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Capastat sulfate

Product Name
Capastat sulfate
CAS No.
1405-37-4
Chemical Name
Capastat sulfate
Synonyms
caprocin;HSDB3211;HSDB 3211;HSDB-3211;capastat sulfate;Capromycinsulfate;Spiramycin sulfate;CAPREOMYCIN SULFATE;CAPREOMYCIN SULPHATE;Capreomicin sulphate
CBNumber
CB4690423
Molecular Formula
C24H44N14O12S
Formula Weight
752.76
MOL File
1405-37-4.mol
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Capastat sulfate Property

Melting point:
>220oC (dec.)
Boiling point:
1377℃
Flash point:
>110°(230°F)
storage temp. 
Sealed in dry,Store in freezer, under -20°C
solubility 
H2O: soluble50mg/mL
form 
powder
color 
White to Off-White
Water Solubility 
Freely soluble in water
Stability:
Hygroscopic
InChIKey
LFFNIXQXRKNZCE-XYHGUWSSSA-N
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Safety

Hazard Codes 
T
Risk Statements 
61-20/21/22
Safety Statements 
53-22-36/37/39-45
WGK Germany 
3
RTECS 
EX8930000
HS Code 
2941901010
Toxicity
LD50 intravenous in mouse: 250mg/kg
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H360May damage fertility or the unborn child

Precautionary statements

P201Obtain special instructions before use.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P308+P313IF exposed or concerned: Get medical advice/attention.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
C4142
Product name
Capreomycin sulfate from Streptomyces capreolus
Packaging
1g
Price
$293
Updated
2024/03/01
Sigma-Aldrich
Product number
1091006
Product name
Capreomycin sulfate from Streptomyces capreolus
Packaging
250mg
Price
$447
Updated
2024/03/01
Alfa Aesar
Product number
J66684
Product name
Capreomycin sulfate
Purity
90%
Packaging
250mg
Price
$50.65
Updated
2024/03/01
Alfa Aesar
Product number
J66684
Product name
Capreomycin sulfate, 90%
Packaging
1g
Price
$130.65
Updated
2024/03/01
Cayman Chemical
Product number
19469
Product name
Capreomycin (sulfate)
Purity
≥700 IU/mg
Packaging
500mg
Price
$73
Updated
2024/03/01
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Capastat sulfate Chemical Properties,Usage,Production

Description

Capreomycin is a polypeptide antibiotic first isolated from S. capreolus. It is cytotoxic to M. tuberculosis (MIC = 10 μg/ml). Capreomycin is more effective against M. tuberculosis when combined with aminoglycoside antibiotics.

Originator

Capastat,Lilly,UK,1966

Uses

antibacterial, tuberculostatic

Uses

Capreomycin sulfate is a salt of a complex of cyclic pentopeptides isolated from Streptomyces capreolus, first reported in 1962. The sulfate salt is the most commonly accessible formulation of capreomycin and is used for pharmaceutical applications. The complex has two major components, IA and IB, with an exocyclic lysine residue, and two minor delysinyl components, IIA and IIB. Capreomycin is a potent antibiotic with activity against mycobateria, and Gram positive and negative organisms. Capreomycin acts by binding to the 23S ribosomal subunit, disrupting protein synthesis.

