CAS 75903-10-5

Fórmula: C45H60N4O11

InChI: InChI=1S/C45H60N4O11/c1-11-18-49-19-16-45(17-20-49)47-33-30-31-38(53)27(7)41-32(30)42(55)44(9,60-41)58-21-15-29(57-10)24(4)40(59-28(8)50)26(6)37(52)25(5)36(51)22(2)13-12-14-23(3)43(56)46-35(39(31)54)34(33)48-45/h12-15,21-22,24-26,29,36-37,40,47,51-54H,11,16-20H2,1-10H3/t22-,24+,25+,26+,29-,36-,37+,40+,44-/m0/s1

Clave InChI: WGJJHCHIIIQECM-CTRLBJGESA-N

SMILES: CCCN1CCC2(CC1)NC3=C4C5=C(C(=NC(=O)C(=CC=C[C@@H]([C@@H]([C@H]([C@H]([C@H]([C@@H]([C@@H]([C@H](C=CO[C@@]6(C(=O)C4=C(O6)C(=C5O)C)C)OC)C)OC(=O)C)C)O)C)O)C)C)C3=N2)O

N-Desisobutyl-N-propyl Rifabutin

Producto controlado

CAS: 75903-10-5

Fórmula: C₄₅H₆₀N₄O₁₁

Forma y color: Neat

Peso molecular: 832.978

Ref: TR-D290080

N-Desisobutyl-N-propyl rifabutin

CAS: 75903-10-5

N-Desisobutyl-N-propyl rifabutin is a synthetic derivative of rifabutin, which is an antibiotic belonging to the rifamycin class. This compound is sourced from modifications of the parent molecule rifabutin, itself derived from the rifamycin family produced by the bacterium Amycolatopsis, traditionally used for its antimicrobial properties. The mode of action involves the inhibition of bacterial RNA polymerase, effectively preventing the transcription process necessary for bacterial replication and protein synthesis. This disruption of RNA synthesis provides potent antimicrobial activity.

Fórmula: C₄₅H₆₀N₄O₁₁

Pureza: Min. 95%

Peso molecular: 832.98 g/mol

Ref: 3D-AD21204