C6374
Caerulomycin A
from Streptomyces caeruleus, ≥98% (HPLC)
别名:
Carulomycin A, Cerulomycin
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关于此项目
经验公式（希尔记法）:
C12H11N3O2
化学文摘社编号:
分子量:
229.23
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
51111800
MDL number:
InChI
1S/C12H11N3O2/c1-17-10-6-9(8-14-16)15-12(7-10)11-4-2-3-5-13-11/h2-8,16H,1H3/b14-8+
SMILES string
COc1cc(\C=N\O)nc(c1)-c2ccccn2
InChI key
JCTRJRHLGOKMCF-RIYZIHGNSA-N
biological source
Streptomyces caeruleus
assay
≥98% (HPLC)
form
powder
antibiotic activity spectrum
fungi
storage temp.
−20°C
Quality Level
Biochem/physiol Actions
Caerulomycins produced by Streptomyces caeruleus are bipyridinic molecules endowed with antibiotic properties. Caerulomycin A was found to have a strong anti-fungal and anti-amoebic activity, and a mild antibacterial activity.
Preparation Note
Caerulomycin A stock solution may be prepared in DMSO or methanol at 1 mg/mL. The stock solution can be further diluted in water to 0.1 mg/mL. Higher concentrations my requrie gentle heating to 40 °C. Dilutions from the stock solution should be freshly prepared.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
Tarek Sammakia et al.
Organic letters, 4(14), 2385-2388 (2002-07-06)
[reaction: see text] The total synthesis of caerulomycin C is described. Key steps in this synthesis utilize 1,2-, 1,3-, and 1,4-halogen dance reactions for the functionalization of the pyridine ring.
Qinheng Lin et al.
Wei sheng wu xue bao = Acta microbiologica Sinica, 51(8), 1032-1041 (2011-11-22)
In order to enable the caerulomyicn biosynthetic study by in vivo gene disruptions, it is crucial to develop a genetic modification system for the producer Actinoalloteichus sp. WH1-2216-6. The spore germination timing and the concentration of MgSO4 in the medium
D K Chatterjee et al.
Zeitschrift fur Parasitenkunde (Berlin, Germany), 70(5), 569-573 (1984-01-01)
The anti-amoebic action of the bipyridyl antibiotic caerulomycin was assessed in vitro and in vivo using various strains of Entamoeba histolytica from polyxenic, axenic and monoxenic cultures. Minimum inhibition concentrations of caerulomycin (metronidazole) were 7.5 (5), 15.6(1.95) and 60 (2.5)
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Instructions
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