Rancinamycin III
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Category | Antibiotics |
Catalog number | BBF-02176 |
CAS | 60925-60-2 |
Molecular Weight | 174.15 |
Molecular Formula | C7H10O5 |
Purity | >97% |
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Description
Rancinamycin III is an antibiotic that has antibacterial properties originally isolated from Str. lincolnensis.
Specification
Synonyms | SCHEMBL16431322 |
IUPAC Name | 3,4,5,6-tetrahydroxycyclohexene-1-carbaldehyde |
Canonical SMILES | C1=C(C(C(C(C1O)O)O)O)C=O |
InChI | InChI=1S/C7H10O5/c8-2-3-1-4(9)6(11)7(12)5(3)10/h1-2,4-7,9-12H |
InChI Key | KQQCGAKRCKYICB-UHFFFAOYSA-N |
Reference Reading
1. Rancinamycins I, II, III and IV structural studies
A D Argoudelis, R W Sprague, S A Mizsak J Antibiot (Tokyo). 1976 Aug;29(8):787-96. doi: 10.7164/antibiotics.29.787.
Rancinamycins are secondary metabolites produced by Streptomyces lincolnensis in a sulfur-depleted culture medium. The structures (except stereochemistry) of the main components of the rancinamycin-complex were determined by the use of IR, UV, PMR, and CMR spectra.
2. Rancinamycins, metabolites produced by Streptomyces lincolnensis in sulfur-depleted media
A D Argoudelis, T R Pyke, R W Sprague J Antibiot (Tokyo). 1976 Aug;29(8):777-86. doi: 10.7164/antibiotics.29.777.
Rancinamycins I, II, III, and IV are secondary metabolites produced by Streptomyces lincolnensis in a sulfur-depleted culture medium. Rancinamycins I, and II, the main components of the mixture, show broad spectrum antibiotic activity in vitro. Subcutaneously injected or orally administered antibiotic afforded no protection for experimentally infected mice against lethal challenges of Staphylococcus aureus. Radioactive tracer studies failed to demonstrate that the rancinamycin were precursors in the biosynthesis of lincomycin.
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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 ╳