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  2. Spiro[2,26-dioxabicyclo[23.3.1]nonacosa-4,18,20-triene-27,2'-[2H]pyran]-3,3',9,13(4'H)-tetrone,22-ethyl-5',6'-dihydro-7,11,14,15-tetrahydroxy-6'-[(2R)-2-hydroxypropyl]-5',6,8,10,12,14,16,28,29-nonamethyl-,(1R,2'S,4E,5'S,6S,6'S,7R,8S,10R,11R,12S,14R,15S,16R,18E,20E,22R,25S,28S,29R)-

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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)-

Spiro[2,26-dioxabicyclo[23.3.1]nonacosa-4,18,20-triene-27,2'-[2H]pyran]-3,3',9,13(4'H)-tetrone,22-ethyl-5',6'-dihydro-7,11,14,15-tetrahydroxy-6'-[(2R)-2-hydroxypropyl]-5',6,8,10,12,14,16,28,29-nonamethyl-,(1R,2'S,4E,5'S,6S,6'S,7R,8S,10R,11R,12S,14R,15S,16R,18E,20E,22R,25S,28S,29R)-

CCC1C=CC=CCC(C)C(O)C(C)(O)C(=O)C(C)C(O)C(C)C(=O)C(C(C(C=CC(=O)OC2C(C(CC1)OC1(OC(CC(O)C)C(CC1=O)C)C2C)C)C)O)C Request for Quotation
Chemical Name: Spiro[2,26-dioxabicyclo[23.3.1]nonacosa-4,18,20-triene-27,2'-[2H]pyran]-3,3',9,13(4'H)-tetrone,22-ethyl-5',6'-dihydro-7,11,14,15-tetrahydroxy-6'-[(2R)-2-hydroxypropyl]-5',6,8,10,12,14,16,28,29-nonamethyl-,(1R,2'S,4E,5'S,6S,6'S,7R,8S,10R,11R,12S,14R,15S,16R,18E,20E,22R,25S,28S,29R)-
CAS Number: 11050-94-5
Product Number: AG008RJV(AGN-PC-0P0R7D)
Synonyms:
MDL No: MFCD00043232
Molecular Formula: C45H72O12
Molecular Weight: 805.0460

Identification/Properties

Computed Properties
Molecular Weight:
805.059g/mol
XLogP3:
6.1
Hydrogen Bond Donor Count:
5
Hydrogen Bond Acceptor Count:
12
Rotatable Bond Count:
3
Exact Mass:
804.502g/mol
Monoisotopic Mass:
804.502g/mol
Topological Polar Surface Area:
197A^2
Heavy Atom Count:
57
Formal Charge:
0
Complexity:
1470
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
18
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
3
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Oligomycin B, a naturally occurring compound derived from Streptomyces bacteria, is a potent inhibitor of ATP synthase, an enzyme crucial for cellular energy production. In chemical synthesis, Oligomycin B finds application as a valuable tool for studying mitochondrial function and investigating cellular metabolism. It can serve as a molecular probe in research focused on understanding the mechanisms of oxidative phosphorylation and energy production pathways within cells. By targeting ATP synthase, Oligomycin B disrupts ATP production, leading to a variety of effects on cellular processes that can be manipulated for research purposes. Its unique mechanism of action makes Oligomycin B a versatile compound in biochemical studies and drug development efforts targeting energy metabolism pathways.