Patent US4968686A successfully refreshed from Google Patents.
← Back to Patent Explorer
US4968686A Expired / Lapsed US ⏱️ 0.0 years remaining

Acyclic pyrrolo [2,3-d]pyrimidine analogs as antiviral agents

Assignee: University of Michigan (System)
•
Filing: 1989-06-21
•
Granted: 1990-11-06
•
Expires: 2009-06-21
📄 Original PDF 🌐 Google Patents 🔄 Sync Now

Abstract

Abstract This invention relates to the use of acyclic substituted pyrrolo[2,3-d]pyrimidine nucleoside analogs in the treatment of viral infections. Such substituted compounds retain antiviral properties present in their parent compounds, yet exhibit significantly decreased levels of cytotoxicity, thereby having therapeutic potential as antiviral agents.

Inventors

  • 👤 Leroy B. Townsend
  • 👤 John G. Drach
  • 👤 Charles Shipman, Jr.
  • 👤 Jeffrey S. Pudlo

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-01 20:10
CPC Classifications
C; C07; C07D; C07D471/00; C07D471/02; C07D471/04

Claims Analysis

Total Claims: 44
Claim 1
Independent Claim 63 words
A compound selected from the group consisting of compounds of the following formula and pharmaceutically acceptable salts thereof: ##STR6## where R 1 is NH 2 , NHOH, OH or H; R 2 is CSNH 2 , Cl, Br, I, F, 2-buten-1-yl, 5-(1-hydroxyethyl or 5-(1-methoxyethyl); R 3 is H, NH 2 or Br; and R 4 is (1,3-dihydroxy-2-propoxy)methyl, (2-hydroxyethoxy)methyl, (2-acetoxyethoxy)methyl, 2-hydroxy-1-(1,3-dihydroxy-2-propoxy)ethyl, (2-phosphonylmethoxy)ethyl or 3-hydroxy-2-phosphonylmethoxypropyl.
Claim 2
Dependent Claim 63 words
A compound selected from the group consisting of compounds of the following formula and pharmaceutically acceptable salts thereof: ##STR6## where R 1 is NH 2 , NHOH, OH or H; R 2 is CSNH 2 , Cl, Br, I, F, 2-buten-1-yl, 5-(1-hydroxyethyl or 5-(1-methoxyethyl); R 3 is H, NH 2 or Br; and R 4 is (1,3-dihydroxy-2-propoxy)methyl, (2-hydroxyethoxy)methyl, (2-acetoxyethoxy)methyl, 2-hydroxy-1-(1,3-dihydroxy-2-propoxy)ethyl, (2-phosphonylmethoxy)ethyl or 3-hydroxy-2-phosphonylmethoxypropyl.
Claim 3
Dependent Claim 25 words
The compound of claim 1 wherein R 1 is NH 2 , R 2 is Cl, R 3 is H and R 4 is (2-hydroxyethoxy)methyl.
Claim 4
Dependent Claim 25 words
The compound of claim 1 wherein R 1 is NH 2 , R 2 is Br, R 3 is H and R 4 is (2-hydroxyethoxy)methyl.
Claim 5
Dependent Claim 25 words
The compound of claim 1 wherein R 1 is NH 2 , R 2 is I, R 3 is H and R 4 is (2-hydroxyethoxy)methyl.
Claim 6
Dependent Claim 25 words
The compound of claim 1 wherein R 1 is NH 2 , R 2 is thiocarboxamide, R 3 is H and R 4 is (2-hydroxyethoxy)methyl.
Claim 7
Dependent Claim 25 words
The compound of claim 1 wherein R 1 is NH 2 , R 2 is Cl, R 3 is H and R 4 is (1,3-dihydroxy-2-propoxy)methyl.
Claim 8
Dependent Claim 25 words
The compound of claim 1 wherein R 1 is NH 2 , R 2 is Br, R 3 is H and R 4 is (1,3-dihydroxy-2-propoxy)methyl.
Claim 9
Dependent Claim 25 words
The compound of claim 1 wherein R 1 is NH 2 , R 2 is I, R 3 is H and R 4 is (1,3-dihydroxy-2-propoxy)methyl.
Claim 10
Dependent Claim 25 words
The compound of claim 1 wherein R 1 is NH 2 , R 2 is thiocarboxamide, R 3 is H and R 4 is (1,3-dihydroxy-2-propoxy)methyl.
Claim 11
Dependent Claim 25 words
