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3β-Hydroxy-5β-pregnane-11,20-dione is a steroidal compound belonging to the pregnane family, characterized by its unique molecular structure featuring a hydroxyl group at the 3β position and a ketone group at both the 11 and 20 positions. This chemical is a derivative of the parent steroid, pregnane, and is known for its potential biological activities, such as anti-inflammatory and immunosuppressive properties. It is synthesized through various chemical reactions and can be found in trace amounts in some natural sources, including plants and animals. Due to its structural complexity and potential therapeutic applications, 3β-Hydroxy-5β-pregnane-11,20-dione has been a subject of interest in the field of medicinal chemistry and drug development.

566-00-7

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566-00-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 566-00-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,6 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 566-00:
(5*5)+(4*6)+(3*6)+(2*0)+(1*0)=67
67 % 10 = 7
So 566-00-7 is a valid CAS Registry Number.

566-00-7Relevant academic research and scientific papers

NEUROACTIVE STEROIDS AND METHODS OF PREPARATION

-

, (2020/01/31)

Disclosed are neuroactive steroid anaesthetic agents, methods for their preparation and compositions comprising the same. The invention provides scaled up and/or GMP methods for preparing neuroactive steroids, such as alfaxalone, alfadolone and alfadolone acetate.

Allopregnanolone and pregnanolone analogues modified in the C ring: Synthesis and activity

Slavíková, Barbora,Bujons, Jordi,Matyá?, Libor,Vidal, Miguel,Babot, Zoila,Kri?tofíková, Zdena,Su?ol, Cristina,Kasal, Alexander

, p. 2323 - 2336 (2013/06/04)

(25R)-3β-Hydroxy-5α-spirostan-12-one (hecogenin) and 11α-hydroxypregn-4-ene-3,20-dione (11α-hydroxyprogesterone) were used as starting materials for the synthesis of a series of 11- and 12-substituted derivatives of 5ξ-pregnanolone (3α-hydroxy-5α- pregnan-20-one and 3α-hydroxy-5β-pregnan-20-one), the principal neurosteroid acting via γ-aminobutyric acid (GABA). These analogues were designed to study the structural requirements of the corresponding GABA A receptor. Their biological activity was measured by in vitro test with [3H]flunitrazepam as radioligand in which allopregnanolone and its active analogues stimulated the binding to the GABAA receptor. Analysis of the SAR data suggests dependence of the flunitrazepam binding activity on the hydrophobic-hydrophilic balance of the groups at the C-ring edge rather than on specific interactions between them and the receptor.

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