Name | [(1S,4R)-4-[2-amino-6-(cyclopropylamino)purin-9-yl]cyclopent-2-en-1-yl]methyl 2-hydroxyacetate |
---|---|
Synonyms |
Abacavir hydroxyacetate
Prurisol UNII-B3C7MG354B Acetic acid,2-hydroxy-,((1S,4R)-4-(2-amino-6-(cyclopropylamino)-9H-purin-9-yl)-2-cyclopenten-1-yl)methyl ester |
Description | Abacavir hydroxyacetate is an orally active inhibitor of IL-20 and PRINS. Abacavir hydroxyacetate reduces proliferation rate of skin in psoriasis as an immune modulator. Abacavir hydroxyacetate can be used for the research of inflammatory skin problems[1][2]. |
---|---|
Related Catalog | |
In Vivo | Abacavir hydroxyacetate (10-20 mg/kg; p.o. once) effectively controls psoriasis of mice[2]. Animal Model: 6 to 8-week-old male and female SCID mice with implantation of psoriatic tissue[2] Dosage: 10 and 20 mg/kg Administration: Oral gavage; 10-20 mg/kg once Result: Decreased the concentration of PRINS and 1L-20, and reduced the lesion area of skin. Showed a better effect than methotrexate in controlling psoriasis. |
References |
Molecular Formula | C16H20N6O3 |
---|---|
Molecular Weight | 344.36800 |
Exact Mass | 344.16000 |
PSA | 128.91000 |
LogP | 0.63860 |