The compound of claim 1 wherein R 1 is NH 2 , R 2 is thiocarboxamide, R 3 is H and R 4 is 2-hydroxy-1-(1,3-dihydroxy-2-propoxy)ethyl.
Claim 12
Dependent Claim 23 words
The compound of claim 1 wherein R 1 is OH, R 2 is Cl, R 3 is H and R 4 is (1,3-dihydroxy-2-propoxy)methyl.
Claim 13
Dependent Claim 23 words
The compound of claim 1 wherein R 1 is NHOH, R 2 is Cl, R 3 is H and R 4 is (1,3-dihydroxy-2-propoxy)methyl.
Claim 14
Dependent Claim 23 words
The compound of claim 1 wherein R 1 is OH, R 2 is Br, R 3 is H and R 4 is (1,3-dihydroxy-2-propoxy)methyl.
Claim 15
Dependent Claim 23 words
The compound of claim 1 wherein R 1 is NHOH, R 2 is Br, R 3 is H and R 4 is (1,3-dihydroxy-2-propoxy)methyl.
Claim 16
Dependent Claim 23 words
The compound of claim 1 wherein R 1 is NHOH, R 2 is I, R 3 is H and R 4 is (1,3-dihydroxy-2-propoxy)methyl.
Claim 17
Dependent Claim 27 words
The compound of claim 1 wherein R 1 is wherein R 1 is OH, R 2 is I, R 3 is H and R 4 is (1,3-dihydroxy-2-propoxy)methyl.
Claim 18
Dependent Claim 12 words
The compound of claim 1 wherein R 3 is NH 2 .
Claim 19
Dependent Claim 10 words
The compound of claim 1 wherein R 3 is Br.
Claim 20
Independent Claim 123 words
A method of treating mammalian cells infected with a mammalian infectious virus selected from the group consisting of human cytomegalovirus and herpes simplex virus, the method comprising the step of contacting said cells with a composition comprising a therapeutically effective amount of a compound selected from the group consisting of compounds of the following formula or a pharmaceutically acceptable salt thereof: ##STR7## where R 1 is NH 2 , NHOH, OH or H; R 2 is CSNH 2 , Cl, Br, I, F, 2-buten-1-yl, 5-(1-hydroxyethyl) or 5-(1-methoxyethyl); R 3 is H, NH 2 or Br; and R 4 is (1,3-dihydroxy-2-propoxy)methyl, (2-hydroxyethoxy)methyl, (2-acetoxyethoxy)methyl, 2-hydroxy-1-(1,3-dihydroxy-2-propoxy)ethyl, (2-phosphonylmethoxy)ethyl or 3-hydroxy-2-phosphonylmethoxypropyl, wherein said contacting of said cells comprises in vivo administration of said composition to the infected mammal.
Claim 21
Independent Claim 123 words
A method of treating mammalian cells infected with a mammalian infectious virus selected from the group consisting of human cytomegalovirus and herpes simplex virus, the method comprising the step of contacting said cells with a composition comprising a therapeutically effective amount of a compound selected from the group consisting of compounds of the following formula or a pharmaceutically acceptable salt thereof: ##STR7## where R 1 is NH 2 , NHOH, OH or H; R 2 is CSNH 2 , Cl, Br, I, F, 2-buten-1-yl, 5-(1-hydroxyethyl) or 5-(1-methoxyethyl); R 3 is H, NH 2 or Br; and R 4 is (1,3-dihydroxy-2-propoxy)methyl, (2-hydroxyethoxy)methyl, (2-acetoxyethoxy)methyl, 2-hydroxy-1-(1,3-dihydroxy-2-propoxy)ethyl, (2-phosphonylmethoxy)ethyl or 3-hydroxy-2-phosphonylmethoxypropyl, wherein said contacting of said cells comprises in vivo administration of said composition to the infected mammal.
Claim 22
Dependent Claim 20 words
The method of claim 19 wherein said contacting of said cells comprises invivo administration of said composition to a mammal.
Claim 23
Dependent Claim 11 words
The method of claim 19 wherein said cells are human cells.
Claim 24
Dependent Claim 11 words
The method of claim 20 wherein said mammal is a human.
