Search Results - "KISO, YOSHIAKI"
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New directions for protease inhibitors directed drug discovery
Published in Biopolymers (01-07-2016)“…ABSTRACT Proteases play crucial roles in various biological processes, and their activities are essential for all living organisms—from viruses to humans…”
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2
Paclitaxel Prodrugs: Toward Smarter Delivery of Anticancer Agents
Published in Journal of medicinal chemistry (14-12-2006)Get full text
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3
Mitocryptide-2: Identification of Its Minimum Structure for Specific Activation of FPR2-Possible Receptor Switching from FPR2 to FPR1 by Its Physiological C-terminal Cleavages
Published in International journal of molecular sciences (15-04-2021)“…Mitocryptides are a novel family of endogenous neutrophil-activating peptides originating from various mitochondrial proteins. Mitocryptide-2 (MCT-2) is one of…”
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The application of bioisosteres in drug design for novel drug discovery: focusing on acid protease inhibitors
Published in Expert opinion on drug discovery (01-10-2012)“…A bioisostere is a powerful concept for medicinal chemistry. It allows the improvement of the stability; oral absorption; membrane permeability; and…”
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Molecular sieving effects of disk-shaped molecules on reverse osmosis and nanofiltration separation
Published in Separation and purification technology (01-02-2017)“…[Display omitted] •The shape of crown ethers was approximated to be a disk.•The calculated rejections corresponded well to the observed rejection.•The…”
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Pore radius estimation based on organic solute molecular shape and effects of pressure on pore radius for a reverse osmosis membrane
Published in Journal of membrane science (01-03-2011)“…▶ The shape of organic solute was represented by molecular length and width. ▶ Rejections of alcohols were successfully simulated by using the shape…”
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7
Effect of molecular shape on rejection of uncharged organic compounds by nanofiltration membranes and on calculated pore radii
Published in Journal of membrane science (15-08-2010)“…We examined the effects of molecular shape on the rejection of uncharged organic compounds by nanofiltration membranes and on pore radii calculated for those…”
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8
Novel and efficient synthesis of difficult sequence-containing peptides through O-N intramolecular acyl migration reaction of O-acyl isopeptides
Published in Chemical communications (Cambridge, England) (2004)“…A novel and efficient method for the synthesis of difficult sequence-containing peptides has been developed based on the synthesis of O-acyl isopeptides…”
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Application of the O-N intramolecular acyl migration reaction in medicinal chemistry
Published in Current medicinal chemistry (01-11-2007)“…The O-N intramolecular acyl migration, also named as an acyl shift or acyl transfer reaction, is well-known in organic and peptide chemistry as a simple…”
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10
Structure of HIV-1 protease in complex with potent inhibitor KNI-272 determined by high-resolution X-ray and neutron crystallography
Published in Proceedings of the National Academy of Sciences - PNAS (24-03-2009)“…HIV-1 protease is a dimeric aspartic protease that plays an essential role in viral replication. To further understand the catalytic mechanism and inhibitor…”
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Synthesis of O-Acyl Isopeptides
Published in Chemical record (01-04-2013)“…O‐Acyl isopeptides, in which the N‐acyl linkage on the hydroxyamino acid residue (e.g., Ser and Thr) is replaced with an O‐acyl linkage, generally possess…”
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12
Mitocryptide-2, a neutrophil-activating cryptide, is a specific endogenous agonist for formyl-peptide receptor-like 1
Published in Biochemical and biophysical research communications (07-01-2011)“…► The cryptides, functional cryptic peptides hidden in protein structures, have become a topic of interest for the global scientific community. ► Mammalian…”
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Design, synthesis, and biological evaluation of novel dipeptide-type SARS-CoV 3CL protease inhibitors: Structure–activity relationship study
Published in European journal of medicinal chemistry (01-07-2013)“…This work describes the design, synthesis, and evaluation of low-molecular weight peptidic SARS-CoV 3CL protease inhibitors. The inhibitors were designed based…”
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14
PARK7 DJ-1 protects against degeneration of nigral dopaminergic neurons in Parkinson’s disease rat model
Published in Neurobiology of disease (01-10-2006)“…DJ-1 has recently been shown to be responsible for onset of familial Parkinson’s disease (PD), PARK7. DJ-1 has been shown to play roles in transcriptional…”
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Mitochondrial protein-derived cryptides: Are endogenous N-formylated peptides including mitocryptide-2 components of mitochondrial damage-associated molecular patterns?
Published in Biopolymers (01-07-2016)“…ABSTRACT Recently, much attention has been paid to “nonclassical” bioactive peptides, which are fragmented peptides simultaneously produced during maturation…”
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Synthesis and structure–activity relationships of benzophenone-bearing diketopiperazine-type anti-microtubule agents
Published in Bioorganic & medicinal chemistry (15-07-2012)“…KPU-105 (4), a potent anti-microtubule agent that contains a benzophenone was derived from the diketopiperazine-type vascular disrupting agent (VDA) plinabulin…”
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17
Compensating Enthalpic and Entropic Changes Hinder Binding Affinity Optimization
Published in Chemical biology & drug design (01-06-2007)“…A common strategy to improve the potency of drug candidates is to introduce chemical functionalities, like hydrogen bond donors or acceptors, at positions…”
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18
Crystal structures of the free and inhibited forms of plasmepsin I (PMI) from Plasmodium falciparum
Published in Journal of structural biology (01-07-2011)“…Plasmepsin I (PMI) is one of the four vacuolar pepsin-like proteases responsible for hemoglobin degradation by the malarial parasite Plasmodium falciparum, and…”
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19
Development of O-acyl isopeptide method
Published in Biopolymers (2007)“…During over a decade of study on aspartic protease inhibitors and water‐soluble prodrugs, in 2003, we discovered that the presence of an O‐acyl instead of…”
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20
Tripeptidic BACE1 inhibitors devised by in-silico conformational structure-based design
Published in Bioorganic & medicinal chemistry letters (15-01-2012)“…Previously reported pentapeptidic BACE1 inhibitors, designed using a substrate-based approach, were used as lead compounds for the further design of…”
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