SK281850B6 - Antimikrobiálne účinné zmesi obsahujúce aminokyseliny, liečivá s ich obsahom a ich použitie - Google Patents

Antimikrobiálne účinné zmesi obsahujúce aminokyseliny, liečivá s ich obsahom a ich použitie Download PDF

Info

Publication number: SK281850B6
Authority: SK; Slovakia
Prior art keywords: cyclopentane; amino; acid; medicaments; acids
Prior art date: 1995-07-19

Application number

SK947-96A

Other languages

English (en)

Slovak (sk)

Other versions

SK94796A3 (en

Inventor

Michael Matzke

Hans-Christian Militzer

Joachim Mittendorf

Franz Kunisch

Axel Schmidt

Wolfgang Sch�Nfeld

Karl Ziegelbauer

Original Assignee

Bayer Aktiengesellschaft

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.)

1995-07-19

Filing date

1996-07-18

Publication date

2001-08-06

1996-07-18 Application filed by Bayer Aktiengesellschaft filed Critical Bayer Aktiengesellschaft

1997-02-05 Publication of SK94796A3 publication Critical patent/SK94796A3/sk

2001-08-06 Publication of SK281850B6 publication Critical patent/SK281850B6/sk

Links

239000000203 mixture Substances 0.000 title claims abstract description 36
239000003814 drug Substances 0.000 title claims abstract description 11
150000001413 amino acids Chemical class 0.000 title description 2
230000000844 anti-bacterial effect Effects 0.000 title 1
235000008206 alpha-amino acids Nutrition 0.000 claims abstract description 13
AGPKZVBTJJNPAG-WHFBIAKZSA-N L-isoleucine Chemical compound CC[C@H](C)[C@H](N)C(O)=O AGPKZVBTJJNPAG-WHFBIAKZSA-N 0.000 claims abstract description 9
229930182844 L-isoleucine Natural products 0.000 claims abstract description 9
RKOUGZGFAYMUIO-RITPCOANSA-N pdl 118 Chemical compound N[C@H]1CC(=C)C[C@H]1C(O)=O RKOUGZGFAYMUIO-RITPCOANSA-N 0.000 claims abstract description 7
QNAYBMKLOCPYGJ-UHFFFAOYSA-N D-alpha-Ala Natural products CC([NH3+])C([O-])=O QNAYBMKLOCPYGJ-UHFFFAOYSA-N 0.000 claims abstract description 5
QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 claims abstract description 5
208000031888 Mycoses Diseases 0.000 claims abstract description 5
229960003767 alanine Drugs 0.000 claims abstract description 5
201000010099 disease Diseases 0.000 claims abstract description 5
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 5
NISGSNTVMOOSJQ-UHFFFAOYSA-N cyclopentanamine Chemical compound NC1CCCC1 NISGSNTVMOOSJQ-UHFFFAOYSA-N 0.000 claims abstract description 4
ONIBWKKTOPOVIA-BYPYZUCNSA-N L-Proline Chemical compound OC(=O)[C@@H]1CCCN1 ONIBWKKTOPOVIA-BYPYZUCNSA-N 0.000 claims abstract description 3
229930182821 L-proline Natural products 0.000 claims abstract description 3
238000004519 manufacturing process Methods 0.000 claims abstract 2
150000001371 alpha-amino acids Chemical class 0.000 claims description 6
239000003937 drug carrier Substances 0.000 claims description 3
LTXATNYXTLWVBT-UHFFFAOYSA-N 2-methylidenecyclopentane-1-carboxylic acid Chemical compound OC(=O)C1CCCC1=C LTXATNYXTLWVBT-UHFFFAOYSA-N 0.000 claims 1
150000001370 alpha-amino acid derivatives Chemical class 0.000 abstract description 7
241001465754 Metazoa Species 0.000 description 10
150000001576 beta-amino acids Chemical class 0.000 description 9
150000001875 compounds Chemical class 0.000 description 9
230000037396 body weight Effects 0.000 description 8
229940024606 amino acid Drugs 0.000 description 7
150000003839 salts Chemical class 0.000 description 7
108010016626 Dipeptides Proteins 0.000 description 6
150000001412 amines Chemical class 0.000 description 6
238000002360 preparation method Methods 0.000 description 6
239000002253 acid Substances 0.000 description 5
230000000843 anti-fungal effect Effects 0.000 description 5
238000001727 in vivo Methods 0.000 description 5
239000000243 solution Substances 0.000 description 5
241000222122 Candida albicans Species 0.000 description 4
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
230000000694 effects Effects 0.000 description 4
208000015181 infectious disease Diseases 0.000 description 4
239000003826 tablet Substances 0.000 description 4
238000012360 testing method Methods 0.000 description 4
-1 β-amino acid compounds Chemical class 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
241000700157 Rattus norvegicus Species 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
150000007513 acids Chemical class 0.000 description 3
235000001014 amino acid Nutrition 0.000 description 3
229940095731 candida albicans Drugs 0.000 description 3
239000002775 capsule Substances 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
239000006187 pill Substances 0.000 description 3
239000000829 suppository Substances 0.000 description 3
229920001817 Agar Polymers 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
241000233866 Fungi Species 0.000 description 2
QNAYBMKLOCPYGJ-UWTATZPHSA-N L-Alanine Natural products C[C@@H](N)C(O)=O QNAYBMKLOCPYGJ-UWTATZPHSA-N 0.000 description 2
ROHFNLRQFUQHCH-YFKPBYRVSA-N L-leucine Chemical compound CC(C)C[C@H](N)C(O)=O ROHFNLRQFUQHCH-YFKPBYRVSA-N 0.000 description 2
