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Roxithromycin

CAS No.
80214-83-1
Chemical Name:
Roxithromycin
Synonyms
Roxid;Rulid;Roxithromycin Solution, 100ppm;Brilid;Overal;RU 965;Surlid;Assoral;Forilin;biaxsig
CBNumber:
CB1707342
Molecular Formula:
C41H76N2O15
Molecular Weight:
837.05
MDL Number:
MFCD00214389
MOL File:
80214-83-1.mol
MSDS File:
SDS
Last updated:2024-11-20 11:41:24

Roxithromycin Properties

Melting point 111-118?C
alpha D25 -77.5 ±2° (c = 0.45 in chloroform)
Boiling point 864.7±75.0 °C(Predicted)
Density 1.25±0.1 g/cm3(Predicted)
Flash point >110°(230°F)
storage temp. Sealed in dry,2-8°C
solubility chloroform: soluble10mg/mL
pka pKa 9.27±0.01(H2O t = 25.0 I = 0.15 (KCl)) (Uncertain)
form powder
color White to off-white
Water Solubility Soluble in water to 18µg/ml
Merck 14,8276
InChIKey RXZBMPWDPOLZGW-HEWSMUCTSA-N
CAS DataBase Reference 80214-83-1
FDA UNII 21KOF230FA
ATC code J01FA06
EPA Substance Registry System Erythromycin, 9-[O-[(2-methoxyethoxy)methyl]oxime], (9E)- (80214-83-1)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P264-P270-P301+P312-P501
Hazard Codes  Xn
Risk Statements  22
Safety Statements  26-24/25
WGK Germany  3
RTECS  KF4990000
HS Code  29415000
NFPA 704
0
1 0

Roxithromycin price More Price(21)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich R4393 Roxithromycin ≥90% (HPLC) 80214-83-1 1g $43.8 2023-01-07 Buy
Sigma-Aldrich R4393 Roxithromycin ≥90% (HPLC) 80214-83-1 10g $182 2023-01-07 Buy
Alfa Aesar J66213 Roxithromycin, 97% 80214-83-1 5g $98 2024-03-01 Buy
Alfa Aesar J66213 Roxithromycin, 97% 80214-83-1 10g $165 2024-03-01 Buy
Cayman Chemical 19465 Roxithromycin ≥95% 80214-83-1 1g $33 2024-03-01 Buy
Product number Packaging Price Buy
R4393 1g $43.8 Buy
R4393 10g $182 Buy
J66213 5g $98 Buy
J66213 10g $165 Buy
19465 1g $33 Buy

Roxithromycin Chemical Properties,Uses,Production

Pharmacological effects

Roxithromycin is a semi-synthetic 14-membered ring macrolide antibiotic. It has similar mechanism of action as erythromycin with its antibacterial effect in vivo being 1-4 times stronger than erythromycin. Its effect against Gram-positive bacteria is slightly worse than erythromycin; the effect against Legionella pneumophila is somehow stronger than erythromycin; for Chlamydia pneumoniae, Mycoplasma pneumoniae and Ureaplasma urealyticum, it has similar or slightly stronger antimicrobial effect compared with erythromycin.
This product can penetrate through the bacterial cell membrane, having reversible binding to bacterial ribosomes 50S subunit at close to the donor ("P" position), blocking the transfer of ribonucleic acid binding to the "P" position as well as blocking the transfer of the peptide chain from the acceptor position ("A" position) to "P" position, thus leading to the inhibition of bacterial protein synthesis and playing an antibacterial effect. It is characterized by faster access to macrophages, alveolar cells and neutrophils. In vitro studies have shown that roxithromycin has broad antibacterial spectrum with similar effect as erythromycin against a variety of Streptococcus (including A, B, C-type streptococcus and Streptococcus pneumoniae, but except G-type and enterococci), Streptococcus pneumoniae, Staphylococcus aureus, Staphylococcus aureus (except MRSA), Staphylococcus epidermidis, Legionella pneumophila, Haemophilus ducreyi, Chlamydia trachomatis, Mycoplasma pneumoniae and oral or vaginal anaerobic bacteria. Neisseria catarrhalis is highly sensitive to roxithromycin. It also has inhibitory effects on Campylobacter, Bordetella pertussis, Haemophilus influenzae, Mycobacterium tuberculosis and Diphtheria bacilli but has no antibacterial activity against other gram-negative bacteria. The in vivo antibacterial activity of this product was significantly stronger than that of erythromycin. It also has significant effect against chlamydia, mycoplasma, ureaplasma urealyticum, Treponema pallidum and Legionella infection. It also has relatively weak effect on the helicobacter, Neisseria gonorrhoeae, meningococcal and Bordetella pertussis. Some bacteria have cross-resistance to erythromycin and this product.

