IL98211A - The use in the C36-rich history of 43-de) acetylglucosaminyl (-43-deoxy-deoxy-tycopenin against bactericidal substances resistant to clicopeptide - Google Patents

The use in the C36-rich history of 43-de) acetylglucosaminyl (-43-deoxy-deoxy-tycopenin against bactericidal substances resistant to clicopeptide

Info

Publication number: IL98211A
Authority: IL; Israel
Prior art keywords: hydrogen; compound; medicament; glycopeptide antibiotics; vancomycin
Prior art date: 1990-05-28

Application number

IL9821191A

Other languages

English (en)

Hebrew (he)

Other versions

IL98211A0 (en

Inventor

Adriano Malabarba

Jurgen Kurt Kettenring

Original Assignee

Lepetit Spa

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1990-05-28

Filing date

1991-05-22

Publication date

1996-10-16

1991-05-22 Application filed by Lepetit Spa filed Critical Lepetit Spa

1992-06-21 Publication of IL98211A0 publication Critical patent/IL98211A0/xx

1996-10-16 Publication of IL98211A publication Critical patent/IL98211A/en

Links

229960001608 teicoplanin Drugs 0.000 title claims abstract description 36
241000894006 Bacteria Species 0.000 title claims abstract description 27
239000003910 polypeptide antibiotic agent Substances 0.000 title claims abstract description 26
-1 acetylglucosaminyl Chemical group 0.000 claims abstract description 96
150000001412 amines Chemical class 0.000 claims abstract description 20
150000001875 compounds Chemical class 0.000 claims description 73
239000001257 hydrogen Substances 0.000 claims description 43
229910052739 hydrogen Inorganic materials 0.000 claims description 43
239000002253 acid Substances 0.000 claims description 40
DDTDNCYHLGRFBM-YZEKDTGTSA-N chembl2367892 Chemical compound CC(=O)N[C@H]1[C@@H](O)[C@H](O)[C@H](CO)O[C@H]1O[C@@H]([C@H]1C(N[C@@H](C2=CC(O)=CC(O[C@@H]3[C@H]([C@H](O)[C@H](O)[C@@H](CO)O3)O)=C2C=2C(O)=CC=C(C=2)[C@@H](NC(=O)[C@@H]2NC(=O)[C@@H]3C=4C=C(O)C=C(C=4)OC=4C(O)=CC=C(C=4)[C@@H](N)C(=O)N[C@H](CC=4C=C(Cl)C(O5)=CC=4)C(=O)N3)C(=O)N1)C(O)=O)=O)C(C=C1Cl)=CC=C1OC1=C(O[C@H]3[C@H]([C@@H](O)[C@H](O)[C@H](CO)O3)NC(C)=O)C5=CC2=C1 DDTDNCYHLGRFBM-YZEKDTGTSA-N 0.000 claims description 35
108010053950 Teicoplanin Proteins 0.000 claims description 32
150000003839 salts Chemical class 0.000 claims description 32
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 22
108010059993 Vancomycin Proteins 0.000 claims description 20
239000003814 drug Substances 0.000 claims description 20
MYPYJXKWCTUITO-LYRMYLQWSA-N vancomycin Chemical compound O([C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1=C2C=C3C=C1OC1=CC=C(C=C1Cl)[C@@H](O)[C@H](C(N[C@@H](CC(N)=O)C(=O)N[C@H]3C(=O)N[C@H]1C(=O)N[C@H](C(N[C@@H](C3=CC(O)=CC(O)=C3C=3C(O)=CC=C1C=3)C(O)=O)=O)[C@H](O)C1=CC=C(C(=C1)Cl)O2)=O)NC(=O)[C@@H](CC(C)C)NC)[C@H]1C[C@](C)(N)[C@H](O)[C@H](C)O1 MYPYJXKWCTUITO-LYRMYLQWSA-N 0.000 claims description 20
229960003165 vancomycin Drugs 0.000 claims description 20
MYPYJXKWCTUITO-UHFFFAOYSA-N vancomycin Natural products O1C(C(=C2)Cl)=CC=C2C(O)C(C(NC(C2=CC(O)=CC(O)=C2C=2C(O)=CC=C3C=2)C(O)=O)=O)NC(=O)C3NC(=O)C2NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(CC(C)C)NC)C(O)C(C=C3Cl)=CC=C3OC3=CC2=CC1=C3OC1OC(CO)C(O)C(O)C1OC1CC(C)(N)C(O)C(C)O1 MYPYJXKWCTUITO-UHFFFAOYSA-N 0.000 claims description 20
125000000217 alkyl group Chemical group 0.000 claims description 18
208000015181 infectious disease Diseases 0.000 claims description 18
125000006239 protecting group Chemical group 0.000 claims description 18
RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims description 17
108010081391 Ristocetin Proteins 0.000 claims description 17
BGTFCAQCKWKTRL-YDEUACAXSA-N chembl1095986 Chemical compound C1[C@@H](N)[C@@H](O)[C@H](C)O[C@H]1O[C@@H]([C@H]1C(N[C@H](C2=CC(O)=CC(O[C@@H]3[C@H]([C@@H](O)[C@H](O)[C@@H](CO)O3)O)=C2C=2C(O)=CC=C(C=2)[C@@H](NC(=O)[C@@H]2NC(=O)[C@@H]3C=4C=C(C(=C(O)C=4)C)OC=4C(O)=CC=C(C=4)[C@@H](N)C(=O)N[C@@H](C(=O)N3)[C@H](O)C=3C=CC(O4)=CC=3)C(=O)N1)C(O)=O)=O)C(C=C1)=CC=C1OC1=C(O[C@@H]3[C@H]([C@H](O)[C@@H](O)[C@H](CO[C@@H]5[C@H]([C@@H](O)[C@H](O)[C@@H](C)O5)O)O3)O[C@@H]3[C@H]([C@@H](O)[C@H](O)[C@@H](CO)O3)O[C@@H]3[C@H]([C@H](O)[C@@H](CO)O3)O)C4=CC2=C1 BGTFCAQCKWKTRL-YDEUACAXSA-N 0.000 claims description 17
229950004257 ristocetin Drugs 0.000 claims description 17
150000007513 acids Chemical class 0.000 claims description 16
125000003074 decanoyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C(*)=O 0.000 claims description 13
238000004519 manufacturing process Methods 0.000 claims description 13
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 11
150000002431 hydrogen Chemical class 0.000 claims description 11
YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims description 10
GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims description 10
125000003277 amino group Chemical group 0.000 claims description 9
230000001588 bifunctional effect Effects 0.000 claims description 8
125000004432 carbon atom Chemical group C* 0.000 claims description 8
125000004433 nitrogen atom Chemical group N* 0.000 claims description 8
125000001424 substituent group Chemical group 0.000 claims description 8
125000001931 aliphatic group Chemical group 0.000 claims description 7
239000003242 anti bacterial agent Substances 0.000 claims description 7
229910052757 nitrogen Inorganic materials 0.000 claims description 7
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims description 6
241000295644 Staphylococcaceae Species 0.000 claims description 6
229940088710 antibiotic agent Drugs 0.000 claims description 6
125000000623 heterocyclic group Chemical group 0.000 claims description 5
108010065152 Coagulase Proteins 0.000 claims description 4
125000005842 heteroatom Chemical group 0.000 claims description 4