KZSNJWFQEVHDMF-BYPYZUCNSA-N L-valine Chemical compound CC(C)[C@H](N)C(O)=O KZSNJWFQEVHDMF-BYPYZUCNSA-N 0.000 description 2
BHHGXPLMPWCGHP-UHFFFAOYSA-N Phenethylamine Chemical compound NCCC1=CC=CC=C1 BHHGXPLMPWCGHP-UHFFFAOYSA-N 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
239000013543 active substance Substances 0.000 description 2
239000008272 agar Substances 0.000 description 2
150000003863 ammonium salts Chemical class 0.000 description 2
229940121375 antifungal agent Drugs 0.000 description 2
239000008298 dragée Substances 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
229960000310 isoleucine Drugs 0.000 description 2
210000003734 kidney Anatomy 0.000 description 2
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
XTEGVFVZDVNBPF-UHFFFAOYSA-N naphthalene-1,5-disulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1S(O)(=O)=O XTEGVFVZDVNBPF-UHFFFAOYSA-N 0.000 description 2
239000000825 pharmaceutical preparation Substances 0.000 description 2
239000000843 powder Substances 0.000 description 2
YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
238000001228 spectrum Methods 0.000 description 2
239000000126 substance Substances 0.000 description 2
239000000725 suspension Substances 0.000 description 2
230000009885 systemic effect Effects 0.000 description 2
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
210000003462 vein Anatomy 0.000 description 2
238000005303 weighing Methods 0.000 description 2
238000005160 1H NMR spectroscopy Methods 0.000 description 1
BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 1
HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 1
108050005273 Amino acid transporters Proteins 0.000 description 1
102000034263 Amino acid transporters Human genes 0.000 description 1
239000004475 Arginine Substances 0.000 description 1
241001480043 Arthrodermataceae Species 0.000 description 1
241001225321 Aspergillus fumigatus Species 0.000 description 1
241000228245 Aspergillus niger Species 0.000 description 1
206010007134 Candida infections Diseases 0.000 description 1
RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 1
208000007163 Dermatomycoses Diseases 0.000 description 1
FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
XBPCUCUWBYBCDP-UHFFFAOYSA-N Dicyclohexylamine Chemical compound C1CCCCC1NC1CCCCC1 XBPCUCUWBYBCDP-UHFFFAOYSA-N 0.000 description 1
241001480036 Epidermophyton floccosum Species 0.000 description 1
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
FFEARJCKVFRZRR-UHFFFAOYSA-N L-Methionine Natural products CSCCC(N)C(O)=O FFEARJCKVFRZRR-UHFFFAOYSA-N 0.000 description 1
ODKSFYDXXFIFQN-BYPYZUCNSA-P L-argininium(2+) Chemical compound NC(=[NH2+])NCCC[C@H]([NH3+])C(O)=O ODKSFYDXXFIFQN-BYPYZUCNSA-P 0.000 description 1
235000019454 L-leucine Nutrition 0.000 description 1
239000004395 L-leucine Substances 0.000 description 1
KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 description 1
FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 description 1
229930195722 L-methionine Natural products 0.000 description 1
KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 1
239000004472 Lysine Substances 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
241000893980 Microsporum canis Species 0.000 description 1
241000699666 Mus <mouse, genus> Species 0.000 description 1
241000699670 Mus sp. Species 0.000 description 1
UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 1
GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
241000700159 Rattus Species 0.000 description 1
240000004808 Saccharomyces cerevisiae Species 0.000 description 1
KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
241001045770 Trichophyton mentagrophytes Species 0.000 description 1
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
241000222126 [Candida] glabrata Species 0.000 description 1
239000012072 active phase Substances 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
239000005557 antagonist Substances 0.000 description 1
230000000845 anti-microbial effect Effects 0.000 description 1
ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 description 1
229940091771 aspergillus fumigatus Drugs 0.000 description 1
230000001588 bifunctional effect Effects 0.000 description 1
230000000740 bleeding effect Effects 0.000 description 1
238000009835 boiling Methods 0.000 description 1
210000004556 brain Anatomy 0.000 description 1
KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
159000000007 calcium salts Chemical class 0.000 description 1
208000032343 candida glabrata infection Diseases 0.000 description 1
201000003984 candidiasis Diseases 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
239000000969 carrier Substances 0.000 description 1
230000034303 cell budding Effects 0.000 description 1
235000015165 citric acid Nutrition 0.000 description 1
229960004106 citric acid Drugs 0.000 description 1
239000000470 constituent Substances 0.000 description 1
