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Filtered Search Results
![eMolecules 87-51-4 | Indole-3-acetic acid | Combi-Blocks | MFCD00005636 | 175.187 | C10H9NO2 | 98.000 | OC(=O)Cc1c[nH]c2ccccc12 | 5g | 205388705](https://assets.fishersci.com/TFS-Assets/CCG/product-images/VN00128114-205388705.PNG-250.jpg)
eMolecules 87-51-4 | Indole-3-acetic acid | Combi-Blocks | MFCD00005636 | 175.187 | C10H9NO2 | 98.000 | OC(=O)Cc1c[nH]c2ccccc12 | 5g | 205388705
Indole-3-acetic acid | Combi-Blocks | 87-51-4 | MFCD00005636 | 175.187 | C10H9NO2 | 98.000 | OC(=O)Cc1c[nH]c2ccccc12 | 5g | 205388705
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Medchemexpress LLC 1H-Indol-5-amine | 5192-03-0 | 132.17 | 10 G
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1H-Indol-5-amine (5-Aminoindole) is an organic compound featuring an indole ring structure. This derivative is a valuable intermediate for synthesizing other active compounds, including 11-aryl-3H-indolo[5,4-b]naphthyridine derivatives. It also serves as a ligand for preparing AI-Sepharose hydrophobic charge induction chromatography media.
- Organic compound with indole ring structure
- Key intermediate for synthesis of active compounds
- Can be used as a ligand for preparing AI-Sepharose chromatography media
- Suitable for protein adsorption and elution
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000380113 BMS-986094 50MG
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Medchemexpress LLC 1-Methyl-1H-indazole-3-carboxylic acid | 50890-83-0 | 176.18 | 25 G
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1-Methyl-1H-indazole-3-carboxylic acid is a biochemical reagent used in life science research. This organic compound, appearing as a white to off-white solid, is stable under recommended storage conditions and is for research use only.
- Functions as a biological material or organic compound
- Stable under recommended storage conditions
- Store at room temperature for up to 3 years
- In solvent, stable at -80°C for 2 years or -20°C for 1 year
- Ships at room temperature for short durations
- Keep in tightly sealed container, cool, well-ventilated area
- Protect from direct sunlight and sources of ignition
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![eMolecules 186407-74-9 | 4-BROMO-1H-INDAZOLE | AstaTech | MFCD05664001 | 197.035 | C7H5BrN2 | 95.000 | Brc1cccc2[nH]ncc12 | 100g | 226993600](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000170276.jpg-250.jpg)
eMolecules 186407-74-9 | 4-BROMO-1H-INDAZOLE | AstaTech | MFCD05664001 | 197.035 | C7H5BrN2 | 95.000 | Brc1cccc2[nH]ncc12 | 100g | 226993600
4-BROMO-1H-INDAZOLE | AstaTech | 186407-74-9 | MFCD05664001 | 197.035 | C7H5BrN2 | 95.000 | Brc1cccc2[nH]ncc12 | 100g | 226993600
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Chem-Impex International, Inc. 1-Methylindole-2-carboxylic acid | 16136-58-6 | MFCD00005801 | 5G
1-Methylindole-2-carboxylic acid, 16136-58-6, MFCD00005801, 5G
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Medchemexpress LLC 5-Bromo-1H-indole-2-carboxylic acid | 7254-19-5 | 240.06 | 1 G
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5-Bromo-1H-indole-2-carboxylic acid is an indole-derived organic compound characterized by the presence of bromine and carboxyl groups. This compound functions as a crucial intermediate in the synthesis of various other active compounds. Additionally, its dimeric form has demonstrated antibacterial properties against Gram-positive bacteria, including Listeria monocytogenes.
