TargetMol

Maridomycin

Product Code:
 
TAR-T25778
Product Group:
 
Inhibitors and Activators
Supplier:
 
TargetMol
Regulatory Status:
 
RUO
Shipping:
 
cool pack
Storage:
 
-20℃
1 / 1
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CodeSizePrice
TAR-T25778-5mg5mg£850.00
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Further Information

Bioactivity:
Maridomycin is a macrolide antibiotic.
CAS:
35775-82-7
Formula:
C41H67NO15
Molecular Weight:
813.979
Purity:
0.98
SMILES:
CCC(=O)O[C@H]1[C@H](C)O[C@H](C[C@@]1(C)O)O[C@@H]1[C@@H](C)O[C@@H](O[C@H]2[C@@H](CC=O)C[C@@H](C)[C@@H](O)C=C[C@@H]3O[C@H]3C[C@@H](C)OC(=O)C[C@H]([C@@H]2OC)C(=O)CC)[C@H](O)[C@H]1N(C)C

References

1. Uyeda M, Mori S, Morita M, Ogata T, Mori M, Shibata M. Microbial transformation of antibiotics. III. Reacylation of 4"-depropionyl maridomycin III into maridomycin V (maridomycin K) by Streptomyces sp. strain no. K-342. J Antibiot (Tokyo). 1977 Dec;30(12):1130-1. PubMed PMID: 599088. 2. Harada S, Muroi M, Kondo M, Tsuchiya K, Matsuzawa T. Chemical modification of maridomycin, a new macrolide antibiotic. Antimicrob Agents Chemother. 1973 Aug;4(2):140-8. PubMed PMID: 4790934; PubMed Central PMCID: PMC444519. 3. Nakahama K, Izawa M, Muroi M, Kishi T, Uchida M. Microbial conversion of antibiotics. I. Deacylation of maridomycin by bacteria. J Antibiot (Tokyo). 1974 Jun;27(6):425-32. PubMed PMID: 4212166. 4. Muroi M, Izawa M, Ono H, Higashide E, Kishi T. Isolation of maridomycins and structure of maridomycin II. Experientia. 1972 May 15;28(5):501-2. PubMed PMID: 5040787.