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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)-

Resistomycin

Oc1cc(O)c2c3c1C(=O)C(c1c3c3c(C2=O)c(O)cc(c3c(c1)O)C)(C)C Request for Quotation
Chemical Name: Resistomycin
CAS Number: 20004-62-0
Product Number: AG0074DU(AGN-PC-0LPKI7)
Synonyms:
MDL No:
Molecular Formula: C22H16O6
Molecular Weight: 376.3588

Identification/Properties

Computed Properties
Molecular Weight:
376.364g/mol
XLogP3:
3.6
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
0
Exact Mass:
376.095g/mol
Monoisotopic Mass:
376.095g/mol
Topological Polar Surface Area:
115A^2
Heavy Atom Count:
28
Formal Charge:
0
Complexity:
893
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
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


Resistomycin, a naturally occurring antibiotic isolated from Streptomyces that demonstrates potent antifungal activity, has shown promise in the field of chemical synthesis. When utilized in chemical reactions, Resistomycin serves as a valuable tool for selectively inhibiting the growth of fungi, allowing for precise control over the synthesis of organic compounds. Its ability to target specific fungal species without impacting other microorganisms makes it a versatile agent for protecting chemical reactions from contamination. Furthermore, Resistomycin's mechanism of action, which involves disrupting fungal cell walls, can be exploited to modulate reaction conditions and enhance product yields in various synthetic processes. By harnessing the unique properties of Resistomycin, chemists can unlock new possibilities in the efficient and controlled synthesis of complex molecules.