- Indole-derived organic compound
- Substituted with bromine and carboxyl groups
- Functions as an important intermediate for synthesis
- Dimeric form exhibits antibacterial activity against Gram-positive bacteria
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![eMolecules 93247-78-0 | Methyl indole-7-carboxylate | Chem-Impex | MFCD00211064 | 175.187 | C10H9NO2 | 98.000 | COC(=O)c1cccc2cc[nH]c12 | 5g | 386897624](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000216636.jpg-250.jpg)
eMolecules 93247-78-0 | Methyl indole-7-carboxylate | Chem-Impex | MFCD00211064 | 175.187 | C10H9NO2 | 98.000 | COC(=O)c1cccc2cc[nH]c12 | 5g | 386897624
Methyl indole-7-carboxylate | Chem-Impex | 93247-78-0 | MFCD00211064 | 175.187 | C10H9NO2 | 98.000 | COC(=O)c1cccc2cc[nH]c12 | 5g | 386897624
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![eMolecules 389122-08-1 | 3-Amino-5-bromo-1H-1,2,4-triazole | Accela ChemBio | MFCD18807020 | 162.978 | C2H3BrN4 | 95.000 | Nc1n[nH]c(Br)n1 | 5g | 802543378](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000216434.jpg-250.jpg)
eMolecules 389122-08-1 | 3-Amino-5-bromo-1H-1,2,4-triazole | Accela ChemBio | MFCD18807020 | 162.978 | C2H3BrN4 | 95.000 | Nc1n[nH]c(Br)n1 | 5g | 802543378
3-Amino-5-bromo-1H-1,2,4-triazole | Accela ChemBio | 389122-08-1 | MFCD18807020 | 162.978 | C2H3BrN4 | 95.000 | Nc1n[nH]c(Br)n1 | 5g | 802543378
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TARGETMOL CHEMICALS INC 9-Methyl salvianolate B 5MG
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Also available in 1 mL, 1 mg, 10 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. 9'-Methyl lithospermate B is a phenolic compound extracted from Radix Salvia miltiorrhizae. Purity 97.25%
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Medchemexpress LLC Quinocetone | 81810-66-4 | MFCD09753267 | 98.0% | 306.32 g/mol | C18H14N2O3 | 50MG
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Quinocetone is an antibacterial quinoxaline derivative supplied as an analytical standard for research and analytical testing. The compound is offered in solid and solution formats, and is characterized by a reported purity of 98.0%, chemical formula C18H14N2O3, and molecular weight 306.32 g/mol.
- Analytical standard suitable for method development and calibration.
- High purity for reliable quantitative results.
- Available in solid and solution formats for flexible use.
- Documented chemical identity with CAS 81810-66-4.
- Appropriate for laboratory research and reference analyses.
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Medchemexpress LLC Fgin 1-27 | 142720-24-9 | 100.0% | 436.60 | C28H37FN2O | 10 MG
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FGIN 1-27 is a selective peripheral benzodiazepine receptor ligand supplied as a high-purity research compound for in vitro and in vivo neuroscience studies. It is provided as a solid and in ready-to-use solution formats, with documented solubility and storage guidance to support experimental workflows.
- High purity suitable for receptor binding and pharmacology assays.
- Solid and solution formats for flexible dosing and formulation.
- Soluble in DMSO; in vivo formulation protocols available.
- Storage conditions provided for long-term and short-term stability.
- Datasheet, certificate of analysis, and safety data available for experimental documentation.
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eMolecules 500-22-1 | pyridine-3-carbaldehyde | Pharmablock - Stock | MFCD00006382 | 107.112 | C6H5NO | 97.000 | O=Cc1cccnc1 | 10g | 384443569
pyridine-3-carbaldehyde | Pharmablock - Stock | 500-22-1 | MFCD00006382 | 107.112 | C6H5NO | 97.000 | O=Cc1cccnc1 | 10g | 384443569
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NC(=O)OCC1c2ccccc2-c2ccccc12 | 250mg | 632274406](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000084647.jpg-250.jpg)
eMolecules 282734-33-2 | tert-Butyl(R)-2-((((9h-fluoren-9-yl)methoxy)carbonyl)amino)-3-iodopropanoate | ChemScene | MFCD11053633 | 493.341 | C22H24INO4 | 95.000 | CC(C)(C)OC(=O)[C@H](CI)NC(=O)OCC1c2ccccc2-c2ccccc12 | 250mg | 632274406
tert-Butyl(R)-2-((((9h-fluoren-9-yl)methoxy)carbonyl)amino)-3-iodopropanoate | ChemScene | 282734-33-2 | MFCD11053633 | 493.341 | C22H24INO4 | 95.000 | CC(C)(C)OC(=O)[C@H](CI)NC(=O)OCC1c2ccccc2-c2ccccc12 | 250mg | 632274406
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Medchemexpress LLC MY-875 | C21H25NO6 | 1 ML
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MY-875 is a competitive inhibitor of microtubulin polymerization with an IC50 value of 0.92 μM. It works by targeting colchicine binding sites and activating the Hippo pathway. This compound induces apoptosis and demonstrates anticancer activity. It is intended for research use only.
- Inhibits microtubulin polymerization
- Targets colchicine binding sites
- Activates the Hippo pathway
- Induces apoptosis
- Exhibits anticancer activity
- Shows significant anti-proliferative activity against cancer cells
- Inhibits cell colony-forming ability
- Arrests cells in the G2/M phase
- Reduces expression of anti-apoptotic proteins
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