Clinical data | |
---|---|
AHFS/Drugs.com | International Drug Names |
ATC code | |
Identifiers | |
| |
CAS Number | |
PubChem CID | |
ChemSpider | |
UNII | |
KEGG | |
CompTox Dashboard (EPA) | |
ECHA InfoCard | 100.047.784 |
Chemical and physical data | |
Formula | C41H67NO15 |
Molar mass | 813.979 g·mol−1 |
3D model (JSmol) | |
Melting point | 155 to 156 °C (311 to 313 °F) |
Solubility in water | Soluble in acidic/low pH water; Very soluble in methanol, chloroform, ethyl acetate, benzene, ethyl ether; Almost completely in ethanol(>95.5) mg/mL (20 °C) |
| |
| |
(verify) |
Midecamycin is a macrolide antibiotic[1] that is synthesized from Streptomyces mycarofaciens.[2]
YouTube Encyclopedic
-
1/4Views:13 8101 36368 27616 162
-
Dược lý học kháng sinh (phần 2): Macrolid, Lincosamid, Chloramphenicol, Streptogramin (nhóm MLSK)
-
Терапия воспалительных заболеваний глаз у детей
-
Học thuốc và dược lý nhanh (phần 1): Kháng sinh
-
Informasi Obat Cefixime Sirup Untuk mengatasi berbagai Infeksi Bakteri Pada Anak
Transcription
Physical Properties
Its melting point may vary depending on the compound type and the source consulted. For example, the Merck Index gives a melting point of 155-156 Celsius for the A1 type while the Japanese Pharmacopoeia reports 153-158 Celsius. The Merck Index also gives a melting point of 122-125 Celsius for the A3 type.[citation needed]
References
- ^ Salhi A, Vindel JA, Brunaud M, Berceaux G, Marin A, Wuatelet C (1977). "Properties of midecamycin, a new macrolide antibiotic". Giornale Italiano di Chemioterapia. 24 (1–2): 67–76. PMID 308022.
- ^ Wang YG, Hutchinson CR (1989). "Cloning of midecamycin biosynthetic genes from Streptomyces mycarofaciens 1748". Chinese Journal of Biotechnology. 5 (4): 191–201. PMID 2491329.