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MIDECAMYCIN

CAS No.
35457-80-8
Chemical Name:
MIDECAMYCIN
Synonyms
medemycin;mydecamycin;medecamycin;sf837;Aboren;Myoxam;Midecin;Momicin;Macropen;MoMicine
CBNumber:
CB5175530
Molecular Formula:
C41H67NO15
Molecular Weight:
813.97
MDL Number:
MFCD00865000
MOL File:
35457-80-8.mol
MSDS File:
SDS
Last updated:2024-03-16 16:33:45

MIDECAMYCIN Properties

Melting point 155℃ -156℃
Boiling point 874℃
alpha D23 -67° (c = 1 in ethanol)
Density 1.1651 (rough estimate)
refractive index 1.6220 (estimate)
Flash point >110°(230°F)
storage temp. Keep in dark place,Inert atmosphere,2-8°C
solubility Chloroform (Slightly), Ethanol (Slightly), Methanol (Slightly)
form Solid
pka 6.9 in 50% aq ethanol
color White to Off-White
Water Solubility Soluble in methanol or ethanol. Insoluble in water
FDA UNII N34Z0Y5UH7
ATC code J01FA03

SAFETY

Risk and Safety Statements

Hazard statements  H413
RTECS  OH4730600

MIDECAMYCIN price More Price(17)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Alfa Aesar J66046 Midecamycin, 900 μg/mg 35457-80-8 500mg $180 2024-03-01 Buy
Alfa Aesar J66046 Midecamycin, 900 μg/mg 35457-80-8 1g $258 2024-03-01 Buy
TRC M343250 Midecamycin(>85%) 35457-80-8 10g $1190 2021-12-16 Buy
Usbiological 017648 Midecamycin 35457-80-8 1g $460 2021-12-16 Buy
Usbiological 257342 Midecamycin 35457-80-8 500mg $468 2021-12-16 Buy
Product number Packaging Price Buy
J66046 500mg $180 Buy
J66046 1g $258 Buy
M343250 10g $1190 Buy
017648 1g $460 Buy
257342 500mg $468 Buy

MIDECAMYCIN Chemical Properties,Uses,Production

Description

Midecamycin, a macrolide antibiotic having a 16-membered lactone ring, was found in the culture broth of Streptomyces mycarofaciens by Meiji Seika Kaisha in 1971. Under specific culture conditions, it is produced by the organism as a single component. Midecamycin shows almost the same antimicrobial spectrum and activity as kitasamycin. Although its serum and urine concentrations are low, it distributes in tissues at high concentration following oral administration.

Chemical Properties

White Solid

Originator

Medemycin,Meiji Seika,Japan,1974

Uses

A broad spectrum antibiotic

Uses

A 16-membered ring macrolide antibiotic used in ophthalmology as well as other medical fields.

Definition

ChEBI: Midecamycin is an organic molecular entity.

Manufacturing Process

The SF-837 strain, namely Streptomyces mycarofaciens identified as ATCC No. 21454 was inoculated to 60 liters of a liquid culture medium containing 2.5% saccharified starch, 4% soluble vegetable protein, 0.3% potassium chloride and 0.3% calcium carbonate at pH 7.0, and then stir-cultured in a jarfermenter at 28°C for 35 hours under aeration. The resulting culture was filtered directly and the filter cake comprising the mycelium cake was washed with dilute hydrochloric acid.
The culture filtrate combined with the washing liquid was obtained at a total volume of 50 liters (potency 150 mcg/ml). The filtrate (pH 8) was then extracted with 25 liters of ethyl acetate and 22 liters of the ethyl acetate phase was concentrated to approximately 3 liters under reduced pressure. The concentrate was diluted with 1.5 liters of water, adjusted to pH 2.0 by addition of 5N hydrochloric acid and then shaken thoroughly. The aqueous phase was separated from the organic phase and this aqueous solution was adjusted to pH 8 by addition of 3N sodium hydroxide and then extracted with 800 rnl of ethyl acetate. The resulting ethyl acetate extract was then shaken similarly together with 500 ml of aqueous hydrochloric acid to transfer the active substances into the latter which was again extracted with 400 ml of ethyl ether at pH 8.The ether extract was dried with anhydrous sodium sulfate and concentrated under reduced pressure to give 16.5 g of light yellow colored powder.
12 g of this crude powder were dissolved in 200 ml of ethyl acetate and the solution was passed through a column of 600 ml of pulverized carbon which had been impregnated with ethyl acetate. The development was carried out using ethyl acetate as the solvent and the active fractions of eluate were collected to a total volume of 2,500 ml, which was then evaporated to dryness under reduced pressure to yield 5 g of a white colored powder. This powder was dissolved in 10 ml of benzene and the insoluble matters were filtered out. The filtered solution in benzene was then subjected to chromatographic isolation by passing through a column of 700 ml of silica gel which had been impregnated with benzene. The development of the active substances adsorbed on the silica gel was effected using a solvent system consisting of benzene-acetone (4:1), and the eluate was collected in fractions of each 20 ml. The active fractions No. 90-380 which gave a single spot in alumina thin layer chromatography and which could be recognized as containing the SF- 837 substance purely in view of the Rf-value of the single spot were combined together to a total volume of 4,000 ml, and then concentrated under reduced pressure to yield 1.5 g of white colored powder of a melting point of 122°C to 124°C which was found by analysis to be the pure SF-837 substance free base.

Therapeutic Function

Antibacterial

Pharmaceutical Applications

A naturally occurring metabolite of Streptomyces mycarofaciens, supplied as the native compound and as midecamycin acetate for oral administration.
It is rapidly and extensively metabolized and is said to exhibit less toxicity than earlier macrolides. It is of limited availability.

