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Progress in the Chemistry of Organic Natural Products / Fortschritte Der Chemie Organischer Naturstoffe Softcover Repri Edition
Contributor(s): Glasenapp-Breiling, M. (Author), Jagtap, P. G. (Author), Kingston, D. G. I. (Author)
ISBN: 3709132282     ISBN-13: 9783709132289
Publisher: Springer
OUR PRICE:   $104.49  
Product Type: Paperback - Other Formats
Published: June 2012
Qty:
Additional Information
BISAC Categories:
- Science | Chemistry - Organic
- Medical | Pharmacology
- Science | Life Sciences - Biochemistry
Dewey: 547
Series: Fortschritte Der Chemie Organischer Naturstoffe Progress in
Physical Information: 0.56" H x 6.14" W x 9.21" (0.84 lbs) 253 pages
 
Descriptions, Reviews, Etc.
Publisher Description:
Of the porphyrinoid structures occurring in nature the most important and most widespread are the red blood pigment heme (1), the green pigment of plant photosynthesis chlorophyll a (2), the bacterial photo- synthetic pigment bacteriochlorophyll a (3), and the "antipernicious" red pigment vitamin BJ2 (4). The basic function of these cofactors are determined by the incorporation of the different metal ions into the macrotetracycles. The different oxidation levels of the macrocyclic ligand system regulate the fine tuning of these functions. The final adaptation of the cofactors to their special molecular environments in the cell compartments is effected by variation of the substitution patterns of the chromophores. HCO, C 3 CO, Phytyl 2 Heme Chlorophyll a CONH, CONH, H, NOC 1, CONH, /I(Y N 3 4 Bacteriochlorophyll a Vitamin B" HO References, pp. 42-51 Naturally Occurring Cyclic Tetrapyrroles 3 Until the mid-1970s the four classic cyclic tetrapyrrolic structures with their porphyrin, chi orin, bacteriochlorin, and corrin skeletons were almost the only representatives in the class of porphyrinoid natural products (1-10). Although other partially reduced porphyrins were conceivable, none of these partially saturated porphyrinoid structures had hitherto been found in nature.