CGP 4832
CGP 4832 is a Rifamycin S (HY-125365) derivative and Antibacterial agent. CGP 4832 inhibits DNA-dependent transcription through DNA-dependent RNA polymerase. CGP 4832 exhibits activity against Gram-positive bacteria comparable to Rifampicin (HY-B0272), but is more potent against certain Gram-negative bacterial species, such as Escherichia coli ETH 2018 (MIC 0.01 µg/mL) and Salmonella AX 5 (MIC 0.5 µg/mL). CGP 4832 can be used for research on Gram-negative bacterial infections.
Nur für Forschungszwecke. Wir verkaufen nicht an Patienten.
- CAS. Nr.: 113303-81-4
- Formel: C49H65N3O15
- Molecular Weight:936.05
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Speicherung:
Please store the product under the recommended conditions in the Certificate of Analysis.
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Biologische Aktivität
Beschreibung
IC50 & Target
[1]|
RNA Polymerase |
In Vitro
The MIC of CGP-4832 (24 h) against Escherichia coli MG1655 in iron-limited RPMI-1640 (0.25 mg/L) is 32-fold lower than that in iron-rich MHII (8 mg/L)[1].
CGP-4832 (24 h) does not show enhanced activity against Acinetobacter baumannii HUMC1 or LAC-4 in iron-limited RPMI-1640 compared with MHII, with MICs of 8 mg/L and 2 mg/L in RPMI-1640, respectively[1].
CGP 4832 (hydroquinone form; 10 min) inhibits DNA-dependent RNA polymerase from Escherichia coli ETH 2018 with ED50 values of 0.09 µg/mL and 0.06 µg/mL for crude and highly purified enzyme, respectively, and no correlation exists between MIC and enzyme inhibition among the bacterial strains tested[2].
CGP 4832 exhibits activity against Gram-positive bacteria comparable to that of Rifampicin (HY-B0272), but is 80-400 times more potent against certain Gram-negative bacterial species, such as Escherichia coli ETH 2018 (MIC 0.01 µg/mL) and Salmonella AX 5 (MIC 0.5 µg/mL)[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS. Nr. 113303-81-4
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Molecular Weight 936.05
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Formel C49H65N3O15
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SMILES
CO[C@H]1/C=C/O[C@@]2(C)OC3=C(C4=C(C(O)=C3C)C(C(NC(/C(C)=C\C=C\[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(CC(OCC5CCCN(C)C5)=O)=O)[C@@H]1C)=O)=C(N6CCOCC6)C4=O)=O)C2=O
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Versand
Room temperature in continental US; may vary elsewhere.
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Speicherung
Please store the product under the recommended conditions in the Certificate of Analysis.
Reinheit & Dokumentation
Verweise
[1]. Lu P, et al. Defining the minimum inhibitory concentration of 22 rifamycins in iron limited, physiologic medium against Acinetobacter baumannii, Escherichia coli, and Klebsiella pneumoniae clinical isolates. PloS one. 2023;18(6):e0287102. [Content Brief]
[2]. Wehrli W, et al. CGP 4832, a new semisynthetic rifamycin derivative highly active against some gram-negative bacteria. The Journal of antibiotics. 1987 Dec;40(12):1733-9. [Content Brief]
Calculators
Konzentration (Stammlösung) × Volumen (Stammlösung) = Konzentration (Ziellösung) × Volumen (Ziellösung)