MIDECAMYCIN Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 137)Suppliers
Supplier Tel Email Country ProdList Advantage
.GZ HONESTCHEM CO.,LTD
+86-15013270415 honestchemical@foxmail.com China 247 58
Shanghai Zheyan Biotech Co., Ltd.
18017610038 zheyansh@163.com CHINA 3620 58
BOC Sciences
+1-631-485-4226 inquiry@bocsci.com United States 19553 58
career henan chemical co
+86-0371-86658258 15093356674; factory@coreychem.com China 29826 58
Shaanxi Dideu Medichem Co. Ltd
+86-29-87569265 +86-18612256290 1056@dideu.com China 3791 58
Hefei TNJ Chemical Industry Co.,Ltd.
0551-65418671 sales@tnjchem.com China 34572 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-89586680 +86-18192503167 1026@dideu.com China 9553 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 29474 58
AFINE CHEMICALS LIMITED
0571-85134551 info@afinechem.com CHINA 15377 58
Baoji Guokang Healthchem co.,ltd
+8615604608665 15604608665 dominicguo@gk-bio.com CHINA 9427 58

View Lastest Price from MIDECAMYCIN manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
MIDECAMYCIN pictures 2021-11-02 MIDECAMYCIN
35457-80-8
US $238.10 / g 100g 99% 200kg Baoji Guokang Healthchem co.,ltd
Midecamycin pictures 2021-07-20 Midecamycin
35457-80-8
US $1.00-1.00 / KG 1g 99% 50tons Shaanxi Dideu Medichem Co. Ltd
Midecamycin pictures 2021-07-09 Midecamycin
35457-80-8
US $1.00 / g 300g 99.8% 20 TONS .GZ HONESTCHEM CO.,LTD
  • MIDECAMYCIN pictures
  • MIDECAMYCIN
    35457-80-8
  • US $238.10 / g
  • 99%
  • Baoji Guokang Healthchem co.,ltd
  • Midecamycin pictures
  • Midecamycin
    35457-80-8
  • US $1.00-1.00 / KG
  • 99%
  • Shaanxi Dideu Medichem Co. Ltd
  • Midecamycin pictures
  • Midecamycin
    35457-80-8
  • US $1.00 / g
  • 99.8%
  • .GZ HONESTCHEM CO.,LTD
midecamycina(sub1) platenomycinb1 LeucoMycin V 3,4B-Dipropanoate MoMicine antibioticsf837 sf837 turimycinp(sub3) LEUCOMYCIN V 3,4B-DIPROPIONATE Aboren Leucomycin V, 3,4B-dipropanoate (9CI) Macropen Medecamycin A1 Medemycin A1 Midecamycin A1 Midecin Momicin Mydecamycin A1 Myoxam Normicina NSC 154011 Oxacyclohexadecane, leucomycin V deriv. Rubimycin SF 837A1 Turimycin P3 YL 704B1 MIDECAMYCIN MIDECAMYCINE midecamycin from streptomyces*mycarofaciens MIDECAMYCIN FROM STREPTOMYCES & Leucomycin V 3,4''-dipropionate Leucomycin V 3,4B-dipropionate antibioticsf837a1 antibioticyl704b1 espinomycina leucomycinv,3,4(supb)-dipropanoate propanoic acid [(11Z,13E)-6-[[(2S,3R,4R,5S,6R)-4-(dimethylamino)-3-hydroxy-5-[[(2S,4R,5R,6R)-4-hydroxy-4,6-dimethyl-5-(1-oxopropoxy)-2-oxanyl]oxy]-6-methyl-2-oxanyl]oxy]-10-hydroxy-5-methoxy-9,16-dime Midecamycin, >98% (4R,5S,6S,7R,9R,10R,11E,13E,16R)-6-(((2S,3R,4R,5S,6R)-4-(Dimethylamino)-3-hydroxy-5-(((2S,4R,5S,6S)-4-hydroxy-4,6-dimethyl-5-(propionyloxy)tetrahydro-2H-pyran-2-yl)oxy)-6-methyltetrahydro-2H-pyran-2-yl)oxy)-10-hydroxy-5-methoxy-9,16-dimethyl-2-oxo-7-(2-ox (4R,5S,6S,7R,9R,10R,11E,13E,16R)-6-(((2S,3R,4R,5S,6R)-4-(Dimethylamino)-3-hydroxy-5-(((2S,4R,5S,6S)-4-hydroxy-4,6-dimethyl-5-(propionyloxy)tetrahydro-2H-pyran-2-yl)oxy)-6-methyltetrahydro-2H-pyran-2-yl)oxy)-10-hydroxy-5-methoxy-9,16-dimethyl-2-oxo-7-(2-oxoethyl)oxacyclohexadeca-11,13-dien-4-yl propionate (2S,3S,4R,6S)-6-{[(2R,3S,4R,5R,6S)-4-(dimethylamino)-5-hydroxy-6-{[(4R,5S,6S,7R,9R,10R,11E,13E,16R)-10-hydroxy-5-methoxy-9,16-dimethyl-2-oxo-7-(2-oxoethyl)-4-(propanoyloxy)-1-oxacyclohexadeca-11,13-dien-6-yl]oxy}-2-methyloxan-3-yl]oxy}-4-hydroxy-2,4-dimethyloxan-3-yl propanoate Midecamycin (>85%) MIDECAMYCIN USP/EP/BP DMUAPQTXSSNEDD-BJXZGPOLSA-N medemycin mydecamycin medecamycin 35457-80-8 3557-80-8 C41H67NO15 Pharmaceuticals Carbohydrates & Derivatives Chiral Reagents Intermediates & Fine Chemicals