Maridomycin
| Code | Size | Price |
|---|
| TAR-T25778-5mg | 5mg | £850.00 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Special offer! Add £1 to your order to get a TargetMol CCK-8 Kit. Read more here. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Quantity:
Prices exclude any Taxes / VAT
Overview
Regulatory Status: RUO
Shipping:
cool pack
Storage:
-20℃
Documents
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.