MetaCyc Compound: 7,9,9'-cis-neurosporene

Synonyms: proneurosporene, 7,9,9'-tri-cis-neurosporene, 7,9,9'-tricis-neurosporene

Superclasses: a lipidan isoprenoida terpenoida tetraterpenoida carotenoida carotene
a secondary metabolitea terpenoida tetraterpenoida carotenoida carotene

Chemical Formula: C40H58

Molecular Weight: 538.9 Daltons

Monoisotopic Molecular Weight: 538.4538518618 Daltons

7,9,9'-<i>cis</i>-neurosporene compound structure


InChI: 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-


Unification Links: ChEBI:62463, KEGG:C19759, PubChem:25244751

Standard Gibbs Free Energy of Change Formation (ΔfG in kcal/mol): 864.46497Inferred by computational analysis [Latendresse13]

Reactions known to consume the compound:

trans-lycopene biosynthesis II (plants) :
7,9,9'-cis-neurosporene + an electron-transfer quinone → prolycopene + an electron-transfer quinol

Reactions known to produce the compound:

trans-lycopene biosynthesis II (plants) :
9,9'-di-cis-ζ-carotene + an electron-transfer quinone → 7,9,9'-cis-neurosporene + an electron-transfer quinol

In Reactions of unknown directionality:

Not in pathways:
7,9,9'-cis-neurosporene = 9'-cis-neurosporene


Latendresse13: Latendresse M. (2013). "Computing Gibbs Free Energy of Compounds and Reactions in MetaCyc."

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Please cite the following article in publications resulting from the use of MetaCyc: Caspi et al, Nucleic Acids Research 42:D459-D471 2014
Page generated by SRI International Pathway Tools version 19.5 on Sun Nov 29, 2015, BIOCYC14B.