502-64-7
Chemical Structure
Neurosporene
- CAS No.: 502-64-7
- Formula:C40H58
- Molecular Weight:538.89
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
InChIKey: ATCICVFRSJQYDV-XILUKMICSA-N
SMILES: C/C(C)=C\CC/C(C)=C/C=C/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/CC/C=C(C)/CC/C=C(C)\C
Biological Activity: Neurosporene is a carotenoid. Neurosporene is an intermediate in the synthesis of Lycopene (HY-N0287). Neurosporene can be isolated from date palm, Kocuria sp. GMA bacteria, and Anthurus archeri fungi. Neurosporene has antioxidant activity. Neurosporene can be used in the research of diseases such as cancer[1][2][3].
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Neurosporene | Neurosporene is a carotenoid. Neurosporene is an intermediate in the synthesis of Lycopene (HY-N0287). Neurosporene can be isolated from date palm, Kocuria sp. GMA bacteria, and Anthurus archeri fungi. Neurosporene has antioxidant activity. Neurosporene can be used in the research of diseases such as cancer. | |||||||||||||||||||||
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- [1]. Nasir M U, et al. A review on the nutritional content, functional properties and medicinal potential of dates[J]. Sci. Lett, 2015, 3(1): 17-22.
- [2]. Ibrahim G S, et al. Bio-production and characterization of carotenoid yellow pigment from Kocuria sp. GMA and exploring its sustainable antioxidant, antimicrobial and antibiofilm properties. Egyptian Journal of Chemistry, 2024, 67(8): 57-68.
- [3]. Czygan F C, et al. Carotinoide der Porter-Lincoln-Reihe in Anthurus archeri (Clathraceae; Basidiom ycetales; Mycophyta)/Carotenoids of the Porter-Lincoln-Series in Anthurus archeri (Clathraceae; Basidiomycetales; Mycophyta). Zeitschrift für Naturforschung C, 1975, 30(3-4): 297-297.
Keywords
