WO1999029716A1 - Derives de l'echinocandine, leur procede de preparation et leur application comme anti-fongiques - Google Patents

Derives de l'echinocandine, leur procede de preparation et leur application comme anti-fongiques Download PDF

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Publication number
WO1999029716A1
WO1999029716A1 PCT/FR1998/002671 FR9802671W WO9929716A1 WO 1999029716 A1 WO1999029716 A1 WO 1999029716A1 FR 9802671 W FR9802671 W FR 9802671W WO 9929716 A1 WO9929716 A1 WO 9929716A1
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WIPO (PCT)
Prior art keywords
formula
radical
compounds
hydrogen atom
carbon atoms
Prior art date
Legal status (The legal status 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 status listed.)
Ceased
Application number
PCT/FR1998/002671
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English (en)
French (fr)
Inventor
Olivier Courtin
Patrick Fauveau
Astrid Markus
Dominique Melon Manguer
Jean-Marc Michel
Laurent Schio
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sanofi Aventis France
Aventis Pharmaceuticals Inc
Original Assignee
Hoechst Marion Roussel
Hoechst Marion Roussel Inc
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.)
Filing date
Publication date
Priority claimed from FR9715628A external-priority patent/FR2772028B1/fr
Priority to UA2000074030A priority Critical patent/UA72200C2/uk
Priority claimed from FR9813361A external-priority patent/FR2784993B1/fr
Priority to BR9813531-7A priority patent/BR9813531A/pt
Priority to AU15659/99A priority patent/AU755033B2/en
Priority to IL13664798A priority patent/IL136647A0/xx
Priority to PL341012A priority patent/PL196889B1/pl
Priority to US09/581,451 priority patent/US6677429B1/en
Priority to EA200000625A priority patent/EA002706B1/ru
Priority to SK839-2000A priority patent/SK286916B6/sk
Priority to EP98959935A priority patent/EP1036090B1/fr
Priority to CA002311295A priority patent/CA2311295A1/fr
Priority to JP2000524307A priority patent/JP4361679B2/ja
Priority to KR1020007006268A priority patent/KR100564872B1/ko
Priority to NZ504614A priority patent/NZ504614A/xx
Priority to APAP/P/2000/001826A priority patent/AP1260A/en
Application filed by Hoechst Marion Roussel, Hoechst Marion Roussel Inc filed Critical Hoechst Marion Roussel
Priority to HU0100263A priority patent/HUP0100263A3/hu
Priority to SI9830834T priority patent/SI1036090T1/sl
Priority to HR20000384A priority patent/HRP20000384B1/xx
Priority to EEP200000336A priority patent/EE04837B1/xx
Priority to DE69834057T priority patent/DE69834057T2/de
Publication of WO1999029716A1 publication Critical patent/WO1999029716A1/fr
Priority to BG104494A priority patent/BG65033B1/bg
Priority to IL136647A priority patent/IL136647A/en
Priority to NO20002959A priority patent/NO327498B1/no
Anticipated expiration legal-status Critical
Priority to AU2003200556A priority patent/AU2003200556B2/en
Priority to US10/666,072 priority patent/US7160983B2/en
Priority to US11/165,458 priority patent/US7285619B2/en
Priority to IL172412A priority patent/IL172412A/en
Priority to CY20061100686T priority patent/CY1105695T1/el
Priority to IL184171A priority patent/IL184171A0/en
Ceased legal-status Critical Current

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Classifications

    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
    • 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
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
    • C07D487/18—Bridged systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
    • C07K7/50—Cyclic peptides containing at least one abnormal peptide link
    • C07K7/54—Cyclic peptides containing at least one abnormal peptide link with at least one abnormal peptide link in the ring
    • C07K7/56—Cyclic peptides containing at least one abnormal peptide link with at least one abnormal peptide link in the ring the cyclisation not occurring through 2,4-diamino-butanoic acid
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides

