Search

Raghavan R Balachandran

from Wexford, PA
Age ~79

Raghavan Balachandran Phones & Addresses

  • Wexford, PA
  • Tuscaloosa, AL
  • Monroeville, PA
  • Allison Park, PA
  • 2548B Pheasant Run Dr, Wexford, PA 15090

Education

Degree: High school graduate or higher

Emails

Resumes

Resumes

Raghavan Balachandran Photo 1

Raghavan Balachandran

View page
Location:
United States
Raghavan Balachandran Photo 2

Raghavan Balachandran

View page

Publications

Us Patents

Analogs Of Discodermolide And Dictyostatin-1, Intermediates Therefor And Methods Of Synthesis Thereof

View page
US Patent:
7122686, Oct 17, 2006
Filed:
Sep 5, 2003
Appl. No.:
10/655916
Inventors:
Dennis P. Curran - Pittsburgh PA, US
Youseung Shin - Pittsburgh PA, US
Billy W. Day - Pittsburgh PA, US
Raghavan Balachandran - Wexford PA, US
Charitha Madiraju - Pittsburgh PA, US
Tiffany Turner - Pittsburgh PA, US
Assignee:
University of Pittsburgh - Pittsburgh PA
International Classification:
C07D 313/00
US Classification:
549266, 560 1
Abstract:
A compound of the following structure:.

Synthesis And Biological Evaluation Of Analogs Of The Antimitotic Marine Natural Product Curacin A

View page
US Patent:
20020037918, Mar 28, 2002
Filed:
Jul 19, 2001
Appl. No.:
09/909076
Inventors:
Peter Wipf - Pittsburgh PA, US
Jonathan Reeves - Pittsburgh PA, US
Billy Day - Pittsburgh PA, US
Raghavan Balachandran - Pittsburgh PA, US
International Classification:
A61K031/381
A61K031/343
A61K031/341
A61K031/085
US Classification:
514/443000, 514/461000, 514/469000, 514/720000, 549/049000, 549/078000, 549/462000, 549/497000, 568/660000
Abstract:
The present invention provides an efficient synthetic strategy for the preparation of analogs that incorporate important structural elements of the marine natural product curacin A, the compositions and various uses of the compositions. The most active of these compounds at nanomolar concentrations inhibit tubulin polymerization, show growth inhibition activity, inhibited colchicines binding to tubulin and block mitotic progression. The compounds of the present invention represent some of the most potent synthetic curacin A analogs synthesized, with an activity profile rivaling that of the natural product despite the simplified structure, greater water solubility, and increased chemical stability.

Analogs Of Discodermolide And Dictyostatin-1, Intermediates Therefor And Methods Of Synthesis Thereof

View page
US Patent:
20060270862, Nov 30, 2006
Filed:
Aug 2, 2006
Appl. No.:
11/497746
Inventors:
Dennis Curran - Pittsburgh PA, US
Youseung Shin - Pittsburgh PA, US
Billy Day - Pittsburgh PA, US
Raghavan Balachandran - Wexford PA, US
Charitha Madiraju - Pittsburgh PA, US
Tiffany Turner - Pittsburgh PA, US
International Classification:
C07D 313/02
C07C 69/73
C07F 9/28
C07F 7/02
US Classification:
549266000, 549216000, 549214000, 560183000
Abstract:
A compound of the following structure: wherein Ris H, an alkyl group, an aryl group, an alkenyl group, an alkynyl group, or a halogen atom; Ris H, an alkyl group, an aryl group, a benzyl group, a trityl group, —SiRRR, CHOR, or COR; R, Rand Rare independently an alkyl group or an aryl group; Ris an alkyl group, an aryl group, an alkoxylalkyl group, —RSiRRRor a benzyl group, wherein Ris an alkylene group; Ris an alkyl group, an allyl group, a benzyl group, an aryl group, an alkoxy group, or —NRR, wherein Rand Rare independently H, an alkyl group or an aryl group; Ris (CH)where n is and integer in the range of 0 to 5, —CHCH(CH)—, —CH═CH—, —CH═C(CH)—, or —C≡C—; Ris (CH)where p is an integer in the range of 4 to 12, —(CHR)(CHR)(CHR)(CHR)(CHR)C(R)═C(R)C(R)═C(R)—, —(CHR)(CHR)(CHR)(CHR)(CHR)CH(R)CH(R)C(R)═C(R)—, —(CHR)(CHR)(CHR)(CHR)(CHR)C(R)═C(R)CH(R)CH(R)—, —(CHR)(CHR)(CHR)(CHR)(CHR)CH(R)CH(R)CH(R)CH(R)—, wherein y1 and y2 are 1 and y3, y4 and y5 are independently 0 or 1, R, R, R, Rand Rare independently H, CH, or OR, and R, R, R, and Rare independently H or CH, wherein Ris H, an alkyl group, an aryl group, a benzyl group, a trityl group, —SiRRR, CHOR, or COR; and Ris H or OR, wherein Ris H, an alkyl group, an aryl group, an aryl group, a benzyl group, a trityl group, —SiRRR, CHOR, or COR; provided that the compound is not dictyostatin 1.
Raghavan R Balachandran from Wexford, PA, age ~79 Get Report