Rutamycin
Rutamycin Basic information
- Product Name:
- Rutamycin
- Synonyms:
-
- oligomycin D
- 26-Demethyloligomycin A
- A-272
- RR-32705
- RRNo-32705
- RutaMycin, 26-deMethyloligoMycin A, A 272, RR 32705, RutaMycin A
- Rutamycin
- Spiro[2,26-dioxabicyclo[23.3.1]nonacosa-4,18,20-triene-27,2'-[2H]pyran]-3,9,13-trione,22-ethyl-3',4',5',6'-tetrahydro-7,11,14,15-tetrahydroxy-6'-[(2R)-2-hydroxypropyl]-5',6,8,10,12,14,16,29-octamethyl-,(1S,2'R,4E,5'S,6S,6'S,7S,8S,10R,11R,12S,14R,15S,16R,18E,20E,22R,25S,29R)-
- CAS:
- 1404-59-7
- MF:
- C44H72O11
- MW:
- 777.042
- Mol File:
- 1404-59-7.mol
Rutamycin Chemical Properties
- Melting point:
- 116-119°
- alpha
- D20 -62° (c = 1.36 in CHCl3)
- Boiling point:
- 883.4±65.0 °C(Predicted)
- Density
- 1.15±0.1 g/cm3(Predicted)
- storage temp.
- Store at -20°C
- solubility
- DMF: soluble; DMSO: soluble; Ethanol: soluble; Methanol: soluble
- form
- A lyophilisate
- pka
- 12.52±0.70(Predicted)
Rutamycin Usage And Synthesis
Description
Oligomycin D is a macrolide antibiotic produced by several species of Streptomyces that inhibits the mitochondrial F1FO-ATPase and is used to uncouple oxidative phosphorylation from electron transport. Oligomycin D is reported to inhibit K-Ras plasma membrane localization in MDCK cells with an IC50 value of 3.49 nM and is cytotoxic to SW620 colon cancer cells with an IC50 value of 36 μM.
Uses
Oligomycin D (rutamycin) is macrocyclic lactone belonging to the oligomycin class but identified from different species of Streptomyces in 1961. Like oligomycin A, oligomycin D inhibits mitochondrial F1F0-ATPase and is an important bioprobe to study the organisation of ATPase on the mitochondrial membrane. Oligomycin D exhibits a broad biological profile including antifungal, antitumor and nematocidal activities.
Uses
Oligomycin D is an inhibitor of mitochondrial F1F0-ATPase.
References
[1] INOUE S. Purification and Characterization of a Novel Protein Activator of Ca2+/Calmodulin-Dependent Protein Kinase I[J]. Biochemical and biophysical research communications, 1995, 215 3: Pages 861-867. DOI: 10.1006/bbrc.1995.2543
[2] SALIM A A, TAN L, HUANG X C, et al. Oligomycins as inhibitors of K-Ras plasma membrane localisation?[J]. Organic & Biomolecular Chemistry, 2015, 2: 711-715. DOI: 10.1039/c5ob02020d
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