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Khalid D. Benbatoul
Observed names:
K Benbatoul,
K D Benbatoul,
K. Benbatoul,
Khalid Benbatoul
Observed institutions:
BC Cancer Agency,
University of California San Diego,
Bristol-Myers Squibb (United States),
Ligand Pharmaceuticals (United States),
Aptose Biosciences (United States),
Vaxiion Therapeutics (United States)
show all 6
OpenAlex ID:
A5080370216
Discovery and characterization of OC144-093, a novel inhibitor of P-glycoprotein-mediated multidrug resistance.
2000
·
M J Newman
, J C Rodarte
, et al.
·
PubMed
·
191
APTO-253 Stabilizes G-quadruplex DNA, Inhibits MYC Expression, and Induces DNA Damage in Acute Myeloid Leukemia Cells
2018
·
Andrea Local
, Hongying Zhang
, et al.
·
Molecular Cancer Therapeutics
·
83
PDF
Antiinflammatory glucocorticoid receptor ligand with reduced side effects exhibits an altered protein–protein interaction profile
2007
·
Jeffrey N. Miner
, Bob Ardecky
, et al.
·
Proceedings of the National Academy of Sciences
·
68
2,4,5-Trisubstituted imidazoles
2000
·
Chengzhi Zhang
, Sepehr Sarshar
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
62
Novel regions of allelic deletion on chromosome 18p in tumors of the lung, brain and breast
1998
·
Yen Tran
, Khalid Benbatoul
, et al.
·
Oncogene
·
54
LGD-5552, an Antiinflammatory Glucocorticoid Receptor Ligand with Reduced Side Effects, in Vivo
2008
·
Francisco J. López
, Robert J. Ardecky
, et al.
·
Endocrinology
·
53
PDF
2,4,5-Trisubstituted imidazoles
2000
·
Sepehr Sarshar
, Chengzhi Zhang
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
44
Quantitation of the change in GADD153 messenger RNA level as a molecular marker of tumor response in head and neck cancer.
1999
·
G Los
, K Benbatoul
, et al.
·
PubMed
·
23
2,4,5-三置換イミダゾール P-糖蛋白質媒介多剤耐性の新規無毒モジュレータ 2
2000
·
C Zhang
, Sepehr Sarshar
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
19
Identification of a potent and rapidly reversible inhibitor of the 20S-proteasome
2004
·
Ashok V. Purandare
, Honghe Wan
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
17
Increase in tumor GADD153 mRNA level following treatment correlates with response to paclitaxel
2000
·
Maida M. de las Alas
, Randolph D. Christen
, et al.
·
Cancer Chemotherapy and Pharmacology
·
11
A Phase 1 a/b Dose Escalation Study of the Mutation Agnostic BTK/FLT3 Inhibitor CG-806 in Patients with Relapsed or Refractory CLL/SLL or Non-Hodgkin's Lymphomas
2020
·
Rafael Bejar
, Hongying Zhang
, et al.
·
Blood
·
8
A Phase 1a/b Dose Escalation Study of the Mutation Agnostic FLT3/BTK Inhibitor Luxeptinib (CG-806) in Patients with Relapsed or Refractory Acute Myeloid Leukemia
2021
·
Aaron D Goldberg
, Maro Ohanian
, et al.
·
Blood
·
5
A Phase 1a/b Dose Escalation Study of the Mutation Agnostic BTK/FLT3 Inhibitor Luxeptinib (CG-806) in Patients with Relapsed or Refractory B-Cell Malignancies
2021
·
Felipe Samaniego
, John M. Burke
, et al.
·
Blood
·
5
Inhibition of c-Myc By Apto-253 As an Innovative Therapeutic Approach to Induce Cell Cycle Arrest and Apoptosis in Acute Myeloid Leukemia
2016
·
Hongying Zhang
, Andrea Local
, et al.
·
Blood
·
5
A Phase 1a/b Dose Escalation Study of the MYC Repressor Apto-253 in Patients with Relapsed or Refractory AML or High-Risk MDS
2020
·
Rafael Bejar
, Hongying Zhang
, et al.
·
Blood
·
4
ChemInform Abstract: 2,4,5‐Trisubstituted Imidazoles: Novel Nontoxic Modulators of P‐Glycoprotein Mediated Multidrug Resistance. Part 2.
2001
·
Chengzhi Zhang
, Sepehr Sarshar
, et al.
·
ChemInform
·
4
Abstract 794: CG'806, a first-in-class pan-FLT3/pan-BTK inhibitor, targets multiple pathways to kill diverse subtypes of acute myeloid leukemia and B-cell malignancy in vitro
2018
·
Hongying Zhang
, Andrea Local
, et al.
·
Cancer Research
·
3
Abstract 4225: CG-806, a first-in-class FLT3/BTK inhibitor, and venetoclax synergize to inhibit cell proliferation and to induce apoptosis in aggressive B-cell lymphomas
2020
·
Nasrin Rastgoo
, Matthew Thayer
, et al.
·
Cancer Research
·
2
CG'806, a First-in-Class Pan-FLT3/Pan-BTK Inhibitor, Exhibits Broader and Greater Potency Than Ibrutinib Against Primary and Cultured Malignant B Cells
2018
·
Hongying Zhang
, Andrea Local
, et al.
·
Blood
·
2
Abstract 44: CG′806, a first-in-class FLT3/BTK inhibitor, exhibits potent activity against AML patient samples with mutant or wild type FLT3, as well as other hematologic malignancy subtypes
2017
·
Stephen E. Kurtz
, Beth Wilmot
, et al.
·
Clinical Cancer Research
·
2
APTO-253 Interaction with G-Quadruplex DNA Is Linked to Inhibition of c-Myc Expression, Induction of DNA Damage, and Generation of Synthetic Lethality in Cells with BRCA1/2 Impairment
2017
·
Andrea Local
, Hongying Zhang
, et al.
·
Blood
·
2
CG '806, a First-in-Class Non-Covalent Pan-FLT3/BTK Inhibitor, Exerts Superior Potency Against B-Cell Malignant Cells
2017
·
Hongying Zhang
, Andrea Local
, et al.
·
Blood
·
2
Abstract CT239: Early clinical findings from a phase 1a/b dose escalation trial to evaluate the safety and tolerability of CG-806 in patients with relapsed or refractory CLL/SLL or non-Hodgkin's lymphomas
2020
·
Hongying Zhang
, Nasrin Rastgoo
, et al.
·
Cancer Research
·
1
Pf203 Cg‐806, Preclinical in Vivo Efficacy and Safety Profile as a Pan‐flt3/pan‐btk Inhibitor
2019
·
H. Zhang
, K. Benbatoul
, et al.
·
HemaSphere
·
1
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Works count:
38
Citation count:
672
H-index:
11
I10-index:
11
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