239000006071 cream Substances 0.000 description 1
238000002425 crystallisation Methods 0.000 description 1
230000008025 crystallization Effects 0.000 description 1
229960002887 deanol Drugs 0.000 description 1
230000037304 dermatophytes Effects 0.000 description 1
ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
239000002552 dosage form Substances 0.000 description 1
210000003238 esophagus Anatomy 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
235000019441 ethanol Nutrition 0.000 description 1
BEFDCLMNVWHSGT-UHFFFAOYSA-N ethenylcyclopentane Chemical compound C=CC1CCCC1 BEFDCLMNVWHSGT-UHFFFAOYSA-N 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000000174 gluconic acid Substances 0.000 description 1
235000012208 gluconic acid Nutrition 0.000 description 1
229950006191 gluconic acid Drugs 0.000 description 1
239000008103 glucose Substances 0.000 description 1
239000008187 granular material Substances 0.000 description 1
230000033687 granuloma formation Effects 0.000 description 1
210000002216 heart Anatomy 0.000 description 1
DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
150000007529 inorganic bases Chemical class 0.000 description 1
238000007689 inspection Methods 0.000 description 1
235000015110 jellies Nutrition 0.000 description 1
239000004310 lactic acid Substances 0.000 description 1
235000014655 lactic acid Nutrition 0.000 description 1
229960000448 lactic acid Drugs 0.000 description 1
229960003136 leucine Drugs 0.000 description 1
210000004185 liver Anatomy 0.000 description 1
239000006210 lotion Substances 0.000 description 1
210000004072 lung Anatomy 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
229960004452 methionine Drugs 0.000 description 1
238000000034 method Methods 0.000 description 1
244000005700 microbiome Species 0.000 description 1
238000002156 mixing Methods 0.000 description 1
229910017604 nitric acid Inorganic materials 0.000 description 1
231100000252 nontoxic Toxicity 0.000 description 1
230000003000 nontoxic effect Effects 0.000 description 1
239000002674 ointment Substances 0.000 description 1
210000004789 organ system Anatomy 0.000 description 1
150000007530 organic bases Chemical class 0.000 description 1
229940116315 oxalic acid Drugs 0.000 description 1
235000006408 oxalic acid Nutrition 0.000 description 1
FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
239000006072 paste Substances 0.000 description 1
230000001717 pathogenic effect Effects 0.000 description 1
RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 1
239000000546 pharmaceutical excipient Substances 0.000 description 1
230000000144 pharmacologic effect Effects 0.000 description 1
229940117803 phenethylamine Drugs 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
230000003389 potentiating effect Effects 0.000 description 1
210000001525 retina Anatomy 0.000 description 1
229960004889 salicylic acid Drugs 0.000 description 1
239000000523 sample Substances 0.000 description 1
238000000926 separation method Methods 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000004334 sorbic acid Substances 0.000 description 1
235000010199 sorbic acid Nutrition 0.000 description 1
229940075582 sorbic acid Drugs 0.000 description 1
210000000952 spleen Anatomy 0.000 description 1
239000007921 spray Substances 0.000 description 1
150000003460 sulfonic acids Chemical class 0.000 description 1
230000001629 suppression Effects 0.000 description 1
230000004083 survival effect Effects 0.000 description 1
239000011975 tartaric acid Substances 0.000 description 1
229960001367 tartaric acid Drugs 0.000 description 1
235000002906 tartaric acid Nutrition 0.000 description 1
230000001225 therapeutic effect Effects 0.000 description 1
238000002560 therapeutic procedure Methods 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
230000014616 translation Effects 0.000 description 1
229960004295 valine Drugs 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
- C07C237/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
- C07C237/04—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
- 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
- A61K38/05—Dipeptides
- 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
- 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
- A61P31/10—Antimycotics
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C229/46—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino or carboxyl groups bound to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
- C07C229/48—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino or carboxyl groups bound to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups and carboxyl groups bound to carbon atoms of the same non-condensed ring
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/06—Systems containing only non-condensed rings with a five-membered ring
- C07C2601/08—Systems containing only non-condensed rings with a five-membered ring the ring being saturated

