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(5Z,7E,22E)-(1S,3R,24R)-25-(5-butyloxazole-2-yl)-26,27-cyclo-9,10-secocholesta-5,7,10(19),22-tetraene-1,3,24-triol is a complex cyclocholesterol derivative with a unique molecular structure. It features a butyloxazole group at the 25th position and hydroxyl groups at the 1st, 3rd, and 24th positions. (5Z,7E,22E)-(1S,3R,24R)-25-(5-butyloxazole-2-yl)-26,27-cyclo-9,10-secocholesta-5,7,10(19),22-tetraene-1,3,24-triol also has a series of conjugated double bonds at the 5th, 7th, 10th, 19th, and 22nd positions. Its structure and functional groups suggest potential roles in various biological processes, such as signaling, membrane function, or other physiological activities. Further research is necessary to fully comprehend its properties and possible applications.

198760-31-5

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198760-31-5 Usage

Uses

Used in Pharmaceutical Industry:
(5Z,7E,22E)-(1S,3R,24R)-25-(5-butyloxazole-2-yl)-26,27-cyclo-9,10-secocholesta-5,7,10(19),22-tetraene-1,3,24-triol is used as a potential therapeutic agent for [application reason] due to its unique structure and functional groups that may play a role in biological processes.
Used in Research and Development:
In the field of research and development, (5Z,7E,22E)-(1S,3R,24R)-25-(5-butyloxazole-2-yl)-26,27-cyclo-9,10-secocholesta-5,7,10(19),22-tetraene-1,3,24-triol is used as a subject for studying [application reason], such as its interaction with cellular receptors, potential effects on cellular signaling pathways, or its role in membrane function.

Check Digit Verification of cas no

The CAS Registry Mumber 198760-31-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,8,7,6 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 198760-31:
(8*1)+(7*9)+(6*8)+(5*7)+(4*6)+(3*0)+(2*3)+(1*1)=185
185 % 10 = 5
So 198760-31-5 is a valid CAS Registry Number.

198760-31-5Downstream Products

198760-31-5Relevant academic research and scientific papers

Practical synthesis of a heterocyclic immunosuppressive vitamin D analogue

Westermann, Juergen,Schneider, Matthias,Platzek, Johannes,Petrov, Orlin

, p. 200 - 205 (2012/12/26)

1α,25-Dlhydroxyvitamin D3 (calcitrioi) 1 and synthetic analogues thereof are highly potent compounds with a wide range of pharmacological activity making them of great interest for the pharmaceutical industry. Herein we report an improved synthesis of the calcitriol analogue 2, which features a novel oxazole-containing side chain. The crucial part of the synthesis was the development of a practical route to the β-keto phosphonate 28, allowing an easy introduction of the unnatural side chain by a Wittig Horner reaction.

NEW VITAMIN D DERIVATIVES WITH CARBO-OR HETEROCYCLIC SUBSTITUENTS AT C-25, A PROCESS FOR THEIR PRODUCTION, INTERMEDIATE PRODUCTS AND THEIR USE FOR PRODUCING MEDICAMENTS

-

, (2008/06/13)

The invention concerns new vitamin D derivatives of general formula (I) a process for their production, their use for production of medicaments, and intermediate products used in the process.

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