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Neurosporene

Neurosporene is a carotenoid pigment. It is an intermediate in the biosynthesis of lycopene and a variety of bacterial carotenoids.[1]

Neurosporene
Names
IUPAC name
7,8-Dihydro-ψ,ψ-carotene
Systematic IUPAC name
(6E,8E,10E,12E,14E,16E,18E,20E,22E,26E)-2,6,10,14,19,23,27,31-Octamethyldotriaconta-2,6,8,10,12,14,16,18,20,22,26,30-dodecaene
Identifiers
  • 502-64-7 Y
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:16833
ChemSpider
  • 4444347
  • 5280789
  • InChI=1S/C40H58/c1-33(2)19-13-23-37(7)27-17-31-39(9)29-15-25-35(5)21-11-12-22-36(6)26-16-30-40(10)32-18-28-38(8)24-14-20-34(3)4/h11-12,15-17,19-22,25-31H,13-14,18,23-24,32H2,1-10H3/b12-11+,25-15+,26-16+,31-17+,35-21+,36-22+,37-27+,38-28+,39-29+,40-30+
    Key: ATCICVFRSJQYDV-XILUKMICSA-N
  • InChI=1/C40H58/c1-33(2)19-13-23-37(7)27-17-31-39(9)29-15-25-35(5)21-11-12-22-36(6)26-16-30-40(10)32-18-28-38(8)24-14-20-34(3)4/h11-12,15-17,19-22,25-31H,13-14,18,23-24,32H2,1-10H3/b12-11+,25-15+,26-16+,31-17+,35-21+,36-22+,37-27+,38-28+,39-29+,40-30+
    Key: ATCICVFRSJQYDV-XILUKMICBV
  • CC(=CCC/C(=C/CC/C(=C/C=C/C(=C/C=C/C=C(\C)/C=C/C=C(\C)/C=C/C=C(\C)/CCC=C(C)C)/C)/C)/C)C
Properties
C40H58
Molar mass 538.904 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

References edit

  1. ^ Scolnik, PA; Walker, MA; Marrs, BL (1980). "Biosynthesis of carotenoids derived from neurosporene in Rhodopseudomonas capsulata". The Journal of Biological Chemistry. 255 (6): 2427–32. doi:10.1016/S0021-9258(19)85909-4. PMID 7358679.



neurosporene, carotenoid, pigment, intermediate, biosynthesis, lycopene, variety, bacterial, carotenoids, namesiupac, name, dihydro, carotenesystematic, iupac, name, octamethyldotriaconta, dodecaeneidentifierscas, number, model, jsmol, interactive, imagechebi,. Neurosporene is a carotenoid pigment It is an intermediate in the biosynthesis of lycopene and a variety of bacterial carotenoids 1 Neurosporene NamesIUPAC name 7 8 Dihydro ps ps caroteneSystematic IUPAC name 6E 8E 10E 12E 14E 16E 18E 20E 22E 26E 2 6 10 14 19 23 27 31 Octamethyldotriaconta 2 6 8 10 12 14 16 18 20 22 26 30 dodecaeneIdentifiersCAS Number 502 64 7 Y3D model JSmol Interactive imageChEBI CHEBI 16833ChemSpider 4444347PubChem CID 5280789InChI InChI 1S C40H58 c1 33 2 19 13 23 37 7 27 17 31 39 9 29 15 25 35 5 21 11 12 22 36 6 26 16 30 40 10 32 18 28 38 8 24 14 20 34 3 4 h11 12 15 17 19 22 25 31H 13 14 18 23 24 32H2 1 10H3 b12 11 25 15 26 16 31 17 35 21 36 22 37 27 38 28 39 29 40 30 Key ATCICVFRSJQYDV XILUKMICSA NInChI 1 C40H58 c1 33 2 19 13 23 37 7 27 17 31 39 9 29 15 25 35 5 21 11 12 22 36 6 26 16 30 40 10 32 18 28 38 8 24 14 20 34 3 4 h11 12 15 17 19 22 25 31H 13 14 18 23 24 32H2 1 10H3 b12 11 25 15 26 16 31 17 35 21 36 22 37 27 38 28 39 29 40 30 Key ATCICVFRSJQYDV XILUKMICBVSMILES CC CCC C C CC C C C C C C C C C C C C C C C C C C C C C CCC C C C C C C CPropertiesChemical formula C 40H 58Molar mass 538 904 g mol 1Except where otherwise noted data are given for materials in their standard state at 25 C 77 F 100 kPa Infobox referencesReferences edit Scolnik PA Walker MA Marrs BL 1980 Biosynthesis of carotenoids derived from neurosporene in Rhodopseudomonas capsulata The Journal of Biological Chemistry 255 6 2427 32 doi 10 1016 S0021 9258 19 85909 4 PMID 7358679 nbsp This article about an organic compound is a stub You can help Wikipedia by expanding it vte Retrieved from https en wikipedia org w index php title Neurosporene amp oldid 1153347773, wikipedia, wiki, book, books, library,

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