Sungsoon Fang

age ~49

from San Diego, CA

Also known as:
  • Sunsoon Fang
  • Sang Sungsoon
Phone and address:
9110 Judicial Dr, San Diego, CA 92122
8584123196

Sungsoon Fang Phones & Addresses

  • 9110 Judicial Dr, San Diego, CA 92122 • 8584123196
  • La Jolla, CA
  • Champaign, IL
  • Urbana, IL

Work

  • Company:
    The salk institute
    Aug 2008
  • Position:
    Postdoctoral research associate

Education

  • Degree:
    Ph.D.
  • School / High School:
    University of Illinois at Urbana-Champaign
    2003 to 2008
  • Specialities:
    Molecular Physiology

Skills

Molecular Biology • Physiology • Type 2 Diabetes • Inflammatory Bowel Disease • Insulin Resistance • Pancreatic Beta Cell • Intestinal Homeostasis • Bile Acid Homeostasis • Cell

Industries

Research

Resumes

Sungsoon Fang Photo 1

Assistant Professor

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Location:
San Diego, CA
Industry:
Research
Work:
The Salk Institute since Aug 2008
Postdoctoral Research Associate

Defense Security Command - Seoul, Korea May 1999 - Jul 2001
Sergeant, Retired
Education:
University of Illinois at Urbana-Champaign 2003 - 2008
Ph.D., Molecular Physiology
Seoul National University 1995 - 1999
B.S., Molecular biology
Daewon Foreign Language High School 1991 - 1994
Skills:
Molecular Biology
Physiology
Type 2 Diabetes
Inflammatory Bowel Disease
Insulin Resistance
Pancreatic Beta Cell
Intestinal Homeostasis
Bile Acid Homeostasis
Cell

Us Patents

  • Analogs Of Fexaramine And Methods Of Making And Using

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  • US Patent:
    20200123113, Apr 23, 2020
  • Filed:
    Sep 10, 2019
  • Appl. No.:
    16/566343
  • Inventors:
    - La Jolla CA, US
    - New South Wales, AU
    Annette Atkins - San Diego CA, US
    Sungsoon Fang - La Jolla CA, US
    Jae Myoung Suh - San Diego CA, US
    Thomas J. Baiga - Escondido CA, US
    Ruth T. Yu - La Jolla CA, US
    John F.W. Keana - Eugene OR, US
    Christopher Liddle - Chertswood, AU
  • Assignee:
    Salk Institute for Biological Studies - La Jolla CA
    The University of Sydney - New South Wales
  • International Classification:
    C07D 231/56
    C07B 59/00
    C07C 233/63
  • Abstract:
    Novel compounds having a formulaembodiments of a method of making the same, and of a composition comprising them are disclosed herein. Also disclosed are embodiments of a method of treating or preventing a metabolic disorder in a subject, comprising administering to a subject (e.g., via the gastrointestinal tract) a therapeutically effective amount of one or more of the disclosed compounds, thereby activating FXR receptors in the intestines, and treating or preventing a metabolic disorder in the subject. Additionally disclosed are embodiments of a method of treating or preventing inflammation in an intestinal region of a subject, comprising administering to the subject (e.g., via the gastrointestinal tract) a therapeutically effective amount of one or more of the disclosed compounds, thereby activating FXR receptors in the intestines, and thereby treating or preventing inflammation in the intestinal region of the subject.
  • Analogs Of Fexaramine And Methods Of Making And Using