Definitions

  • the present invention relates to new derivatives of echinocandins, their preparation process and their application as antifungals.
  • the subject of the invention is, and, in all the forms of isomers possible and their mixtures, the compounds of formula (I): 0
  • R 1 and R 2 identical or different from each other represent a hydrogen atom, a hydroxyl radical, an alkyl radical containing up to 8 linear, branched or cyclic carbon atoms, optionally interrupted by an oxygen atom optionally substituted by an 0 atom
  • halogen an OH radical, an N z a , a and bb radical identical or different from each other, 5 representing a hydrogen atom or an alkyl radical containing up to 8 carbon atoms, a and b possibly forming with the nitrogen atom a heterocycle possibly containing one or more heteroatoms additional,
  • R a represents a radical XR a , X representing an oxygen atom or an NH or N-alkyl radical containing up to 8 carbon atoms and R a represents a hydrogen atom, a linear, branched or cyclic alkyl radical containing up to with 8 carbon atoms optionally substituted by one or more halogen atoms, by one or more OH, C0 2 H, C0 2 alk, .a 'radicals by a radical
  • a 'and b' can form a heterocycle possibly containing one or more additional heteroatoms and / or by a heterocycle containing one or more hetero-
  • d, e, f and g represent a hydrogen atom or an alkyl radical containing up to 8 carbon atoms, f and g which may further represent an acyl radical containing up to 8 carbon atoms, e and f can also form a ring optionally containing one or more heteroatoms, R3 represents a hydrogen atom, a methyl or hydroxyl radical
  • R4 represents a hydrogen atom or a hydroxyl radical
  • R represents a linear or branched or cyclic chain containing up to 30 carbon atoms, possibly containing- one or more heteroatoms, one or more heterocycles or a linear, branched or cyclic acyl radical containing up to 30 carbon atoms optionally containing one or more heteroatoms and / or one or more heterocycles,
  • T represents a hydrogen atom, a methyl radical, a CH 2 CONH 2 , CH 2 C ⁇ N radical, a (CH 2 ) 2 NH 2 or (CH 2 ) 2 Nalc + X ⁇ radical,
  • X being a halogen atom and having an alkyl radical containing up to 8 carbon atoms
  • Y represents a hydrogen atom, a hydroxyl radical or a halogen atom or an OS03H radical or one of the salts thereof radical
  • W represents a hydrogen atom or an OH radical
  • Z represents a hydrogen atom or a methyl radical
  • addition salts with acids there may be mentioned those formed with mineral acids, such as hydrochloric, hydrobromic, sulfuric or phosphoric acids or with organic acids such as formic, acetic, trifluoroacetic, propionic, benzoic acid, maleic, fumaric, succinic, tartaric, citric, oxalic, glycolic, aspartic, alkanesulfonic, such as methane or ethane sulfonic acids, arylsulfonic such as benzene or paratoluenesulfonic acids.
  • mineral acids such as hydrochloric, hydrobromic, sulfuric or phosphoric acids
  • organic acids such as formic, acetic, trifluoroacetic, propionic, benzoic acid, maleic, fumaric, succinic, tartaric, citric, oxalic, glycolic, aspartic, alkanesulfonic, such as methane or ethane sulfonic acids, aryl
  • the alkyl, alkenyl or alkynyl radical is preferably a methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, terbutyl, decyl or dodecyl, vinyl, allyl, ethynyl, propynyl, cyclobutyl, cyclopentyl or cyclohexyl radical,
  • the halogen is preferably fluorine or chlorine or bromine
  • the aryl radical is preferably the phenyl radical
  • the heterocyclic radical is preferably the pyrrolyl, pyrrolidinyl, pyridyle, pyrazinyl, pyrimidyl, piperidinyl, piperazinyl, quinuclidinyl, oxazolyl, isoxazolyl, morpholinyl, indolyl, imidazolyl radical, benzimida zolyle, triazolyle, thiazolyle, azURIdinyle, aziridinyle.