Indications

This product is applicable to the purulent Streptococcus caused pharyngitis and tonsillitis, susceptible bacteria-caused sinusitis, otitis media, acute bronchitis, acute exacerbation of chronic bronchitis, Mycoplasma pneumoniae or Chlamydia pneumoniae caused pneumonia; Chlamydia trachomatis caused urinary reproductive system infections (urethritis and cervicitis); sensitive bacteria caused infection of skin soft tissue and other parts of the body; it can also used for non-specific and gonococcal genital infection, Legionella caused infection and Pediatric Infections.
Roxithromycin is characterized by acid resistance and excellent oral absorption with T1/2 being 12 to 14 hours which is 6 times higher than erythromycin. It has wide distribution in the body and is able to reach high concentration in both the upper and lower respiratory tract, reproductive tract and skin and maintain for a long time. Most of the metabolism occurs in vivo.
Roxithromycin clinical evaluation: the curing rate of chlamydia urethritis, cervicitis clinical and bacteriological was 93% to 97%; the efficacy against genital infection is similar to doxycycline; the cure rate for skin infection is 90% or more; the effectiveness for the treatment of respiratory infections is 83% and 50% while the effectiveness for the treatment of pneumonia and dental infections are 79% and 85%.

Chemical properties

It appears as White crystalline powder, odorless, bitter taste. It is easily soluble in ethanol or acetone, more easily soluble in methanol or ether but almost do not dissolve in water. [Α] D23-77.5 ° ± 2 ° (c = 0.45, chloroform).

Uses

1.  It belongs to macrolide antibiotics, being a kind of erythromycin derivative with the antibacterial spectrum being similar as erythromycin but having a 6 times stronger effect on erythromycin with high bioavailability. It is used for the treatment of respiratory tract infection, such as pneumonia, acute bronchitis, acute infection of chronic bronchitis, atypical pneumonia, and genitourinary system infection, skin and soft tissue infections, having good therapeutic effect and tolerance with smaller adverse reactions than erythromycin.
2.  As the new generation of macrolide antibiotics;
3.  The product belongs to a new generation of macrolide antibiotics, mainly used for Gram-positive bacteria, anaerobes, chlamydia and mycoplasma. Its antibacterial activity in vitro is similar as erythromycin with its in vivo effect being 1-4 times stronger than erythromycin. Pharmacological effects and indications 1, it has strong bactericidal effect on Gram-negative bacteria and some Gram-negative bacteria (meningococcus, Neisseria gonorrhoeae, influenza bacilli, pertussis, Brucella) and spirochetes, Mycoplasma pneumoniae and Rickettsia. Legionella is sensitive to it; its effect against mycoplasma and chlamydia is further enhanced.
4.  2, antibacterial mechanism: it can bind to the bacterial ribosome 50S subunit, through blocking the peptidyl transfer and MRNA displacement, further inhibiting the protein synthesis. 3, this product has excellent oral absorption and quick efficacy with stronger bioavailability and plasma concentrations than erythromycin. According to reports, oral administration of 150 mg can lead to a peak plasma concentration of up to 6.6~7.9 ug/ml while the value for erythromycin under the same conditions is only 0.2~0.4ug/ml; roxithromycin is mainly distributed in body fluids and tissues, with high and durable tissue concentration and cell concentration. Moreover, it has a half-life of up to 12 h while the value for erythromycin is only 1.5~2.0h. 4, in clinical medicine, it is the first-choice drug for the treatment of drug-resistance Staphylococcus aureus and hemolytic streptococcus. In veterinary clinical practice, it is used for the treatment of penicillin-resistant staphylococcus aureus caused severe infection, pneumonia, uterine inflammation and poultry chronic respiratory disease. 5, the goods are mainly used for the treatment of livestock and poultry chronic respiratory disease with good efficacy in the treatment of livestock and poultry staphylococcus and streptococcal disease, chlamydia, spirocheal disease (swine dysentery), infectious pleurisy and rhinitis. 6, indications: avian neck swelling, local heat, pain, difficulty breathing, mouth and nose flow white foam, mucous membranes and skin cyanosis and other symptoms.

Production method

Take erythromycin as raw materials for reaction with hydroxylamine hydrochloride in triethylamine and methanol, generating oxime, followed by reaction with methoxy ethoxymethyl chloride in acetone to derive roxithromycin.

Description

Roxithromycin, an oxime ether derivative of erythromycin, is a new macrolide antibiotic of high potency and long duration. Its in v i m activity spectrum is similar to that of erythromycin, but is superior to the latter against Legionella, Mycoplasma and Chlamydia.

