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About This Item
Tapasztalati képlet (Hill-képlet):
C9H9NO
CAS-szám:
Molekulatömeg:
147.17
MDL-szám:
UNSPSC kód:
12352100
PubChem Substance ID:
NACRES:
NA.22
Forma:
powder
Teszt:
99%
Javasolt termékek
Minőségi szint
Teszt
99%
Forma
powder
bp
181-183 °C/24 mmHg (lit.)
mp
69-70 °C (lit.)
oldhatóság
ethanol: 50 mg/mL, clear, faintly yellow
SMILES string
COc1cccc2[nH]ccc12
InChI
1S/C9H9NO/c1-11-9-4-2-3-8-7(9)5-6-10-8/h2-6,10H,1H3
Nemzetközi kémiai azonosító kulcs
LUNOXNMCFPFPMO-UHFFFAOYSA-N
Alkalmazás
4-Methoxyindole was used for comparing the complexation reaction of β-cyclodextrin (β-CD) with pindolol using reversed-phase liquid chromatography.
Reactant for preparation of:
- GABA analogs
- Sodium-Dependent Glucose Co-transporter 2 (SGLT2) Inhibitors for the Management of Hyperglycemia in Diabetes
- Anticancer agents
- Integrase strand-transfer inhibitors (INSTIs)
- Inhibitor of Proliferation of Colon Cancer Cells
- Isomeridianin G as GSK-3ß inhibitors
- HIV-1 integrase inhibitors
- Inhibitors of mitogen activated protein kinase-activated protein kinase 2 (MK-2)
Figyelmeztetés
Warning
Figyelmeztető mondatok
Óvintézkedésre vonatkozó mondatok
Veszélyességi osztályok
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Célzott szervek
Respiratory system
Tárolási osztály kódja
11 - Combustible Solids
WGK
WGK 3
Lobbanási pont (F)
Not applicable
Lobbanási pont (C)
Not applicable
Egyéni védőeszköz
dust mask type N95 (US), Eyeshields, Gloves
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Carmen Gazpio et al.
Journal of pharmaceutical and biomedical analysis, 37(3), 487-492 (2005-03-03)
The complexation with beta-cyclodextrin (beta-CD) has been investigated using reversed-phase liquid chromatography. The compounds tested have been pindolol and, for comparison purposes, indole and 4-methoxyindole. The retention behaviour has been analysed on a Kromasil 100 C18 column and the mobile
Brenden Barco et al.
Frontiers in plant science, 10, 1775-1775 (2020-02-23)
The plant kingdom produces hundreds of thousands of specialized bioactive metabolites, some with pharmaceutical and biotechnological importance. Their biosynthesis and function have been studied for decades, but comparatively less is known about how transcription factors with overlapping functions and contrasting
Brenden Barco et al.
Nature communications, 10(1), 3444-3444 (2019-08-03)
Plants synthesize numerous ecologically specialized, lineage-specific metabolites through biosynthetic gene duplication and functional specialization. However, it remains unclear how duplicated genes are wired into existing regulatory networks. We show that the duplicated gene CYP82C2 has been recruited into the WRKY33 regulon
Thomas Heine et al.
Applied biochemistry and biotechnology, 181(4), 1590-1610 (2016-11-11)
The enantioselective epoxidation of styrene and related compounds by two-component styrene monooxygenases (SMOs) has targeted these enzymes for development as biocatalysts. In the present work, we prepare genetically engineered fusion proteins that join the C-terminus of the epoxidase (StyA) to
Jung Min Song et al.
International journal of pharmaceutics, 477(1-2), 96-101 (2014-10-15)
Indole-3-carbinol (I3C), a constituent of commonly consumed Brassica vegetables, has been shown to have anticancer effects in a variety of preclinical models of lung cancer. However, it has shown only limited efficacy in clinical trials, likely due to its poor
Tudóscsoportunk valamennyi kutatási területen rendelkezik tapasztalattal, beleértve az élettudományt, az anyagtudományt, a kémiai szintézist, a kromatográfiát, az analitikát és még sok más területet.
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