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Micronomicin sulfate - ≥98.0%, high purity , CAS No.66803-19-8

    Grade & Purity:
  • ≥98%
In stock
Item Number
M650470
Grouped product items
SKU Size
Availability
Price Qty
M650470-50mg
50mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$45.90
M650470-100mg
100mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$50.90

Antibiotics Disease Research Antibacterial Antibiotics Disease Research Anti-inflammation/Immunoregulatory Antibiotics Other Antibiotics

Basic Description

Synonyms AKOS025401575 | Antibiotic XK-62-2 sulfate | DTXCID0028535 | (2R,3R,4R,5R)-2-(((1S,2S,3R,4S,6R)-4,6-diamino-3-(((2R,3R,6S)-3-amino-6-((methylamino)methyl)tetrahydro-2H-pyran-2-yl)oxy)-2-hydroxycyclohexyl)oxy)-5-methyl-4-(methylamino)tetrahydro-2H-pyran-3,
Specifications & Purity ≥98%
Biochemical and Physiological Mechanisms Micronomicin sulfate (Gentamicin C2b sulfate) is an aminoglycoside antibiotic isolated from Micromonospora . Micronomicin sulfate is a broad-spectrum antibiotic close to the gentamicin-type antibiotics , exhibits a high activity against Pseudomonas , Prot
Storage Temp Store at 2-8°C,Desiccated
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description

Micronomicin sulfate (Gentamicin C2b sulfate) is an aminoglycoside antibiotic isolated from Micromonospora . Micronomicin sulfate is a broad-spectrum antibiotic close to the gentamicin-type antibiotics , exhibits a high activity against Pseudomonas , Proteus , Klebsiella pneumoniae , Serratia , etc ( MIC =0.001-8.3 μg/ml)

In Vitro

Micronomicin has a potent antibacterial activity, it is active against Staphylococcus aureus FDA 209 P, Staphylococcus aureus with the minimal inhibitory values of 0.01 μg/ml. It is also against Escherichia coli St.M. 589, Baker 2, F 14-BK, and R5/W677 with the minimal inhibitory values of 0.75 μg/ml, 0.3 μg/ml, 0.03 μg/ml and 0.03 μg/ml. And it is active against Pseudomonas aeruginosa strains and lebsiella pneumoniae strains (MICs = 0.03-17.5 μg/ml). MCE has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

Micronomicin sulfate is highly active against various bacterial infections in mice, and has an intravenous acute LD 50 in mice of 93 mg/kg . Micronomicin sulfate (intravenous injection; 4-100 mg/kg; 30 days) is injected for subacute toxicity study. The wistar rats dies at the dose level of 100 mg/kg (10 out of 30 animals): renal disorders and ataxia. The renal histological disorders occurrs mainly at the dose levels of 25 mg/kg and over. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Wistar ratsDosage: 4, 10, 25, 63 mg/kg and 100 mg/kg Administration: Intravenous injection; 30 days Result: Led to death of rat at 100 mg/kg.

Form:Solid

IC50& Target:Aminoglycoside

Taxonomic Classification

Taxonomy Tree

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 2-deoxystreptamine aminoglycosides  O-glycosyl compounds  Aminocyclitols and derivatives  Cyclohexanols  Cyclohexylamines  Oxanes  Monosaccharides  Organic sulfuric acids  Tertiary alcohols  1,2-aminoalcohols  Dialkylamines  Oxacyclic compounds  Acetals  Monoalkylamines  Hydrocarbon derivatives  Organopnictogen compounds  Organic oxides  
Molecular Framework Aliphatic heteromonocyclic compounds
Substituents Amino cyclitol glycoside - 2-deoxystreptamine aminoglycoside - Glycosyl compound - O-glycosyl compound - Aminocyclitol or derivatives - Cyclohexanol - Cyclohexylamine - Sulfuric acid - Cyclitol or derivatives - Monosaccharide - Oxane - Organic sulfuric acid or derivatives - Tertiary alcohol - Cyclic alcohol - Secondary alcohol - 1,2-aminoalcohol - Secondary amine - Organoheterocyclic compound - Acetal - Oxacycle - Secondary aliphatic amine - Alcohol - Organic oxide - Hydrocarbon derivative - Primary aliphatic amine - Organopnictogen compound - Organic nitrogen compound - Amine - Primary amine - Organonitrogen compound - Aliphatic heteromonocyclic 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

Names and Identifiers

IUPAC Name (2R,3R,4R,5R)-2-[(1S,2S,3R,4S,6R)-4,6-diamino-3-[(2R,3R,6S)-3-amino-6-(methylaminomethyl)oxan-2-yl]oxy-2-hydroxycyclohexyl]oxy-5-methyl-4-(methylamino)oxane-3,5-diol;sulfuric acid
INCHI InChI=1S/C20H41N5O7.H2O4S/c1-20(28)8-29-19(14(27)17(20)25-3)32-16-12(23)6-11(22)15(13(16)26)31-18-10(21)5-4-9(30-18)7-24-2;1-5(2,3)4/h9-19,24-28H,4-8,21-23H2,1-3H3;(H2,1,2,3,4)/t9-,10+,11-,12+,13-,14+,15+,16-,17+,18+,19+,20-;/m0./s1
InChIKey MQDGQSCLOYLSEK-SCFBDNQUSA-N
Smiles CC1(COC(C(C1NC)O)OC2C(CC(C(C2O)OC3C(CCC(O3)CNC)N)N)N)O.OS(=O)(=O)O
Isomeric SMILES C[C@@]1(CO[C@@H]([C@@H]([C@H]1NC)O)O[C@H]2[C@@H](C[C@@H]([C@H]([C@@H]2O)O[C@@H]3[C@@H](CC[C@H](O3)CNC)N)N)N)O.OS(=O)(=O)O
PubChem CID 171808
Molecular Weight 561.7

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

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

Chemical and Physical Properties

Solubility H2O : 50 mg/mL (Need ultrasonic)
Molecular Weight 561.700 g/mol
XLogP3
Hydrogen Bond Donor Count 10
Hydrogen Bond Acceptor Count 16
Rotatable Bond Count 7
Exact Mass 561.268 Da
Monoisotopic Mass 561.268 Da
Topological Polar Surface Area 283.000 Ų
Heavy Atom Count 37
Formal Charge 0
Complexity 688.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 12
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

Solution Calculators

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