2A,3A-EPOXY-16B-(1-PYRROLIDINYL)-5A-ANDROSTAN-17B-OL

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Reagent Code: #139719
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CAS Number 119302-19-1

science Other reagents with same CAS 119302-19-1

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Weight 359.55 g/mol
Formula C₂₃H₃₇NO₂
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MDL Number MFCD14155627
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Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of steroidal drugs with potential neuroactive and hormonal properties. Its unique epoxy and pyrrolidinyl functional groups enable selective interactions with steroid receptors, making it valuable in developing agents that modulate central nervous system activity. It has been investigated for its potential in treating hormonal imbalances and neurodegenerative conditions due to its ability to cross the blood-brain barrier and influence neurosteroid pathways. Additionally, its structural features are exploited in structure-activity relationship (SAR) studies to optimize potency and selectivity in new steroid-based therapeutics.

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inventory 5g
10-20 days ฿8,680.00

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2A,3A-EPOXY-16B-(1-PYRROLIDINYL)-5A-ANDROSTAN-17B-OL
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Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of steroidal drugs with potential neuroactive and hormonal properties. Its unique epoxy and pyrrolidinyl functional groups enable selective interactions with steroid receptors, making it valuable in developing agents that modulate central nervous system activity. It has been investigated for its potential in treating hormonal imbalances and neurodegenerative conditions due to its ability to cross the bl

Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of steroidal drugs with potential neuroactive and hormonal properties. Its unique epoxy and pyrrolidinyl functional groups enable selective interactions with steroid receptors, making it valuable in developing agents that modulate central nervous system activity. It has been investigated for its potential in treating hormonal imbalances and neurodegenerative conditions due to its ability to cross the blood-brain barrier and influence neurosteroid pathways. Additionally, its structural features are exploited in structure-activity relationship (SAR) studies to optimize potency and selectivity in new steroid-based therapeutics.

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