Chemical Properties

White Solid

Originator

Roussel (France)

Uses

anesthetic (local)

Uses

Semisynthetic erythromycin derivative. Antibacterial

Uses

Roxithromycin was one of the new generation erythromycins introduced in the 1980s. Improved acid stability was achieved by converting the 9-keto group to the more stable oxime and alkylation of the oxime to provide the methoxyethoxymethyl ether oxime. In vivo, roxithromycin exhibits higher tissue levels and a longer half-life while being slightly less potent than erythromycin in vitro.

Definition

ChEBI: Roxithromycin is semisynthetic derivative of erythromycin A. It has a role as an antibacterial drug. It is an erythromycin derivative, a macrolide and a semisynthetic derivative. It is functionally related to an erythromycin A.

brand name

Rulide (Hoechst-Roussel).

Antimicrobial activity

Activity against common pathogens is comparable to that of erythromycin. It is active against L. monocytogenes, C. jejuni, H. ducreyi, G. vaginalis, Bord. pertussis, C. diphtheriae, B. burgdorferi, H. pylori, the M. avium complex, Chlamydia spp., and U. urealyticum.

Pharmaceutical Applications

A semisynthetic derivative of erythromycin A formulated for oral use.

Pharmacokinetics

Oral absorption:50–55%
Cmax 150 mg oral : 7.9 mg/L after 1.9 h
300 mg oral :10.8 mg/L after 1.5 h
Plasma half-life :10.5–11.9 h
Plasma protein binding :c. 90%
absorption and metabolism
Absorption is not affected by food. Oral administration with antacids or H2-receptor antagonists does not significantly affect bioavailability. In a direct comparison, the area under the time–concentration curve (AUC) produced by a 150 mg dose was 16 times greater than that produced by 250 mg erythromycin A. Behavior in children is broadly similar to that in adults, repeated doses of 2.5 mg/kg producing age-independent mean peak plasma concentrations around 10 mg/L at 1–2 h, but the apparent elimination half-life was longer (approximately 20 h).
It is saturably bound to α-acid glycoprotein in plasma. The plasma clearance appears to be dose dependent or plasma concentration dependent.
DistributionIt is widely distributed, but does not reach the CSF. Concentrations close to the simultaneous serum level have been found in tonsillar, lung, prostatic and other tissues. It achieves high levels in skin.
Distribution
It is widely distributed, but does not reach the CSF. Concentrations close to the simultaneous serum level have been found in tonsillar, lung, prostatic and other tissues. It achieves high levels in skin.
Metabolism and excretion
Less than 5% of the administered dose is eliminated as degradation products. Rather more than half the dose appears in the feces and only 7–10% (including metabolites) in the urine: up to 15% is eliminated via the lungs. Renal clearance increased in volunteers as the dose was raised from 150 to 450 mg, and is decreased in elderly subjects. In patients in whom the creatinine clearance was <10 mL/min, the apparent elimination half-life rose to around 15.5 h and total body clearance was significantly reduced. The apparent elimination half-life was somewhat increased in patients with hepatic cirrhosis.

Side effects

It is generally well tolerated, adverse effects being described in 3–4% of patients, mostly gastrointestinal disturbance (abdominal pain, nausea and diarrhea). Headache, weakness, dizziness, rash and reversible changes in liver function tests and increased eosinophils and platelets have also been described.

3970-21-6
13127-18-9
80214-83-1
Synthesis of Roxithromycin from 2-Methoxyethoxymethyl chloride and ERYTHROMYCIN OXIME

Roxithromycin Preparation Products And Raw materials

Global( 585)Suppliers
Supplier Tel Email Country ProdList Advantage
Hebei Weibang Biotechnology Co., Ltd
+8615531157085 abby@weibangbio.com China 8810 58
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+86-13131129325 sales1@chuanghaibio.com China 5892 58
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+8618092446649 sarah@tnjone.com China 1143 58
Henan Suikang Pharmaceutical Co.,Ltd.
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+8615858145714 FandaChem@Gmail.com China 9206 55
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+undefined-21-51877795 ivan@atkchemical.com China 32957 60
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18017610038 zheyansh@163.com CHINA 3619 58
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View Lastest Price from Roxithromycin manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Roxithromycin pictures 2024-11-28 Roxithromycin
80214-83-1
US $0.00-0.00 / kg 1kg 99% 20tons Sinoway Industrial co., ltd.
Roxithromycin pictures 2024-11-28 Roxithromycin
80214-83-1
US $0.00 / kg 25kg 99% 1tons Henan Suikang Pharmaceutical Co.,Ltd.
Roxithromycin pictures 2024-11-27 Roxithromycin
80214-83-1
US $0.00 / Kg/Drum 25KG 96.0%~102.0%; EP9.0/CP2015 10tons/month WUHAN FORTUNA CHEMICAL CO., LTD
  • Roxithromycin pictures
  • Roxithromycin
    80214-83-1
  • US $0.00-0.00 / kg
  • 99%
  • Sinoway Industrial co., ltd.
  • Roxithromycin pictures
  • Roxithromycin
    80214-83-1
  • US $0.00 / kg
  • 99%
  • Henan Suikang Pharmaceutical Co.,Ltd.
  • Roxithromycin pictures
  • Roxithromycin
    80214-83-1
  • US $0.00 / Kg/Drum
  • 96.0%~102.0%; EP9.0/CP2015
  • WUHAN FORTUNA CHEMICAL CO., LTD

