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3β-acetoxy-16α-bromo-5α-androstan-17-one is a steroidal compound characterized by its unique molecular structure. It features a 5α-androstan core, which is a type of steroid with a cycloalkane ring system. The 3β-acetoxy group indicates the presence of an acetate ester at the 3β position, while the 16α-bromo group signifies a bromine atom attached at the 16α position. The 17-one functional group denotes a ketone at the 17 position. 3β-acetoxy-16α-bromo-5α-androstan-17-one is of interest in the field of organic chemistry, particularly in the study of steroidal compounds and their potential applications in medicine and pharmaceuticals. Its specific structure may also be relevant to research on hormone synthesis and regulation.

1242-55-3

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1242-55-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1242-55-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,4 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1242-55:
(6*1)+(5*2)+(4*4)+(3*2)+(2*5)+(1*5)=53
53 % 10 = 3
So 1242-55-3 is a valid CAS Registry Number.

1242-55-3Relevant academic research and scientific papers

Development of Selective Steroid Inhibitors for the Glucose-6-phosphate Dehydrogenase from Trypanosoma cruzi

Fredo Naciuk, Fabrício,Do Nascimento Faria, Jéssica,Gonc?lves Eufrásio, Amanda,Torres Cordeiro, Artur,Bruder, Marjorie

, p. 1250 - 1256 (2020)

Chagas disease is a parasitic infection affecting millions of people across Latin America, imposing a dramatic socioeconomic burden. Despite the availability of drugs, nifurtimox and benznidazole, lack of efficacy and incidence of side-effects prompt the identification of novel, efficient, and affordable drug candidates. To address this issue, one strategy could be probing the susceptibility of Trypanosoma parasites toward NADP-dependent enzyme inhibitors. Recently, steroids of the androstane group have been described as highly potent but nonselective inhibitors of parasitic glucose-6-phosphate dehydrogenase (G6PDH). In order to promote selectivity, we have synthesized and evaluated 26 steroid derivatives of epiandrosterone in enzymatic assays, whereby 17 compounds were shown to display moderate to high selectivity for T. cruzi over the human G6PDH. In addition, three compounds were effective in killing intracellular T. cruzi forms infecting rat cardiomyocytes. Altogether, this study provides new SAR data around G6PDH and further supports this target for treating Chagas disease.

Microwave induced selective enolization of steroidal ketones and efficient acetylation of sterols in semisolid state

Marwah, Padma,Marwah, Ashok,Lardy, Henry A.

, p. 2273 - 2287 (2007/10/03)

Under microwave irradiation steroidal enones, more specifically, position three carbonyls were efficiently and selectively converted to the corresponding enol acetates in the presence of additional enolizable carbonyl functions at other positions, using acetic anhydride and a catalytic amount of toluene-p-sulfonic acid. Acetylation of hydroxyl groups of the sterols, including those at the hindered positions, was near quantitative. Strictly anhydrous conditions were not a pre-requisite for acetylation and the reaction system easily tolerated up to 10% (v/v) moisture.

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