|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 second generation cephalosporin antibiotic
An insoluble broad spectrum anti-parasitic drug; considered a dangerous good
A bacteriostatic sulfonamide antibiotic; acts as a folic acid synthesis inhibitor
Pseudoerythromycin A enol ether
A degradation product of erythromycin formed by a complex internal rearrangement of erythromycin A on exposure to neutral to weakly alkaline conditions; devoid ...
An acid degradation product produced by selective hydrolysis of the more labile forosamine saccharide in the 17-position of 3-ethoxy-5,6-dihydrospinosyn J, the ...
The first of the semi-synthetic tetracyclines; a pro-drug of tetracycline; has broad spectrum gram positive activity in vivo
The salt of the semi-synthetic cyclic lipopeptide, micafungin; inhibits the synthesis of β-(1,3)-D-glucan, an essential component of the cell wall of susceptibl...
A semi-synthetic 4”-epimethylamino analogue of avermectin B1b prepared by oxidation of the 4”-hydroxy moiety and reductive amination; members of the avermectin/...
Avermectin B1a monosaccharide
An acid degradation product produced by selective hydrolysis of the terminal saccharide unit of avermectin; a potent inhibitor of nematode larval development; d...
A sparingly soluble (4.1 mg/ml) fungicidal polyene antifungal
An irreversible base degradation product of doramectin found in animal treated with doramectin and in the environment; an anthelmintic in animal health
A secondary degradation product formed by epimerisation of tetracycline and dehydration at the C6 position to aromatise the B ring; an important standard for mo...
Milbemycin A4 oxime
A semi-synthetic macrocyclic lactone prepared by the oxidation and oximation of a mixture of milbemycin A4; the major component (~70%) in the commercial product...
A semi-synthetic analogue of erythromycin prepared by reduction of erythromycin oxime; a potent antibiotic
A salt prepared from doxycycline taking advantage of the basic dimethylamino group which protonates and readily forms a salt in hydrochloric acid solutions; the...
A semi-synthetic derivative of lipstatin, a metabolite isolated from streptomyces toxytricini; a potent, irreversible inhibitor of pancreatic lipase; blocks the...
Erythromycin A enol ether
A degradation product of erythromycin formed under acidic conditions by C6–OH internal attack on the C9 ketone to produce a cyclic enol ether; an important stan...
A salt prepared from demeclocycline taking advantage of the basic dimethylamino group; shows broad spectrum antibacterial and antiprotozoan activity by binding ...
A macrolide antibiotic pro-drug of 9S-erythromycylamine, a close analogue of erythromycin in which the 9-keto group is replaced with an amino group in the S-con...
Azlocillin sodium salt
An extended spectrum beta-lactam antibiotic derived from ampicillin