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Cefradine

Cefradine Structure
CAS No.
38821-53-3
Chemical Name:
Cefradine
Synonyms
CEPHRADINE;CEPHRADINE COMPACTED;Anspor;velosef;CEFRADIN;cephradin;Cefradine CRS;Cefro;Cefrag;sefril
CBNumber:
CB2341505
Molecular Formula:
C16H19N3O4S
Molecular Weight:
349.4
MOL File:
38821-53-3.mol
MSDS File:
SDS
Modify Date:
2024/4/3 17:07:09

Cefradine Properties

Melting point 140-142 C
Boiling point 898℃
Density 1.2794 (rough estimate)
refractive index 1.6320 (estimate)
Flash point >110°(230°F)
storage temp. Keep in dark place,Inert atmosphere,2-8°C
solubility 1 M NH4OH: soluble50mg/mL
pka 2.63, 7.27(at 25℃)
form powder
color White
Water Solubility Soluble in water
Stability Light Sensitive
CAS DataBase Reference 38821-53-3(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07,GHS08
Signal word  Danger
Hazard statements  H315-H317-H319-H334-H335
Precautionary statements  P280-P302+P352-P305+P351+P338
Hazard Codes  Xi,Xn
Risk Statements  36/37/38-42/43-20/21/22
Safety Statements  26-36-45-36/37-22
WGK Germany  1
RTECS  XI0336000
HS Code  29419054
NFPA 704
0
2 0

Cefradine price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) C8395 Cephradine ≥90.0% (Cephradine, HPLC) 38821-53-3 500MG ₹10446.13 2022-06-14 Buy
Sigma-Aldrich(India) C8395 Cephradine ≥90.0% (Cephradine, HPLC) 38821-53-3 1G ₹17514.85 2022-06-14 Buy
Sigma-Aldrich(India) C8395 Cephradine ≥90.0% (Cephradine, HPLC) 38821-53-3 5G ₹68619.68 2022-06-14 Buy
Product number Packaging Price Buy
C8395 500MG ₹10446.13 Buy
C8395 1G ₹17514.85 Buy
C8395 5G ₹68619.68 Buy

Cefradine Chemical Properties,Uses,Production

Description

Cefradine is an orally bioavailable β-lactam cephalosporin antibiotic. It is active against S. pyogenes, E. coli, K. pneumoniae, and E. cloacae (MICs = 0.04, 9.4, 9.4, and 6.3 μg/ml, respectively). Cefradine is also active against clinical isolates of S. aureus (MICs = 0.8-6 μg/ml) and S. pyogenes (MICs = 0.1-0.4 μg/ml), as well as H. influenzae, E. coli, and K. pneumoniae (MICs = 6.2-12.5 μg/ml). It increases survival in mouse models of systemic lethal infection by S. pyogenes, E. coli, K. pneumoniae, or E. cloacae (ED50s = 5, 37, 122, and 50 mg/kg, respectively), as well as by penicillin-susceptible or -resistant strains of S. aureus (ED50s = 18 and 91 mg/kg, respectively). Formulations containing cefradine have previously been used in the treatment of respiratory and urinary tract infections, skin infections, and otitis media.

Chemical Properties

Solid

Uses

Cephalosporin antibacterial.

Definition

ChEBI: A cephalosporin with a methyl substituent at position 3, and a (2R)-2-amino-2-cyclohexa-1,4-dien-1-ylacetamido substituent at position 7, of the cephem skeleton.

Application

Cephradine was synthesized by the Squibb Institute of Medical Research in 1971. It shows almost the same antibacterial activity and pharmacokinetic properties as cephalexin. Cephradine has been used for therapy of urinary and respiratory tract infections caused by Staphylococcus, Streptococcus, Escherichia coli, Klebsiella, and Proteus mirabilis.

Antimicrobial activity

Cephradine. A semisynthetic cephalosporin available in both oral and injectable forms. The antibacterial spectrum and susceptibility to β-lactamases are almost identical to those of cefalexin .
It is almost completely absorbed when given by mouth. A 500 mg oral dose achieves a concentration of about 18–20 mg/L after 1 h. The peak is delayed and reduced by food, but the half-life is not altered. Intramuscular administration of 1 g results a plasma concentration of 10–12 mg/L within 2 h. The plasma half-life is around 1 h and protein binding low.
Concentrations of up to 40% of those simultaneously found in the serum have been demonstrated in lung tissue. Penetration into the CSF is poor. Levels in sputum were about 20% of those simultaneously present in the plasma following a 1 g oral dose and similar levels have been found in bone. Breast milk concentrations approaching 1 mg/L have been found after 500 mg orally every 6 h and similar concentrations have been found in amniotic fluid. Cord blood concentration is said to be similar to that in the maternal blood.
It is excreted unchanged in the urine mostly in the first 6 h, achieving concentrations exceeding 1 g/L. Probenecid markedly increases the plasma concentration and delays the peak.
There is some biliary excretion. The parenteral forms may give rise to local pain or thrombophlebitis. Other side effects common to cephalosporins have been described. In some patients Candida vaginitis has been troublesome.
Clinical use is similar to that of cefalexin, but it has been largely superseded by later cephalosporins.

