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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)-

Teicoplanin A2

OC[C@H]1O[C@@H](Oc2c3cc4cc2Oc2ccc(cc2Cl)C[C@@H]2C(=O)N[C@H](C(=O)N[C@H]4C(=O)N[C@H]4C(=O)N[C@@H]([C@@H](c5ccc(O3)c(Cl)c5)O[C@@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3NC(=O)C)O)O)C(=O)N[C@@H](c3c(c5cc4ccc5O)c(cc(c3)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@@H]3O)O)O)C(=O)O)c3cc(O)cc(c3)Oc3cc([C@H](C(=O)N2)N)ccc3O)[C@@H]([C@H]([C@@H]1O)O)NC(=O)CCCCCCC(C)C Request for Quotation
Chemical Name: Teicoplanin A2
CAS Number: 91032-26-7
Product Number: AG00GWMA(AGN-PC-00T4IH)
Synonyms:
MDL No:
Molecular Formula: C88H97Cl2N9O33
Molecular Weight: 1879.6583

Identification/Properties

Computed Properties
Molecular Weight:
1879.674g/mol
XLogP3:
0.3
Hydrogen Bond Donor Count:
24
Hydrogen Bond Acceptor Count:
34
Rotatable Bond Count:
19
Exact Mass:
1877.557g/mol
Monoisotopic Mass:
1877.557g/mol
Topological Polar Surface Area:
662A^2
Heavy Atom Count:
132
Formal Charge:
0
Complexity:
3940
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
23
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


Teicoplanin A2-2 is a powerful antibiotic isolated from the fermentation of Actinoplanes teichomyceticus. Beyond its antimicrobial properties, Teicoplanin A2-2 also exhibits potential applications in chemical synthesis. In organic chemistry, Teicoplanin A2-2 can serve as a chiral resolving agent, allowing researchers to selectively separate enantiomers. This ability is particularly valuable in drug development, where enantiomeric purity is crucial for maintaining desired pharmacological effects and minimizing side effects. Additionally, Teicoplanin A2-2 can be employed in asymmetric synthesis to catalyze various reactions with high enantioselectivity. Such applications highlight the versatility and importance of Teicoplanin A2-2 in advancing synthetic methodologies and delivering structurally complex molecules with precision.