CAS 100324-63-8
:25-DESACETYL RIFABUTIN
Description:
25-Desacetyl Rifabutin, with the CAS number 100324-63-8, is a derivative of rifabutin, an antibiotic primarily used in the treatment of tuberculosis and certain mycobacterial infections. This compound is characterized by its structural modification, which involves the removal of an acetyl group from rifabutin, resulting in altered pharmacological properties. It exhibits antibacterial activity, particularly against Mycobacterium avium complex, and is often utilized in patients with HIV/AIDS who are at risk for opportunistic infections. The substance is known for its ability to inhibit bacterial RNA synthesis by binding to the bacterial DNA-dependent RNA polymerase. Additionally, 25-desacetyl rifabutin may have different bioavailability and metabolic pathways compared to its parent compound, influencing its therapeutic efficacy and safety profile. As with many antibiotics, resistance can develop, necessitating careful monitoring of its use in clinical settings. Overall, 25-desacetyl rifabutin represents an important component in the arsenal against mycobacterial diseases, particularly in immunocompromised populations.
Formula:C44H60N4O10
InChI:InChI=1/C44H60N4O10/c1-11-23(4)48-18-16-44(17-19-48)46-32-29-30-38(52)27(8)40-31(29)41(54)43(9,58-40)57-20-15-28(56-10)24(5)36(50)26(7)37(51)25(6)35(49)21(2)13-12-14-22(3)42(55)45-34(39(30)53)33(32)47-44/h12-15,20-21,23-26,28,35-37,47,49-52H,11,16-19H2,1-10H3,(H,45,55)/b13-12+,20-15+,22-14-/t21-,23?,24+,25+,26-,28-,35-,36+,37?,43-/m0/s1
Synonyms:- 25-O-Deacetyl Rifabutin
- 25-O-Deacetylrifamycin
- (9S,12E,14S,15S,16S,17R,19R,20S,21S)-6,16,18,20-tetrahydroxy-14-methoxy-7,9,15,17,19,21,25-heptamethyl-1'-(1-methylpropyl)-26H-spiro[9,4-(epoxypentadeca[1,11,13]trienoimino)furo[2',3':7,8]naphtho[1,2-d]imidazole-2,4'-piperidine]-5,10,26(3H,9H)-trione
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Found 5 products.
25-O-Deacetyl Rifabutin
CAS:Controlled ProductFormula:C44H60N4O10Color and Shape:NeatMolecular weight:804.9725-O-Deacetyl rifabutin
CAS:<p>25-O-Deacetyl rifabutin is an antibiotic derivative, which is sourced from the semi-synthetic modification of rifabutin, a compound originally derived from the fermentation of the bacterium Amycolatopsis mediterranei. This derivative works by inhibiting bacterial RNA synthesis. It achieves this by specifically targeting the DNA-dependent RNA polymerase enzyme, which is essential for bacterial transcription. The mechanism involves binding to the beta-subunit of the polymerase, thereby blocking the elongation of the RNA chain, which ultimately leads to the death of the bacterial cell.</p>Formula:C44H60N4O10Purity:Min. 95%Color and Shape:Purple PowderMolecular weight:804.97 g/mol




