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Tokiko Asami
Observed name:
Asami, Tokiko
Institution:
Carna Biosciences (Japan)
Observed institutions:
Carna Biosciences (Japan),
Kobe University
ORCID:
0000-0001-6783-4091
Observed ORCID:
0000-0001-6783-4091
OpenAlex ID:
A5081638860
Design and Synthesis of Novel Amino-triazine Analogues as Selective Bruton’s Tyrosine Kinase Inhibitors for Treatment of Rheumatoid Arthritis
2018
·
Wataru Kawahata
, Tokiko Asami
, et al.
·
Journal of Medicinal Chemistry
·
36
Discovery of novel furanone derivatives as potent Cdc7 kinase inhibitors
2017
·
Takayuki Irie
, Tokiko Asami
, et al.
·
European Journal of Medicinal Chemistry
·
30
Discovery of AS-1763: A Potent, Selective, Noncovalent, and Orally Available Inhibitor of Bruton’s Tyrosine Kinase
2021
·
Wataru Kawahata
, Tokiko Asami
, et al.
·
Journal of Medicinal Chemistry
·
29
A novel meta‐cleavage dioxygenase that cleaves a carboxyl‐group‐substituted 2‐aminophenol: Purification and characterization of 4‐amino‐3‐hydroxybenzoate 2,3‐dioxygenase from Bordetella sp. strain 10d
2002
·
Shinji Takenaka
, Tokiko Asami
, et al.
·
European Journal of Biochemistry
·
17
PDF
Design and synthesis of novel pyrimidine analogs as highly selective, non-covalent BTK inhibitors
2017
·
Wataru Kawahata
, Tokiko Asami
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
15
Discovery of AS-0141, a Potent and Selective Inhibitor of CDC7 Kinase for the Treatment of Solid Cancers
2021
·
Takayuki Irie
, Tokiko Asami
, et al.
·
Journal of Medicinal Chemistry
·
12
Abstract B152: CB1763, a highly selective, novel non-covalent BTK inhibitor, targeting ibrutinib-resistant BTK C481S mutant
2018
·
Tokiko Asami
, Wataru Kawahata
, et al.
·
Molecular Cancer Therapeutics
·
7
TR-FRET binding assay targeting unactivated form of Bruton’s tyrosine kinase
2015
·
Tokiko Asami
, Wataru Kawahata
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
6
‘Turn On/Off’ fluorescence probe for the screening of unactivated Bruton’s tyrosine kinase
2015
·
Wataru Kawahata
, Tokiko Asami
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
4
Impact of Docirbrutinib (AS-1763) Treatment in CLL: Preclinical Data and Early Clinical Biomarkers
2024
·
Natalia Timofeeva
, Breana Herrera
, et al.
·
Blood
·
2
Abstract C93: The design and synthesis of a novel fluorogenic probe targeting inactive forms of Burton's tyrosine kinase for high-throughput binding assay.
2011
·
Wataru Kawahata
, Tokiko Asami
, et al.
·
Molecular Cancer Therapeutics
·
1
Abstract C94: A novel binding assay to identify inhibitors that bind to inactive forms of Bruton's tyrosine kinase based on fluorescence resonance energy transfer.
2011
·
Tokiko Asami
, Wataru Kawahata
, et al.
·
Molecular Cancer Therapeutics
·
1
Docirbrutinib is a pan-mutant BTK inhibitor and inhibits B-cell receptor signaling in chronic lymphocytic leukemia cells in preclinical and early clinical investigations
2026
·
Natalia Timofeeva
, Breana Herrera
, et al.
·
Blood Cancer Journal
Characterization and Preclinical Evaluation of AS-1763, an Oral, Potent and Selective Noncovalent BTK Inhibitor, in Chronic Lymphocytic Leukemia
2023
·
Shady I. Tantawy
, Natalia Timofeeva
, et al.
·
Blood
PDF
Abstract 1400: AS-1763: a highly potent, noncovalent and next generation BTK inhibitor for the treatment of patients with B-cell malignancies having C481S mutation in BTK
2022
·
Wataru Kawahata
, Tokiko Asami
, et al.
·
Cancer Research
CCDC 2083520: Experimental Crystal Structure Determination
2021
·
Irie, Takayuki
, Asami, Tokiko
, et al.
·
The Cambridge Structural Database
Abstract 3232: Development of novel Btk inhibitor, CB988 targering ibrutinib-resistant Btk C481S mutant
2017
·
Wataru Kawahata
, Tokiko Asami
, et al.
·
Cancer Research
Abstract A180: Discovery of furanone derivatives as novel Cdc7 inhibitors with anti-tumor activity
2015
·
Takayuki Irie
, Tokiko Asami
, et al.
·
Molecular Cancer Therapeutics
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Works count:
18
Citation count:
160
H-index:
7
I10-index:
6
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