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11α,16α-Dihydroxypregn-4-ene-3,20-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55622-61-2

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55622-61-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55622-61-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,6,2 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 55622-61:
(7*5)+(6*5)+(5*6)+(4*2)+(3*2)+(2*6)+(1*1)=122
122 % 10 = 2
So 55622-61-2 is a valid CAS Registry Number.

55622-61-2Upstream product

55622-61-2Downstream Products

55622-61-2Relevant academic research and scientific papers

Mammalian Cells Engineered To Produce New Steroids

Spady, Emma S.,Wyche, Thomas P.,Rollins, Nathanael J.,Clardy, Jon,Way, Jeffrey C.,Silver, Pamela A.

, p. 1827 - 1833 (2018)

Steroids can be difficult to modify through traditional organic synthesis methods, but many enzymes regio- and stereoselectively process a wide variety of steroid substrates. We tested whether steroid-modifying enzymes could make novel steroids from non-native substrates. Numerous genes encoding steroid-modifying enzymes, including some bacterial enzymes, were expressed in mammalian cells by transient transfection and found to be active. We made three unusual steroids by stable expression, in HEK293 cells, of the 7α-hydroxylase CYP7B1, which was selected because of its high native product yield. These cells made 7α,17α-dihydroxypregnenolone and 7β,17α-dihydroxypregnenolone from 17α-hydroxypregnenolone and produced 11α,16α-dihydroxyprogesterone from 16α-hydroxyprogesterone. The last two products were the result of CYP7B1-catalyzed hydroxylation at previously unobserved sites. A Rosetta docking model of CYP7B1 suggested that these substrates’ D-ring hydroxy groups might prevent them from binding in the same way as the native substrates, bringing different carbon atoms close to the active ferryl oxygen atom. This new approach could potentially use other enzymes and substrates to produce many novel steroids for drug candidate testing.

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