Batrachotoxin (BTX)


Avaibility : disponibles
Chemical Names
BTX; Batrachotoxin (7CI, 8CI); Batrachotoxinin A, 20-(2,4-dimethyl-1H-pyrrole-3-carboxylate).
Structure C31H42N2O6
RTECS No. CR3990000
Merck Index No
(13th Ed.)

What is Batrachotoxin (BTX)?

Purchase Batrachotoxin Online is a significant exploration device in pharmacology on account of its activity of holding voltage-gated sodium channels open just as its particular impacts at other ligand-restricting destinations. It was regularly utilized in particle channel and ligand research.

Batrachotoxin has no current clinical uses for two essential reasons. In the first place, batrachotoxin is exceptionally harmful and risky to use for clinical purposes. Engineered structures with changed properties would need to be produced for clinical preliminaries. Second, there are no financially accessible wellsprings of batrachotoxins or economically suitable manufactured pathways. Most accessible loads of batrachotoxin were gathered from wild-got Phyllobates frogs by John Daly numerous years prior. Work in significant locales of Colombia is as of now troublesome or unthinkable, so these stocks can’t be renewed. No financially practical wellsprings of batrachotoxin are known from New Guinea, however extra exploration on a definitive wellspring of batrachotoxins may clarify new sources.

General Information

The neurotoxin batrachotoxin (BTX) is an individual from a group of steroidal alkaloids called batrachotoxins. The batrachotoxin family incorporates (among different synthetic substances) batrachotoxin, homobatrachotoxin, batrachotoxinin A, and pseudobatrachotoxin (insecure, converts to batrachotoxinin An on standing) (7). These poisons were first found in poison dart frogs of the variety Phyllobates (8); the name given to this gathering of synthetic substances was gotten from the greek word for frog, “batrachos” (9). Batrachotoxin, the (20-alpha)- 2,4-dimethylpyrrole-3-carboxylate of batrachotoxinin-A, can be tested utilizing an altered Ehrlich reagent (discovery limit under 50 ng) (7); Ehrlich reagent is a corrosive arrangement of p-dimethyl amino benzaldehyde (10). The design of BTX incorporates a steroid skeleton and an oxazapane ring (13), which are demonstrated on the construction beneath.

By weight, batrachotoxin is quite possibly the most intense characteristic poisons known (9) since it ties to and irreversibly opens voltage-gated sodium channels (9,15); the appropriate capacity of these sodium channels is needed for the transmission of electrical signs through nerve and muscle cells (2). The movement of BTX relies upon temperature, arriving at its greatest at 37 degrees Celsius (4). The accompanying rundown gives a portion of the properties of this intense poison.

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10μg, 20

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