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Medicinal Chemistry (AREA)
General Health & Medical Sciences (AREA)
Pharmacology & Pharmacy (AREA)
Animal Behavior & Ethology (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Epidemiology (AREA)
Proteomics, Peptides & Aminoacids (AREA)
Gastroenterology & Hepatology (AREA)
General Chemical & Material Sciences (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Chemical Kinetics & Catalysis (AREA)
Oncology (AREA)
Engineering & Computer Science (AREA)
Bioinformatics & Cheminformatics (AREA)
Immunology (AREA)
Communicable Diseases (AREA)
Genetics & Genomics (AREA)
Biophysics (AREA)
Biochemistry (AREA)
Molecular Biology (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Peptides Or Proteins (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Medicinal Preparation (AREA)
Pyrrole Compounds (AREA)

SK947-96A 1995-07-19 1996-07-18 Antimikrobiálne účinné zmesi obsahujúce aminokyseliny, liečivá s ich obsahom a ich použitie SK281850B6 (sk)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19526274A DE19526274A1 (de)	1995-07-19	1995-07-19	Verbesserung der Verträglichkeit von pharmazeutisch wirksamen beta-Aminosäuren

Publications (2)

Publication Number	Publication Date
SK94796A3 SK94796A3 (en)	1997-02-05
SK281850B6 true SK281850B6 (sk)	2001-08-06

Family

ID=7767189

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
SK947-96A SK281850B6 (sk)	1995-07-19	1996-07-18	Antimikrobiálne účinné zmesi obsahujúce aminokyseliny, liečivá s ich obsahom a ich použitie
SK1421-2000A SK284733B6 (sk)	1995-07-19	1996-07-18	Dipeptid, spôsob jeho výroby, liečivo túto látku obsahujúce a jej použitie

