer therapeutics, 2018-12, Vol.17 (12), p.2796-2810

2018

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Targeting Aurora kinase A and JAK2 prevents GVHD while maintaining Treg and antitumor CTL function

Science translational medicine, 2017-01, Vol.9 (372)

2017

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Outcome and safety of upper pole versus non-upper pole single puncture PCNL for staghorn stones: a systematic review and meta-analysis [version 1; peer review: 2 approved with reservations]

F1000 research, 2019, Vol.8, p.537

2019

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Abstract 4547: Preparation of peptide-based Shp2 substrates with phosphatase activity-dependent fluorescence

Cancer research (Chicago, Ill.), 2015-08, Vol.75 (15_Supplement), p.4547-4547

2015

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Abstract 3697: Development of a focused non-hydrolyzable phosphopeptide library based on a high affinity SHP2 substrate

Cancer research (Chicago, Ill.), 2015-08, Vol.75 (15_Supplement), p.3697-3697

2015

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Facing Industry Revolution 4.0 for Millennial Accountants

International journal of innovative technology and exploring engineering, 2019-11, Vol.9 (1), p.1037-1042

2019

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Intracellular protein degradation of BRD4 by dBET1 reveals conserved in vivo cereblon function in human and mouse T-cells

The Journal of immunology (1950), 2017-05, Vol.198 (1_Supplement), p.52-52.18

2017

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Kesadaran Wajib Pajak, Sanksi Perpajakan dan Kualitas Pelayanan Perpajakan terhadap Kepatuhan Wajib Pajak dalam Membayar Pajak Bumi dan Bangunan

Bifunctional building blocks in the Ugi-azide condensation reaction: a general strategy toward exploration of new molecular diversity

Construction of functionalized tricyclic dihydropyrazino-quinazolinedione chemotypes via an Ugi/N-acyliminium ion cyclization cascade

Oxidations of pyrrolidines and piperidines to afford CH-functionalized isopropyl-1-carboxylate congeners

Parsonage-turner syndrome after COVID-19 vaccination in a 25-year-old woman: A case report

Structural Insights into JAK2 Inhibition by Ruxolitinib, Fedratinib, and Derivatives Thereof

Spontaneous intracerebral hemorrhage after anticoagulation therapy in a 57-year-old man with SARS-COV-2 infection: A case report

Concise One-Pot Preparation of Unique Bis-Pyrrolidinone Tetrazoles

Concise route to a series of novel 3-(tetrazol-5-yl)quinoxalin-2(1H)-ones

Differential BET Bromodomain Inhibition by Dihydropteridinone and Pyrimidodiazepinone Kinase Inhibitors

2-Butyl-11-phenyl-5,10-dihydro-1H-benzo[e]imidazo[1,5-a][1,4]diazepine-1,3(2H)-dione

Abstract 4879: Mutation selectivity of the allosteric SHP2 inhibitor SHP099

2-Propyl 3,3-dibromo-2-hydroxypyrrolidine-1-carboxylate

Targeting Aurora kinase A and JAK2 prevents GVHD while maintaining T reg and antitumor CTL function

Ligand-mediated protein degradation reveals functional conservation among sequence variants of the CUL4-type E3 ligase substrate receptor cereblon

Potent Dual BET Bromodomain-Kinase Inhibitors as Value-Added Multitargeted Chemical Probes and Cancer Therapeutics

Synthesis of tetrazolo-fused benzodiazepines and benzodiazepinones by a two-step protocol using an Ugi-azide reaction for initial diversity generation

Targeting the BRD4-HOXB13 Coregulated Transcriptional Networks with Bromodomain-Kinase Inhibitors to Suppress Metastatic Castration-Resistant Prostate Cancer

Targeting Aurora kinase A and JAK2 prevents GVHD while maintaining Treg and antitumor CTL function

Outcome and safety of upper pole versus non-upper pole single puncture PCNL for staghorn stones: a systematic review and meta-analysis [version 1; peer review: 2 approved with reservations]

Abstract 4547: Preparation of peptide-based Shp2 substrates with phosphatase activity-dependent fluorescence

Abstract 3697: Development of a focused non-hydrolyzable phosphopeptide library based on a high affinity SHP2 substrate

Facing Industry Revolution 4.0 for Millennial Accountants

Intracellular protein degradation of BRD4 by dBET1 reveals conserved in vivo cereblon function in human and mouse T-cells

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