Cephalosporin C sodium salt
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
| Category | Antibiotics |
| Catalog number | BBF-04162 |
| CAS | 51762-04-0 |
| Molecular Weight | 437.40 |
| Molecular Formula | C16H20N3NaO8S |
Ordering Information
| Catalog Number | Size | Price | Stock | Quantity |
|---|---|---|---|---|
| BBF-04162 | 1 g | $298 | In stock |
Online Inquiry
Add to cartDescription
Cephalosporin C sodium salt is the salt form of cephalosporin C, which is an antibiotic isolated from fungi of the genus Acremonium.
Specification
| Related CAS | 61-24-5 (free acid) |
| Synonyms | Sodium cephalosporin C |
| Storage | Store at -20°C |
| IUPAC Name | sodium;(6R,7R)-3-(acetyloxymethyl)-7-[(5-amino-5-carboxypentanoyl)amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate |
| Canonical SMILES | CC(=O)OCC1=C(N2C(C(C2=O)NC(=O)CCCC(C(=O)O)N)SC1)C(=O)[O-].[Na+] |
| InChI | InChI=1S/C16H21N3O8S.Na/c1-7(20)27-5-8-6-28-14-11(13(22)19(14)12(8)16(25)26)18-10(21)4-2-3-9(17)15(23)24;/h9,11,14H,2-6,17H2,1H3,(H,18,21)(H,23,24)(H,25,26);/q;+1/p-1/t9?,11-,14-;/m1./s1 |
| InChI Key | HZWLVUKHUSRPCG-BJIHTTGYSA-M |
Properties
| Appearance | Solid |
| Antibiotic Activity Spectrum | Gram-positive bacteria |
Reference Reading
1.Use of alpha-aminoadipic acid for the biosynthesis of penicillin N and cephalosporin C by a Cephalosporium sp.
Warren SC, Newton GG, Abraham EP. Biochem J. 1967 Jun;103(3):891-901.
1. l-alpha-Amino[6-(14)C]adipic acid has been prepared from the dl-amino acid by oxidation of the l-isomer with l-amino acid oxidase to alpha-oxo[6-(14)C]adipic acid and by transamination of the latter with l-glutamic acid in an extract of a Cephalosporium sp. prepared by ultrasonic treatment of the mycelium. 2. The optical configuration of small amounts of (14)C-labelled alpha-aminoadipic acid from the mycelium of the Cephalosporium sp. has been determined by treatment with l-amino acid oxidase and measurement of the proportion of radioactivity subsequently retained on a column of a strong cation-exchange resin. 3. alpha-Aminoadipic acid which had been labelled in the mycelium from [1-(14)C]acetate appeared to contain more than 99% of the l-isomer. 4. l-alpha-Amino[(14)C]adipic acid (sodium salt) was taken up much more rapidly than the d-isomer, or alpha-oxo[6-(14)C]adipic acid, by suspensions of washed mycelium of the Cephalosporium sp.
Recommended Products
| BBF-05880 | N-Me-L-Ala-maytansinol | Inquiry |
| BBF-03755 | Actinomycin D | Inquiry |
| BBF-05886 | Notoginsenoside R1 | Inquiry |
| BBF-03428 | Tubermycin B | Inquiry |
| BBF-01829 | Deoxynojirimycin | Inquiry |
| BBF-01732 | Mevastatin | Inquiry |
Bio Calculators
* Our calculator is based on the following equation:
Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2
* Total Molecular Weight:
g/mol
Tip: Chemical formula is case sensitive. C22H30N4O √ c22h30n40 ╳
