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16β-piperidino-5α-androstane-3,17-dione is a synthetic steroidal compound that belongs to the class of androgens, which are male sex hormones. This specific compound is characterized by the presence of a piperidino group at the 16β position and a double bond between carbons 3 and 17, along with a ketone group at both the 3 and 17 positions. It is structurally derived from the naturally occurring hormone testosterone, but with modifications that alter its chemical properties and potential biological effects. The compound may be of interest in scientific research due to its potential applications in the study of androgen receptors and their role in various physiological processes. However, it is important to note that the compound's specific uses, effects, and safety profile are not well-established and would require further investigation and clinical studies.

3136-46-7

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3136-46-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3136-46-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,3 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3136-46:
(6*3)+(5*1)+(4*3)+(3*6)+(2*4)+(1*6)=67
67 % 10 = 7
So 3136-46-7 is a valid CAS Registry Number.

3136-46-7Downstream Products

3136-46-7Relevant academic research and scientific papers

Synthesis and neuromuscular blocking activity of 16β-piperidino epiandrosterone derivatives

Dubey, Sonal,Jindal,Piplani, Poonam,Young, Louse C.,Fathi, Behrooz,Harvey, Alan L.

, p. 229 - 240 (2007/10/03)

This study reports the synthesis of steroidal quaternary ammonium compounds 11 and 12, with quaternary nitrogen at position 3 and 16 of the steroid nucleus in 5α-epiandrosterone series; along with their neuromuscular blocking activity using chick biventer cervicis muscle preparation. The compound 12 was found to be five times more potent than 11 in reducing twitch response to nerve stimulations, indicating the importance of extended interonium distances and 17-acetoxy function for potent antagonist activity. Birkhaeuser Boston 2006.

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