HINDERED CIS ISOMERS OF VITAMIN A AND RETINENE: THE STRUCTURE OF THE NEO-B ISOMER
- 15 July 1955
- journal article
- research article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 41 (7) , 438-451
- https://doi.org/10.1073/pnas.41.7.438
Abstract
Neo-B isomer of vitamin A and retinene, a hindered cis form, is the precursor of the visual pigments rhodopsin and iodopsin. This paper shows it to be a monocis isomer, therefore either 7 cis or 11-cis. The 11-cis isomer was synthesized and found to possess very different properties from neo-b. It may be called "neo-c." Neo-b isomer must therefore be 7-cis. Its properties are in specific agreement with this structure. The formation of theneo-b isomer raises special problems chemically and physiologically. Nothing is known of its biological occurrence or function outside the eye.This publication has 9 references indexed in Scilit:
- IODOPSINThe Journal of general physiology, 1955
- Crystalline Neoretinene bScience, 1954
- THE MOLAR EXTINCTION OF RHODOPSINThe Journal of general physiology, 1953
- GEOMETRICAL ISOMERS OF RETINENEThe Journal of general physiology, 1953
- CIS-TRANS ISOMERS OF VITAMIN A AND RETINENE IN THE RHODOPSIN SYSTEMThe Journal of general physiology, 1952
- The Mechanism of Rhodopsin SynthesisProceedings of the National Academy of Sciences, 1951
- Zur cis‐trans‐Isomerisierung von CarotinoidenHelvetica Chimica Acta, 1949
- Studies on vitamin ABiochemical Journal, 1948
- Synthese des Vitamin AHelvetica Chimica Acta, 1947