  • the salt of the SO 3 H radical there may be mentioned the sodium and potassium salts or also the amine salts.
  • n represents an integer between 1 and 8 and especially those in which n represents the number 2 and Y 'represents a hydrogen atom or an alkyl radical containing up to 8 carbon atoms, and those in which R2 represents a radical
  • the invention also particularly relates to the compounds of formula (I) in which R2 represents a radical
  • Y '' represents a hydrogen atom or an alkyl radical containing up to 8 carbon atoms and p represents an integer varying from 1 to 8, and especially the compounds in which p represents the number 2.
  • a subject of the invention is very particularly the compounds in which RI represents a hydrogen atom.
  • the compounds of formula (I) have interesting antifungal properties; they are particularly active on Candida albicans and other Candida such as Candida glabrata, krusei, tropicalis, pseudotropicalis, parapsilosis and Aspergillus fumigatus, Aspergillus flavus, Cryptococcus neoformans.
  • the compounds of formula (I) can be used as medicaments in humans or animals, in particular for combating digestive, urinary, vaginal or skin candidiasis, cryptococcosis, for example neuromenengees, pulmonary or skin cryptococcosis, bronchopulmonary and pulmonary aspergillosis and invasive aspergillosis of the munodepressed i.
  • the compounds of the invention can also be used in the prevention of fungal diseases in congenital or acquired immune depressed people.
  • the compounds of the invention are not limited to pharmaceutical use, they can also be used as fungicides in fields other than pharmaceutical.
  • the subject of the invention is therefore, as antifungal compounds, the compounds of formula (I) as well as their addition salts with acids.
  • a subject of the invention is also the compounds of formula (I), as medicaments.
  • the invention particularly relates to pharmaceutical compositions containing as active principle at least one compound of formula (I) or one of its addition salts with pharmaceutically acceptable acids. These compositions can be administered by the oral, rectal, parenteral route or by the local route as a topical application to the skin and the mucous membranes, but the preferred route is the oral route.
  • compositions can be solid or liquid and present in pharmaceutical forms commonly used in human medicine, such as, for example, simple or coated tablets, capsules, granules, suppositories, injections, ointments, creams, gels; they are prepared according to the usual methods.
  • the active ingredient (s) can be incorporated therein into excipients usually used in these pharmaceutical compositions, such as talc, gum arabic, lactose, starch, magnesium stearate, cocoa butter, aqueous vehicles or no, fatty substances of animal or vegetable origin, paraffinic derivatives, glycols, various wetting agents, dispersants or emulsifiers, preservatives.
  • compositions can also be in the form of a powder intended to be dissolved extemporaneously in a suitable vehicle, for example sterile pyrogen-free water.
  • the dose administered is variable depending on the condition treated, the subject in question, the route of administration and the product considered. It can be, for example, between 50 mg and 300 mg per day orally, in adults for the products of Examples 8, 9, 11, 13 and 14.
  • the subject of the invention is also a process for preparing the compounds of formula (I), characterized in that a compound of formula (II) is subjected:
  • RI and R2 retain their previous meaning and if desired the action of a reducing agent and / or an amine functionalizing agent, and / or an acid to form the salt of the product obtained , and / or an agent for separating the various isomers obtained, and thus obtains the desired compound of formula (I)
