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Merck
CN

SBR00082

Isepamicin Sulfate

≥68%, powder

Synonym(s):

Isepamicin monosulfate, Isepamicin sulfate

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About This Item

Empirical Formula (Hill Notation):
C22H45N5O16S
CAS Number:
67814-76-0
Molecular Weight:
667.68
UNSPSC Code:
51101500
NACRES:
NA.41

Key Documents

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InChI

InChI=1S/C22H43N5O12.H2O4S/c1-22(35)6-36-20(15(33)18(22)26-2)39-17-8(27-19(34)9(28)4-23)3-7(25)16(14(17)32)38-21-13(31)12(30)11(29)10(5-24)37-21;1-5(2,3)4/h7-18,20-21,26,28-33,35H,3-6,23-25H2,1-2H3,(H,27,34);(H2,1,2,3,4)/t7-,8+,9-,10+,11+,12-,13+,14-,15+,16+,17-,18+,20+,21+,22-;/m0./s1

InChI key

DDXRHRXGIWOVDQ-MGAUJLSLSA-N

SMILES string

C[C@@]1(CO[C@@H]([C@@H]([C@H]1NC)O)O[C@H]2[C@@H](C[C@@H]([C@H]([C@@H]2O)O[C@@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CN)O)O)O)N)NC(=O)[C@H](CN)O)O.OS(=O)(=O)O

assay

≥68%

form

powder

color

white to off-white

antibiotic activity spectrum

Gram-negative bacteria, Gram-positive bacteria

mode of action

protein synthesis | inhibits

storage temp.

2-8°C

Quality Level

100

General description

Isepamicin Sulfate is a semisynthetic aminoglycoside antibiotic derived from gentamicin with a spectrum of activity against Gram-positive bacteria, Gram-negative bacteria, and fungi.

Biochem/physiol Actions

Sepamicin Sulfate inhibits bacterial protein synthesis by binding to the bacterial 30S ribosomal subunit, leading to the misreading of genetic information and inhibition of protein synthesis, and ultimately, bacterial cell death.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H315,H319

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
0000372597
0000372597

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