http://rdf.ncbi.nlm.nih.gov/pubchem/patent/NZ-509165-A

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filingDate 1999-07-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0ff2e498ffd0143cc4014c04900481ad
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d256a3f3fe5bb3b06d03ef59c19267da
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publicationDate 2003-08-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber NZ-509165-A
titleOfInvention Glycopeptide antobiotics, combinatorial libraries of glycopeptide antibiotics and methods of producing same
abstract A glycopeptide of the formula A1-A2-A3-A4-A5-A6-A7 wherein: each dash is a covalent bond A1 comprises a modified or unmodified alpha-amino acid residue, alkyl, aryl, aralkyl, alkanoyl, aroyl, aralkanoyl, heterocyclic, heterocyclic-carbonyl, heterocyclic-alkyl, heterocyclic-alkyl-carbonyl, alkylsulfonyl, arylsulfonyl, guanidinyl, carbamoyl, or xanthyl; A2 to A7 comprise a modified or unmodified alpha-amino acid residue, whereby (i) the group A1 is linked to an amino group on the group A2, (ii) each of the groups A2, A4 and A6 bears an aromatic side chain, which aromatic side chains are cross-linked together by two or more covalent bonds, and (iii) the group A7 bears a terminal carboxyl, ester, amide, or N-substituted amide group; wherein one or more of the groups A1 to A7 is linked via a glycosidic bond to one or more glycosidic groups each having one or more sugar residues; wherein at least one of said sugar residues is a disaccharide modified to bear one or more substituents of the formula YXR, N+(R1)=CR2R3, N=PRIR2R3, N+R1R2R3 or P+R1R2R3 in which the group Y is a single bond, O, NR1 or S; the group X is O, NR1, S, SO2, C(0)0, C(O)S, C(S)O, C(S)S, C(NR1)O, C(O)NR1, or halo (in which case Y and R are absent); and R, R1, R2, and R3 are independently hydrogen, alkyl, aryl, aralkyl, alkanoyl, aroyl, aralkanoyl, heterocyclic, heterocyclic-carbonyl, heterocyclic-alkyl, heterocyclic-alkyl-carbonyl, alkylsulfonyl or arylsulfonyl; and any pharmaceutically acceptable salts thereof; provided that at least one of the substituents of the formula YXR is not hydroxyl; X and Y are not both O ; X and Y are not S and O, or O and S, respectively; and if two or more of said substituents are present, they can be the same or different. Provided that when A4 is linked to a disaccharide having a glucose residue that bears an N-substituted aminohexose residue, then said glucose residue is modified to bear at least one of said substituents YXR, N+(R1)=CR2R3, N=PR1R2R3, N+R1R2R3 or P+R1R2 R3. Also described is a chemical library comprising a plurality of the glycopeptides, a method for preparing the substituted glycopeptides and a glycopeptide antibiotic bearing at least on disaccharide group, said disaccharide group comprising two saccharide groups, a first of said saccharide groups bearing at least one amino or substituted amino group, and a second of said saccharide groups modified to bear at least one substituent which is not hydroxyl, or a pharmaceutically acceptable salt thereof.
priorityDate 1998-07-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID1068
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID22017113
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID12821434
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID432898608
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID159393904
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCA9CFS1
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID15896766
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID450934603
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID425999247
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID2733084
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID69020
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID592570
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID19800382
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21894497
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID1351
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID424346164
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID457282502
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID453625043
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419474315
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21301321
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID22242641
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID1280
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415803777
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID456491178
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID410440257
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID66049
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6364
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426406759
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419580480
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21918305
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ8NUT2
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID19791191
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID60464
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID432672554

Total number of triples: 315.