Apramycin sulfate salt - 10mM in Water , CAS No.65710-07-8

CAS: 65710-07-8 Cat. No.: A425315 Peso molecular: 637.66 Número EC: 265-890-7 PubChem CID: 3081544

GRADE & PURITY 10mM in Water

Synonyms

Apramycin Sulfate, Antibiotic for Culture Media Use Only | W-104790 | (2R,3R,4S,5S,6S)-5-amino-2-(((2R,3S,4R,4aR,6S,7R,8aS)-7-amino-6-(((1R,2R,3S,4R,6S)-4,6-diamino-2,3-dihydroxycyclohexyl)oxy)-4-hydroxy-3-(methylamino)octahydropyrano[3,2-b]pyran-2-yl)oxy

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Specifications

Sinónimos

Apramycin Sulfate, Antibiotic for Culture Media Use Only | W-104790 | (2R, 3R, 4S, 5S, 6S)-5-amino-2-(((2R, 3S, 4R, 4aR, 6S, 7R, 8aS)-7-amino-6-(((1R, 2R, 3S, 4R, 6S)-4, 6-diamino-2, 3-dihydroxycyclohexyl)oxy)-4-hydroxy-3-(methylamino)octahydropyrano[3, 2-b]pyran-2-yl)oxy

Especificaciones y pureza

10mM in Water

Mecanismos bioquímicos y fisiológicos

Aminoglycoside antibiotic agent. Potent protein synthesis inhibitor. Inhibits translocation. Shows bactericidal effects in vivo. Orally active.

Condiciones de almacenamiento de almacenamiento

Store at -80°C

Enviado en

Dry ice packs + Cold packs

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Nombres e identificadores

• Sonrisas canónicas: CNC1C(C2C(CC(C(O2)OC3C(CC(C(C3O)O)N)N)N)OC1OC4C(C(C(C(O4)CO)N)O)O)O.OS(=O)(=O)O
• IUPAC Name: (2R,3R,4S,5S,6S)-2-[[(2R,3S,4R,4aR,6S,7R,8aS)-7-amino-6-[(1R,2R,3S,4R,6S)-4,6-diamino-2,3-dihydroxycyclohexyl]oxy-4-hydroxy-3-(methylamino)-2,3,4,4a,6,7,8,8a-octahydropyrano[3,2-b]pyran-2-yl]oxy]-5-amino-6-(hydroxymethyl)oxane-3,4-diol;sulfuric acid
• InChIKey: WGLYHYWDYPSNPF-RQFIXDHTSA-N
• INCHI: 1S/C21H41N5O11.H2O4S/c1-26-11-14(30)18-8(33-20(11)37-21-16(32)13(29)10(25)9(4-27)34-21)3-7(24)19(36-18)35-17-6(23)2-5(22)12(28)15(17)31;1-5(2,3)4/h5-21,26-32H,2-4,22-25H2,1H3;(H2,1,2,3,4)/t5-,6+,7-,8+,9-,10-,11+,12+,13+,14-,15-,16-,17-,18+,19+,20-,21-;/m1./s1
• Isómeros SMILES: CN[C@H]1[C@H]([C@@H]2[C@H](C[C@H]([C@H](O2)O[C@@H]3[C@H](C[C@H]([C@@H]([C@H]3O)O)N)N)N)O[C@@H]1O[C@@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)N)O)O)O.OS(=O)(=O)O
• WGK Alemania: 3
• CAS alternativo: 37321-09-8
• PubChem CID: 3081544
• Peso molecular: 637.66

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Clase Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates
        • Level5 Aminosaccharides
          • Level6 Aminoglycosides
            • Level7 Aminocyclitol glycosides

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Clase: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Aminosaccharides - Aminoglycosides
• Direct Parent: Aminocyclitol glycosides
• Alternative Parents: Hexoses Aminocyclitols and derivatives Cyclohexanols Cyclohexylamines Oxanes Organic sulfuric acids 1,3-aminoalcohols 1,2-aminoalcohols Oxacyclic compounds Acetals Dialkylamines Hydrocarbon derivatives Monoalkylamines Organic oxides Organopnictogen compounds Primary alcohols
• Molecular Framework: Aliphatic heteropolycyclic compounds
• Substituents: Amino cyclitol glycoside - Hexose monosaccharide - Aminocyclitol or derivatives - Cyclohexanol - Cyclohexylamine - Sulfuric acid - Cyclitol or derivatives - Monosaccharide - Oxane - Organic sulfuric acid or derivatives - 1,3-aminoalcohol - Cyclic alcohol - Secondary alcohol - 1,2-aminoalcohol - Secondary amine - Acetal - Organoheterocyclic compound - Oxacycle - Secondary aliphatic amine - Primary alcohol - Organic oxide - Hydrocarbon derivative - Primary aliphatic amine - Organopnictogen compound - Organic nitrogen compound - Amine - Alcohol - Primary amine - Organonitrogen compound - Aliphatic heteropolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as aminocyclitol glycosides. These are organic compounds containing an amicocyclitol moiety glycosidically linked to a carbohydrate moiety. There are two major classes of aminoglycosides containing a 2-streptamine core. They are called 4,5- and 4,6-disubstituted 2-deoxystreptamines.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Propiedades químicas y físicas

