US2010056629A1PendingUtilityA1
Retrovirus-infection inhibitor
Est. expiryNov 17, 2026(~0.3 yrs left)· nominal 20-yr term from priority
A61P 31/18A61P 43/00A61K 31/202A61P 31/14A61P 31/12
31
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Claims
Abstract
An infection inhibitor of retrovirus, particularly human immunodeficiency virus, comprising, as an active ingredient, at least one compound selected from the group consisting of a compound represented by the formula (I) (GGA) or a salt thereof, a compound represented by the formula (II) (NIK-333) or a salt thereof, and derivatives thereof.
Claims
exact text as granted — not AI-modified1 . A retrovirus-infection inhibitor comprising, as an active ingredient, at least one compound selected from the group consisting of a compound represented by the formula (I) or a salt thereof, a compound represented by the formula (II) or a salt thereof, and derivatives thereof:
2 . The inhibitor of claim 1 , wherein the active ingredient is a compound represented by the formula (I) or a salt thereof, or a compound represented by the formula (II) or a salt thereof.
3 . The inhibitor of claim 1 , wherein the retrovirus is a human immunodeficiency virus.
4 . The inhibitor claim 1 , wherein the inhibition of retrovirus infection is based on a CXCR4 expression lowering action.
5 . A therapeutic agent for HIV infection, comprising, as an active ingredient, at least one compound selected from the group consisting of a compound represented by the formula (I) or a salt thereof, a compound represented by the formula (II) or a salt thereof, and derivatives thereof.
6 . A method of suppressing retrovirus infection, comprising administering an effective amount of at least one compound selected from the group consisting of a compound represented by the formula (I) or a salt thereof, a compound represented by the formula (II) or a salt thereof, and derivatives thereof to a subject in need of the administration.
7 . The method of claim 6 , wherein a compound represented by the formula (I) or a salt thereof, or a compound represented by the formula (II) or a salt thereof is administered in an effective amount to the subject.
8 . The method of claim 6 , wherein the retrovirus is a human immunodeficiency virus.
9 . The method of claim 6 , wherein the suppression of retrovirus infection is based on a CXCR4 expression lowering action.
10 . A therapeutic method of HIV infection, comprising administering an effective amount of at least one compound selected from the group consisting of a compound represented by the formula (I) or a salt thereof, a compound represented by the formula (II) or a salt thereof, and derivatives thereof to a subject in need of the administration.
11 . The inhibitor of claim 2 , wherein the inhibition of retrovirus infection is based on a CXCR4 expression lowering action.
12 . The inhibitor of claim 3 , wherein the inhibition of retrovirus infection is based on a CXCR4 expression lowering action.
13 . The method of claim 7 , wherein the suppression of retrovirus infection is based on a CXCR4 expression lowering action.
14 . The method of claim 8 , wherein the suppression of retrovirus infection is based on a CXCR4 expression lowering action.Join the waitlist — get patent alerts
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