Family Applications After (1)

Application Number	Title	Priority Date	Filing Date
SK1421-2000A SK284733B6 (sk)	1995-07-19	1996-07-18	Dipeptid, spôsob jeho výroby, liečivo túto látku obsahujúce a jej použitie

Country Status (44)

Country	Link
US (1)	US5935988A (cs)
EP (2)	EP1043332B1 (cs)
JP (2)	JP3891503B2 (cs)
KR (1)	KR100433968B1 (cs)
CN (1)	CN1115145C (cs)
AR (1)	AR003465A1 (cs)
AT (2)	ATE344274T1 (cs)
AU (1)	AU713555B2 (cs)
BG (1)	BG62134B1 (cs)
BR (1)	BR9603124A (cs)
CA (1)	CA2181308A1 (cs)
CO (1)	CO4700525A1 (cs)
CU (1)	CU22820A3 (cs)
CZ (2)	CZ287896B6 (cs)
DE (3)	DE19526274A1 (cs)
DK (2)	DK1043332T3 (cs)
DZ (1)	DZ2073A1 (cs)
EE (1)	EE03803B1 (cs)
ES (2)	ES2154761T3 (cs)
GR (1)	GR3035601T3 (cs)
HR (1)	HRP960303B1 (cs)
HU (1)	HUP9601977A3 (cs)
IL (1)	IL118869A (cs)
MA (1)	MA23940A1 (cs)
MX (1)	MX9602836A (cs)
NO (1)	NO315926B1 (cs)
NZ (1)	NZ299008A (cs)
PE (1)	PE9398A1 (cs)
PL (1)	PL184861B1 (cs)
PT (2)	PT754678E (cs)
RO (1)	RO118656B1 (cs)
RS (1)	RS49520B (cs)
RU (1)	RU2181123C2 (cs)
SA (1)	SA96170491B1 (cs)
SG (1)	SG47158A1 (cs)
SI (2)	SI0754678T1 (cs)
SK (2)	SK281850B6 (cs)
SV (1)	SV1996000062A (cs)
TN (1)	TNSN96100A1 (cs)
TR (1)	TR199600583A2 (cs)
TW (1)	TW496737B (cs)
UA (1)	UA46725C2 (cs)
YU (1)	YU20050685A (cs)
ZA (1)	ZA966111B (cs)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US6191306B1 (en) *	1999-08-03	2001-02-20	Eastman Chemical Company	Process for the preparation of cyclopropylglycine
KR20010073441A (ko) *	2000-01-14	2001-08-01	최인도	패류종묘 착상판의 제조방법
US8394813B2 (en)	2000-11-14	2013-03-12	Shire Llc	Active agent delivery systems and methods for protecting and administering active agents
US7169752B2 (en)	2003-09-30	2007-01-30	New River Pharmaceuticals Inc.	Compounds and compositions for prevention of overdose of oxycodone
US20060014697A1 (en)	2001-08-22	2006-01-19	Travis Mickle	Pharmaceutical compositions for prevention of overdose or abuse
US7105486B2 (en) *	2002-02-22	2006-09-12	New River Pharmaceuticals Inc.	Abuse-resistant amphetamine compounds
US7659253B2 (en) *	2002-02-22	2010-02-09	Shire Llc	Abuse-resistant amphetamine prodrugs
US7700561B2 (en) *	2002-02-22	2010-04-20	Shire Llc	Abuse-resistant amphetamine prodrugs
SI1644019T2 (en) *	2003-05-29	2018-04-30	Shire Llc	Abuse resistant amphetamine compounds

