CAS 17650-86-1
:Amicetin
Description:
Amicetin, with the CAS number 17650-86-1, is a chemical compound that belongs to the class of aminoglycoside antibiotics. It is primarily known for its antibacterial properties, particularly against a range of Gram-negative bacteria. The structure of Amicetin features an amino sugar moiety, which is characteristic of aminoglycosides, allowing it to bind to bacterial ribosomes and inhibit protein synthesis, thereby exerting its antimicrobial effects. This compound is often utilized in clinical settings for treating infections, although its use may be limited due to potential side effects and the emergence of antibiotic resistance. In terms of physical properties, Amicetin is typically a white to off-white powder, soluble in water, which facilitates its administration in various formulations. Safety and handling precautions are essential, as with many antibiotics, to mitigate risks of toxicity and environmental impact. Overall, Amicetin represents a significant tool in the arsenal against bacterial infections, although careful consideration of its application is necessary in modern medicine.
Formula:C29H42N6O9
InChI:InChI=1S/C29H42N6O9/c1-15-19(44-26-24(38)23(37)22(34(4)5)16(2)43-26)10-11-21(42-15)35-13-12-20(33-28(35)41)32-25(39)17-6-8-18(9-7-17)31-27(40)29(3,30)14-36/h6-9,12-13,15-16,19,21-24,26,36-38H,10-11,14,30H2,1-5H3,(H,31,40)(H,32,33,39,41)/t15-,16-,19+,21-,22-,23+,24-,26-,29+/m1/s1
InChI key:InChIKey=HDNVYHWHCVTDIV-ZENIWSRCSA-N
SMILES:O=C1N(C=CC(NC(=O)C2=CC=C(NC([C@@](CO)(C)N)=O)C=C2)=N1)[C@@H]3O[C@H](C)[C@@H](O[C@@H]4[C@H](O)[C@@H](O)[C@H](N(C)C)[C@@H](C)O4)CC3
Synonyms:- 4-[[(2S)-2-Amino-3-hydroxy-2-methyl-1-oxopropyl]amino]-N-[1-[(2R,5S,6R)-5-[[4,6-dideoxy-4-(dimethylamino)-α-<span class="text-smallcaps">D</span>-glucopyranosyl]oxy]tetrahydro-6-methyl-2H-pyran-2-yl]-1,2-dihydro-2-oxo-4-pyrimidinyl]benzamide
- Allomycin
- Amicetin
- Benzamide, 4-[(2-amino-3-hydroxy-2-methyl-1-oxopropyl)amino]-N-[1-[5-[[4,6-dideoxy-4-(dimethylamino)-α-<span class="text-smallcaps">D</span>-glucopyranosyl]oxy]tetrahydro-6-methyl-2H-pyran-2-yl]-1,2-dihydro-2-oxo-4-pyrimidinyl]-, [2R-[2α(S*),5β,6α]]-
- Benzamide, 4-[[(2S)-2-amino-3-hydroxy-2-methyl-1-oxopropyl]amino]-N-[1-[(2R,5S,6R)-5-[[4,6-dideoxy-4-(dimethylamino)-α-<span class="text-smallcaps">D</span>-glucopyranosyl]oxy]tetrahydro-6-methyl-2H-pyran-2-yl]-1,2-dihydro-2-oxo-4-pyrimidinyl]-
- Hydracrylanilide, 2-amino-4′-[[1,2-dihydro-2-oxo-1-[2,3,6-trideoxy-4-O-[4,6-dideoxy-4-(dimethylamino)-α-<span class="text-smallcaps">D</smallcap>-glucopyranosyl]-β-<smallcap>D</span>-erythro-hexopyranosyl]-4-pyrimidinyl]carbamoyl]-2-methyl-
- N-[1-(5-{[4,6-dideoxy-4-(dimethylamino)hexopyranosyl]oxy}-6-methyltetrahydro-2H-pyran-2-yl)-2-oxo-1,2-dihydropyrimidin-4-yl]-4-[(2-methylseryl)amino]benzamide
- N-{1-[(2R,5S,6R)-5-{[4,6-dideoxy-4-(dimethylamino)-alpha-D-glucopyranosyl]oxy}-6-methyltetrahydro-2H-pyran-2-yl]-2-oxo-1,2-dihydropyrimidin-4-yl}-4-[(2-methyl-L-seryl)amino]benzamide
- NSC 5340
- Sacromycin
- Benzamide, 4-[(2-amino-3-hydroxy-2-methyl-1-oxopropyl)amino]-N-[1-[5-[[4,6-dideoxy-4-(dimethylamino)-α-D-glucopyranosyl]oxy]tetrahydro-6-methyl-2H-pyran-2-yl]-1,2-dihydro-2-oxo-4-pyrimidinyl]-, [2R-[2α(S*),5β,6α]]-
- Benzamide, 4-[[(2S)-2-amino-3-hydroxy-2-methyl-1-oxopropyl]amino]-N-[1-[(2R,5S,6R)-5-[[4,6-dideoxy-4-(dimethylamino)-α-D-glucopyranosyl]oxy]tetrahydro-6-methyl-2H-pyran-2-yl]-1,2-dihydro-2-oxo-4-pyrimidinyl]-
- Hydracrylanilide, 2-amino-4′-[[1,2-dihydro-2-oxo-1-[2,3,6-trideoxy-4-O-[4,6-dideoxy-4-(dimethylamino)-α-D-glucopyranosyl]-β-D-erythro-hexopyranosyl]-4-pyrimidinyl]carbamoyl]-2-methyl-
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Found 2 products.
Amicetin
CAS:Amicetin, a potent antibiotic, is effective against gram-positive bacteria by inhibiting protein synthesis [1] [2] [3].Formula:C29H42N6O9Color and Shape:SolidMolecular weight:618.68Amicetin
CAS:<p>Amicetin is a type of antibiotic, which is derived from bacterial sources, specifically from Streptomyces species. It functions primarily by inhibiting protein synthesis in susceptible bacteria, achieved through interfering with the aminoacyl-tRNA binding process on the ribosome. This mechanism disrupts the translation process, thereby preventing bacterial growth and replication.</p>Formula:C29H42N6O9Purity:Min. 95%Molecular weight:618.68 g/mol

