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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.
"