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Spiramycin

Spiramycin Structure
CAS No.
8025-81-8
Chemical Name:
Spiramycin
Synonyms
LEUCOMYCIN;espiramicin;Spiramycine;Spiramycin Ep;KITASAMYCIN BASE;5337r.p.;r.p.5337;rovamycin;nsc-64393;provamycin
CBNumber:
CB0396400
Molecular Formula:
C43H74N2O14
Molecular Weight:
843.05
MOL File:
8025-81-8.mol
Modify Date:
2024/6/13 17:03:25

Spiramycin Properties

Melting point 126-128 °C
Boiling point 914℃
alpha D20 -80° (methanol)
refractive index 81 ° (C=2, 10% AcOH)
Flash point >110°(230°F)
storage temp. 2-8°C
solubility ethanol: 50 mg/mL, clear to slightly hazy, light-yellow
form powder
color white to light yellow
optical activity [α]/D -85 to -80° in water (Specific rotation (dry basis))
Water Solubility Soluble in methanol. Slightly soluble in water
Merck 14,8752
CAS DataBase Reference 8025-81-8

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H303
Precautionary statements  P270-P301+P312-P403-P501c
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36-24/25
WGK Germany  1
RTECS  WG9400000
10
HS Code  29419090
Toxicity LD50 in rats (mg/kg): 9400 orally; 1000 s.c.; 170 i.v. (Sous)
NFPA 704
0
2 0

Spiramycin price More Price(5)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) S9132 Spiramycin 8025-81-8 1G ₹8757.43 2022-06-14 Buy
Sigma-Aldrich(India) S9132 Spiramycin 8025-81-8 5G ₹26542.9 2022-06-14 Buy
Sigma-Aldrich(India) 46745 Spiramycin from Streptomyces sp. VETRANAL?, analytical standard, mixture of isomers 8025-81-8 100MG ₹5618.18 2022-06-14 Buy
TCI Chemicals (India) S0575 Spiramycin 8025-81-8 5G ₹7700 2022-05-26 Buy
TCI Chemicals (India) S0575 Spiramycin 8025-81-8 25G ₹9800 2022-05-26 Buy
Product number Packaging Price Buy
S9132 1G ₹8757.43 Buy
S9132 5G ₹26542.9 Buy
46745 100MG ₹5618.18 Buy
S0575 5G ₹7700 Buy
S0575 25G ₹9800 Buy

Spiramycin Chemical Properties,Uses,Production

Description

Spiramycin was found in the culture broth of Streptomyces ambofaciens by Rhone Poulenc in 1954 and its acetate was synthesized by Kyowa Hakko Kogyo Co. in 1965. This antibiotic consists of three closely related macrolide components, I, II, and III, whose ratio is 2 : 1 : 1. Spiramycin shows almost the same antimicrobial spectrum and activity as the other macrolides, but its acetate, acetylspiramycin, has much better pharmacokinetic properties and activity in vivo.

Chemical Properties

An antibiotic substance.

Uses

Spiramycin I (foromacidin A) is the major analogue of a complex of 16-membered macrocyclic lactones produced by S. ambofaciens and S. spiramyceticus that have broad spectrum antibiotic activity. Spiramycins are unusual among the macrocyclic lactones in that they contain two basic sugars. Spiramycin complex has been used in both human and animal health but its use has not been widespread.

Antimicrobial activity

Enterobacteriaceae are resistant. Spiramycin is also active against anaerobic species: Actinomyces israelii (MIC 2–4 mg/L), Cl. perfringens (MIC 2–8 mg/L) and Bacteroides spp. (MIC 4–14 mg/L). It is also active against Tox. gondii.

Hazard

Poison; moderately toxic; teratogen; muta- gen; can cause hypermotility, diarrhea, nausea, or vomiting.

Pharmaceutical Applications

A fermentation product of Streptomyces ambofaciens, composed of several closely related compounds. Spiramycin 1 is the major component (c. 63%); spiramycins 2 and 3 are the acetate and monopropionate esters, respectively. It is available for oral administration and as spiramycin adipate for intravenous infusion. Spiramycins are relatively stable in acid conditions. A derivative, acetylspiramycin, is available in Japan.