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB8716278D0 (en) *	1987-07-10	1987-08-19	Fujisawa Pharmaceutical Co	Antimicrobial agent
JPH02174753A (ja) *	1988-08-25	1990-07-06	Fujisawa Pharmaceut Co Ltd	シス―２―アミノシクロペンタンカルボン酸誘導体およびその製法ならびに抗菌剤
RU2030422C1 (ru) *	1990-04-27	1995-03-10	Фармацевтическое акционерное общество "Феррейн"	Способ получения карнозина
DE4302155A1 (de) *	1993-01-27	1994-07-28	Bayer Ag	Verwendung von Cyclopentan- und -penten-beta-Aminosäuren
AU673824B2 (en) *	1992-05-29	1996-11-28	Bayer Aktiengesellschaft	Cyclopentane- and -pentene-beta-amino acids
US5631291A (en) *	1992-05-29	1997-05-20	Bayer Aktiengesellschaft	Cyclopentane- and -pentene-β-amino acids
GB9216441D0 (en) *	1992-08-03	1992-09-16	Ici Plc	Fungicidal process
WO1995007022A1 (en) *	1993-09-07	1995-03-16	Zeneca Limited	Fungicides
DE19548825C2 (de) *	1995-12-27	1999-03-25	Rolf Dr Hermann	Neue, substituierte Cyclopentylaminderivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel
DE19604225A1 (de) *	1996-02-06	1997-08-07	Bayer Ag	Stoffzusammensetzungen aus alpha-Aminosäuren und Cyclohexen-beta-aminosäuren

1995
- 1995-07-19 DE DE19526274A patent/DE19526274A1/de not_active Withdrawn
1996
- 1996-06-28 HR HR960303A patent/HRP960303B1/xx not_active IP Right Cessation
- 1996-07-08 EP EP00110958A patent/EP1043332B1/de not_active Expired - Lifetime
- 1996-07-08 EP EP96110967A patent/EP0754678B1/de not_active Expired - Lifetime
- 1996-07-08 ES ES96110967T patent/ES2154761T3/es not_active Expired - Lifetime
- 1996-07-08 DK DK00110958T patent/DK1043332T3/da active
- 1996-07-08 ES ES00110958T patent/ES2275460T3/es not_active Expired - Lifetime
- 1996-07-08 PT PT96110967T patent/PT754678E/pt unknown
- 1996-07-08 DE DE59611398T patent/DE59611398D1/de not_active Expired - Fee Related
- 1996-07-08 AT AT00110958T patent/ATE344274T1/de not_active IP Right Cessation
- 1996-07-08 PT PT00110958T patent/PT1043332E/pt unknown
- 1996-07-08 DK DK96110967T patent/DK0754678T3/da active
- 1996-07-08 DE DE59606266T patent/DE59606266D1/de not_active Expired - Fee Related
- 1996-07-08 AT AT96110967T patent/ATE198469T1/de not_active IP Right Cessation
- 1996-07-08 SI SI9630243T patent/SI0754678T1/xx unknown
- 1996-07-08 SI SI9630749T patent/SI1043332T1/sl unknown
- 1996-07-12 RS YU41796A patent/RS49520B/sr unknown
- 1996-07-12 AU AU59488/96A patent/AU713555B2/en not_active Ceased
- 1996-07-12 CU CU1996063A patent/CU22820A3/es unknown