    view source
  • US Patent:
    20190084939, Mar 21, 2019
  • Filed:
    Nov 27, 2018
  • Appl. No.:
    16/200861
  • Inventors:
    - La Jolla CA, US
    - New South Wales, AU
    Annette Atkins - San Diego CA, US
    Sungsoon Fang - La Jolla CA, US
    Jae Myoung Suh - San Diego CA, US
    Thomas J. Baiga - Escondido CA, US
    Ruth T. Yu - La Jolla CA, US
    John F.W. Keana - Eugene OR, US
    Christopher Liddle - Chertswood, AU
  • Assignee:
    Salk Institute for Biological Studies - La Jolla CA
    The University of Sydney - Sydney
  • International Classification:
    C07D 231/56
    C07C 233/63
    C07B 59/00
  • Abstract:
    Novel compounds having a formulaembodiments of a method of making the same, and of a composition comprising them are disclosed herein. Also disclosed are embodiments of a method of treating or preventing a metabolic disorder in a subject, comprising administering to a subject (e.g., via the gastrointestinal tract) a therapeutically effective amount of one or more of the disclosed compounds, thereby activating FXR receptors in the intestines, and treating or preventing a metabolic disorder in the subject. Additionally disclosed are embodiments of a method of treating or preventing inflammation in an intestinal region of a subject, comprising administering to the subject (e.g., via the gastrointestinal tract) a therapeutically effective amount of one or more of the disclosed compounds, thereby activating FXR receptors in the intestines, and thereby treating or preventing inflammation in the intestinal region of the subject.
  • Analogs Of Fexaramine And Methods Of Making And Using

    view source
  • US Patent:
    20170066724, Mar 9, 2017
  • Filed:
    Sep 12, 2016
  • Appl. No.:
    15/263033
  • Inventors:
    - La Jolla CA, US
    - Sydney, AU
    Annette Atkins - San Diego CA, US
    Sungsoon Fang - La Jolla CA, US
    Jae Myoung Suh - San Diego CA, US
    Thomas J. Baiga - Escondido CA, US
    Ruth T. Yu - La Jolla CA, US
    John F.W. Keana - Eugene OR, US
    Christopher Liddle - Chertswood, AU
  • Assignee:
    Salk Institute for Biological Studies - La Jolla CA
    The University of Sydney - Sydney
  • International Classification:
    C07D 231/56
    C07B 59/00
    C07C 233/63
  • Abstract:
    Novel compounds having a formulaembodiments of a method of making the same, and of a composition comprising them are disclosed herein. Also disclosed are embodiments of a method of treating or preventing a metabolic disorder in a subject, comprising administering to a subject (e.g., via the gastrointestinal tract) a therapeutically effective amount of one or more of the disclosed compounds, thereby activating FXR receptors in the intestines, and treating or preventing a metabolic disorder in the subject. Additionally disclosed are embodiments of a method of treating or preventing inflammation in an intestinal region of a subject, comprising administering to the subject (e.g., via the gastrointestinal tract) a therapeutically effective amount of one or more of the disclosed compounds, thereby activating FXR receptors in the intestines, and thereby treating or preventing inflammation in the intestinal region of the subject.
  • Methods Of Using Fexaramine And Agents That Increase Sympathetic Nervous System Activity To Promote Browning Of White Adipose Tissue

    view source
  • US Patent:
    20150258052, Sep 17, 2015
  • Filed:
    Mar 13, 2015
  • Appl. No.:
    14/657078
  • Inventors:
    - La Jolla CA, US
    - Ann Arbor MI, US
    Annette Atkins - San Diego CA, US
    Sungsoon Fang - La Jolla CA, US
    Jae Myoung Suh - San Diego CA, US
    Ruth T. Yu - La Jolla CA, US
    Alan R. Saltiel - Ann Arbor MI, US
  • Assignee:
    Salk Institute for Biological Studies - La Jolla CA
    The Regents of the University of Michigan - Ann Arbor MI
  • International Classification:
    A61K 31/216
    A61K 31/137
    A61K 31/4704
    A61K 9/00
    A61K 45/06
  • Abstract:
    Provided are methods of promoting browning of white adipose tissue (WAT) in a subject. Such methods can include administering to a subject (e.g., via the gastrointestinal tract) a therapeutically effective amount of fexaramine in combination with a therapeutically effective amount of a compound that mimics or increases sympathetic nervous system activity (e.g., one or more beta-adrenergic agonists and/or compounds that increase epinephrine secretion).

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