(2R)-4-amino-N-[(1R,2S,3S,4R,5S)-5-amino-2-{[(2S,3R,4S,5S,6R)-4-amino-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4-{[(2R,3R,4S,5S,6R)-6-(aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3-hydroxycyclohexyl]-2-hydroxybutanamide; sulfuric acid

• ChemBase编号: 132535
• 分子式: C22H45N5O17S
• 平均质量: 683.681
• 单一同位素质量: 683.25311601
• SMILES: C1[C@@H]([C@H]([C@@H]([C@H]([C@@H]1NC(=O)[C@@H](CCN)O)O[C@@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O)N)O)O)O[C@@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CN)O)O)O)N.OS(=O)(=O)O
• Canonical SMILES: OS(=O)(=O)O.NCC[C@H](C(=O)N[C@@H]1C[C@H](N)[C@H]([C@@H]([C@H]1O[C@H]1O[C@H](CO)[C@H]([C@@H]([C@H]1O)N)O)O)O[C@H]1O[C@H](CN)[C@H]([C@@H]([C@H]1O)O)O)O
• InChI: InChI=1S/C22H43N5O13.H2O4S/c23-2-1-8(29)20(36)27-7-3-6(25)18(39-22-16(34)15(33)13(31)9(4-24)37-22)17(35)19(7)40-21-14(32)11(26)12(30)10(5-28)38-21;1-5(2,3)4/h6-19,21-22,28-35H,1-5,23-26H2,(H,27,36);(H2,1,2,3,4)/t6-,7+,8+,9+,10+,11-,12+,13+,14+,15-,16+,17-,18+,19-,21+,22+;/m0./s1
• InChIKey: HIBICIOPDUTNRR-BOEHXBESSA-N

名称和登记号

名称

• IUPAC标准名: (2R)-4-amino-N-[(1R,2S,3S,4R,5S)-5-amino-2-{[(2S,3R,4S,5S,6R)-4-amino-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4-{[(2R,3R,4S,5S,6R)-6-(aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3-hydroxycyclohexyl]-2-hydroxybutanamide; sulfuric acid
• IUPAC传统名: (2R)-4-amino-N-[(1R,2S,3S,4R,5S)-5-amino-2-{[(2S,3R,4S,5S,6R)-4-amino-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4-{[(2R,3R,4S,5S,6R)-6-(aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3-hydroxycyclohexyl]-2-hydroxybutanamide; sulfuric acid
• 别名: Amikacin sulfate salt; Amikacin sulfate salt

登记号

• CAS号: 149022-22-0; 39831-55-5
• MDL号: MFCD00167477; MFCD00167475
• PubChem SID: 24890648; 162226812
• PubChem CID: 16218872

理论计算性质

• Acid pKa: 12.104234
• 质子受体: 17
• 质子供体: 13
• LogD (pH = 5.5): -20.16644
• LogD (pH = 7.4): -15.099279
• Log P: -8.584383
• 摩尔折射率: 129.841 cm^3
• 极化性: 54.552784 Å^3
• 极化表面积: 331.94 Å^2
• 可自由旋转的化学键: 10
• 里宾斯基五规则: false

分子性质

安全信息

• RTECS编号: WK1961200
• 德国WGK号: 2
• 个人保护装置: Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
• 保存温度: 2-8°C

产品相关信息

• 纯度: 95+%

详细说明

Sigma Aldrich - A2324

Biochem/physiol Actions
Antibacterial spectrum: Gram-negative and gram-positive bacteria.
Amikacin prevents bacterial protein synthesis by binding to the 30S ribosome subunit and inducing mRNA misreading.
Other Notes
Aminoglycoside antibiotic. Derivative of kanamycin.
Quality
Amikacin:Sulfate ratio 1:1.8
Application
Amikacin is an aminoglycoside antibiotic commonly used in the treatment of drug-resistant mycobacteria 1. It is used to study organism-directed delivery of antibiotics as well as drug resistance 2.