CAS 17092-92-1
:(-)-Dihidroactinidiolida
Descripción:
(-)-Dihidroactinidiolida es un compuesto orgánico que se encuentra de forma natural, clasificado como un lactona, específicamente un éster cíclico. Se deriva de la fruta del kiwi (Actinidia deliciosa) y es conocido por su agradable aroma afrutado, que contribuye a su uso en aplicaciones de sabor y fragancia. El compuesto tiene un centro quiral, lo que resulta en su designación como el enantiómero (-), que es significativo en el contexto de sus propiedades sensoriales y su posible actividad biológica. Su estructura molecular presenta un anillo de seis miembros, que es característico de muchas lactonas, y exhibe solubilidad en disolventes orgánicos. (-)-Dihidroactinidiolida ha despertado interés en los campos de la ciencia de los alimentos y la perfumería debido a su atractivo perfil de aroma. Además, la investigación sobre sus posibles beneficios para la salud y aplicaciones en la síntesis de productos naturales continúa expandiéndose, destacando su relevancia tanto en entornos industriales como académicos. Al igual que con muchos compuestos orgánicos, se deben observar precauciones de seguridad y manejo al trabajar con esta sustancia.
Fórmula:C11H16O2
InChI:InChI=1S/C11H16O2/c1-10(2)5-4-6-11(3)8(10)7-9(12)13-11/h7H,4-6H2,1-3H3/t11-/m1/s1
Clave InChI:InChIKey=IMKHDCBNRDRUEB-LLVKDONJSA-N
SMILES:C[C@@]12C(=CC(=O)O1)C(C)(C)CCC2
Sinónimos:- (+/-)-(2,6,6,-Trimethyl-2-hydroxycyclohexylidene)acetic acid gamma-lactone
- (2,6,6-Trimethyl-2-Hydroxycyclohexylidene)Acetic Acid Lactone
- (7AR)-4,4,7a-trimethyl-2,4,5,6,7,7a-hexahydro-1-benzofuran-2-one
- (7aR)-5,6,7,7a-Tetrahydro-4,4,7a-trimethyl-2(4H)-benzofuranone
- (R)-5,6,7,7a-Tetrahydro-4,4,7a-trimethyl-2(4H)-benzofuranone
- (R)-Dihydroactinidiolide
- 2(4H)-Benzofuranone, 5,6,7,7a-tetrahydro-4,4,7a-trimethyl-
- 2(4H)-Benzofuranone, 5,6,7,7a-tetrahydro-4,4,7a-trimethyl-, (7aR)-
- 2(4H)-Benzofuranone, 5,6,7,7a-tetrahydro-4,4,7a-trimethyl-, (R)-
- 2(4H)-Benzofuranone, 5,6,7,7a-tetrahydro-4,4,7a-trimethyl-, (S)-
- 4,4,7a-Trimethyl-5,6,7,7a-tetrahydro-1-benzofuran-2(4H)-one
- 5,6,7,7a-Tetrahydro-4,4,7a-trimethyl-2(4H)-benzofuranone
- Actinidiolide, dihydro-
- Nsc 357087
- (R)-5,6,7,7a-Tetrahydro-4,4,7a-trimethylbenzofuran-2(4H)-one
- (R)-4,4,7a-Trimethyl-5,6,7,7a-tetrahydrobenzofuran-2(4H)-one
- dihydroactindiolide
- FEMA 4020
- 2(4H)-Benzofuranone, 5,6,7,7a-tetrahydro-4,4,7a-trimethyl-(8CI)
- 4,4,7a-trimethyl-6,7-dihydro-5H-1-benzofuran-2-one
- (7aR)-4,4,7a-trimethyl-6,7-dihydro-5H-benzofuran-2-one
- (S)-2,6,6-Trimethyl-2-hydroxycyclohexylidene)acetic acid lactone
- (S)-dihydroactinidiolide
- (7aR)-5,6,7,7a-Tetrahydro-4,4,7aα-trimethyl-2(4H)-benzofuranone
- (R)-5,6,7,7a-tetrahydro-4,4,7atrimethyl-2(4H)-Benzofuranone
- 2(4H)-Benzofuranone,5,6,7,
- (R)-5,6,7,7alpha-Tetrahydro-4,4,7a-trimethyl-2(4H)-benzofuranone
- 2(4H)-Benzofuranone
- (2,6,6-Trimethyl-2-hydroxycyclohexylidene)acetic acid lacton
- 4,4,7a-Trimethyl-5,6,7,7a-tetrahydrobenzofuran-2(4H)-one(R-Dihydroactinidiolide)
- (2,6,6-TriMethyl-2-hydroxycyclohexylidene)acetic acid laCLone
- Dihydrokiwi lactone
- Dihydroactinidioli
- Ver más sinónimos
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95
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Encontrado 7 productos.
2(4H)-Benzofuranone, 5,6,7,7a-tetrahydro-4,4,7a-trimethyl-, (7aR)-
CAS:Fórmula:C11H16O2Pureza:98%Forma y color:SolidPeso molecular:180.2435(2,6,6-Trimethyl-2-hydroxycyclohexylidene)acetic acid lactone
CAS:(2,6,6-Trimethyl-2-hydroxycyclohexylidene)acetic acid lactonePureza:98% 99%eePeso molecular:180.24g/molDihydroactinidiolide
CAS:Dihydroactinidiolide (R-(-)Dihydro actinidiolide)is avolatileterpene. It has a sweet,tea-likeodorand is used as a fragrance.Fórmula:C11H16O2Pureza:99.94%Forma y color:Less Crystal Colorless CrystalPeso molecular:180.24R-Dihydroactinidiolide
CAS:Producto controladoFórmula:C11H16O2Forma y color:NeatPeso molecular:180.2444,4,7a-Trimethyl-5,6,7,7a-tetrahydrobenzofuran-2(4H)-one
CAS:Fórmula:C11H16O2Pureza:95.0%Forma y color:SolidPeso molecular:180.247R-Dihydroactinidiolide
CAS:<p>R-Dihydroactinidiolide is a carotenoid found in tobacco. It has been shown to inhibit the growth of neuroblastoma cells and other carcinoma cell lines in vitro, as well as to induce DNA damage and apoptosis in these cells. The surface methodology used for this study provides evidence that dihydroactinidiolide binds to specific receptors on the surface of cancer cells, which may be involved in the genotoxic effects observed. R-Dihydroactinidiolide can be metabolized by various enzymes into different metabolites with different biochemical properties and biological activities. This process involves cleavage of the acetate side chain by an enzyme called lipoxygenase, followed by oxidation of one or more double bonds on the ring system. The reaction mechanism is not yet known.</p>Fórmula:C11H16O2Pureza:Min. 95%Forma y color:PowderPeso molecular:180.24 g/mol





