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N- (1- carboxy- 2- methylbutyl)benzisothiazolone

expels zinc from zinc fingers of HIV nucleocapsid protein; structure in first source

Also Known As:

3-methyl-2-(3-oxo-3H-benz(d)isothiazol-2-yl)pentanoic acid; CMBB-BIT; PD 161374; PD-161374

Networked: 1 relevant articles (1 outcomes, 0 trials/studies)

Relationship Network

Bio-Agent Context: Research Results

Organic Chemicals: 133
- Sulfur Compounds: 278
  - Thiazoles: 392
    - N-(1-carboxy-2-methylbutyl)benzisothiazolone: 1
Heterocyclic Compounds: 198
- 1-Ring Heterocyclic Compounds
  - Azoles: 2138
    - Thiazoles: 392
      - N-(1-carboxy-2-methylbutyl)benzisothiazolone: 1

Experts

1.	Domagala, J: 1 article (02/2001)
2.	Gogliotti, R: 1 article (02/2001)
3.	Gracheck, S: 1 article (02/2001)
4.	Heldsinger, A: 1 article (02/2001)
5.	McQuade, T: 1 article (02/2001)
6.	Sharmeen, L: 1 article (02/2001)

Related Diseases

1.	HIV Infections (HIV Infection) 02/01/2001 - "PD 161374 inhibited acute HIV infection and it was effective when added during the early phase of HIV infection. "