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Cat. No.: HY-N14758

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6"'-Deamino-6"'-hydroxyparomomycin I

6"'-Deamino-6"'-hydroxyparomomycin I is an amino glycosyl antibiotic that can be produced by Streptomyces rimosus forma paromomycinus A67 15. It is active against both Gram-positive and Gram-negative bacteria. 6"'-Deamino-6"'-hydroxyparomomycin I can be used as an intermediate in the biosynthesis of paromomycin.

For research use only. We do not sell to patients.

CAS No.: 78524-72-8
Formula: C₂₃H₄₄N₄O₁₅
Molecular Weight:616.61

Storage:

Please store the product under the recommended conditions in the Certificate of Analysis.

Data Sheet (275 KB)

6"'-Deamino-6"'-hydroxyparomomycin I Chemical Structure

CAS No.: 78524-72-8

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Use of MCE Products

Fluorescent Dye

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Biological Activity

Description

All Antibiotic Isoforms :

Chemical Information

CAS No. 78524-72-8
Molecular Weight 616.61
Formula C₂₃H₄₄N₄O₁₅
SMILES

O[C@H]([C@@H]([C@H](O1)CO)O[C@H]2O[C@H]([C@H]([C@@H]([C@H]2N)O)O)CO)[C@@H]1O[C@H]([C@H]([C@@H](C[C@@H]3N)N)O)[C@@H]3O[C@H]4O[C@@H]([C@H]([C@@H]([C@H]4N)O)O)CO
Structure Classification
- Others
Initial Source
- Microorganisms
mutant of Streptomyces rimosus forma paromomycinus
Shipping

Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation

Select Batch:

Purity: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (275 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Handling Instructions (2659 KB)

References

[1]. Autissier D, et al. 6"'-Deamino-6"'-hydroxy derivatives, as intermediates in the biosynthesis of neomycin and paromomycin. J Antibiot (Tokyo). 1981 May;34(5):536-43. [Content Brief]

[2]. Toda S, NAKAGAWA S, NAITO T, et al. AMINOGLYCOSIDE ANTIBIOTICS. XV CHEMICAL CONVERSION OF NEOMYCIN B TO PAROMOMYCIN I, 6'''-DEAMINO-6'''-HYDROXYNEOMYCIN B AND 6'''-DEAMINO-6'''-HYDROXY-PAROMOMYCIN I. The Journal of Antibiotics, 1983, 36(1): 87-91.

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Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

Keywords

6"'-Deamino-6"'-hydroxyparomomycin I

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6"'-Deamino-6"'-hydroxyparomomycin I

All Antibiotic Isoforms

Biological Activity

Chemical Information

Purity & Documentation

References

Calculators

Help & FAQs

6"'-Deamino-6"'-hydroxyparomomycin I Related Classifications

HY-N14758 Related Classifications