CAS 1968-05-4

3,3'-Diindolilmetano

Descripción:

3,3'-Diindolilmetano (DIM) es un compuesto orgánico derivado del indol, formado específicamente a través de la dimerización del indol-3-carbinol, que se encuentra en verduras crucíferas como el brócoli y las coles de Bruselas. Se caracteriza por sus dos anillos de indol conectados por un puente de metileno. Se conoce que el DIM tiene potenciales beneficios para la salud, particularmente en el contexto de la prevención del cáncer y el equilibrio hormonal, ya que puede influir en el metabolismo del estrógeno y exhibir propiedades antiinflamatorias. El compuesto es típicamente un sólido cristalino de color amarillo a naranja y es soluble en disolventes orgánicos, pero tiene una solubilidad limitada en agua. Su fórmula molecular es C18H16N2, y tiene un peso molecular relativamente bajo. El DIM ha despertado interés en la investigación nutricional y farmacéutica debido a sus propiedades bioactivas, y los estudios han explorado su papel en la modulación de diversas vías biológicas, incluyendo la apoptosis y la regulación del ciclo celular. Sin embargo, se necesita más investigación para comprender completamente sus mecanismos y potencial terapéutico.

Fórmula: C₁₇H₁₄N₂

InChI: InChI=1S/C17H14N2/c1-3-7-16-14(5-1)12(10-18-16)9-13-11-19-17-8-4-2-6-15(13)17/h1-8,10-11,18-19H,9H2

Clave InChI: InChIKey=VFTRKSBEFQDZKX-UHFFFAOYSA-N

SMILES: C(C=1C=2C(NC1)=CC=CC2)C=3C=4C(NC3)=CC=CC4

Sinónimos:

• 1H-Indole, 3,3′-methylenebis-
• 3,3'-Methylenebisindole
• 3,3'-methanediylbis(1H-indole)
• 3,3'Diindolemethane
• 3,3-Methylenediindole
• 3,3′-Bisindolylmethane
• 3,3′-Methanediyldi(1H-indole)
• 3,3′-Methylenebis[1H-indole]
• 3-[(1H-Indol-3-yl)methyl]-1H-indole
• Arundine
• Bis(1H-indol-3-yl)methane
• Bis(3-indolyl)methane
• Cervicon-DIM
• DIM
• DIM (AhR agonist)
• DIM (diindolylmethane)
• Di(1H-indol-3-yl)methane
• Diindolylmethane
• Diindoylmethane
• Hb 236
• Indole, 3,3′-methylenedi-
• Infemin
• 3,3-Diindolylmethane

3,3'-Methylenediindole

CAS: 1968-05-4

Fórmula: C₁₇H₁₄N₂

Pureza: >98.0%(N)

Forma y color: White to Light yellow to Light red powder to crystal

Peso molecular: 246.31

Ref: 3B-M1399

3,3'-Diindolylmethane

CAS: 1968-05-4

3,3'-Diindolylmethane (DIM), a small molecule compound, is a proposed Y preventive agent.

Fórmula: C₁₇H₁₄N₂

Pureza: 99.09%

Forma y color: Solid

Peso molecular: 246.31

Ref: TM-T2991

3,3'-Diindolylmethane

CAS: 1968-05-4

3,3'-Diindolylmethane

Fórmula: C₁₇H₁₄N₂

Pureza: ≥98%

Peso molecular: 246.31

Ref: 54-BUP14951

3,3'-Bisindolylmethane

CAS: 1968-05-4

Fórmula: C₁₇H₁₄N₂

Pureza: 98%

Forma y color: Solid

Peso molecular: 246.3065

Ref: IN-DA003BAM

3,3-MethylenedIIndole

CAS: 1968-05-4

3,3-MethylenedIIndole

Fórmula: C₁₇H₁₄N₂

Pureza: >98%

Peso molecular: 246.31

Ref: 54-OR1010762

3,3''-Diindolylmethane

CAS: 1968-05-4

Fórmula: C₁₇H₁₄N₂

Pureza: ≥ 98.0% (anhydrous basis)