125000000400 lauroyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
125000001402 nonanoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
DQJCDTNMLBYVAY-ZXXIYAEKSA-N (2S,5R,10R,13R)-16-{[(2R,3S,4R,5R)-3-{[(2S,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5-(ethylamino)-6-hydroxy-2-(hydroxymethyl)oxan-4-yl]oxy}-5-(4-aminobutyl)-10-carbamoyl-2,13-dimethyl-4,7,12,15-tetraoxo-3,6,11,14-tetraazaheptadecan-1-oic acid Chemical compound NCCCC[C@H](C(=O)N[C@@H](C)C(O)=O)NC(=O)CC[C@H](C(N)=O)NC(=O)[C@@H](C)NC(=O)C(C)O[C@@H]1[C@@H](NCC)C(O)O[C@H](CO)[C@H]1O[C@H]1[C@H](NC(C)=O)[C@@H](O)[C@H](O)[C@@H](CO)O1 DQJCDTNMLBYVAY-ZXXIYAEKSA-N 0.000 claims description 3
CIISBYKBBMFLEZ-UHFFFAOYSA-N 1,2-oxazolidine Chemical compound C1CNOC1 CIISBYKBBMFLEZ-UHFFFAOYSA-N 0.000 claims description 3
CZSRXHJVZUBEGW-UHFFFAOYSA-N 1,2-thiazolidine Chemical compound C1CNSC1 CZSRXHJVZUBEGW-UHFFFAOYSA-N 0.000 claims description 3
OGYGFUAIIOPWQD-UHFFFAOYSA-N 1,3-thiazolidine Chemical compound C1CSCN1 OGYGFUAIIOPWQD-UHFFFAOYSA-N 0.000 claims description 3
FQUYSHZXSKYCSY-UHFFFAOYSA-N 1,4-diazepane Chemical compound C1CNCCNC1 FQUYSHZXSKYCSY-UHFFFAOYSA-N 0.000 claims description 3
108010015899 Glycopeptides Proteins 0.000 claims description 3
102000002068 Glycopeptides Human genes 0.000 claims description 3
WYNCHZVNFNFDNH-UHFFFAOYSA-N Oxazolidine Chemical compound C1COCN1 WYNCHZVNFNFDNH-UHFFFAOYSA-N 0.000 claims description 3
ZSIQJIWKELUFRJ-UHFFFAOYSA-N azepane Chemical compound C1CCCNCC1 ZSIQJIWKELUFRJ-UHFFFAOYSA-N 0.000 claims description 3
BRNULMACUQOKMR-UHFFFAOYSA-N thiomorpholine Chemical compound C1CSCCN1 BRNULMACUQOKMR-UHFFFAOYSA-N 0.000 claims description 3
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 8
150000003254 radicals Chemical class 0.000 claims 7
ONOBXDPYDHTSBQ-UHFFFAOYSA-N 2,3,4,7-tetrahydro-1h-diazepine Chemical compound C1CC=CCNN1 ONOBXDPYDHTSBQ-UHFFFAOYSA-N 0.000 claims 2
WPWHSFAFEBZWBB-UHFFFAOYSA-N 1-butyl radical Chemical compound [CH2]CCC WPWHSFAFEBZWBB-UHFFFAOYSA-N 0.000 claims 1
239000003153 chemical reaction reagent Substances 0.000 abstract description 12
150000002148 esters Chemical class 0.000 abstract description 12
150000001408 amides Chemical group 0.000 abstract description 9
229920000768 polyamine Polymers 0.000 abstract description 8
RENMDAKOXSCIGH-UHFFFAOYSA-N Chloroacetonitrile Chemical compound ClCC#N RENMDAKOXSCIGH-UHFFFAOYSA-N 0.000 abstract description 4
244000005700 microbiome Species 0.000 abstract description 4
241001505901 Streptococcus sp. 'group A' Species 0.000 abstract description 2
239000000203 mixture Substances 0.000 description 31
238000000034 method Methods 0.000 description 28
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 21
238000006243 chemical reaction Methods 0.000 description 20
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical group CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 16
239000007858 starting material Substances 0.000 description 16
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 15
239000000047 product Substances 0.000 description 14
239000007795 chemical reaction product Substances 0.000 description 13
239000000243 solution Substances 0.000 description 13
238000002360 preparation method Methods 0.000 description 12
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QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
238000004128 high performance liquid chromatography Methods 0.000 description 8
239000003960 organic solvent Substances 0.000 description 8
238000011176 pooling Methods 0.000 description 8
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 7
238000009903 catalytic hydrogenation reaction Methods 0.000 description 7
230000000694 effects Effects 0.000 description 7
239000012458 free base Substances 0.000 description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
LCTCUBQFWLTHNS-MDZDMXLPSA-N 61036-64-4 Chemical compound CCCCC\C=C\CCC(=O)NC1C(O)C(O)C(CO)OC1OC(C(=C1)OC=2C(=CC(=CC=2)C(OC2C(C(O)C(O)C(CO)O2)NC(C)=O)C2C(NC(C3=CC(O)=CC(OC4C(C(O)C(O)C(CO)O4)O)=C3C=3C(O)=CC=C(C=3)C(NC3=O)C(=O)N2)C(=O)OC)=O)Cl)=C(OC=2C(=CC(=CC=2)C(O)C(C(N2)=O)NC(=O)C(N)C=4C=C(O5)C(O)=CC=4)Cl)C=C1C3NC(=O)C2C1=CC(O)=C(C)C5=C1 LCTCUBQFWLTHNS-MDZDMXLPSA-N 0.000 description 6
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
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108700001961 teicoplanin A2 Proteins 0.000 description 6
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125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 5
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125000002252 acyl group Chemical group 0.000 description 4
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GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 3
229910052500 inorganic mineral Inorganic materials 0.000 description 3
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238000001228 spectrum Methods 0.000 description 3
XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 2
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HSDAJNMJOMSNEV-UHFFFAOYSA-N benzyl chloroformate Chemical compound ClC(=O)OCC1=CC=CC=C1 HSDAJNMJOMSNEV-UHFFFAOYSA-N 0.000 description 1
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235000015424 sodium Nutrition 0.000 description 1
CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
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WSWCOQWTEOXDQX-MQQKCMAXSA-N sorbic acid group Chemical group C(\C=C\C=C\C)(=O)O WSWCOQWTEOXDQX-MQQKCMAXSA-N 0.000 description 1
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125000005270 trialkylamine group Chemical group 0.000 description 1
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239000011701 zinc Substances 0.000 description 1
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Classifications

- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G23/00—Compounds of titanium
- C01G23/04—Oxides; Hydroxides
- C01G23/047—Titanium dioxide
- C01G23/053—Producing by wet processes, e.g. hydrolysing titanium salts
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
- A61K38/14—Peptides containing saccharide radicals; Derivatives thereof, e.g. bleomycin, phleomycin, muramylpeptides or vancomycin
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
- B01J21/06—Silicon, titanium, zirconium or hafnium; Oxides or hydroxides thereof
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82B—NANOSTRUCTURES FORMED BY MANIPULATION OF INDIVIDUAL ATOMS, MOLECULES, OR LIMITED COLLECTIONS OF ATOMS OR MOLECULES AS DISCRETE UNITS; MANUFACTURE OR TREATMENT THEREOF
- B82B3/00—Manufacture or treatment of nanostructures by manipulation of individual atoms or molecules, or limited collections of atoms or molecules as discrete units
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G23/00—Compounds of titanium
- C01G23/04—Oxides; Hydroxides
- C01G23/047—Titanium dioxide
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Inorganic Chemistry (AREA)
Environmental & Geological Engineering (AREA)
Medicinal Chemistry (AREA)
Pharmacology & Pharmacy (AREA)
Nanotechnology (AREA)
Crystallography & Structural Chemistry (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Geology (AREA)
General Life Sciences & Earth Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Materials Engineering (AREA)
Bioinformatics & Cheminformatics (AREA)
Immunology (AREA)
Oncology (AREA)
Communicable Diseases (AREA)
Gastroenterology & Hepatology (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Epidemiology (AREA)
Manufacturing & Machinery (AREA)
Proteomics, Peptides & Aminoacids (AREA)
Peptides Or Proteins (AREA)
Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