  • ISi- (CH 3 ) 3 or any other Lewis acid can be used.
  • a more particular subject of the invention is the compounds of formula (IV), the preparation of which is given below in the experimental part.
  • PREPARATION 1 1- [N2 - (12 -methyl-1-oxotetradecyl) -4-oxo-L- omithine] 4- [4- (4-h.hydroxyphenyl) -L- threonine] -5 -L-serine ⁇ chinocandine B.
  • EXAMPLE 5 (Z) 1- [4- [(2-hydroxyethoxy) imino] -N2 - (12 - ethyl- 1-oxotetradecyl) -L-ornithine] 4 - [4- (4-hydroxyphenyl) -L-threonine] -5-L-serine echinocandin B and corresponding E isomer.
  • EXAMPLE 8 (Z) 1- [(S) -N2- (12-methyl-1-oxotetradecyl) 4- [[((3-piperidinyl) oxy] imino] -L-ornithine) hydrochloride 4- [4- (4-hydroxyphenyl) -L-threonine] -5-L-serine ⁇ chinocandine B.
  • a mixture of 1 g of product from stage A and 25 ml of acetonitrile is heated to 55 ° C. in the presence of active 4A siliporite. 430 ml of trimethylsilane iodide are added. The mixture is stirred for 45 minutes and then 150 ⁇ l of a 30% aqueous sodium thiosulfate solution are added. The mixture is stirred for 40 minutes at 20 ° C. and concentrated. The dry extract is taken up in water, stirred for 1 hour at 20 ° C. wrung and washed. A product is obtained which is chromatographed on silica eluting with a methylene chloride-methanol-water mixture (86/13/1). 497 mg of sought product is obtained. Yield 42%.
  • Stage C 1- [4- [(aminoiminomethyl) hydrazono] -N2 - [[4 - [4 - [4 - (pentyloxy) -phenyl] -1-piperazinyl] phenyl] carbonyl] -L- ornithine] -4- [4- (4-hydroxyphenyl) -L-threonine] -5-L-serine- echinocandin B
  • a suspension containing 400 mg of product from stage B, 4.8 ml of n-butanol and 221 mg of aminoguanidine hydrochloride is heated at 130 ° C. for 3 hours. Concentrate and obtain 705 mg of a product which is chromatographed on silica eluting with a methylene chloride mixture of methanol 85/15, then with semi-preparative HPCL (kromasil C18) with an acetonitrile / water / trifluoroacetic acid mixture ( 40.60.0.02). 64 mg of sought product is thus obtained.
  • EXAMPLE 16 1- [4- [(2 -aminoethyl) amino] -N2 - [4- [4 "- (pentyloxy) [1,1 ': 4', 1" -terphenyl] -4-yl] carbonyl] -L-ornithine] -4- [4- (4 -hydroxypheny1) -L-threonine] - 5 -L- serine- echinocandin B (isomer A and isomer B).
  • the medium is incubated at 25 ° C for 1 hour and the reaction ended by adding TCA to a final concentration of 5%.
  • the reaction mixture is transferred to a pre-humidified fiberglass filter.
  • the filter is washed, dried and its radioactivity is counted.
  • Mulundocandin is used as a positive control
  • the control of the vehicle is carried out with the same amount of 1% DMSO.
  • B - activity on the Aspergillus fumigatus enzyme The enzyme is prepared according to the process de Beaulieu et al. (Antimicrob. Agents Chenother 38, 937-944, 1994.
  • the protocol used is identical to the protocol described above for the enzyme Candida albicans except that no dithiotreitol is used in the mixture reactive.
  • the products show good activity on this test.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Molecular Biology (AREA)
  • Genetics & Genomics (AREA)
  • Biophysics (AREA)
  • Biochemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • Environmental Sciences (AREA)
  • Zoology (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Wood Science & Technology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Peptides Or Proteins (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Detergent Compositions (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
PCT/FR1998/002671 1997-12-10 1998-12-09 Derives de l'echinocandine, leur procede de preparation et leur application comme anti-fongiques Ceased WO1999029716A1 (fr)

