The objectives of this proposal are: 1. The synthesis of diverse multi-chain host compounds of a type previously unknown to mankind and which are potentially interesting to biological and medicinal chemists. The host compounds include multi-armed aromatics as well as cyclodextrin-based derivatives. 2. The examination of these host compounds and their ability to perturb the physical-chemical properties (e.g. solubility, spectra, transport, reactivity, etc.) of biologically interesting molecules trapped inside the multi-chain network. 3. The attachment of catalytic groups onto the hosts thereby creating organic molecules which can both bind guests and promote their reactivity as occurs in enzyme-substrate systems. Preliminary results are extremely encouraging: (1) One of our new compounds can induce dramatic rheological changes of water at very low concentrations (4 x 10-3 M). (2) """"""""Hexapus"""""""", a six-armed compound, solubilizes cholesterol in water. (3) A fully alkylated cyclodextrin dissolves in heptane and benzene and acts as an ionophore.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM021457-09
Application #
3270514
Study Section
Bio-Organic and Natural Products Chemistry Study Section (BNP)
Project Start
1977-12-01
Project End
1986-08-31
Budget Start
1985-09-01
Budget End
1986-08-31
Support Year
9
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Emory University
Department
Type
Schools of Arts and Sciences
DUNS #
042250712
City
Atlanta
State
GA
Country
United States
Zip Code
30322
Sybachin, A V; Efimova, A A; Litmanovich, E A et al. (2007) Complexation of polycations to anionic liposomes: composition and structure of the interfacial complexes. Langmuir 23:10034-9
Yaroslavov, A A; Udalykh OYu; Melik-Nubarov, N S et al. (2001) Conventional and gemini surfactants embedded within bilayer membranes: contrasting behavior. Chemistry 7:4835-43
Yaroslavov, A A; Sukhishvili, S A; Obolsky, O L et al. (1996) DNA affinity to biological membranes is enhanced due to complexation with hydrophobized polycation. FEBS Lett 384:177-80
Menger, F M; Guo, Y; Lee, A S (1994) Synthesis of a lipid/peptide/drug conjugate: N4-(acylpeptidyl)-ara-C. Bioconjug Chem 5:162-6
Epand, R M; Epand, R F; Leon, B T et al. (1991) Evidence for the regulation of the activity of protein kinase C through changes in membrane properties. Biosci Rep 11:59-64
Charp, P A; Zhou, Q Z; Wood Jr, M G et al. (1988) Synthetic branched-chain analogues of distearoylphosphatidylcholine: structure-activity relationship in inhibiting and activating protein kinase C. Biochemistry 27:4607-12
Zhou, Q Z; Raynor, R L; Wood Jr, M G et al. (1988) Structure-activity relationship of synthetic branched-chain distearoylglycerol (distearin) as protein kinase C activators. Biochemistry 27:7361-5