Azirinomycin
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| Category | Others |
| Catalog number | BBF-00244 |
| CAS | 31772-89-1 |
| Molecular Weight | 99.09 |
| Molecular Formula | C4H5NO2 |
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Description
Azirinomycin is produced by the strain of Streptomyces aureus. It has anti-gram positive and negative bacterial activity.
Specification
| Synonyms | 3-Methyl-2H-azirine-2-carboxylic acid; 2H-AZIRINE-2-CARBOXYLIC ACID, 3-METHYL- |
| IUPAC Name | 3-methyl-2H-azirine-2-carboxylic acid |
| Canonical SMILES | CC1=NC1C(=O)O |
| InChI | InChI=1S/C4H5NO2/c1-2-3(5-2)4(6)7/h3H,1H3,(H,6,7) |
| InChI Key | NHCHAEIJXKFNRU-UHFFFAOYSA-N |
Properties
| Appearance | Dull Yellow Oil |
| Antibiotic Activity Spectrum | gram-positive bacterial; gram-negative bacteria |
Reference Reading
1. [Asymmetric syntheses of azacycloalkanes by one-pot [1+2+n] cyclization]
Shingo Harada Yakugaku Zasshi. 2013;133(9):975-82. doi: 10.1248/yakushi.13-00157.
Enantio- and diastereoselective one-pot synthesis of three- to seven-membered cis-azaheterocycles was achieved using a triggered asymmetric conjugate addition reaction of lithium amide with an enoate, followed by C- and N-alkylation of the resulting lithium 3-aminoenolate with α, ω-dihaloalkane, which can be regarded as a [1+2+n] cyclization. The usefulness of the developed methodology was clearly demonstrated by the short-step asymmetric syntheses of azirinomycin ester, nemonapride, and kopsinine.
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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 ╳
