Enramycin B (Enduracidin B), Lipodepsipeptide antibiotic agent (ab143613)
Key features and details
- Lipodepsipeptide antibiotic agent. MurG inhibitor.
- CAS Number: 34304-21-7
- Purity: >= 83%
Soluble in 0.1% formic acid in H2O
- Form / State: Solid
- Source: Synthetic
Overview
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Product name
Enramycin B (Enduracidin B), Lipodepsipeptide antibiotic agent -
Description
Lipodepsipeptide antibiotic agent. MurG inhibitor. -
Biological description
Lipodepsipeptide antibiotic agent. MurG inhibitor. Inhibits peptidoglycan synthesis. Active against multi-drug resistant Gram-positive bacteria in vivo. -
Purity
>= 83% -
CAS Number
34304-21-7 -
Chemical structure
Properties
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Chemical name
(2S)-N-[(2Z,4E)-10-Methyl-1-oxo-2,4-undecadien-1-yl]-L-α-aspartyl-L-threonyl-(2R)-2-(4-hydroxyphenyl)glycyl-D-ornithyl-D-allothreonyl-(2S)-2-(4-hydroxyphenyl)glycyl-(2R)-2-(4-hydroxyphenyl)glycyl-L-allothreonyl-N5-(aminocarbonyl)-L-ornithyl-3-[(5R)-2-amino-4,5-dihydro-1H-imidazol-5-yl]-D-alanyl-(2S)-2-(4-hydroxyphenyl)glycyl-D-seryl-(2S)-2-(3,5-dichloro-4-hydroxyphenyl)glycylglycyl-3-[(5R)-2-amino-4,5-dihydro-1H-imidazol-5-yl]-L-alanyl-D-alanyl-2-(4-hydroxyphenyl)
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Molecular weight
2369.33 -
Molecular formula
C108H140Cl2N26O31 -
PubChem identifier
16132291 -
Storage instructions
Store at +4°C. The product can be stored for up to 12 months. -
Solubility overview
Soluble in 0.1% formic acid in H2O
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Handling
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one week. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.
Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
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SMILES
CCC(C)CCCCC=CC=CC(=O)NC(CC(=O)O)C(=O)NC1C(OC(=O)C(NC(=O)C(NC(=O)C(NC(=O)CNC(=O)C(NC(=O)C(NC(=O)C(NC(=O)C(NC(=O)C(NC(=O)C(NC(=O)C(NC(=O)C(NC(=O)C(NC(=O)C(NC(=O)C(NC1=O)C2=CC=C(C=C2)O)CCCN)C(C)O)C3=CC=C(C=C3)O)C4=CC=C(C=C4)O)C(C)O)CCCNC(=O)N)CC5CNC(=N5)N)C6=CC=C(C=C6)O)CO)C7=CC(=C(C(=C7)Cl)O)Cl)CC8CNC(=N8)N)C)C9=CC=C(C=C9)O)C -
Source
Synthetic
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Research areas