Forma y color: White to off-white crystalline powder

Peso molecular: 246.31

Ref: 7W-GK6642

3,3'-Diindolylmethane

Producto controlado

CAS: 1968-05-4

Applications 3,3'-Diindolylmethane is an activator of Chk2 that causes G2/M cell cycle arrest in various cancer cell lines. 3,3'-Diindolylmethane is an antiproliferative and inducer of apoptosis; promotes proteasomal degradation of Cdc25C and Cdk1. Inhibits phosphorylation of EGFR and downstream activation of ERK.
References Kandala, et al.: Mol.Pharmacol., 78, 297 (2010), Kandala, et al.: J. Pharmacol. Exp. Ther., 341 24 (2012),

Fórmula: C₁₇H₁₄N₂

Forma y color: Neat

Peso molecular: 246.31

Ref: TR-D455190

Bis (3-indolyl)methane

CAS: 1968-05-4

Fórmula: C₁₇H₁₄N₂

Pureza: 98%

Forma y color: Solid, White to pale reddish yellow powder

Peso molecular: 246.313

Ref: 10-F024220

3,3'-Diindolymethane (synthetic)

CAS: 1968-05-4

3,3'-Diindolylmethane, also known as DIM, is natural compound derived from indole. In a recent study, DIM was evaluated as a potential agent for preventing biofilm formation by Streptococcus mutans, which is a major cause of dental caries. The researchers found that DIM significantly inhibited biofilm formation (by 92%) and reduced the production of extracellular polymeric substances (EPS), which are important for biofilm stability particularly under acidic conditions. The study suggests that 3,3'-diindolylmethane has anti-biofilm and anti-virulence properties against S. mutans, and it is a potential candidate for reducing biofilm formation and preventing dental caries.
It has been also reported that 3,3'-diindolymethane can act as a chemopreventive agent. DIM has estrogenic effects without interacting with the binding domain of the estrogen receptors. This study found that DIM could suppress cell growth and disrupt cell cycle progression of young adult mouse colonocytes (YAMCs) in vitro. Moreover, DIM altered gene expression associated with apoptosis and cell proliferation, and it induced transcriptional activity of the estrogen receptor (ER), which was inhibited by an ER antagonist.

Fórmula: C₁₇H₁₄N₂

Pureza: Min. 95%

Forma y color: Powder

Peso molecular: 246.31 g/mol

Ref: 3D-FD14886

3,3'-Diindolylmethane

CAS: 1968-05-4

3,3'-Diindolylmethane

Fórmula: C₁₇H₁₄N₂

Pureza: 98%

Peso molecular: 246.31

Ref: IN-DG8848

3,3'-Diindolymethane (natural)

CAS: 1968-05-4

3,3'-Diindolylmethane, also known as DIM, is natural compound derived from indole. In a recent study, DIM was evaluated as a potential agent for preventing biofilm formation by Streptococcus mutans, which is a major cause of dental caries. The researchers found that DIM significantly inhibited biofilm formation (by 92%) and reduced the production of extracellular polymeric substances (EPS), which are important for biofilm stability particularly under acidic conditions. The study suggests that 3,3'-diindolylmethane has anti-biofilm and anti-virulence properties against S. mutans, and it is a potential candidate for reducing biofilm formation and preventing dental caries. It has been also reported that 3,3'-diindolymethane can act as a chemopreventive agent. DIM has estrogenic effects without interacting with the binding domain of the estrogen receptors. This study found that DIM could suppress cell growth and disrupt cell cycle progression of young adult mouse colonocytes (YAMCs) in vitro. Moreover, DIM altered gene expression associated with apoptosis and cell proliferation, and it induced transcriptional activity of the estrogen receptor (ER), which was inhibited by an ER antagonist.

Fórmula: C₁₇H₁₄N₂

Pureza: Min. 95%

Forma y color: Powder

Peso molecular: 246.31 g/mol

Ref: 3D-FD14887