Pre-exposure prophylaxis of hiv infections
US-2024041906-A1 · Feb 8, 2024 · US
US2016129035A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016129035-A1 |
| Application number | US-201414895719-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jun 3, 2014 |
| Priority date | Jun 4, 2013 |
| Publication date | May 12, 2016 |
| Grant date | — |
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A drug combination against acid-fast bacillus , including: an inhibitor for WecA or an ortholog thereof; and at least one of an inhibitor for MurX or an ortholog thereof and an RNA synthesis inhibitor, wherein the inhibitor for WecA or an ortholog thereof is used in combination with the at least one of an inhibitor for MurX or an ortholog thereof and an RNA synthesis inhibitor; a screening method for a drug against acid-fast bacillus ; and an inhibitor for WecA or an ortholog thereof.
Opening claim text (preview).
1 . A method for treating an individual infected with acid-fast bacillus , comprising: administering, to the individual, an inhibitor for WecA or an ortholog thereof, and at least one of an inhibitor for MurX or an ortholog thereof and an RNA synthesis inhibitor. 2 . The method according to claim 1 , wherein the inhibitor for WecA or an ortholog thereof contains a compound expressed by the following Structural Formula (1), and the inhibitor for MurX or an ortholog thereof contains a compound expressed by the following Structural Formula (2): where in Structural Formula (2), “Me” is a methyl group. 3 . The method according to claim 1 , wherein the inhibitor for WecA or an ortholog thereof contains tunicamycin, and the RNA synthesis inhibitor contains rifampicin. 4 . A screening method for a drug against acid-fast bacillus , the method comprising: measuring activity of a test substance against WecA or an ortholog thereof. 5 . A method for inhibiting WecA or an ortholog thereof, comprising: administering a compound expressed by the following Structural Formula (1):
with ribosyl as the saccharide radical · CPC title
Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin · CPC title
for tuberculosis · CPC title
Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca · CPC title
having two nitrogen atoms, e.g. dilazep · CPC title
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