Infinity Pharmaceuticals,
Inc., announced today that the Journal of Medicinal Chemistry (Volume 49,
Issue 15 (July 27, 2006), pages 4606-4615), an official peer-reviewed
journal of the American Chemical Society, has published a paper describing
Infinity's novel, water-soluble Hsp90 inhibitor, IPI-504, for the treatment
of a broad range of cancers. IPI-504, Infinity's lead oncology drug
candidate, is currently being evaluated in two separate Phase I clinical
trials for the treatment of multiple myeloma and gastrointestinal stromal
tumors (GIST).
"This publication demonstrates what we believe is the innovative power
of Infinity's chemistry expertise in small molecule drug discovery," said
James Porter, Ph.D., corresponding and co-lead author with Jie Ge, Ph.D.
and Emmanuel Normant, Ph.D., all members of Infinity's IPI-504 project
team. "The discovery and development of IPI-504 represents a great
accomplishment by the entire IPI-504 team and exhibits an exemplary
interdisciplinary effort by all to identify and characterize this potent
inhibitor of Hsp90."
"The discovery of a water-soluble derivative of 17-AAG
(17-Allylamino-17-demethoxy-geldanamycin) represents a significant
breakthrough in Hsp90 inhibition," said Julian Adams, Ph.D., Infinity's
President and Chief Scientific Officer. "The 17-AAG pharmacophore, while a
potent inhibitor of Hsp90, historically has suffered from pharmacological
deficiencies -- including poor solubility -- which have necessitated the
use of complex organic formulations with inherent patient safety concerns.
The availability of a potent, water-soluble derivative of 17-AAG allows
Infinity, for the first time, to test the true potential of 17-AAG and its
derivatives in inhibiting Hsp90, an important cancer target."
Overview of Published Paper
The published paper describes the discovery of IPI-504, a highly
soluble hydroquinone hydrochloride salt of 17-AAG. The paper delineates the
synthesis, biochemical binding affinity to Hsp90, and cellular activity of
IPI-504. The hydroquinone hydrochloride salt is a potent inhibitor of Hsp90
and its excellent aqueous solubility addresses the pharmaceutical
deficiencies historically associated with 17-AAG. In addition, although the
molecule was designed to be a soluble prodrug of 17-AAG, it was found to be
an active, more potent inhibitor of Hsp90. Various hydroquinone analogs of
17-AAG and its metabolites were also prepared to investigate the structure
activity relationship of hydroquinone binding to Hsp90.
About IPI-504
IPI-504 is Infinity's novel, proprietary agent that has demonstrated in
preclinical studies the ability to potently and selectively inhibit Hsp90,
thereby killing cancer cells. IPI-504 preferentially targets and
accumulates in tumor tissues, sparing healthy tissues. In preclinical
studies, it has demonstrated a broad potential to treat a variety of
cancers as both a single agent as well as in combination with existing
anti-cancer drugs. IPI-504 is currently delivered in a [patient-friendly],
water-based formulation.
Infinity is currently conducting two Phase I clinical with intravenous
formulations of IPI-504. In July 2005, Infinity initiated the first of
these Phase I clinical trials in refractory multiple myeloma. In December
2005, Infinity initiated the second Phase I clinical trials with IPI-504 in
refractory gastrointestinal stromal tumors (GIST).
About Infinity Pharmaceuticals, Inc.
Infinity is an innovative cancer drug discovery and development company
that is seeking to leverage its strength in small molecule drug
technologies to bring important new medicines to patients. The company
recently announced a definitive agreement to merge with Discovery Partners
International, Inc. (Nasdaq: DPII).
Additional Information about the DPI-Infinity Merger and Where to Find
It
In connection with the proposed merger between Discovery Partners
International, Inc. (DPI) and Infinity, DPI filed a registration statement
on Form S-4 on May 24, 2006 with the SEC, that contains a proxy
statement/prospectus. Investors and security holders of DPI and Infinity
are urged to read the proxy statement/prospectus (including any amendments
or supplements to the proxy statement/prospectus) regarding the proposed
merger because it contains important information about DPI, Infinity and
the proposed merger. Security holders will be able to obtain a copy of the
proxy statement/prospectus, as well as other filings containing information
about DPI and Infinity, without charge, at the SEC's Internet site
(sec). Copies of the proxy statement/prospectus can also be
obtained, without charge, by directing a request to Discovery Partners
International, Inc., 9640 Towne Centre Drive, San Diego, CA 92121,
Attention: Investor Relations, Telephone: (858) 455-8600.
Participants in the Solicitation
DPI and its directors and executive officers and Infinity and its
directors and executive officers may be deemed to be participants in the
solicitation of proxies from the stockholders of DPI in connection with the
proposed merger of DPI with Infinity. Information regarding the special
interests of these directors and executive officers in the merger
transaction is included in the proxy statement/prospectus referred to
above. Additional information regarding the directors and executive
officers of DPI is also included in DPI's proxy statement for its 2006
Annual Meeting of Stockholders, which was filed with the SEC on April 6,
2006. This document is available free of charge at the SEC's web site
( sec ) and from Investor Relations at DPI at the address described above.
Infinity Pharmaceuticals, Inc.
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