Discovery and Development of Novel Glucose Dependent Partial Glucokinase Activato

Award Information
Agency:
Department of Health and Human Services
Branch
n/a
Amount:
$201,930.00
Award Year:
2010
Program:
SBIR
Phase:
Phase I
Contract:
1R43DK088457-01
Award Id:
96055
Agency Tracking Number:
DK088457
Solicitation Year:
n/a
Solicitation Topic Code:
NIDDK
Solicitation Number:
n/a
Small Business Information
CALASIA PHARMACEUTICALS, INC., 6330 Nancy Ridge Drive, SAN DIEGO, CA, 92121
Hubzone Owned:
N
Minority Owned:
N
Woman Owned:
N
Duns:
831901231
Principal Investigator:
DUNCANMCREE
() -
Business Contact:
() -
sprasad@calasiapharma.com
Research Institute:
n/a
Abstract
DESCRIPTION (provided by applicant): Type 2 diabetes (T2DM) is a chronic metabolic disease that affects the quality and longevity of life. Currently it is estimated that about 246 million people worldwide and diabetic and their number is expected to increa se to 380 million by 2025. Further, the agents used to treat T2DM fail to exhibit the desired efficacy in Type 2 diabetics. Therefore, there is a significant unmet medical need for new and more efficacious antidiabetic agents that would display effective a nd sustained glucose lowering over number of years. Glucokinase Activators (GKAs) have emerged as a new class of pharmaceutical agents that have exhibited efficacy in a variety of animal models of Type 2 diabetes and several GKAs have entered clinical tria ls. Unfortunately, severe and debilitating adverse drug reactions were recently observed during clinical trials that studied the effects of GKA treatment in T2DM patients. In detail, GKA treatment resulted in hypoglycemia due to inappropriate insulin secre tion and necessitated glucose infusion rescue therapy. Glucose independent insulin secretion is a hallmark of both the sulfonylureas and meglitinides insulin secretagogues that can result in hypoglycemia. Likewise, excessive activation of GKA would also re sult in inappropriate insulin secretion and hypoglycemia. Thus, we hypothesize that partial activation of GK will have a reduced potential for hypoglycemia in a clinical setting. Towards the identification of partial GKAs, Sorrento Technologies team has so lved multiple crystal structures of human GK 9hGK) ternary complexes (hGK:glucose:GKA) using either full or partial GKAs bound to the allosteric site and glucose bound to the active site. From the resulting 3-dimentional information, a detailed structural model of full or partial GK activation is being developed. We intend to use this structural information to guide our identification of novel potent GKAs that only partially activate GK. In detail, novel GKAs will be evolved from either crystallographic and /or nanocalorimetry fragment-based screening. The evolution of fragment ligands into partial GKAs will be aided by both biochemical mode of activation analysis as well as Sorrento Technologies' rapid procedure to generate high quality structural data of no vel hGK:glucose:GKA ternary complexes. After identification of several lead K-system GKA series, we intend to implement structure guided medicinal chemistry campaign to develop a partial GKAs with pharmaceutical like properties.

* information listed above is at the time of submission.

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