MedKoo Cat#: 584789 | Name: Minimycin

Description:

WARNING: This product is for research use only, not for human or veterinary use.

Minimycin is a nucleoside antibiotic.

Chemical Structure

Minimycin
Minimycin
CAS#32388-21-9

Theoretical Analysis

MedKoo Cat#: 584789

Name: Minimycin

CAS#: 32388-21-9

Chemical Formula: C9H11NO7

Exact Mass: 245.0536

Molecular Weight: 245.19

Elemental Analysis: C, 44.09; H, 4.52; N, 5.71; O, 45.68

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
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Related CAS #
No Data
Synonym
Minimycin
IUPAC/Chemical Name
2H-1,3-Oxazine-2,4(3H)-dione, 5-beta-D-ribofuranosyl-
InChi Key
REFHNSOTFKKRAI-GBNDHIKLSA-N
InChi Code
InChI=1S/C9H11NO7/c11-1-4-5(12)6(13)7(17-4)3-2-16-9(15)10-8(3)14/h2,4-7,11-13H,1H2,(H,10,14,15)/t4-,5-,6-,7+/m1/s1
SMILES Code
O=C(N1)OC=C([C@H]2[C@@H]([C@@H]([C@@H](CO)O2)O)O)C1=O
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>3 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 245.19 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1: Isono K, Suhadolnik RJ. Biosynthesis of the C-nucleoside, minimycin: asymmetric incorporation of glutamate and acetate into the oxazine ring. J Antibiot (Tokyo). 1977 Mar;30(3):272-3. PubMed PMID: 863787. 2: Kusakabe Y, Nagatsu J, Shibuya M, Kawaguchi O, Hirose C. Minimycin, a new antibiotic. J Antibiot (Tokyo). 1972 Jan;25(1):44-7. PubMed PMID: 5010645. 3: Isono K, Uzawa J. 13C-NMR evidence for the biosynthetic incorporation of acetate into minimycin and compounds related to Krebs cycle. FEBS Lett. 1977 Aug 1;80(1):53-6. PubMed PMID: 891969. 4: Isono K, Suhadolnik RJ. The biosynthesis of the nucleoside antibiotics: minimycin formation by Streptomyces hygroscopicus. Ann N Y Acad Sci. 1975 Aug 8;255:390-401. PubMed PMID: 1059367. 5: Sasaki K, Kusakabe Y, Esumi S. The structure of minimycin, a novel carbon-linked nucleoside antibiotic related to -pseudouridine. J Antibiot (Tokyo). 1972 Mar;25(3):151-4. PubMed PMID: 5034811. 6: De Bernardo S, Weigele M. Synthesis of oxazinomycin (minimycin). J Org Chem. 1977 Jan 7;42(1):109-12. PubMed PMID: 830847. 7: Walker MG, Blum R, Fagan LM. Minimycin: a miniature rule-based system. MD Comput. 1985 Jul-Aug;2(4):21-7, 46. PubMed PMID: 3916115. 8: Tymiak AA, Culver CA, Goodman JF, Seiner VS, Sykes RB. Oxazinomycin produced by a Pseudomonas species. J Antibiot (Tokyo). 1984 Apr;37(4):416-8. PubMed PMID: 6725147. 9: Buchanan JG. The C-nucleoside antibiotics. Fortschr Chem Org Naturst. 1983;44:243-99. Review. PubMed PMID: 6360831. 10: Kitani S, Kinoshita H, Nihira T, Yamada Y. In vitro analysis of the butyrolactone autoregulator receptor protein (FarA) of Streptomyces lavendulae FRI-5 reveals that FarA acts as a DNA-binding transcriptional regulator that controls its own synthesis. J Bacteriol. 1999 Aug;181(16):5081-4. PubMed PMID: 10438782; PubMed Central PMCID: PMC93999. 11: Srivastava PC, Robins RK. Synthesis and biological activity of certain derivatives of oxazinomycin and related oxadiazole nucleosides. J Med Chem. 1981 Oct;24(10):1172-7. PubMed PMID: 6276541. 12: Viti C, Pace A, Giovannetti L. Characterization of Cr(VI)-resistant bacteria isolated from chromium-contaminated soil by tannery activity. Curr Microbiol. 2003 Jan;46(1):1-5. PubMed PMID: 12432455. 13: Ruengjitchatchawalya M, Nihira T, Yamada Y. Purification and characterization of the IM-2-binding protein from Streptomyces sp. strain FRI-5. J Bacteriol. 1995 Feb;177(3):551-7. PubMed PMID: 7836286; PubMed Central PMCID: PMC176627.