Clinical Use

Cephradine (Anspor, Velosef) is the only cephalosporinderivative available in both oral and parenteral dosageforms. It closely resembles cephalexin chemically (it maybe regarded as a partially hydrogenated derivative ofcephalexin) and has very similar antibacterial and pharmacokineticproperties.
It occurs as a crystalline hydrate that is readily soluble inwater. Cephradine is stable to acid and absorbed almostcompletely after oral administration. It is minimally proteinbound and excreted almost exclusively through the kidneys.It is recommended for the treatment of uncomplicated urinarytract and upper respiratory tract infections caused bysusceptible organisms. Cephradine is available in both oraland parenteral dosage forms.

Cefradine Preparation Products And Raw materials

Global( 635)Suppliers
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CHEMXTREE STANDARDS +919872732255 Punjab, India 96 58 Inquiry
OCEAN TRADING CORPORATION +91(22) 24921669 New Delhi, India 6211 58 Inquiry
Medilink Pharmachem +91 (79) 3007-0133 New Delhi, India 424 50 Inquiry
ORCHID PHARMA LIMITED +91–44–2744 4471/72/73/74/75/76/77/78 New Delhi, India 32 58 Inquiry
A.J Chemicals 91-9810153283 New Delhi, India 6124 58 Inquiry
CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
Pharmaffiliates Analytics and Synthetics P. Ltd +91-172-5066494 Haryana, India 6773 58 Inquiry
SynZeal Research Pvt Ltd +1 226-802-2078 Gujarat, India 6522 58 Inquiry
M/S JINDAL PHARMA 09779700777 Punjab, India 2 58 Inquiry
Planters International Company 09844020673 Karnataka, India 55 58 Inquiry
CEPHRADINE HYDRATE CEFRADINE sefril sq11436 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[(amino-1,4-cyclohexadien-1-ylacetyl)amino]-3-methyl-8-oxo-, [6R-[6α,7β(R*)]]- 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2R)-amino-1,4-cyclohexadien-1-ylacetyl]amino]-3-methyl-8-oxo-, (6R,7R)- 7-[D-a-Amino-(1,4-cyclohexadienyl)acetamide]-3-desacetoxycephalosphoranic acid Cefradex Cefrag Cefro Cesporan Dimacef Easkacef Ecosporina Lenzacef Lisacef Megacef Samedrin Velocef CEPHRADINE MICRONISED POWDER (6r-(6alpha,7))-((amino-1,4-cyclohexadien-1-ylacetyl)amino)-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid CEPHRADINE APPROX. 90% (HPLC) Cephradine (base and/or unspecified salts) Cefril Escacef Cephradine,Cefradin Cephradine Monohydrate CoMpacted/Powder Cefradine API 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylicacid, 7-[[(2R)-2-aMino-2-(1,4-cyclohexadien-1-yl)acetyl]aMino]-3-Methyl-8-oxo-,(6R,7R)- The setting of the Cephradine, >=90% Cefradine Impurity Soluble Cefradine (6R-(6alpha,7))-((Amino-1,4-cyclohexadien-1-ylacetyl)amino)-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic aci Cefradine IMP cephradine(compacted)cephradine(compacted) good quantity Cefradine Cefradine CAS # 38821-53-3 Cefradine Cefradine (6r-(6-alpha,7-beta(r*)))-ien-1-ylacetyl)amino)-3-methyl-8-oxo (6r-6alpha,7beta(r*)))-ien-1-ylacetyl)amino)-3-methyl-8-ox 5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylicacid,7-((amino-1,4-cyclohexad 7-[d-2-amino-2-(1,4-cyclohexadien-1-yl)acetamido]-3-methyl-8-oxo-5-thia-1-azab 7-[d-2-amino-2-(1,4-cyclohexadienyl)acetamide]desacetoxycephalosporanicacid eskacef icyclo[4.2.0]-oct-2-ene-2-caboxylicacid (6R,7R)-7-[[(2R)-2-amino-2-(1,4-cyclohexadien-1-yl)acetyl]amino]-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid CEPHRADINE Manufacturer 38821-53-3 For Antibiotic Cefradine(non-sterile) (6R,7R)-7-[[2-amino-2-(1-cyclohexa-1,4-dienyl)-1-oxoethyl]amino]-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid Cefradine for peak identification CRS Cephradine, Velosef (6R,7R)-7-((R)-2-Amino-2-(cyclohexa-1,4-dien-1-yl)acetamido)-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid CEPHRADINE ARGININE STERILE CEFRADINE (COMPACTED) Cefradine USP/EP/BP (6R,7R)-7-[[(2R)-Amino(cyclohexa-1,4-dienyl)acetyl]amino]-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid Cefradine (C0690000)