all-trans-Canthaxanthin (E 161g) - analytical standard, Moligand™ , CAS No.514-78-3

CAS: 514-78-3 Cat. No.: A135943 Formule: C₄₀H₅₂O₂ Poids moléculaire: 564.84 Numéro CE: 208-187-2

GRADE & PURITY Analytical standard, Moligand™

Synonyms

.BETA.-CAROTENE-4,4'-DIONE | CANTHAXANTHIN [FCC] | DTXCID002727 | 4,4'-DIKETO-.BETA.-CAROTENE | Canthaxanthin, tech. | NSC 374110 | UNII-4C3C6403MU | NCGC00095896-01 | Ro 1-9915 | Carotene-4,4'-dione, beta- | 2,4,4-trimethyl-3-[(1E,3E,5E,7E,9E,11E,13E,15E

Storage

Protected from light,Store at -20°C,Argon charged

Shipped In

Ice chest + Ice pads

Vue d’ensemble

All-trans-Canthaxanthin is a red-orange carotenoid with various biological activities, such as antioxidant, antitumor properties.

Specifications

Synonymes

.BETA.-CAROTENE-4,4'-DIONE | CANTHAXANTHIN [FCC] | DTXCID002727 | 4,4'-DIKETO-.BETA.-CAROTENE | Canthaxanthin, tech. | NSC 374110 | UNII-4C3C6403MU | NCGC00095896-01 | Ro 1-9915 | Carotene-4,4'-dione, beta- | 2,4,4-trimethyl-3-[(1E,3E,5E,7E,9E,11E,13E,15E

Spécifications et pureté

analytical standard, Moligand™

Conditions de stockage de stockage

Protected from light,Store at -20°C,Argon charged

Expédié en

Ice chest + Ice pads

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Grade

Étalon d'analyse, Moligand™

Noms et identifiants

• Pubchem Sid: 528771958
• Sourires canoniques: CC1=C(C(CCC1=O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(C(=O)CCC2(C)C)C)C)C
• IUPAC Name: 2,4,4-trimethyl-3-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-(2,6,6-trimethyl-3-oxocyclohexen-1-yl)octadeca-1,3,5,7,9,11,13,15,17-nonaenyl]cyclohex-2-en-1-one
• InChIKey: FDSDTBUPSURDBL-DKLMTRRASA-N
• INCHI: 1S/C40H52O2/c1-29(17-13-19-31(3)21-23-35-33(5)37(41)25-27-39(35,7)8)15-11-12-16-30(2)18-14-20-32(4)22-24-36-34(6)38(42)26-28-40(36,9)10/h11-24H,25-28H2,1-10H3/b12-11+,17-13+,18-14+,23-21+,24-22+,29-15+,30-16+,31-19+,32-20+
• Isomères SMILES: CC1=C(C(CCC1=O)(C)C)/C=C/C(=C/C=C/C(=C/C=C/C=C(/C=C/C=C(/C=C/C2=C(C(=O)CCC2(C)C)C)\C)\C)/C)/C
• Poids moléculaire: 564.84
• Reaxy-Rn: 3124143
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3124143&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Classe Prenol lipids
      • Subclass Tetraterpenoids
        • Level5 Carotenoids
          • Level6 Xanthophylls

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Classe: Prenol lipids
• Subclass: Tetraterpenoids
• Intermediate Tree Nodes: Carotenoids
• Direct Parent: Xanthophylls
• Alternative Parents: Cyclohexenones Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic homomonocyclic compounds
• Substituents: Xanthophyll - Cyclohexenone - Cyclic ketone - Ketone - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as xanthophylls. These are carotenoids containing an oxygenated carotene backbone. Carotenes are characterized by the presence of two end-groups (mostly cyclohexene rings, but also cyclopentene rings or acyclic groups) linked by a long branched alkyl chain. Carotenes belonging form a subgroup of the carotenoids family. Xanthophylls arise by oxygenation of the carotene backbone.
• External Descriptors: C40 isoprenoids (tetraterpenes)

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

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ALOX15 Tchem Arachidonate 15-lipoxygenase (7108 Activities)

Discover Target: ALOX15

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GCN5 Histone acetyltransferase GCN5 (89 Activities)

Discover Target: GCN5

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Mapt Microtubule-associated protein tau (6 Activities)

Discover Target: Mapt

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FTL Ferritin light chain (43324 Activities)

Discover Target: FTL

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Mécanismes d'action

Propriétés chimiques et physiques

• Sensibilité: Air sensitive; Light sensitive
• Point de fusion (°C): 201.6-201.7 °C
• Poids moléculaire: 564.800 g/mol
• XLogP3: 11.400
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 10
• Exact Mass: 564.397 Da
• Monoisotopic Mass: 564.397 Da
• Topological Polar Surface Area: 34.100 Ų
• Heavy Atom Count: 42
• Formal Charge: 0
• Complexity: 1270.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 9
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 9
• Covalently-Bonded Unit Count: 1