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      Indole-3-carbinol

      • Product Name: Indole-3-carbinol
      • CAS: 700-06-1
      • Purity:
      • Appearance: Off-white powder

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      Factory Supply industrial standard Indole-3-carbinol 700-06-1 In Stock

      • Molecular Formula:C9H9NO
      • Molecular Weight:147.177
      • Appearance/Colour:Off-white powder 
      • Melting Point:96-99 °C(lit.) 
      • Refractive Index:1.5670 (estimate) 
      • Boiling Point:360.6 °C at 760 mmHg 
      • PKA:15.10±0.10(Predicted) 
      • Flash Point:171.9 °C 
      • PSA:36.02000 
      • Density:1.272 g/cm3 
      • LogP:1.66020 

      Indole-3-carbinol(Cas 700-06-1) Usage

      Preparation

      Using indole, phosphorus oxychloride and N,N-dimethylformamide as raw materials, indole-3-carbaldehyde was synthesized by Vilsmeier-Haack reaction with a yield of 87.1%.

      Synthesis Reference(s)

      Canadian Journal of Chemistry, 31, p. 775, 1953 DOI: 10.1139/v53-106The Journal of Organic Chemistry, 61, p. 1493, 1996 DOI: 10.1021/jo951219c

      Biochem/physiol Actions

      Inhibits cancinogenesis at the initiation stage. Has be shown to inhibit carcinogenesis in several animal species, but it enhances tumor incidence if administered at a post-initiation stage. Found in cruciferous vegetables.

      Anticancer Research

      I3C is a bioactive compound majorly found in Brassica vegetables including broccoli,cauliflower, and collard greens. I3C and its derivative diindolylmethane (DIM)have been investigated for cancer prevention and treatment of breast, prostate, andovarian cancers. I3C partially modulates the tyrosine kinase/PI3K/Akt signalingpathway which leads to the prevention of lung adenocarcinoma which is induced byusing tobacco carcinogen in A/J mice. DIM transduces signaling via aryl hydrocarbon(Ah) receptor, NF-κB/Wnt/Akt/mTOR signaling pathways, cell cycle arrest,modulated cytochrome P450 enzymes, and altered angiogenetic and invasive,metastatic, and epigenetic behavior of cancer cells. Combination of DIM and I3Cinduces Nrf2-mediated phase II drug metabolizing genes (GSTm2, UGT1A1, andNQO1) and antioxidant genes (HO-1, SOD-1) (Weng et al. 2008; 2012).

      Sources

      Indole-3-carbinol (I3C) is a bioactive phytochemical found abundantly in cruciferous vegetables such as broccoli, cabbage, green peas, cauliflower, and Brussels sprouts.[1]

      Categories and Type

      I3C is classified as a bioactive phytochemical and belongs to the group of indole compounds.

      Mechanism of Action

      I3C and its metabolites alter multiple signaling pathways controlling cellular events such as oxidation, inflammation, proliferation, differentiation, apoptosis, angiogenesis, and immunity. DIM, a metabolite of I3C, is particularly involved in modulating aryl hydrocarbon receptor (AHR) signaling.[3]

      Production Methods

      I3C is naturally occurring and is produced when raw cruciferous vegetables are consumed or processed. It can also be obtained through extraction and purification processes for use in dietary supplements or pharmaceuticals.

      Definition

      ChEBI: Indole-3-carbinol is an indolyl alcohol carrying a hydroxymethyl group at position 3. It is a constituent of the cruciferous vegetables and had anticancer activity.

      Application

      Indole-3-carbinol (I3C) is a secondary plant metabolite of 3-methylindole produced in Brassica family vegetables. It is an inhibitor of Amyloid-beta deposition and Inhibits cancinogenesis at the initiation stage. Indole-3-carbinol is used in cancer prevention, specifically for breast, cervical and colon cancers. It has also been widely used to address lupus.