Priority Applications (28)

Application Number Priority Date Filing Date Title
UA2000074030A UA72200C2 (uk) 1997-12-10 1998-09-12 Похідні ехінокандину, спосіб їх одержання, їх застосування, проміжні сполуки та фармацевтична композиція
HR20000384A HRP20000384B1 (en) 1997-12-10 1998-12-09 Echinocandin derivatives, preparation method and application as anti-fungla agents
EEP200000336A EE04837B1 (et) 1997-12-10 1998-12-09 Ehhinokandiini derivaadid, nende valmistamismeetod ja kasutamine antimükootikumidena
HU0100263A HUP0100263A3 (en) 1997-12-10 1998-12-09 Echinocandin derivatives, preparation method and application as anti-fungal agents
IL13664798A IL136647A0 (en) 1997-12-10 1998-12-09 Echinocandin derivatives, preparation method and application as anti-fungal agents
PL341012A PL196889B1 (pl) 1997-12-10 1998-12-09 Pochodne echinokandyny, sposób wytwarzania pochodnej echinokandyny, jej zastosowanie jako substancji przeciwgrzybicznej oraz zawierająca ją kompozycja farmaceutyczna
US09/581,451 US6677429B1 (en) 1997-12-10 1998-12-09 Echinocandin derivatives, preparation method and application as anti-fungal agents
EA200000625A EA002706B1 (ru) 1997-12-10 1998-12-09 Производные эхинокандина, способ их получения и их применение в качестве противогрибковых средств
SK839-2000A SK286916B6 (sk) 1997-12-10 1998-12-09 Deriváty echinokandínu, spôsob ich prípravy a ich aplikácia ako antifungálnych činidiel
EP98959935A EP1036090B1 (fr) 1997-12-10 1998-12-09 Derives de l'echinocandine, leur procede de preparation et leur application comme anti-fongiques
CA002311295A CA2311295A1 (fr) 1997-12-10 1998-12-09 Derives de l'echinocandine, leur procede de preparation et leur application comme anti-fongiques
JP2000524307A JP4361679B2 (ja) 1997-12-10 1998-12-09 エキノカンジン誘導体、それらの製造方法及びそれらの抗真菌剤としての使用
KR1020007006268A KR100564872B1 (ko) 1997-12-10 1998-12-09 에키노칸딘 유도체, 그의 제조 방법 및 항진균제로서의 응용
NZ504614A NZ504614A (en) 1997-12-10 1998-12-09 Echinocandin derivatives and application as anti-fungal agents
APAP/P/2000/001826A AP1260A (en) 1997-12-10 1998-12-09 Echinocandin derivatives, preparation method and application as anti-fungal agents.
BR9813531-7A BR9813531A (pt) 1997-12-10 1998-12-09 "derivados da equinocandina, seu processo de preparo e sua aplicação como antifúngicos"
SI9830834T SI1036090T1 (sl) 1997-12-10 1998-12-09 Derivati ehinokandina, postopek za njihovo pripravo in njihova uporaba kot protiglivicna sredstva
DE69834057T DE69834057T2 (de) 1997-12-10 1998-12-09 Echinocandinderivate, deren herstellung und deren verwendung zur bekämpfung von pilzen
AU15659/99A AU755033B2 (en) 1997-12-10 1998-12-09 Echinocandin derivatives, preparation method and application as anti-fungal agents
BG104494A BG65033B1 (bg) 1997-12-10 2000-05-31 Производни на ехинокандин, метод за тяхното получаване и използването им като противогъбично средство
IL136647A IL136647A (en) 1997-12-10 2000-06-08 History of Echinocandin, method of preparation and use as antifungal preparations
NO20002959A NO327498B1 (no) 1997-12-10 2000-06-09 Echinocandinderivater, fremgangsmate for fremstilling av slike, antifungale forbindelser og farmasoytiske preparater inneholdende disse forbindelser.
AU2003200556A AU2003200556B2 (en) 1997-12-10 2003-02-12 Echinocandin derivative and their preparation method
US10/666,072 US7160983B2 (en) 1997-12-10 2003-09-19 Echinocandin derivatives, their method of preparation and their application as anti-fungal agents
US11/165,458 US7285619B2 (en) 1997-12-10 2005-06-23 Echinocandin derivatives, their method of preparation and their application as anti-fungal agents
IL172412A IL172412A (en) 1997-12-10 2005-12-06 History of Echinocandin, method of preparation and use as antifungal preparations
CY20061100686T CY1105695T1 (el) 1997-12-10 2006-05-30 Παραγωγα της εχινοκανδινης, μεθοδος παρασκευης τους και εφαρμογη τους σαν αντι-μυκητιασικα
IL184171A IL184171A0 (en) 1997-12-10 2007-06-24 Echinocandin derivatives, preparation method and application as anti-fungal agents

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
FR97/15628 1997-12-10
FR9715628A FR2772028B1 (fr) 1997-12-10 1997-12-10 Nouveaux derives de l'echinocandine, leur procede de preparation et leur application comme fongicides
FR98/13361 1998-10-26
FR9813361A FR2784993B1 (fr) 1998-10-26 1998-10-26 Nouveaux derives de l'echinocandine, leur procede de preparation et leur application comme fongicides

Related Child Applications (4)

Application Number Title Priority Date Filing Date
US09/581,451 A-371-Of-International US6677429B1 (en) 1997-12-10 1998-12-09 Echinocandin derivatives, preparation method and application as anti-fungal agents
US09581451 A-371-Of-International 1998-12-09
US09581541 A-371-Of-International 1998-12-09
US10/666,072 Division US7160983B2 (en) 1997-12-10 2003-09-19 Echinocandin derivatives, their method of preparation and their application as anti-fungal agents

