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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)-

Platensimycin

O=C(Nc1c(O)ccc(c1O)C(=O)O)CC[C@]1(C)C(=O)C=CC23C1C1CC(C2)C(O1)(C3)C Request for Quotation
Chemical Name: Platensimycin
CAS Number: 835876-32-9
Product Number: AG004TTQ(AGN-PC-0WAHX0)
Synonyms:
MDL No:
Molecular Formula: C24H27NO7
Molecular Weight: 441.4737

Identification/Properties

Computed Properties
Molecular Weight:
441.48g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
5
Exact Mass:
441.179g/mol
Monoisotopic Mass:
441.179g/mol
Topological Polar Surface Area:
133A^2
Heavy Atom Count:
32
Formal Charge:
0
Complexity:
888
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
6
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


Platensimycin is a potent antibiotic compound that has garnered significant attention in the field of chemical synthesis. Its unique structure and mechanism of action make it a valuable tool for the development of new pharmaceuticals and other bioactive compounds. In chemical synthesis, Platensimycin can be utilized as a versatile building block or as a catalyst for specific reactions. Its ability to selectively inhibit bacterial fatty acid biosynthesis makes it a valuable tool for studying and modulating complex biological pathways. By incorporating Platensimycin into synthetic routes, chemists can access structurally diverse molecules with potential therapeutic applications. Its broad spectrum of activity and relatively simple chemical structure make it an attractive target for synthetic chemists looking to develop novel drug candidates or probe biological systems.