      General Description

      Indole-3-carbinol is a novel secondary plant metabolite produced in cruciferous vegetables, such as cabbage, cauliflower and brussels sprouts.

      InChI:InChI=1/C9H9NO/c11-6-7-5-10-9-4-2-1-3-8(7)9/h1-5,10-11H,6H2

      700-06-1 Relevant articles

      -

      Clerin,Bruice

      , p. 5571 (1974)

      -

      Reduction of Aldehydes with Formic acid in Ethanol using Immobilized Iridium Nanoparticles on a Triazine-phosphanimine Polymeric Organic Support

      Panahi, Farhad,Haghighi, Fatemeh,Khalafi-Nezhad, Ali

      , (2020/07/06)

      A novel triazine-phosphanimine polymeric...

      Chemoselective transfer hydrogenation of aromatic and heterocyclic aldehydes by green chemically prepared cobalt oxide nanoparticles

      Krishnaveni,Lakshmi,Kaveri,Kadirvelu

      , (2020/09/16)

      A new surfactant (quercetin) assisted hy...

      Efficient Synthesis and Biological Activity of Novel Indole Derivatives as VEGFR-2 Tyrosine Kinase Inhibitors

      Zhang,Xu,Wang,Kang

      , p. 3006 - 3016 (2018/02/21)

      A series of novel indole derivatives wer...

      Facile Installation of 2-Reverse Prenyl Functionality into Indoles by a Tandem N-Alkylation-Aza-Cope Rearrangement Reaction and Its Application in Synthesis

      Chen, Xiaobei,Fan, Huaqiang,Zhang, Shilei,Yu, Chenguang,Wang, Wei

      supporting information, p. 716 - 723 (2016/01/12)

      An unprecedented tandem N-alkylation-ion...

      700-06-1 Process route

      Indole-3-carboxaldehyde
      487-89-8,1228547-52-1

      Indole-3-carboxaldehyde

      indole-3-carbinol
      700-06-1

      indole-3-carbinol

      Conditions
      Conditions Yield
      With sodium tetrahydroborate; In methanol; at 0 ℃; for 1h;
      100%
      With formic acid; In ethanol; at 80 ℃; for 12h; Catalytic behavior;
      91%
      With ammonia; calcium; In tetrahydrofuran; at -33 ℃; for 2h; other reagents: lithium, sodium, liq. ammonia;
      80%
      With tricobalt tetraoxide; In isopropyl alcohol; at 50 ℃; for 0.5h; chemoselective reaction; Green chemistry;
      80%
      With sodium tetrahydroborate; In methanol; for 1h; Ambient temperature;
      57%
      With ethanol; platinum; Hydrogenation;
      With sodium borate; ethanol;
      With methanol; sodium borate;
      With 1,4-dioxane; sodium borate;
      With tetrahydrofuran; lithium borate;
      With sodium tetrahydroborate;
      With cytochrome P450BM-3 F87A/T268A variant; NADPH; at 37 ℃; pH=7.4; aq. phosphate buffer; Enzymatic reaction;
      With sodium hydroxide; In isopropyl alcohol; at 82 ℃; for 2h;
      88 %Chromat.
      With sodium tetrahydroborate; In tetrahydrofuran; ethanol; at 20 ℃; for 3h;
      3-methoxycarbonylindole
      942-24-5

      3-methoxycarbonylindole

      indole-3-carbinol
      700-06-1

      indole-3-carbinol

      Conditions
      Conditions Yield
      3-methoxycarbonylindole; With pentadec-3-en-2-one; trimethylsilyl trifluoromethanesulfonate; triphenylphosphine; In dichloromethane; at -78 - 0 ℃; for 1h; Inert atmosphere;
      With diisobutylaluminium hydride; In hexane; dichloromethane; at -78 ℃; Inert atmosphere;
      With potassium carbonate; In methanol; hexane; dichloromethane; at 20 ℃; for 0.5h; Inert atmosphere;
      84%

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