Pharmacokinetics

Oral absorption: Variable
Cmax 1 g oral: 2.8 mg/L after 2 h
Plasma half-life:4–8h
Volume of distribution :383 L
Plasma protein binding :15%
In healthy volunteers given 2 g orally followed by 1 g every 6 h, peak plasma levels were 1.0–6.7 mg/L. After 1 g orally the AUC was 10.8 mg.h/L, with an apparent elimination halflife of 2.8 h. It is widely distributed in the tissues. It does not reach the CSF. Levels 12 h after a dose of 1 g were 0.25 mg/L in serum, 5.3 mg/L in bone and 6.9 mg/L in pus. Levels of 10.6 mg/L have been found 4 h after dosing in saliva, and concentrations at least equal to those in the serum are seen in bronchial secretions. A concentration of 27 mg/g was found in prostate tissues after repeated dosage. Only 5–15% is recovered from the urine. Most is metabolized, but significant quantities are eliminated via the bile, in which concentrations up to 40 times those in the serum may be found.

Side effects

Spiramycin is generally well tolerated, the most common adverse reactions being gastrointestinal disturbances, notably abdominal pain, nausea and vomiting, rashes and sensitization following contact.

Spiramycin Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 363)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
CHEMSWORTH +91-261-2397244 New Delhi, India 6707 30 Inquiry
A.J Chemicals 91-9810153283 New Delhi, India 6124 58 Inquiry
TCI Chemicals (India) Pvt. Ltd. 1800 425 7889 New Delhi, India 6778 58 Inquiry
SynZeal Research Pvt Ltd +1 226-802-2078 Gujarat, India 6522 58 Inquiry
Triveni chemicals 08048762458 New Delhi, India 6093 58 Inquiry
Pharmaffiliates Analytics and Synthetics P. Ltd +91-172-5066494 Haryana, India 6773 58 Inquiry
Chandra Prabhu Pharma Services 08048372381Ext 506 Maharashtra, India 19 58 Inquiry
Harshada Corporation 08048372248Ext 946 Mumbai, India 3 58 Inquiry
Add Biotec 91-22-26731400 Maharashtra, India 49 58 Inquiry

Spiramycin Spectrum

SPIRAMYCIN rovamycin provamycin FORMACIDINE foromacidin sequamycin spiramycin from streptomyces sp. Spiramycin solution spiramycin standard solution Spiramyein SPIRAMYCIN VETRANAL, 100 MG SpiramycinBaseEp97 2-[12-[5-(4,5-Dihydroxy-4,6-dimethyl-oxan-2-yl)oxy-4-dimethylamino-3-hydroxy-6-methyl-oxan-2-yl]oxy-8-(5-dimethylamino-6-methyl-oxan-2-yl)oxy-14-hydroxy-13-methoxy-2,9-dimethyl-16-oxo-1-oxacyclohexadeca-4,6-dien-11-yl]acetaldehyde Pharmagrade Spiramycin,Formacidine SpiraMycin API SpiraMycin(SpiraMycin base) SpiraMycin 0.1 foromacidine 5337r.p. antibiotic799 nsc-64393 r.p.5337 rovamycine 2-[(4R,6S,7R,9R,10R,11E,13E,16R)-6-[[5-[(4,5-dihydroxy-4,6-dimethyl-2-oxanyl)oxy]-4-(dimethylamino)-3-hydroxy-6-methyl-2-oxanyl]oxy]-10-[[5-(dimethylamino)-6-methyl-2-oxanyl]oxy]-4-hydroxy-5-methoxy-9 Spiramycin Solution, 1000ppm Spiramycin, >=3900 IU/mg Spiramycin CRS Spiramycin> foromacidin spiramycin Spiramycin USP/EP/BP Spiramycin (S1100000) *Spiramycin*Q: What is *Spiramycin* Q: What is the CAS Number of *Spiramycin* Q: What is the storage condition of *Spiramycin* Q: What are the applications of *Spiramycin* 3-Dihydrobenzofuranyl-5-acetic acid LEUCOMYCIN KITASAMYCIN BASE Spiramycine espiramicin Spiramycin Ep High purity spiramycin Spiramycin/Spiramycin alkaloids Dopamine Impurity 60 8025-81-8 C40H67NO14 C43H74N2O14 BioChemical Antibiotics Antibiotics A to Z Antibiotics N-S Pharmaceutical intermediates Inhibitors Peptide Synthesis/Antibiotics Miscellaneous Natural Products Antibacterial Antibiotics for Research and Experimental Use Biochemistry Macrolides (Antibiotics for Research and Experimental Use) Macrolides