• Punto de inflamación (°F): 230°F
• Punto de inflamación (°C): >110℃
• Punto de ebullición (°C): 823℃
• Punto de fusión (°C): 168℃
• Peso molecular: 637.700 g/mol
• Hydrogen Bond Donor Count: 13
• Hydrogen Bond Acceptor Count: 20
• Rotatable Bond Count: 6
• Exact Mass: 637.248 Da
• Monoisotopic Mass: 637.248 Da
• Topological Polar Surface Area: 367.000 Ų
• Heavy Atom Count: 42
• Formal Charge: 0
• Complexity: 841.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 17
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 2

XLogP3

Referencias

1. Lu Qi, Shanshan Liu, Zhen Yan, Min Qiao, Haonan Peng, Liping Ding.  (2023)  A cross-reactive fluorescent ensemble based on perylene derivative/surfactant assemblies for discrimination of multiple aminoglycoside antibiotics in aqueous solution.  JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY,      [PMID:] [10.1016/j.jphotochem.2023.115128]

2. Su Ping, Chen Xiaonan, He Zhangjing, Yang Yi.  (2017)  Preparation of polyclonal antibody and development of a biotin-streptavidin-based ELISA method for detecting kanamycin in milk and honey.  CHEMICAL RESEARCH IN CHINESE UNIVERSITIES,  33  (6): (876-881).  [PMID:] [10.1007/s40242-017-7168-9]

3. Ye Tai, Luo Zheng, Che Yueyue, Yuan Min, Cao Hui, Hao Liling, Zhang Qian, Xie Yongxin, Zhang Kaisen, Xu Fei.  (2024)  An inverted tetrahedron-mediated DNA walker for sulfadimethoxine detection.  MICROCHIMICA ACTA,  191  (12): (1-10).  [PMID:39496845] [10.1007/s00604-024-06810-6]

4. Chuntong Liu, Haiyan Qi, Tao Jing, Jun Li, Ming Zhao, Lixin Qiu, Qiuying Li.  (2024)  Efficient electrochemical synthesis of green fluorescent carbon dots for curcumin detection in common foods.  JOURNAL OF FOOD COMPOSITION AND ANALYSIS,      [PMID:] [10.1016/j.jfca.2024.106130]

5. Tai Ye, Long Bai, Jinsong Yu, Weiyan Shi, Min Yuan, Juncheng Wang, Hui Cao, Liling Hao, Xiuxiu Wu, Fengqin Yin, Fei Xu.  (2024)  Fluorescent nanozyme for the dual-mode detection of tetracycline: Aggregation-induced luminescence and boosting peroxidase-like activity.  FOOD CONTROL,      [PMID:] [10.1016/j.foodcont.2024.111109]

6. Haohao Chen, Min Yuan, Fengqin Yin, Hui Cao, Xiuxiu Wu, Liling Hao, Weiyan Shi, Tai Ye, Fei Xu.  (2025)  Freezing-driven assembly of DNA walking machine facilitate G4 nanowires growth for electrochemical detection of kanamycin.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2025.113237]

7. Tingting Wang, Huaizhi Yang, Qiushuang Sheng, Ying Ding, Jian Zhang, Feng Chen, Jianfeng Wang, Lei Song, Xuming Deng.  (2025)  Isoferulic acid facilitates effective clearance of hypervirulent Klebsiella pneumoniae through targeting capsule.  PLoS Pathogens,  21  (1): (e1012787).  [PMID:39761301] [10.1371/journal.ppat.1012787]

8. Lihua Yang, Hang Zhai, Tingting Tian, Botong Liu, Xianpu Ni, Huanzhang Xia*.  (2025)  Combinatorial biosynthesis of novel gentamicin derivatives with nonsense mutation readthrough activity and low cytotoxicity.  Frontiers in Pharmacology,      [PMID:40342992] [10.3389/fphar.2025.1575840]

9. Huanhuan Zhang, Fengjun Sun, Wei Feng, Yan Qian.  (2025)  Polymyxin B combined with amikacin delays the resistance of Klebsiella pneumoniae to polymyxin B by modulating the expression of NlpE.  INFECTION GENETICS AND EVOLUTION,      [PMID:40480594] [10.1016/j.meegid.2025.105780]

10. Haobo Xing, Qingming Hou, Zhenhua Wang, Shanfei Zhang, Shangxia Song, Lulu Du, Chenghua Gao, Yunfei Li, Fubao Sun.  (2026)  Enhanced Monensin Biosynthesis in Streptomyces cinnamonensis with Multigene Integration and Overexpression of Newly Identified Genes.  BIOCHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.bej.2026.110118]