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CATVU LUONG, PHARMD
PHARMD
Pharmacist
NPI: 1295337046Individual
Specialties, Licenses & Credentials
PharmacistPrimary
Pharmacist
Code: 183500000X
53562(TX)
Research & Publications (13)
Dissecting and designing inhibitor selectivity determinants at the S1 site using an artificial Ala190 protease (Ala190 uPA).
PMID 15522303·J Mol Biol·2004
4-observational
Structural snapshots of human HDAC8 provide insights into the class I histone deacetylases.
PMID 15242608·Structure·2004
8-other
The structure of the extracellular region of human hepsin reveals a serine protease domain and a novel scavenger receptor cysteine-rich (SRCR) domain.
PMID 12962630·Structure·2003
8-other
Elaborate manifold of short hydrogen bond arrays mediating binding of active site-directed serine protease inhibitors.
PMID 12742021·J Mol Biol·2003
7-preclinical
Contribution of multicentered short hydrogen bond arrays to potency of active site-directed serine protease inhibitors.
PMID 12296731·J Am Chem Soc·2002
8-other
4-Aminoarylguanidine and 4-aminobenzamidine derivatives as potent and selective urokinase-type plasminogen activator inhibitors.
PMID 12113833·Bioorg Med Chem Lett·2002
8-other
2-(2-Hydroxy-3-alkoxyphenyl)-1H-benzimidazole-5-carboxamidine derivatives as potent and selective urokinase-type plasminogen activator inhibitors.
PMID 12113832·Bioorg Med Chem Lett·2002
8-other
Engineering inhibitors highly selective for the S1 sites of Ser190 trypsin-like serine protease drug targets.
PMID 11731301·Chem Biol·2001
7-preclinical
Exploiting subsite S1 of trypsin-like serine proteases for selectivity: potent and selective inhibitors of urokinase-type plasminogen activator.
PMID 11689072·J Med Chem·2001
7-preclinical
Development of serine protease inhibitors displaying a multicentered short (<2.3 A) hydrogen bond binding mode: inhibitors of urokinase-type plasminogen activator and factor Xa.
PMID 11495587·J Med Chem·2001
8-other
Development of potent and selective factor Xa inhibitors.
PMID 11459634·Bioorg Med Chem Lett·2001
8-other
A novel serine protease inhibition motif involving a multi-centered short hydrogen bonding network at the active site.
PMID 11292354·J Mol Biol·2001
8-other
Structural basis for selectivity of a small molecule, S1-binding, submicromolar inhibitor of urokinase-type plasminogen activator.
PMID 10779411·Chem Biol·2000
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 3133 E LEMMON AVE
DALLAS, TX 75204 - Phone
- (214) 599-2108
Quick Facts
- NPI
- 1295337046
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 13
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