Roxithromycin Spectrum

ROXITHROMYCIN Roxithromycin CP2000 ERYTHROMYCIN 9-(-O-[2-METHOXYETHOXY]METHYLOXIME) ERYTHROMYCIN, 9-[O-[(2-METHOXYETHOXY)METHYL]OXIME], (9E)- Roxithromycin EP RoxithromycinEp/Bp/CpC41H76N2O15 RoxithromycinC41H76N2O15 (9E)-9-[O-[(2-Methoxyethoxy)methyl]oxime] Erythromycin Assoral Roxl-150 Roxithromycin (Roxl-150) 10% water-soluble roxithromycin Roxithromycin solution,1000ppm ROM erythromycin(Water soluble) 70% water-soluble roxithromycin Brilid Claramid Forilin Overal Rossitrol Rotramin Roxeptin Roxithromycin A RU 28965 RU 965 Surlid biaxsig ROXITHROMYCIN,BP,EP Erythromycin, 9-[O-[(2-methoxyethoxy)methyl]oxime], (9E)- (9CI) 5-(3,4,6-Trideoxy-3-dimethylamino-beta-D-xylo-hexopyranosyloxy)-3-(2,6-dideoxy-3-C-methyl-3-O-methyl-alpha-L-ribo-hexopyranosyloxy)-6,11,12-trihydroxy-9-(2-methoxyethoxy)methoxyimino-2,4,6,8,10,12-hexamethylpentadecan-13-olide water-soluble roxithromycin70% aaram.D.Forilin 9-[O-(2-Methoxyethoxy)methyloxime]erythromycin 9-Deoxo-9-[(2-methoxyethoxy)methoxyimino]erythromycin 9-Deoxo-9-[[(2-methoxyethoxy)methyl]oxyimino]erythromycin Roxithromycin,Erythromycin 9-(-O-[2-methoxyethoxy]methyloxime) (3R,4S,5S,6R,7R,9R,11S,12R,13S,14R)-6-{[(2S,3R,4S,6R)-4-(diMethylaMino)-3-hydroxy-6-Methyloxan-2-yl]oxy}-14-ethyl-7,12,13-trihydroxy-4-{[(2R,4R,5S,6S)-5-hydroxy-4-Methoxy-4,6-diMethyloxan-2-yl]oxy}-3,5,7,9,11,13-hexaMethyl-10-(2,4,7-trioxa-1-azaoctan-1-yl RoxithroMycin API Roxithromycin id (3R,4S,5S,6R,7R,9R,10E,11S,12R,13S,14R)-6-[[4-(dimethylamino)-3-hydroxy-6-methyl-2-oxanyl]oxy]-14-ethyl-7,12,13-trihydroxy-4-[(5-hydroxy-4-methoxy-4,6-dimethyl-2-oxanyl)oxy]-10-(2-methoxyethoxymethoxy (E)-roxithromycin Roxithromycin CRS Roxithromycin for system suitability CRS (3R,4S,5S,6R,7R,9R,11S,12R,13S,14R,E)-6-(((2S,3R,4S,6R)-4-(Dimethylamino)-3-hydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-14-ethyl-7,12,13-trihydroxy-4-(((2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyltetrahydro-2H-pyran-2-yl)oxy)-10-(((2-methoxyethoxy)methoxy)imino)-3,5,7,9,11,13-hexamethyloxacyclotetradecan-2-one Roxithromycin USP/EP/BP Roxithromycin (1.0 mg/mL in Methanol) (3R,4S,5S,6R,7R,9R,11S,12R,13S,14R,E)-6-(((2S,3R,4S,6R)-4-(Dimethylamino)-3-hydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-14-ethyl-7,12,13-trihydroxy-4-(((2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyltetrahydro-2H-pyran-2-yl)oxy)-10-(((2-methoxyethoxy)met Roxithromycin-13CD3 RoxithromycinQ: What is Roxithromycin Q: What is the CAS Number of Roxithromycin Q: What is the storage condition of Roxithromycin Q: What are the applications of Roxithromycin Roxithromycin Solution, 100ppm Roxid Rulid Oxithromycin Roxithromycin in Methanol C16860000 Roxithromycin Roxithromycin 100 μg/ml Methanol 80214-83-1 80241-83-1