- 1996-07-12 US US08/679,027 patent/US5935988A/en not_active Expired - Fee Related
- 1996-07-12 YU YU20050685A patent/YU20050685A/sh unknown
- 1996-07-16 TR TR96/00583A patent/TR199600583A2/xx unknown
- 1996-07-16 CA CA002181308A patent/CA2181308A1/en not_active Abandoned
- 1996-07-16 TW TW085108582A patent/TW496737B/zh not_active IP Right Cessation
- 1996-07-16 RO RO96-01451A patent/RO118656B1/ro unknown
- 1996-07-16 IL IL11886996A patent/IL118869A/en not_active IP Right Cessation
- 1996-07-16 MA MA24315A patent/MA23940A1/fr unknown
- 1996-07-16 NZ NZ299008A patent/NZ299008A/en unknown
- 1996-07-17 UA UA96072884A patent/UA46725C2/uk unknown
- 1996-07-17 DZ DZ960117A patent/DZ2073A1/fr active
- 1996-07-17 BG BG100716A patent/BG62134B1/bg unknown
- 1996-07-17 SG SG1996010277A patent/SG47158A1/en unknown
- 1996-07-18 TN TNTNSN96100A patent/TNSN96100A1/fr unknown
- 1996-07-18 PE PE1996000543A patent/PE9398A1/es not_active Application Discontinuation
- 1996-07-18 PL PL96315330A patent/PL184861B1/pl not_active IP Right Cessation
- 1996-07-18 MX MX9602836A patent/MX9602836A/es not_active IP Right Cessation
- 1996-07-18 ZA ZA9606111A patent/ZA966111B/xx unknown
- 1996-07-18 CO CO96037937A patent/CO4700525A1/es unknown
- 1996-07-18 BR BR9603124A patent/BR9603124A/pt active Search and Examination
- 1996-07-18 NO NO19963000A patent/NO315926B1/no unknown
- 1996-07-18 JP JP20641096A patent/JP3891503B2/ja not_active Expired - Fee Related
- 1996-07-18 SK SK947-96A patent/SK281850B6/sk unknown
- 1996-07-18 SK SK1421-2000A patent/SK284733B6/sk unknown
- 1996-07-18 CZ CZ19962143A patent/CZ287896B6/cs not_active IP Right Cessation
- 1996-07-18 EE EE9600109A patent/EE03803B1/xx not_active IP Right Cessation
- 1996-07-18 KR KR1019960028961A patent/KR100433968B1/ko not_active Expired - Fee Related
- 1996-07-19 RU RU96115341/04A patent/RU2181123C2/ru not_active IP Right Cessation
- 1996-07-19 HU HU9601977A patent/HUP9601977A3/hu unknown
- 1996-07-19 CN CN96108880A patent/CN1115145C/zh not_active Expired - Fee Related
- 1996-07-19 SV SV1996000062A patent/SV1996000062A/es not_active Application Discontinuation
- 1996-07-19 AR ARP960103667A patent/AR003465A1/es unknown
- 1996-12-11 SA SA96170491A patent/SA96170491B1/ar unknown
2000
- 2000-07-10 CZ CZ20002554A patent/CZ288204B6/cs not_active IP Right Cessation
2001
- 2001-03-20 GR GR20010400447T patent/GR3035601T3/el not_active IP Right Cessation
2006
- 2006-09-27 JP JP2006263475A patent/JP2007056026A/ja active Pending

