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

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

7 Citations

COA

Grade & Purity:

10mM in Water

Cas Number: 65710-07-8
Molecular Weight: 637.66
EC Number: 265-890-7
PubChem CID: 3081544

In stock

Item Number

A425315

Grouped product items
SKU	Size	Availability	Price	Qty
A425315-1ml	1ml	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$38.90

Aminoglycoside antibiotic agent. Potent protein synthesis inhibitor.

View related series

Antibiotic (1629) Bacterial (3013) Compound libraries (12325)

Basic Description

Synonyms	Apramycin sulfate \| 65710-07-8 \| Apramycin sulphate \| Apramycin (sulfate) \| UNII-8UYL6NAZ3Q \| 8UYL6NAZ3Q \| AI3-29795 \| EINECS 265-890-7 \| 410097-64-2 \| Apramycin, sulfate (2:5) \| (+)-APRAMYCIN SULFATE \| APRAMYCIN SULFATE (MART.) \| APRAMYCIN SULFATE [MART.] \| (2R,3R,4S,5S,6S)-2-[[(
Specifications & Purity	10mM in Water
Biochemical and Physiological Mechanisms	Aminoglycoside antibiotic agent. Potent protein synthesis inhibitor. Inhibits translocation. Shows bactericidal effects in vivo. Orally active.
Storage Temp	Store at -80°C
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.

Taxonomic Classification

Taxonomy Tree

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

Kingdom	Organic compounds
Superclass	Organic oxygen compounds
Class	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
Description	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
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

Names and Identifiers

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
INCHI	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
InChIKey	WGLYHYWDYPSNPF-RQFIXDHTSA-N
Smiles	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
Isomeric 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 Germany	3
Alternate CAS	37321-09-8
PubChem CID	3081544
Molecular Weight	637.66

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Chemical and Physical Properties

Flash Point(°F)	230°F
Flash Point(°C)	>110℃
Boil Point(°C)	823℃
Melt Point(°C)	168℃
Molecular Weight	637.700 g/mol
XLogP3
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 Å²
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

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Lu Qi, Shanshan Liu, Zhen Yan, Min Qiao, Haonan Peng, Liping Ding. (2024) 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, 446 (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).
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).
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, 130 (106130).
5. Tai Ye, Long Bai, Jinsong Yu, Weiyan Shi, Min Yuan, Juncheng Wang, Hui Cao, Liling Hao, Xiuxiu Wu, Fengqin Yin, Fei Xu. (2025) Fluorescent nanozyme for the dual-mode detection of tetracycline: Aggregation-induced luminescence and boosting peroxidase-like activity. FOOD CONTROL, 171 (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, 212 (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).

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