Live face video vs. spoof face video: Use of moiré patterns to detect replay video attacks

K Patel, H Han, AK Jain, G Ott - 2015 International Conference …, 2015 - ieeexplore.ieee.org
With the wide deployment of face recognition systems in applications from border control to
mobile device unlocking, the combat of face spoofing attacks requires increased attention; …

Total synthesis of (−)-macrolactin A

AB Smith, GR Ott - Journal of the American Chemical Society, 1996 - ACS Publications
In 1989 Fenical et al. reported the isolation and planar structures of macrolactins AF, highly
unsaturated macrolides produced in culture by a taxonomically unclassifiable deep-sea …

Total syntheses of (−)-macrolactin A,(+)-macrolactin E, and (−)-macrolactinic acid: an exercise in Stille cross-coupling chemistry

AB Smith, GR Ott - Journal of the American Chemical Society, 1998 - ACS Publications
The total syntheses of the potent antiviral agent (−)-macrolactin A (1) and two related family
members, (+)-macrolactin E (5) and (−)-macrolactinic acid (7), have been achieved, …

Discovery of clinical candidate CEP-37440, a selective inhibitor of focal adhesion kinase (FAK) and anaplastic lymphoma kinase (ALK)

GR Ott, M Cheng, KS Learn, J Wagner… - Journal of medicinal …, 2016 - ACS Publications
Analogues structurally related to anaplastic lymphoma kinase (ALK) inhibitor 1 were optimized
for metabolic stability. The results from this endeavor not only led to improved metabolic …

Combined inhibition of atypical PKC and histone deacetylase 1 is cooperative in basal cell carcinoma treatment

…, MA Fry, NM Urman, SX Atwood, J Roffey, GR Ott… - JCI …, 2017 - pmc.ncbi.nlm.nih.gov
Advanced basal cell carcinomas (BCCs) circumvent Smoothened (SMO) inhibition by activating
GLI transcription factors to sustain the high levels of Hedgehog (HH) signaling required …

CEP-28122, a highly potent and selective orally active inhibitor of anaplastic lymphoma kinase with antitumor activity in experimental models of human cancers

M Cheng, MR Quail, DE Gingrich, GR Ott… - Molecular cancer …, 2012 - aacrjournals.org
Anaplastic lymphoma kinase (ALK) is constitutively activated in a number of human cancer
types due to chromosomal translocations, point mutations, and gene amplification and has …

Potent, selective, orally bioavailable inhibitors of tumor necrosis factor-α converting enzyme (TACE): Discovery of indole, benzofuran, imidazopyridine and …

Z Lu, GR Ott, R Anand, RQ Liu, MB Covington… - Bioorganic & medicinal …, 2008 - Elsevier
Potent and selective inhibitors of tumor necrosis factor-α converting enzyme (TACE) were
discovered with several new heterocyclic P1′ groups in conjunction with cyclic β-amino …

Multigram Synthesis of the C29− C51 Subunit and Completion of the Total Synthesis of Altohyrtin C (Spongistatin 2)

…, R Scott, MM Claffey, CJ Hayes, GR Ott - Journal of the …, 2003 - ACS Publications
A multigram synthesis of the C29−C51 subunit of altohyrtin C (spongistatin 2) has been
accomplished. Union of this intermediate with the C1−C28 fragment and further elaboration …

2,7-Disubstituted-pyrrolo[2,1-f][1,2,4]triazines: New Variant of an Old Template and Application to the Discovery of Anaplastic Lymphoma Kinase (ALK) Inhibitors with …

GR Ott, GJ Wells, TV Thieu, MR Quail… - Journal of medicinal …, 2011 - ACS Publications
A novel 2,7-disubstituted-pyrrolo[2,1-f][1,2,4]triazine scaffold has been designed as a new
kinase inhibitor platform mimicking the bioactive conformation of the well-known …

Technically extended multiparameter optimization (TEMPO): an advanced robust scoring scheme to calculate central nervous system druggability and monitor lead …

AK Ghose, GR Ott, RL Hudkins - ACS Chemical Neuroscience, 2017 - ACS Publications
At the discovery stage, it is important to understand the drug design concepts for a CNS
drug compared to those for a non-CNS drug. Previously, we published on ideal CNS drug …