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Purine nucleoside 5'-phosphate (mono, di or tri) 3'(2')-diphosphates and processes for their preparation

Assignee: Sanraku Ocean Co Ltd
•
Filing: 1977-04-27
•
Granted: 1979-02-27
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Expires: 1997-04-27
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Abstract

Abstract New purine nucleoside 5'-phosphate (mono, di or tri) 3'(2')-diphosphates and the sodium, lithium and potassium salts thereof are elaborated by the enzymatic transfer of pyrophosphoryl group from ATP (adenosine triphosphate), dATP (deoxyadenosine triphosphate) and pppApp (adenosine 5'-triphosphate 3'(2') diphosphate) to specified 5'-purine nucleotides, and a new nucloetide pyrophosphotransferase used for this enzyme reaction is produced by actinomycetes and other microorganisms and recovered from the culture filtrate and mycelium by the conventional methods for recovering enzymes. These compounds are useful for treating leukemia L1210 in mice.

Inventors

  • 👤 Toyokazu Nishino
  • 👤 Yasutaro Hamagishi
  • 👤 Toshikazu Oki
  • 👤 Sawao Murao

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-23 16:50
CPC Classifications
C; C07; C07H; C07H21/00; C07H21/02; A; A61; A61K; A61K38/00; A61K38/16; A61K38/43; A61K38/45; C07H19/00; C07H19/02; C07H19/04; C07H19/16; C07H19/20; C12; C12N; C12N9/00; C12N9/10; C12N9/12; C12P; C12P19/00; C12P19/26; C12P19/28; C12P19/30; C12P19/32; Y; Y10; Y10S; Y10S435/00; Y10S435/8215; Y10S435/822; Y10S435/886; Y10S435/908

Claims Analysis

Total Claims: 6
Claim 1
Independent Claim 73 words
A purine nucleoside 5'-(mono, di or tri) phosphate 3'(2')-diphosphate and the corresponding purine nucleoside 5'-(di or tri) phosphate 3'(2')-monophosphate and the salts thereof selected from the group consisting of adenosine-5'-monophosphate 3'(2')-diphosphate(pApp), adenosine-5'-diphosphate 3'(2')-diphosphate(ppApp), adenosine-5'-triphosphate 3'(2')-diphosphate(pppApp), guanosine-5'-monophosphate 3'(2')-diphosphate(pGpp), inosine-5'-monophosphate 3'(2')-diphosphate(pIpp), inosine-5'-diphosphate 3'(2')-diphosphate(ppIpp), inosine-5'-triphosphate 3'(2')-diphosphate(pppIpp), β,γ-methylene adenosine 5'-triphosphate 3'(2')-diphosphate(p(CH 2 )ppApp), guanosine-5'-triphosphate 3'(2')-monophosphate(pppGp), inosine-5'-diphosphate 3'(2')-monophosphate(ppIp), inosine-5'-triphosphate 3'(2')-monophosphate(pppIp), β,γ-methylene adenosine-5'-triphosphate 3'(2')-monophosphate(p(CH 2 )ppAp) and β,γ-methylene guanosine-5'-triphosphate 3'(2')-monophosphate(p(CH 2 )ppGp) and lithium, potassium and sodium salts thereof.
Claim 2
Dependent Claim 73 words
A purine nucleoside 5'-(mono, di or tri) phosphate 3'(2')-diphosphate and the corresponding purine nucleoside 5'-(di or tri) phosphate 3'(2')-monophosphate and the salts thereof selected from the group consisting of adenosine-5'-monophosphate 3'(2')-diphosphate(pApp), adenosine-5'-diphosphate 3'(2')-diphosphate(ppApp), adenosine-5'-triphosphate 3'(2')-diphosphate(pppApp), guanosine-5'-monophosphate 3'(2')-diphosphate(pGpp), inosine-5'-monophosphate 3'(2')-diphosphate(pIpp), inosine-5'-diphosphate 3'(2')-diphosphate(ppIpp), inosine-5'-triphosphate 3'(2')-diphosphate(pppIpp), β,γ-methylene adenosine 5'-triphosphate 3'(2')-diphosphate(p(CH 2 )ppApp), guanosine-5'-triphosphate 3'(2')-monophosphate(pppGp), inosine-5'-diphosphate 3'(2')-monophosphate(ppIp), inosine-5'-triphosphate 3'(2')-monophosphate(pppIp), β,γ-methylene adenosine-5'-triphosphate 3'(2')-monophosphate(p(CH 2 )ppAp) and β,γ-methylene guanosine-5'-triphosphate 3'(2')-monophosphate(p(CH 2 )ppGp) and lithium, potassium and sodium salts thereof.
Claim 3
Dependent Claim 42 words
A pharmaceutical composition for intraperitoneal administration to animals comprising a substance according to claim 1 in a concentration sufficient to suppress an accumulation of abdominal dropsy without causing toxicity to the recipient in vivo in combination with a pharmaceutically acceptable nontoxic carrier.
Claim 4
Dependent Claim 42 words
A method for chemotherapeutically treating an animal bearing ascites tumor including an accumulation of abdominal dropsy, which comprises administering a compound according to claim 1 to said animal in a dosage sufficient to lower said accumulation without causing toxicity to said animal.
Claim 5
Dependent Claim 11 words
A pharmaceutical composition of claim 2 wherein said animals are rodents.
Claim 6
Dependent Claim 11 words
A method of claim 3 wherein said animal is a rodent.

References Cited (Backward Citations)

US3413282A Cited
US3407190A Cited
US3457254A Cited
US3423399A Cited
US3475409A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1982-02-26 1982-08-28 1983-02-27 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1986-02-26 1986-08-28 1987-02-27 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1990-02-26 1990-08-28 1991-02-27 $7700.00 Window Closed / Lapsed

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