Carbazomycinal
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| Category | Others |
| Catalog number | BBF-00484 |
| CAS | 103744-20-3 |
| Molecular Weight | 255.27 |
| Molecular Formula | C15H13NO3 |
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Description
It is produced by the strain of Streptoverticillum sp. KCC U-0166. It can inhibit the formation of aerial hyphae.
Specification
| Synonyms | Carbazomycin E; SCHEMBL16432825; 9H-Carbazole-1-carboxaldehyde,4-hydroxy-3-methoxy-2-methyl |
| IUPAC Name | 4-hydroxy-3-methoxy-2-methyl-9H-carbazole-1-carbaldehyde |
| Canonical SMILES | CC1=C(C2=C(C3=CC=CC=C3N2)C(=C1OC)O)C=O |
| InChI | InChI=1S/C15H13NO3/c1-8-10(7-17)13-12(14(18)15(8)19-2)9-5-3-4-6-11(9)16-13/h3-7,16,18H,1-2H3 |
| InChI Key | BEJNHSBULWLOJS-UHFFFAOYSA-N |
Properties
| Appearance | Light Yellow Crystal |
| Boiling Point | 512.6 °C at 760 mmHg |
| Melting Point | 224 °C |
| Density | 1.369 g/cm3 |
| Solubility | Soluble in Methanol |
Reference Reading
1. Carbazomycins C, D, E and F, minor components of the carbazomycin complex
T Naid, T Kitahara, M Kaneda, S Nakamura J Antibiot (Tokyo). 1987 Feb;40(2):157-64. doi: 10.7164/antibiotics.40.157.
Carbazomycins C (III), D (IV), E (V) and F (VI), the minor components of the carbazomycin complex, were isolated from the cultured broth of Streptoverticillium ehimense together with carbazomycins A (II) and B (I). Among them, III and IV were shown to be new substances and their structures were elucidated as 4-hydroxy-3,6-dimethoxy-1,2-dimethylcarbazole and 3,4,6-trimethoxy-12-dimethylcarbazole, respectively, by spectroscopic and chemical means. The other components, V and VI, were found to contain an aldehyde function and were identified as carbazomycinal and 6-methoxycarbazomycinal, respectively. The antimicrobial activity of III and IV are also reported.
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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 ╳
