|Description||4-Bromo-calcimycin, a halogenated analog of A-2318, is a non-Fluorescent Ca2+ ionophore which could be commonly used in fluorescent probes experiments as a modutor of the quantitation of free Ca2+.|
|Appearance||Slight yellow crystals|
|Synonyms||4-Bromo-A23187; 4-Bromocalcimycin; 4-Benzoxazolecarboxylic acid, 6-bromo-5-(methylamino)-2-(((2S,3S,6S,8S,9R,11R)-3,9,11-trimethyl-8-((1S)-1-methyl-2-oxo-2-(1H-pyrrol-2-yl)ethyl)-1,7-dioxaspiro(5.5)undec-2-yl)methyl)-|
|Solubility||DMSO, Methanol, Dichloromethane|
|Storage||Refrigerate upon arrival, at +2°C to +8°CUse the original container to store the product.Keep the lid tightly closed.Avoid exposing to strong direct light.May be kept deep frozen.|
|Application||Nonfluorescent calcium ionophore used as a calibration standard for determining cytoplasmic calcium ions by fluorescent probes.|
|Melting Point||205 °C-210 °C|
A semi-synthetic milbemycin derived from nemadectin; an anthelmintic for internal parasite control; binds selectively to parasite glutamate-gated chloride ion c...
A semi-synthetic tetracycline prepared by dehydration of the 6-hydroxy group of chlortetracycline to yield an exocyclic 6-methylene; a close structural analogue...
The hydrochloride salt of a rare semi-synthetic tetracycline; prepared by hydrogenolysis of the chloro and benzylic hydroxy moieties of declomycin; acts by reve...
KT5555, a benzodiazocin compound, has been found to be a tyrosine kinase inhibitor of multi target like JAK2, FLT3 and TrkA. It was also found to exhibit effect...
Kanamycin B sulfate
An aminoglycoside antibiotic often used to select for bacteria which have been successfully transformed with a plasmid conferring kanamycin resistanc
An extended spectrum beta-lactam in the carboxypenicillin family; can be combined with clavulanate potassium for greater efficacy against beta-lactam resistant ...
A freely soluble aminoglycoside antibiotic similar in structure to streptomycin
A semi-synthetic avermectin derivative prepared by selective hydrolysis and oximation of doramectin; a potent nematocide used for the treatment of endo- and exo...
A semi-synthetic lincosamide prepared from clindamycin by hydrolysing the propyl N-methylproline and re-annealing a 4-ethylpipecolic acid; a broad spectrum anti...
A semi-synthetic macrocyclic lactone prepared by the oxidation; used therapeutically for the prevention of intestinal parasites in dogs
Amoxicillin sodium salt
An extended spectrum beta-lactam antibiotic; similar in structure to ampicillin
A sparingly soluble (4.1 mg/ml) fungicidal polyene antifungal
A first generation cephalosporin antibiotic; slightly soluble in aqueous solution (1.789 mg/ml)
An irreversible base degradation product of ivermectin found in animals treated with ivermectin and in the environment
The major component in the second generation spinosyn family of bio-insecticides marketed as spinetoram; a semi-synthetic compound prepared by selective ethylat...
Dihydrostreptomycin sulfate (1:x)
A semi-synthetic pleuromutilin formed by selective reduction of the ethene to ethyl; exhibits comparable antibiotic potency to pleuromutilin
Milbemycin A3 oxime
A semi-synthetic macrocyclic lactone prepared by the oxidation and oximation of a mixture of milbemycin A3; the minor component (~30%) in the commercial product...
A base-catalysed intermediate in the decomposition of doramectin; formed by epimerisation at the 2-position which ultimately rearranges irreversibly to the isom...
A semi-synthetic chloramphenicol analogue in which the dichloroacetamide is replaced with dibromoacetamide; possesses weak antibiotic activity