IL9821191A 1990-05-28 1991-05-22 The use in the C36-rich history of 43-de) acetylglucosaminyl (-43-deoxy-deoxy-tycopenin against bactericidal substances resistant to clicopeptide IL98211A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
EP90110102		1990-05-28

Publications (2)

Publication Number	Publication Date
IL98211A0 IL98211A0 (en)	1992-06-21
IL98211A true IL98211A (en)	1996-10-16

Family

ID=8204033

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL9821191A IL98211A (en)	1990-05-28	1991-05-22	The use in the C36-rich history of 43-de) acetylglucosaminyl (-43-deoxy-deoxy-tycopenin against bactericidal substances resistant to clicopeptide

Country Status (10)

Country	Link
EP (1)	EP0460448B1 (fr)
JP (1)	JPH04235187A (fr)
KR (1)	KR910019628A (fr)
AT (1)	ATE128626T1 (fr)
AU (1)	AU647122B2 (fr)
DE (1)	DE69113513T2 (fr)
DK (1)	DK0460448T3 (fr)
IE (1)	IE72144B1 (fr)
IL (1)	IL98211A (fr)
ZA (1)	ZA913987B (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE4304716A1 (de) *	1993-02-16	1994-08-18	Melzer Wolfgang	Lokal applizierbares Arzneimittel mit verzögerter Freisetzung
US6392012B1 (en)	1998-12-23	2002-05-21	Advanced Medicine, Inc.	Glycopeptide derivatives and pharmaceutical compositions containing the same
KR100891014B1 (ko) *	2007-07-06	2009-04-03	대한민국	특이 항원의 면역 반응을 이용한 반코마이신 내성엔테로코커스의 감염 진단 방법

