5-Bromoindole-3-carboxaldehyde
5-Bromoindole-3-carboxaldehyde structure
|
Common Name | 5-Bromoindole-3-carboxaldehyde | ||
|---|---|---|---|---|
| CAS Number | 877-03-2 | Molecular Weight | 224.054 | |
| Density | 1.7±0.1 g/cm3 | Boiling Point | 395.5±22.0 °C at 760 mmHg | |
| Molecular Formula | C9H6BrNO | Melting Point | 204-207 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 193.0±22.3 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
|
Synthesis and antifungal activity of novel streptochlorin analogues.
Eur. J. Med. Chem. 92 , 776-83, (2015) Streptochlorin, first isolated as a new antibiotic in 1988 from the lipophilic extracts of the mycelium of a Streptomyces sp, is an indole natural products with a variety of biological activities. Based on the methods developed for the synthesis of pimprinine... |
|
|
Antibiotic metabolites from a marine pseudomonad.
Antimicrob. Agents Chemother. 11(3) , 411-4, (1977) An antibiotic-producing pseudomonad was isolated from a seawater sample from a La Jolla, Calif., tidepool. The pseudomonad produces two novel antibacterial compounds, 2-n-pentyl-4-quinolinol and 2-n-heptyl-4-quinolinol. It also synthesizes indole-3-carboxalde... |
|
|
5,5'-Dibromo-bis(3'-indolyl)methane induces Kruppel-like factor 4 and p21 in colon cancer cells.
Mol. Cancer Ther. 7(7) , 2109-20, (2008) Bis(3'-indolyl)methane (DIM) is a metabolite of the phytochemical indole-3-carbinol, and both compounds exhibit a broad spectrum of anticancer activities. We have developed a series of synthetic symmetrical ring-substituted DIM analogues, including 5,5'-dibro... |