CAS 160369-85-7
:α-Neuraminic acid, N-acetyl-2-O-(5-bromo-4-chloro-1H-indol-3-yl)-, sodium salt (1:1)
Description:
α-Neuraminic acid, N-acetyl-2-O-(5-bromo-4-chloro-1H-indol-3-yl)-, sodium salt (1:1) is a synthetic compound that combines elements of sialic acid with an indole derivative. This compound features a neuraminic acid backbone, which is a nine-carbon sugar acid known for its role in biological processes, particularly in cell recognition and signaling. The presence of the N-acetyl group enhances its stability and solubility in biological systems. The indole moiety, substituted with bromine and chlorine, introduces unique electronic and steric properties, potentially influencing its biological activity and interactions. As a sodium salt, it is likely to exhibit increased solubility in aqueous environments, making it suitable for various biochemical applications. This compound may be of interest in research related to glycoproteins, cell adhesion, and possibly in the development of therapeutic agents targeting specific biological pathways. However, detailed studies would be necessary to fully elucidate its properties, reactivity, and potential applications in medicinal chemistry or biochemistry.
Formula:C19H21BrClN2O9·Na
InChI:InChI=1/C19H22BrClN2O9.Na/c1-7(25)23-15-10(26)4-19(18(29)30,32-17(15)16(28)11(27)6-24)31-12-5-22-9-3-2-8(20)14(21)13(9)12;/h2-3,5,10-11,15-17,22,24,26-28H,4,6H2,1H3,(H,23,25)(H,29,30);/q;+1/p-1/t10-,11-,15-,16-,17?,19-;/m1./s1
InChI key:InChIKey=IZESFRHTHSKBEU-GNZCRVNMSA-N
SMILES:O([C@@]1(C(O)=O)O[C@@]([C@@H]([C@@H](CO)O)O)([C@H](NC(C)=O)[C@@H](O)C1)[H])C=2C=3C(NC2)=CC=C(Br)C3Cl.[Na]
Synonyms:- 5-Bromo-4-Chloro-3-Indolyl-Alpha-D-N-Acetylneuraminic Acid Sodium Salt
- 5-Bromo-4-chloro-3-indolyl-α-D-N-acetylneuraminic acid sodium salt
- 5-Bromo-4-chloro-3-indoxyl-alpha-D-N-acetylneuraminic acid,sodium salt
- <span class="text-smallcaps">D</smallcap>-glycero-α-<smallcap>D</span>-galacto-2-Nonulopyranosidonic acid, 5-bromo-4-chloro-1H-indol-3-yl 5-(acetylamino)-3,5-dideoxy-, monosodium salt
- α-Neuraminic acid, N-acetyl-2-O-(5-bromo-4-chloro-1H-indol-3-yl)-, monosodium salt
- α-Neuraminic acid, N-acetyl-2-O-(5-bromo-4-chloro-1H-indol-3-yl)-, sodium salt (1:1)
- D-glycero-α-D-galacto-2-Nonulopyranosidonic acid, 5-bromo-4-chloro-1H-indol-3-yl 5-(acetylamino)-3,5-dideoxy-, monosodium salt
- 5-bromo-4-chloro-3-indolyl A-D-N-*acetylneuramini
- 5-bromo-4-chloro-3-indolyl α-D-N-*acetylneuramini
- 5-Bromo-4-chloro-3-indolyl α-D-N-acetylneuraminic acid sodium salt ,98%
- X-Neu5Ac
- 5-BroMo-4-chloro-3-indolyl a-d-n(-20`C)
- N-Acetyl-2-O-(5-broMo-4-chloro-1H-indol-3-yl)-α-neuraMinic Acid MonosodiuM Salt
- 5-Bromo-4-chloro-3-indolyl-a-D-N-acetylneuraminic Acid, Na
- X-NEUNAC
- 5-broMo-4-chloro-1H-indol-3-yl 5-(AcetylaMino)-3,5-dideoxy-D-glycero-α-D-galacto-2-nonulopyranosidonic Acid MonosodiuM Salt
- X-NANA.Na
- 5-Bromo-4-chloro-3-indolyl N-acetyl-a-D-N-acetylneuraminic acid sodium salt
- 5-Bromo-4-chloro-3-indolyl-α-D-N-acetylneuraminic Acid, Sodium Sal
- 5-bromo-4-chloro-3-indolyl-alpha-D-N-acetylneuraminic acid
- See more synonyms
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Found 8 products.
5-Bromo-4-chloro-3-indolyl N-acetyl-a-D-neuraminic acid sodium salt
CAS:Formula:C19H21BrClN2O9NaPurity:≥ 90.0% (HPLC)Color and Shape:White to off-white powderMolecular weight:559.725-Bromo-4-chloro-3-indolyl α-D-N-acetylneuraminic acid sodium salt
CAS:5-Bromo-4-chloro-3-indolyl α-D-N-acetylneuraminic acid sodium saltFormula:C19H21BrClN2O9·NaPurity:By hplc: 99.9 area-% (Typical Value in Batch COA)Color and Shape: slightly yellow powderMolecular weight:559.72481g/molX-NeuNAc
CAS:X-NeuNAc (5-Bromo-4-chloro-3-indolyl-alpha-D-N-acetylneuraminic acid sodium salt) is a new chromogenic assay substrate of neuraminidase activity in bacterialFormula:C19H21BrClN2NaO9Purity:98.76% - 99.99%Color and Shape:SolidMolecular weight:559.725-Bromo-4-chloro-3-indolyl-α-D-N-acetylneuraminic Acid, Sodium Salt
CAS:Controlled Product<p>Stability Moisture, Temperature sensitive<br>Applications Used as a substrate for the detection of sialidase-like enzyme in screening of enzymes, studying physiological activities of gangliosides, and recombinant technologies.<br>References Biorg. Med. Chem., 1, 147 (1993)<br></p>Formula:C19H21BrClN2O9·NaColor and Shape:NeatMolecular weight:559.725-Bromo-4-chloro-3-indoxyl-α-D-N-acetylneuraminic acid, sodium salt
CAS:Chromogenic substrate for neuraminidase yielding a blue precipitate upon cleavage.Formula:C19H21BrClN2NaO9Purity:Min. 98.0 Area-%Molecular weight:559.74 g/mol5-Bromo-4-Chloro-3-Indoxyl-a-D-N-Acetylneuraminic Acid Sodium Salt extrapure (X-NANA.Na), 98%
CAS:Formula:C19H21BrClN2O9NaMolecular weight:559.72