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB8704847D0 (en) *	1987-03-02	1987-04-08	Lepetit Spa	Substituted alkylamides of teicoplanin compounds
ATE134646T1 (de) *	1988-12-27	1996-03-15	Lepetit Spa	C63-amidderivate von 34-de(acetylglucosaminyl)-34-deoxy-teicoplanine

1991
- 1991-05-20 AU AU77203/91A patent/AU647122B2/en not_active Ceased
- 1991-05-21 EP EP91108165A patent/EP0460448B1/fr not_active Expired - Lifetime
- 1991-05-21 AT AT91108165T patent/ATE128626T1/de not_active IP Right Cessation
- 1991-05-21 DE DE69113513T patent/DE69113513T2/de not_active Expired - Fee Related
- 1991-05-21 DK DK91108165.1T patent/DK0460448T3/da active
- 1991-05-22 IL IL9821191A patent/IL98211A/en active IP Right Grant
- 1991-05-24 JP JP3148092A patent/JPH04235187A/ja active Pending
- 1991-05-27 IE IE179891A patent/IE72144B1/en not_active IP Right Cessation
- 1991-05-27 KR KR1019910008655A patent/KR910019628A/ko not_active Ceased
- 1991-05-27 ZA ZA913987A patent/ZA913987B/xx unknown

Also Published As

Publication number	Publication date
EP0460448A2 (fr)	1991-12-11
AU647122B2 (en)	1994-03-17
EP0460448A3 (en)	1992-04-29
IL98211A0 (en)	1992-06-21
ATE128626T1 (de)	1995-10-15
JPH04235187A (ja)	1992-08-24
ZA913987B (en)	1992-04-29
EP0460448B1 (fr)	1995-10-04
KR910019628A (ko)	1991-12-19
AU7720391A (en)	1991-11-28
DE69113513T2 (de)	1996-03-28
DK0460448T3 (da)	1995-11-20
IE72144B1 (en)	1997-03-26
DE69113513D1 (de)	1995-11-09
IE911798A1 (en)	1991-12-04

Legal Events

Date	Code	Title
1997-03-18	FF	Patent granted
1997-06-10	KB	Patent renewed
1997-09-30	KB	Patent renewed

Publication	Publication Date	Title
US5750509A (en)	1998-05-12	Amide derivatives of antibiotic A 40926
EP0596929B1 (fr)	1995-07-26	Derives amides de l'antibiotique a 40926
EP0376041B1 (fr)	1996-02-28	Dérivés amides en C63 des 34-de(acétylglucosaminyl)-34-déoxyteicoplanines
KR960014104B1 (ko)	1996-10-14	테이코플라닌 화합물의 치환 알킬아미드
EP0465481B1 (fr)	1993-11-18	Nouveaux derives d'alkylamides substitues de teicoplanine
EP0216775B1 (fr)	1989-05-03	Derives d'esters d'acides carboxyliques de la deglucoteicoplanine
US5194424A (en)	1993-03-16	C63 -amide derivatives of 34-de(acetylglucosaminyl)-34-deoxy-teicoplanin and their use as medicaments against bacteria resistant to glycopeptide antibiotics
US5500410A (en)	1996-03-19	Substituted alkylamide derivatives of teicoplanin
AU647122B2 (en)	1994-03-17	C63-amide derivatives of 34-de(acetylglucosaminyl)-34-deoxy- teicoplanin and their use as medicaments against bacteria resistant to glycopeptide antibiotics
NZ231468A (en)	1992-07-28	63 c-amido-teicoplanin antibiotic derivatives and their preparation from 63 c-carboxy-teicoplanin derivatives
US5185320A (en)	1993-02-09	O56 -alkyl derivatives of aglycone and pseudo aglycones of teicoplanin
US5438117A (en)	1995-08-01	Hexapeptides deriving from aglucoteicoplanin and a process for preparing them
EP0563062B1 (fr)	1996-01-10	Hexapeptides derives de l'aglucoteicoplanine, et procede de preparation