SBIR/STTR Research Award

Akylating agent Water-soluble Sulfonyl Hydrazine Prodrug

Award identifier 4344f5394bbdbc14009cd35dd7d03d4b3bf5df7a2127a079cd9a352d65e37e4eAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$100,000

Program and phase

SBIR · Phase I

Award year

2001

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
VION PHARMACEUTICALS, INC.
Proposal award date
Not reported
Contract end date
Not reported
UEI
Not reported
Solicitation number
Not reported
Topic code
Not reported

Research abstract

DESCRIPTION (provided by applicant): 1,2-Bis(methylsulfonyl)-1-(2-chloroethyl)-2-(methylaminocarbonyl) hydrazine (101M) is an alkylating agent that is cytotoxic to cancer cells. Various alkylating agents are approved for the treatment of cancer including cyclophosphamide, busulfan, melphalan, nitrogen mustard, chlorambucil, and the nitrosoureas. The clinical activity and toxicity of these agents are well characterized. I01M is distinguished from currently approved agents by its relative specificity for alkylation of the O/6 position of guanine, a low frequency of induced single-strand breaks in DNA, and the formation of methyl isocyanate that diminishes the cellular enzyme, O/6 alkylguanine DNA alkyltransferase. Despite the in vivo activity displayed by 101M, the therapeutic potential of this compound may be limited by its poor water-solubility. Therefore to improve its water solubility and therapeutic index, the synthesis and biological evaluation of four phosphate- and two glutamic acid-bearing prodrugs will be attempted. Phase I research will focus on (1) the synthesis of four phosphate and two glutamic acid bearing water-soluble analogs; (2) the determination of the stability and water-solubility as well as in vivo bioavailability of the newly synthesized analogs; and (3) the in vitro activation of the novel drugs via incubation with enzymes, such as alkaline phosphatase and carboxypeptidase G2 (CPG2). Phase II effort will focus on (1) the in vivo evaluation of these prodrugs, and (2) the development of these prodrugs for clinical trials. PROPOSED COMMERCIAL APPLICATION: Successful completion of Phase I and Phase II studies will provide water-soluble prodrugs of 101M, which may possess desirable pharmaceutical properties and may be employed as antitumor agents against a variety of cancers.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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