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Micronomicin

Product Name
Micronomicin
CAS No.
52093-21-7
Chemical Name
Micronomicin
Synonyms
DE 020;KW 1062;XK 62-2;Sagamicin;Santemycin;MICRONOMYCIN;Micronomicin;Gentamicin C2b;Antibiotic XK 62-2;Antibiotic KW 1062
CBNumber
CB31179195
Molecular Formula
C20H41N5O7
Formula Weight
463.57
MOL File
52093-21-7.mol
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Micronomicin Property

Melting point:
260° (dec)
alpha 
D20 +116° (c = 1 in water)
Boiling point:
567.39°C (rough estimate)
Density 
1.2416 (rough estimate)
refractive index 
1.7600 (estimate)
storage temp. 
4°C, stored under nitrogen
pka
13.29±0.70(Predicted)
Water Solubility 
Water : 250 mg/mL (539.29 mM; Need ultrasonic)
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Safety

Toxicity
LD50 i.v. in mice: 93 mg/kg (Okachi)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Usbiological
Product number
278497
Product name
Gentamicin C2b
Packaging
1mg
Price
$835
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
API0011937
Product name
MICRONOMICIN
Purity
95.00%
Packaging
1G
Price
$1428
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
API0011937
Product name
MICRONOMICIN
Purity
95.00%
Packaging
5MG
Price
$502.22
Updated
2021/12/16
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Micronomicin Chemical Properties,Usage,Production

Description

Micronomicin, formerly called sagamicin, was found in the culture broth of Micromonospora sagamiensis var. nonreducans by Kyowa Hakko Kogyo Company and Abbott Laboratories in 1974. The compound is identical with one of the minor components contained in gentamicin, gentamicin C2b, but it is produced as a single component. Its amino group at the 6 -position is methylated and is not subject to the enzymatic acetylation caused by resistant bacteria, including Pseudomonas aeruginosa. Micronomicin is less toxic than gentamicin to the renal and aural systems.

Originator

Sagamicin,Kyowa Hakko,Japan,1982

Uses

Gentamicin C2b (micronomicin) is a trisaccharide pentaaminoglycoside antibiotic belonging to the gentamicin class. Gentamicin C2b was isolated from Micromonospora sagamiensis var. nonreductans by researchers at Kyowa Hakko Kogyo in 1974. Gentamicin C2b has broad activity against Gram positive and Gram negative bacteria. More recently, gentamicin C2b has been shown to induce neuromuscular blockage.

Uses

Gentamicin C2b is a component of Gentamicin Sulphate Complex C. Gentamicin (G360600) is an antibiotic from bacteria Micromonospora purpurea and used to treat respiratory and urinary tract, blood, bone and soft tissues infections.

Definition

ChEBI: Gentamicin C2b is an aminoglycoside.

