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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Oligomycin A, 26-hydroxy-28-oxo-

CC[C@H]1/C=C/C=C/C[C@@H](C)[C@H](O)[C@@](C)(O)C(=O)[C@@H](C)[C@H](O)[C@@H](C)C(=O)[C@H]([C@@H]([C@H](/C=C/C(=O)O[C@@H]2[C@@H]([C@H](CC1)O[C@@]1(O[C@@H](C[C@H](O)C)[C@H](CC1=O)C)[C@]2(C)O)C)C)O)C Request for Quotation
Chemical Name: Oligomycin A, 26-hydroxy-28-oxo-
CAS Number: 110231-34-0
Product Number: AG0094DY(AGN-PC-0P0DAV)
Synonyms:
MDL No:
Molecular Formula: C45H72O13
Molecular Weight: 821.0454

Identification/Properties

Computed Properties
Molecular Weight:
821.058g/mol
XLogP3:
4.9
Hydrogen Bond Donor Count:
6
Hydrogen Bond Acceptor Count:
13
Rotatable Bond Count:
3
Exact Mass:
820.497g/mol
Monoisotopic Mass:
820.497g/mol
Topological Polar Surface Area:
217A^2
Heavy Atom Count:
58
Formal Charge:
0
Complexity:
1520
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
18
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
3
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Oligomycin E, a natural product derived from Streptomyces bacteria, is valued for its versatility in chemical synthesis applications. This highly potent compound is renowned for its ability to inhibit the flow of protons across mitochondrial membranes, making it a crucial tool in biochemical research. In chemical synthesis, Oligomycin E is utilized as a selective inhibitor of mitochondrial ATP synthase, providing researchers with a targeted approach to studying energy production mechanisms within cells. By effectively disrupting ATP synthesis, Oligomycin E enables scientists to investigate various cellular processes and pathways, offering valuable insights into bioenergetics and metabolism. Its unique mechanism of action and exceptional purity make Oligomycin E an indispensable resource in the field of chemical synthesis, driving innovation and advancement in biochemistry and biotechnology.