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For example, cyanocobalamin can be converted to its analog cobalamins via reduction to B 12s, followed by the addition of the corresponding alkyl halides, acyl halides, alkene or alkyne. Steric hindrance is the major limiting factor in the synthesis of the B 12 coenzyme analogs. For example, no reaction occurs between neopentyl chloride and B
"B12" and "Cbl" redirect here. For other uses of B12, see B12 (disambiguation). For the musical group, see Carbon Based Lifeforms. Pharmaceutical compound Vitamin B12 General skeletal formula of cobalamins Stick model of cyanocobalamin (R = CN) based on the crystal structure Clinical data Other names Vitamin B12, vitamin B-12, cobalamin AHFS / Drugs.com Monograph MedlinePlus a605007 License ...
In women aged between 19 and 64 years, the mean serum vitamin B 12 concentration was slightly lower than men (298 pmol/L), with 3.3% having low vitamin B 12 concentrations < 150 pmol/L. [161] In Germany, a national survey in 1998 was conducted in 1,266 women of childbearing age.
In enzymology, a cyanocobalamin reductase (cyanide-eliminating) (EC 1.16.1.6) is an enzyme that catalyzes the chemical reaction cob(I)alamin + cyanide + NADP + ⇌ {\displaystyle \rightleftharpoons } cyanocob(III)alamin + NADPH + H +
Cyanocobalamin is usually converted to hydroxocobalamin in the serum, whereas hydroxocobalamin is converted to either methylcobalamin or adenosylcobalamin. Cobalamins circulate bound to serum proteins called transcobalamins (TC) and haptocorrins. Hydroxocobalamin has a higher affinity to the TC II transport protein than cyanocobalamin, or ...
Aerobic pathway that requires oxygen and in which cobalt is inserted late in the pathway; [6] [7] found in Pseudomonas denitrificans and Rhodobacter capsulatus.; Anaerobic pathway in which cobalt insertion is the first committed step towards cobalamin synthesis; [8] [9] [10] found in Salmonella typhimurium, Bacillus megaterium, and Propionibacterium freudenreichii subsp. shermanii.
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