Manufacturing Process

A. Culturing of MK-65: In this example, Micromonospora sagamiensis MK-65 ATCC 21826 (FERM-P No. 1530) is used as the seed strain. One loopful of the seed strain is inoculated into 30 ml of a first seed medium in a 250 mlErlenmeyer flask. The first seed medium has the following composition:
Percent Dextrin 1 Glucose 1 Peptone 0.5 Yeast extract 0.5 CaCO3(pH: 7.2 before sterilization) 0.1
Culturing is carried out with shaking at 30°C for 5 days. 30 ml of the seed culture is then inoculated into 300 ml of a second seed medium, of the same composition as the first seed medium, in a 2 liter-Erlenmeyer flask provided with baffles. The second seed culturing is carried out with shaking at 30°C for 2 days. Then 1.5 liters of the second seed culture (corresponding to the content of 5 flasks) is inoculated into 15 liters of a third seed medium of the same composition as set forth above, in a 30 liter-glass jar fermenter. Culturing in the jar fermenter is carried out with aeration (15 liters/minute) and stirring (350 rpm) at 30°C for 2 days. Then, 15 liters of the third seed culture is inoculated into 60 liters of a fourth seed medium of the same composition as set forth above, in a 300 liter-fermenter. Culturing in the fermenter is carried out with aeration (60 liters/minute) and stirring (150 rpm) at 30°C for 2 days. Finally, 60 liters of the fourth seed culture is inoculated into 600 liters of a fermentation medium having the following composition in a 1,000 liter-fermenter.
Percent Dextrin 5 Soybean meal 4 CaCO3 (pH: 7.2 before sterilization) 0.7
Culturing in the fermenter is carried out with aeration (600 liters/minute) and stirring 150 rpm) at 35°C for 5 days.
B. Isolation of crude antibiotic: After the completion of fermentation, the culture liquor is adjusted to a pH of 2.0 with 12 N sulfuric acid and stirred for 30 minutes. Then, about 10 kg of a filter aid, Radiolite No. 600 (product of Showa Kagaku Kogyo Co., Ltd., Japan) is added thereto and the microbial cells are removed by filtration. The filtrate is adjusted to a pH of 8.0 with 6N sodium hydroxide and passed through a column packed with about 50 liters of a cation exchange resin, Amberlite IRC-50 (ammonia form). The active substance is adsorbed on the resin and the eluate is discarded. After washing the resin with water, the active substance is eluted out with 1N aqueous ammonia. The eluate is obtained in fractions and the activity of each of the fractions is determined against Bacillus subtilis No. 10707 by a paper disk method using an agar plate.
Active fractions are combined and concentrated in vacuo to about 5 liters. The concentrate is then adjusted to a pH of 8.0 with 6N sulfuric acid and passed through a column packed with 1 liter of an anion exchange resin, Dowex 1X2 (OH-form). The column is washed with about 5 liters of water and the effluent and the washings containing active substance are combined and are concentrated to 1/15 by volume. The concentrate is adjusted to a pH of 10.5 with 6 N sodium hydroxide and 5 volumes of acetone is added thereto. The resultant precipitate is removed by filtration and the filtrate is concentrated to 500 ml. The concentrate is adjusted to a pH of 4.5 with 6 N sulfuric acid and 2.5 liters of methanol is added thereto. After cooling, a white precipitate is obtained. The precipitate is separated by filtration and washed with methanol. After drying in vacuo, about 300 g of white powder is obtained.
The white powder is a mixture of the sulfate of gentamicin C1a, and the sulfate of XK-62-2, and exhibits an activity of 620 units/mg (the activity of 1 mg of pure product corresponds to 1,000 units).
C. Isolation and purification of XK-62-2: 100 g of the white powder obtained in the above step B are placed to form a thin, uniform layer on the upper part of a 5 cm x 150 cm column packed with about 3 kg of silica gel advancely suspended in a solvent of chloroform, isopropanol and 17% aqueous ammonia(2:1:1 by volume). Thereafter, elution is carried out with the same solvent at a flow rate of about 250 ml/hour. The eluate is separated in 100 ml portions. The active fraction is subjected to paper chromatography to examine the components eluted. XK-62-2 is eluted in fraction Nos. 53-75 and gentamicin C1ais eluted in fraction Nos. 85-120. The fraction Nos. 53-75 are combined and concentrated under reduced pressure to sufficiently remove the solvent. The concentrate is then dissolved in a small amount of water. After freezedrying the solution, about 38 g of a purified preparate of XK-62-2 (free base) is obtained. The preparate has an activity of 950 units/mg. Likewise, fraction Nos. 85-120 are combined and concentrated under reduced pressure to sufficiently remove the solvent. The concentrate is then dissolved in a small amount of water. After freeze-drying the solution, about 50 g of a purified preparate of gentamicin C1a (free base) is obtained. The activity of the preparate is about 980 units/mg.

Therapeutic Function

Antibiotic

Antimicrobial activity

Antibacterial and pharmacokinetic properties are similar to those of its precursor gentamicin C1a but it is more resistant to AAC(6′). Dosage is similar to that for gentamicin, and should be controlled by blood level determinations. It is available in Japan.

Micronomicin Preparation Products And Raw materials

Raw materials

Preparation Products

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Micronomicin Suppliers

Shijiazhuang Ruitian Biochemical Co. Ltd
Tel
0311-89102030 18031153398
Email
3212842192@qq.com
Country
China
ProdList
166
Advantage
58
Beijing HuaMeiHuLiBiological Chemical
Tel
010-56205725
Fax
010-65763397
Email
waley188@sohu.com
Country
China
ProdList
12338
Advantage
58
ChemStrong Scientific Co.,Ltd
Tel
0755-0755-66853366 13670046396
Fax
0755-28363542
Email
sales@chem-strong.com
Country
China
ProdList
17982
Advantage
56
Lynnchem
Tel
86-(0)29-85992781 17792393971
Email
info@lynnchem.com
Country
China
ProdList
4587
Advantage
58
Novachemistry
Tel
44-20819178-90 02081917890
Fax
(0)2080432064
Email
info@novachemistry.com
Country
United Kingdom
ProdList
4381
Advantage
58
Shenzhen Polymeri Biochemical Technology Co., Ltd.
Tel
+86-400-002-6226 13028896684
Email
sales@rrkchem.com
Country
China
ProdList
55827
Advantage
58
TOSUN PHARM
Tel
020-61855200 13326451905
Email
2881290884@qq.com
Country
China
ProdList
7487
Advantage
58
BOC Sciences
Tel
+16314854226
Email
inquiry@bocsci.com
Country
United States
ProdList
19743
Advantage
58
TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
Country
United States
ProdList
19892
Advantage
58
Dideu Industries Group Limited
Tel
+86-29-89586680 +86-15129568250
Email
1026@dideu.com
Country
China
ProdList
29016
Advantage
58
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View Lastest Price from Micronomicin manufacturers

Shaanxi Dideu Medichem Co. Ltd
Product
Micronomicin 52093-21-7
Price
US $1.00-1.00/KG
Min. Order
1g
Purity
99%
Supply Ability
50tons
Release date
2020-05-07
Hebei Lingding Biotechnology Co., Ltd.
Product
Micronomicin 52093-21-7
Price
US $95.00-79.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
9000kg/per week
Release date
2021-08-23

52093-21-7, MicronomicinRelated Search:


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  • Gentamicin C2b (Component of Gentamicin Sulphate Complex C)
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