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WO1999029716A1 true WO1999029716A1 (fr) 1999-06-17

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PCT/FR1998/002671 Ceased WO1999029716A1 (fr) 1997-12-10 1998-12-09 Derives de l'echinocandine, leur procede de preparation et leur application comme anti-fongiques

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KR (1) KR100564872B1 (https=)
CN (1) CN1284084A (https=)
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SA (1) SA99191248B1 (https=)
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TR (1) TR200001655T2 (https=)
TW (1) TW446541B (https=)
UA (1) UA72200C2 (https=)
UY (1) UY25292A1 (https=)
WO (1) WO1999029716A1 (https=)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000024694A1 (en) * 1998-10-28 2000-05-04 Eli Lilly And Company Photochemical process for making 1-deoxy-2-keto derivatives
WO2000075178A1 (fr) * 1999-06-09 2000-12-14 Aventis Pharma S.A. Nouveaux derives de l'echinocandine, leur procede de preparation et leur application comme antifongiques
WO2000075177A1 (fr) * 1999-06-09 2000-12-14 Aventis Pharma S.A. Nouveaux derives de l'echinocandine, leur procede de preparation et leur application comme antifongiques
FR2833596A1 (fr) * 2001-12-14 2003-06-20 Aventis Pharma Sa Procede de preparation de derives d'echinocandine

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UA72200C2 (uk) * 1997-12-10 2005-02-15 Авентіс Фарма С.А. Похідні ехінокандину, спосіб їх одержання, їх застосування, проміжні сполуки та фармацевтична композиція
CN101659693B (zh) * 2008-08-27 2012-11-21 上海医药工业研究院 制备纽莫康定b0的方法
CN101659692B (zh) * 2008-08-27 2012-07-04 上海医药工业研究院 制备棘球康定b的方法

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WO1996008267A1 (en) * 1994-09-16 1996-03-21 Merck & Co., Inc. Semi-synthetic lipopeptides, compositions containing said lipopeptides, and methods of use
WO1996013272A1 (en) * 1994-10-31 1996-05-09 Merck & Co., Inc. Aza cyclohexapeptide compounds
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Cited By (11)

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Publication number Priority date Publication date Assignee Title
WO2000024694A1 (en) * 1998-10-28 2000-05-04 Eli Lilly And Company Photochemical process for making 1-deoxy-2-keto derivatives
WO2000075178A1 (fr) * 1999-06-09 2000-12-14 Aventis Pharma S.A. Nouveaux derives de l'echinocandine, leur procede de preparation et leur application comme antifongiques
WO2000075177A1 (fr) * 1999-06-09 2000-12-14 Aventis Pharma S.A. Nouveaux derives de l'echinocandine, leur procede de preparation et leur application comme antifongiques
FR2794746A1 (fr) * 1999-06-09 2000-12-15 Hoechst Marion Roussel Inc Nouveaux derives de l'echinocandine, leur procede de preparation et leur application comme anti-fongiques
FR2794747A1 (fr) * 1999-06-09 2000-12-15 Hoechst Marion Roussel Inc Nouveaux derives de l'echinocandine, leur procede de preparation et leur application comme anti-fongiques
US7005417B1 (en) 1999-06-09 2006-02-28 Aventis Pharma S.A. Echinocandin derivatives, method for preparing same and use as antifungal agents
US7022669B1 (en) 1999-06-09 2006-04-04 Aventis Pharma S.A. Echinocandin derivatives, method for preparing same and application as antifungal agents
US7192920B2 (en) * 1999-06-09 2007-03-20 Aventis Pharma Sa Derivatives of echinocandine, their preparation process and their use as antifungals
FR2833596A1 (fr) * 2001-12-14 2003-06-20 Aventis Pharma Sa Procede de preparation de derives d'echinocandine
WO2003054001A3 (fr) * 2001-12-14 2004-01-22 Aventis Pharma Sa Procede de preparation de derives d'echinocandines et leurs compositions
EA007964B1 (ru) * 2001-12-14 2007-02-27 Авентис Фарма С.А. Способ получения эхинокандиновых соединений

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