Also Published As

Publication number	Publication date
JP2007056026A (ja)	2007-03-08
KR100433968B1 (ko)	2004-08-30
CN1115145C (zh)	2003-07-23
HRP960303A2 (en)	1998-02-28
JP3891503B2 (ja)	2007-03-14
DE59606266D1 (de)	2001-02-08
KR970006312A (ko)	1997-02-19
DK0754678T3 (da)	2001-02-05
UA46725C2 (uk)	2002-06-17
PL315330A1 (en)	1997-01-20
NO315926B1 (no)	2003-11-17
ATE198469T1 (de)	2001-01-15
EP1043332A1 (de)	2000-10-11
IL118869A (en)	2002-03-10
HU9601977D0 (en)	1996-09-30
HUP9601977A2 (en)	1997-05-28
SK94796A3 (en)	1997-02-05
AU713555B2 (en)	1999-12-02
EP0754678B1 (de)	2001-01-03
BG62134B1 (bg)	1999-03-31
NO963000D0 (no)	1996-07-18
EE9600109A (et)	1997-02-17
ZA966111B (en)	1997-02-03
TW496737B (en)	2002-08-01
EE03803B1 (et)	2002-08-15
ES2275460T3 (es)	2007-06-16
AU5948896A (en)	1997-01-23
YU20050685A (sh)	2006-08-17
DK1043332T3 (da)	2007-03-12
AR003465A1 (es)	1998-08-05
NO963000L (no)	1997-01-20
HRP960303B1 (en)	2001-08-31
CZ288204B6 (en)	2001-05-16
CZ214396A3 (en)	1997-02-12
RU2181123C2 (ru)	2002-04-10
SK284733B6 (sk)	2005-10-06
ES2154761T3 (es)	2001-04-16
SI0754678T1 (en)	2001-04-30
SG47158A1 (en)	1998-03-20
BG100716A (bg)	1997-04-30
JPH09202761A (ja)	1997-08-05
CU22820A3 (es)	2003-01-29
GR3035601T3 (en)	2001-06-29
BR9603124A (pt)	1998-04-22
EP1043332B1 (de)	2006-11-02
RO118656B1 (ro)	2003-08-29
EP0754678A3 (de)	1997-12-17
MA23940A1 (fr)	1997-04-01
IL118869A0 (en)	1996-10-31
YU41796A (sh)	1999-06-15
TR199600583A2 (tr)	1997-02-21
DE19526274A1 (de)	1997-01-23
SV1996000062A (es)	1997-06-26
DZ2073A1 (fr)	2002-07-22
TNSN96100A1 (fr)	2005-03-15
NZ299008A (en)	1998-05-27
HUP9601977A3 (en)	1998-04-28
ATE344274T1 (de)	2006-11-15
PT754678E (pt)	2001-04-30
PE9398A1 (es)	1998-04-15
US5935988A (en)	1999-08-10
SA96170491B1 (ar)	2006-09-20
CN1143496A (zh)	1997-02-26
CZ287896B6 (cs)	2001-03-14
EP0754678A2 (de)	1997-01-22
DE59611398D1 (de)	2006-12-14
CA2181308A1 (en)	1997-01-20
PL184861B1 (pl)	2003-01-31
MX9602836A (es)	1997-01-31
CO4700525A1 (es)	1998-12-29
PT1043332E (pt)	2007-01-31
RS49520B (sr)	2006-10-27
SI1043332T1 (sl)	2007-04-30
HK1005131A1 (en)	1998-12-24

Publication	Publication Date	Title
EP2124550B1 (en)	2017-04-19	Oxabicycloheptanes and oxabicycloheptenes, their preparation and use
CS208663B2 (en)	1981-09-15	Method of making the new r,s-n-/2-phenyl-2-hydroxyethyl0 -1-alkyl-3-/4-substituted phenyl/propylamines
EP3992177B1 (en)	2024-05-08	Derivative compound introducing biphenyl group into novel aminoalkanoic acid and antifungal pharmaceutical composition comprising same
SK281850B6 (sk)	2001-08-06	Antimikrobiálne účinné zmesi obsahujúce aminokyseliny, liečivá s ich obsahom a ich použitie
JP2022512652A (ja)	2022-02-07	Ｐ２ｘ３拮抗薬での皮膚掻痒症の治療
EP2094675B1 (en)	2011-04-06	A salt of 3-benzyl-2-methyl-2,3,3a,4,5,6,7,7a-octahydrobenzo[d]isoxazol-4-one
EP2848606A2 (en)	2015-03-18	Fluoro-substituted (3r, 4r, 5s)-5-guanidino-4-acylamino-3-(pentan-3-yloxy) cyclohexene-1-carboxylic acids, esters thereof and a method for the use thereof
SU655280A3 (ru)	1979-03-30	Фунгицидное средство
US12569454B2 (en)	2026-03-10	Nucleophilic chemicals useful in the treatment of cisplatin-induced sensory neuropathy and ototoxicity
US8058468B2 (en)	2011-11-15	Carbamate antibiotics
HK1005131B (en)	2001-06-29	Improvement of physiological tolerance of pharmaceutical active beta-amio acids
WO2004024755A2 (de)	2004-03-25	Sarcolysyl-derivate und verfahren zu deren herstellung
JP2009533428A (ja)	2009-09-17	筋肉内抗ウイルス処置
AU2018273599B2 (en)	2020-10-22	Polysubstituted pyrimidines inhibiting the formation of prostaglandin E2, a method of production thereof and use thereof
ZA202304845B (en)	2024-01-31	Pharmaceutical composition comprising an antimicrobial agent and method for the preparation thereof
HK1140375A (en)	2010-10-15	Oxabicycloheptanes and oxabicycloheptenes, their preparation and use