Uses

Thought to inhibit protein synthesis by inhibiting normal ribosomal functions

Manufacturing Process

A culture of NRRL 2773 is produced by growing the organism on a nutrient agar slant having the following composition:
Oatmeal-Tomato Paste Agar
Tomato paste 20Grams
Precooked oatmeal 20Grams
Agar 15Grams
Tap water, added to make a final volume of 1 liter.
The slant is inoculated with spores of NRRL 2773 and is incubated for 10 days at about 30°C. The culture growth on the slant is covered with 6 ml of nutrient broth, and the slant is scraped gently to remove the organisms to provide an aqueous suspension. Employing aseptic techniques, the inoculum obtained from one 1-inch agar slant is used to inoculate a 2-liter Erlenmeyer flask containing a 500-ml portion of a sterilized vegetative culture medium having the following composition: soluble starch, 10 g; peptones, 5 g; beef extract, 5 g; sodium chloride, 5 g; yeast extract, 2.5 g; and tap water, 1,100 ml. The incubation is carried on at 28°C for 48 hours with shaking at 250 cycles per minute on a rotary shaker having a 1-inch stroke.
To produce a larger quantity of vegetative inoculum, 500 ml of the vegetative inoculum is added aseptically to a stainless steel 350-gallon fermentation tank containing 250 gallons of sterile medium having the following composition (weight/volume): glucose, 1.5%; yeast, 1.5%; and antifoam (Polyglycol No. 2000, Dow Chemical Co.), 0.02%. The inoculum is allowed to grow for about 22 hours at a temperature of 30°C. Throughout the growth period, the medium is aerated with sterile air at the rate of 17 cfm and is agitated with two 16-inch impellers rotating at 160 revolutions per minute. To a 1,700- gallon stainless steel fermentor are added 1,100 gallons of a medium having the following composition (weight/volume):
Peptone No. 159 Medium
Glucose 2.5%
Molasses 1.0%
Peptones 4.0%
Calcium carbonate 0.2%
Hydrolyzed casein 0.6%
Antifoam (Polyglycol No. 2000, Dow Chemical Co.) 0.005
The medium after sterilization is inoculated with 100 gallons of the inoculum grown in the fermentation tank. The fermentation is carried on at 30°C for about five days. The foam is controlled by the addition, when needed, of Larex No. 1 (an antifoam product, Swift and Co.). Throughout the fermentation, the medium is aerated by the addition of sterile air at the rate of 96 cfm and is agitated with two 22-inch impellers operated at 140 revolutions per minute. At the end of the fermentation, 240 lb of Dicalite 476 (a perlite filter product, Great Lakes Carbon Corporation) are added to 1,000 gallons of the antibiotic broth, and the mixture is stirred and filtered. The filter cake is washed with tap water and the wash water and the filtrate are combined to provide a total volume of 1,000 gallons.
To 500 gallons of the combined liquids are added 132 lb of Darco G-60. The mixture is stirred thoroughly and filtered, and the filtrate is discarded, The carbon filter cake is washed with 200 liters of tap water, the wash water being discarded. The washed carbon cake on which the capreomycin is adsorbed is further washed with 200 liters of 0.05 N aqueous hydrochloric acid. The acid wash is discarded. The washed carbon cake is eluted during a one-hour period with 400 liters of an aqueous acetone mixture containing 1.65 liters of 11.7 N hydrochloric acid and 80 liters of acetone. The filter cake is further eluted by washing the cake with 200 liters of an aqueous acetone mixture containing 825 ml of 11.7 N hydrochloric acid and 40 liters of acetone during a 15- minute period. The combined eluates, having a total volume of 575 liters, are concentrated in vacuo to 52.5 liters.
The concentrate is added with stirring to 525 liters of acetone and the acetone mixture is permitted to stand overnight at room temperature, during which time an oily precipitate of capreomycin separates. The supernatant is decanted and discarded, and the oily precipitate which remains is dissolved in 20 liters of distilled water. The aqueous solution is concentrated in vacuo to 12 liters to remove any residual acetone. The aqueous concentrate containing capreomycin is filtered to remove a small amount of a precipitate, which is discarded.
The filtrate containing the capreomycin is added to 240 liters of methanol with stirring. The methanolic solution of capreomycin is acidified by the addition of one liter of 10 N sulfuric acid, whereupon the precipitation of the sulfuric acid addition salt of capreomycin commences. The mixture is permitted to stand overnight for more complete precipitation. The supernatant is removed by decanting and filtering. The precipitate, consisting of the capreomycin disulfate, is washed with 10 liters of methanol and is dried in vacuo. Yield: 2,510 grams.

brand name

Capastat Sulfate (Lilly).

Therapeutic Function

Antitubercular

General Description

Capreomycin was found as an antituberculotic antibiotic by Herr et al. of Eli Lilly & Co. in the culture broth of Streptomyces capreolus NRRL2773 in 1962. It shows no cross-resistance with streptomycin and is used against tuberculosis caused by streptomycinresistant Mycobacterium or for patients with adverse side effects caused by streptomycin.

Capastat sulfate Preparation Products And Raw materials

Raw materials

Preparation Products

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Capastat sulfate Suppliers

Hubei widely chemical technology Co., Ltd.
Tel
027-83991130 18627774460
Fax
027-83991130
Email
1718093273@QQ.COM
Country
China
ProdList
1891
Advantage
58
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
94838
Advantage
76
JinYan Chemicals(ShangHai) Co.,Ltd.
Tel
13817811078
Fax
86-021-50426522,50426273
Email
sales@jingyan-chemical.com
Country
China
ProdList
9984
Advantage
60
Adamas Reagent, Ltd.
Tel
400-6009262 16621234537
Fax
021-64823266
Email
zhangsn@titansci.com
Country
China
ProdList
14113
Advantage
59
BEST-REAGENT
Tel
400-1166-196 18981987031
Fax
028-84555506 800101999
Email
cdhxsj@163.com
Country
China
ProdList
11726
Advantage
57
Sinopharm Chemical Reagent Co,Ltd.
Tel
86-21-63210123
Fax
86-21-63290778 86-21-63218885
Email
sj_scrc@sinopharm.com
Country
China
ProdList
9823
Advantage
79
Wuhan Fortuna Chemical Co., Ltd
Tel
027-027-59207852 13308628970
Fax
QQ3130921841
Email
buy@fortunachem.com
Country
China
ProdList
2893
Advantage
58
Dalian Meilun Biotech Co., Ltd.
Tel
0411-62910999 13889544652
Email
sales@meilune.com
Country
China
ProdList
4647
Advantage
58
ShangHai YuanYe Biotechnology Co., Ltd.
Tel
021-61312847 13636370518
Fax
021-55068248
Email
shyysw007@163.com
Country
China
ProdList
4941
Advantage
60
AILY INTL CHEMICAL CORP LTD
Tel
025-83208295 18913388297
Fax
+86-2583208202
Country
China
ProdList
132
Advantage
50
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View Lastest Price from Capastat sulfate manufacturers

Shaanxi TNJONE Pharmaceutical Co., Ltd
Product
Capreomycin Sulfate 1405-37-4
Price
US $0.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
20tons
Release date
2024-04-29
Shaanxi Dideu Medichem Co. Ltd
Product
Capastat sulfate 1405-37-4
Price
US $1.00-1.00/KG
Min. Order
1g
Purity
99%
Supply Ability
50tons
Release date
2020-05-07
WUHAN FORTUNA CHEMICAL CO., LTD
Product
Capastat sulfate 1405-37-4
Price
US $0.00/Kg/Bag
Min. Order
5KG
Purity
≥700IU/mg; BP
Supply Ability
100KGS
Release date
2021-07-23

1405-37-4, Capastat sulfateRelated Search:


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  • BioChemical
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  • CAPASTAT
  • A - KAntibiotics
  • Antibacterial
  • Antibiotics A to
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