IP Library Granted Patent US 8,450,366
Granted Patent B2
US 8,450,366 · App. 12/803,611 · Granted May 28, 2013

Isobenzofuran analogs of sclerophytin A

Inventor: Matthias C. McIntosh (Fayetteville, AR)
Assignee: Board of Trustees of the University of Arkansas
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Quick Facts
Patent No.
US 8,450,366
App. No.
12/803,611
Granted
May 28, 2013
Kind
B2
Abstract

Isobenzofuran analogs of sclerophytin A are prepared in a highly concise fashion via an aldol-cycloaldol sequence. The analogs exhibit IC 50 's as low as 1 μM in growth inhibitory studies against KB3 cells using an MTT assay. Preferred analogs have one of the following structural formulas, where R is hydrogen or a substituted or unsubstituted lower alkyl group and Ar is a substituted or unsubstituted aryl group.

Claims (16)

1. A compound having a structural formula selected from the following:

wherein R represents 14, substituted lower alkyl, or unsubstituted lower alkyl; Ar represents a substituted or unsubstituted aryl; and pharmaceutically acceptable esters and salts thereof.

2. A compound of claim 1 , wherein R=methyl, ethyl, cyclopropylmethyl or cyclopentylmethyl.

3. A compound of claim 1 , wherein Ar=2-Br-phenyl, 3-Br-phenyl, 2,3-di-Cl-phenyl, 2,4-di-Cl-phenyl, 1-naphthyl, 2-pyridyl, 2-furyl, or 2-fluorophenyl.

4. A compound of claim 1 having structure 10, wherein Ar=2-fluorophenyl.

5. A method of converting (S)-(+)-carvone to an aryl glycolate compound thereof, comprising:

(i) reacting (S)-(+)-carvone with an arylaldehyde in an aldol condensation reaction to afford an aryl anti-alcohol; and

(ii) etherifying the aryl anti-alcohol to afford said aryl glycolate compound.

6. The method of claim 5 , further comprising cyclizing said aryl glycolate to afford an isobenzofuran having the structural formula

wherein R represents H, substituted lower alkyl, or unsubstituted lower alkyl; and Ar represents a substituted or unsubstituted aryl.

7. The method of claim 6 , further comprising converting by oxidative rearrangement said isobenzofuran to an enone having the structural formula

wherein R represents H, substituted lower alkyl, or unsubstituted lower alkyl; and Ar represents a substituted or unsubstituted aryl.

8. The method of claim 5 , further comprising converting by β-lactonization-decarboxylation said aryl glycolate to a diene having the structural formula

wherein Ar represents a substituted or unsubstituted aryl.

9. A method of inhibiting cell growth comprising contacting cancerous cells with a growth inhibiting amount of a compound of claim 1 , wherein the cancerous cells comprise leukemia, prostate, or non-small cell lung cancer cells.

10. A method of inhibiting cell proliferation in a patient comprising administering to the patient a proliferation-inhibiting amount of a compound of claim 1 , wherein the patient suffers from cancer comprising leukemia, prostate, or non-small cell lung cancer.

Assignments (3)
CONFIRMATORY LICENSE Recorded Aug 19, 2021
From: UNIVERSITY OF ARKANSAS AT FAYETTEVILLE
To: NATIONAL INSTITUTES OF HEALTH - DIRECTOR DEITR
Reel/Frame 057230/0137 →
CONFIRMATORY LICENSE Recorded Sep 1, 2015
From: UNIVERSITY OF ARKANSAS AT FAYETTEVILLE
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 036515/0870 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 30, 2012
From: MCINTOSH, MATTHIAS C
To: BOARD OF TRUSTEES OF THE UNIVERSITY OF ARKANSAS
Reel/Frame 028285/0637 →
Continuity (2)
Provisional Application 61269875 · Jun 30, 2009
Related Publication 20100331370A1 · Dec 30, 2010