6-Bromo-1H-indole-3-acetic acid methyl ester
CAS No. 152213-63-3
6-Bromo-1H-indole-3-acetic acid methyl ester( Methyl 2-(6-bromo-1H-indol-3-yl)acetate | Methyl 6-Bromoindole-3-acetate )
Catalog No. M29547 CAS No. 152213-63-3
6-Bromo-1H-indole-3-acetic acid methyl ester is a marine derived natural products found in Pseudosuberites hyalinus.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 28 | In Stock |
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| 10MG | 28 | In Stock |
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| 100MG | Get Quote | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product Name6-Bromo-1H-indole-3-acetic acid methyl ester
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NoteResearch use only, not for human use.
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Brief Description6-Bromo-1H-indole-3-acetic acid methyl ester is a marine derived natural products found in Pseudosuberites hyalinus.
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Description6-Bromo-1H-indole-3-acetic acid methyl ester is a marine derived natural products found in Pseudosuberites hyalinus.
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In Vitro——
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In Vivo——
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SynonymsMethyl 2-(6-bromo-1H-indol-3-yl)acetate | Methyl 6-Bromoindole-3-acetate
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PathwayOthers
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TargetOther Targets
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Recptor——
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Research Area——
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Indication——
Chemical Information
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CAS Number152213-63-3
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Formula Weight268.11
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Molecular FormulaC11H10BrNO2
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Purity>98% (HPLC)
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Solubility——
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SMILESO=C(OC)CC1=CNC=2C=C(Br)C=CC21
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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L-Anserine nitrate s...
L-Anserine Nitrate Salt is a dipeptide found in most animal tissues. In model systems it is a potent antioxidant and scavener of hydroxyl radicals.
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[Ile161]MAGE - A2 (1...
[Ile161]MAGE - A2 (157-166)
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Pseudo RACK1
Activator of protein kinase C; attached to cell permeabilization Antennapedia domain vector peptide. Consists of peptide derived from the C2 domain of PKC β linked by a disulfide bridge to the Antennapedia domain vector peptide. The Antennapedia peptide is actively taken up by intact cells, at 4 or 37°C, ensuring rapid and effective uptake of the activator peptide. Once inside the cell, the disulfide bonds are subjected to reduction in the cytoplasm leading to release of the activator peptide.
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