MedKoo Cat#: 592809 | Name: Amicetin B

Description:

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

Amicetin B is a new amicetin-like antibiotic.

Chemical Structure

Amicetin B
Amicetin B
CAS# 43043-15-8

Theoretical Analysis

MedKoo Cat#: 592809

Name: Amicetin B

CAS#: 43043-15-8

Chemical Formula: C25H35N5O7

Exact Mass: 517.2536

Molecular Weight: 517.58

Elemental Analysis: C, 58.01; H, 6.82; N, 13.53; O, 21.64

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.
Bulk Inquiry
Related CAS #
No Data
Synonym
Amicetin B
IUPAC/Chemical Name
Benzamide, 4-amino-N-(1-(5-((4,6-dideoxy-4-(dimethylamino)-alpha-D-glucopyranosyl)oxy)tetrahydro-6-methyl-2H-pyran-2-yl)-1,2-dihydro-2-oxo-4-pyrimidinyl)-, (2R-(2-alpha,5-beta,6-alpha))-
InChi Key
NFOMJDXALJABQF-SIPWQYCSSA-N
InChi Code
InChI=1S/C25H35N5O7/c1-13-17(37-24-22(32)21(31)20(29(3)4)14(2)36-24)9-10-19(35-13)30-12-11-18(28-25(30)34)27-23(33)15-5-7-16(26)8-6-15/h5-8,11-14,17,19-22,24,31-32H,9-10,26H2,1-4H3,(H,27,28,33,34)/t13-,14+,17+,19-,20+,21-,22+,24+/m0/s1
SMILES Code
O=C(NC(C=CN1[C@@H]2CC[C@@H](O[C@@H]3[C@@H]([C@H]([C@H](N(C)C)[C@@H](C)O3)O)O)[C@H](C)O2)=NC1=O)C4=CC=C(N)C=C4
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
2934.99.03.00
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 517.58 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: Bu YY, Yamazaki H, Ukai K, Namikoshi M. Anti-mycobacterial nucleoside antibiotics from a marine-derived Streptomyces sp. TPU1236A. Mar Drugs. 2014 Dec 17;12(12):6102-12. doi: 10.3390/md12126102. PubMed PMID: 25522318; PubMed Central PMCID: PMC4278220. 2: SENSI P, GRECO AM, GALLO GG, ROLLAND G. Isolation and structure determination of a new amicetin-like antibiotic: amicetin B. Antibiot Chemother (Northfield). 1957 Dec;7(12):645-52. PubMed PMID: 24544597. 3: Konstantinova NV, Fedorova GB, Borisova VN, Shapovalova SP, Malkova IV. [Isolation and identification of the antibiotics amicetin and nebramycin formed by a Streptomyces coeruleoaurantiacus 4009 culture]. Antibiotiki. 1982 Jun;27(6):403-9. Russian. PubMed PMID: 7114825. 4: Duvall EJ, Mongkolsuk S, Kim UJ, Lovett PS, Henkin TM, Chambliss GH. Induction of the chloramphenicol acetyltransferase gene cat-86 through the action of the ribosomal antibiotic amicetin: involvement of a Bacillus subtilis ribosomal component in cat induction. J Bacteriol. 1985 Feb;161(2):665-72. PubMed PMID: 3918021; PubMed Central PMCID: PMC214934. 5: Weisblum B, Demohn V. Erythromycin-inducible resistance in Staphylococcus aureus: survey of antibiotic classes involved. J Bacteriol. 1969 May;98(2):447-52. PubMed PMID: 5784204; PubMed Central PMCID: PMC284837. 6: Swaminathan V, Smith JL, Sundaralingam M, Coutsogeorgopoulos C, Kartha G. Crystal and molecular structure of the antibiotic blasticidin S hydrochloride pentahydrate. Biochim Biophys Acta. 1981 Oct 27;655(3):335-41. PubMed PMID: 7284390. 7: Rogers EJ, Ambulos NP Jr, Gu Z, Lovett PS. Parallel induction strategies for cat-86: separating chloramphenicol induction from protein synthesis inhibition. Mol Microbiol. 1993 Jun;8(6):1063-9. PubMed PMID: 7689687.