Claim 25
Dependent Claim 11 words
The method of claim 19 wherein the virus is human cytomegalovirus.
Claim 26
Dependent Claim 14 words
The method of claim 19 wherein the virus is herpes simplex virus type 1.
Claim 27
Dependent Claim 27 words
The method of claim 19 wherein R 1 is NH 2 , R 2 is a halogen group, R 3 is H and R 4 is (1,3-dihydroxy-2-propoxy)methyl.
Claim 28
Dependent Claim 25 words
The method of claim 19 wherein R 1 is NHOH, R 2 is a halogen group, R 3 is H and R 4 is (1,3-dihydroxy-2-propoxy)methyl.
Claim 29
Dependent Claim 27 words
The method of claim 19 wherein R 1 is NH 2 , R 2 is a halogen group, R 3 is H and R 4 is (2-hydroxyethoxy)methyl.
Claim 30
Dependent Claim 10 words
The method of claim 25 wherein R 2 is Cl.
Claim 31
Dependent Claim 10 words
The method of claim 25 wherein R 2 is Br.
Claim 32
Dependent Claim 10 words
The method of claim 25 wherein R 2 is I.
Claim 33
Dependent Claim 10 words
The method of claim 26 wherein R 2 is Cl.
Claim 34
Dependent Claim 10 words
The method of claim 26 wherein R 2 is Br.
Claim 35
Dependent Claim 10 words
The method of claim 26 wherein R 2 is I.
Claim 36
Dependent Claim 10 words
The method of claim 27 wherein R 2 is Cl.
Claim 37
Dependent Claim 10 words
The method of claim 27 wherein R 2 is Br.
Claim 38
Dependent Claim 10 words
The method of claim 27 wherein R 2 is I.
Claim 39
Dependent Claim 27 words
The method of claim 19 wherein R 1 is NH 2 , R 2 is CSNH 2 , R 3 is H and R 4 is (1,3-dihydroxy-2-propoxy)methyl.
Claim 40
Dependent Claim 27 words
The method of claim 19 wherein R 1 is NH 2 , R 2 is CSNH 2 , R 3 is H and R 4 is (2-hydroxyethoxy)methyl.
Claim 41
Dependent Claim 12 words
The method of claim 19 wherein R 3 is NH 2 .
Claim 42
Dependent Claim 10 words
The method of claim 19 wherein R 3 is Br.
Claim 43
Dependent Claim 70 words
A composition comprising a compound selected from the group consisting of compounds of the following formula and pharmaceutically acceptable salts thereof: ##STR8## where R 1 is NH 2 , NHOH, OH or H; R 2 CSNH 2 , Cl, Br, I, F, 2-buten-1-yl, 5-(1-hydroxyethyl) or 5-(1-methoxyethoxy); R 3 is H, NH 2 or Br; and R 4 is (1,3-dihydroxy-2-propoxy)methyl, (2-hydroxyethoxy)methyl, (2-acetoxyethoxy)methyl, 2-hydroxy-1-(1,3-dihydroxy-2-propoxy)ethyl, (2-phosphonylmethoxy)ethyl or 3-hydroxy-2-phosphonylmethoxypropyl; and a pharmaceutically acceptable carrier.
Claim 44
Dependent Claim 70 words
A composition comprising a compound selected from the group consisting of compounds of the following formula and pharmaceutically acceptable salts thereof: ##STR8## where R 1 is NH 2 , NHOH, OH or H; R 2 CSNH 2 , Cl, Br, I, F, 2-buten-1-yl, 5-(1-hydroxyethyl) or 5-(1-methoxyethoxy); R 3 is H, NH 2 or Br; and R 4 is (1,3-dihydroxy-2-propoxy)methyl, (2-hydroxyethoxy)methyl, (2-acetoxyethoxy)methyl, 2-hydroxy-1-(1,3-dihydroxy-2-propoxy)ethyl, (2-phosphonylmethoxy)ethyl or 3-hydroxy-2-phosphonylmethoxypropyl; and a pharmaceutically acceptable carrier.

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1993-11-05 1994-05-07 1994-11-06 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1997-11-05 1998-05-07 1998-11-06 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2001-11-05 2002-05-07 2002-11-06 $7700.00 Window Closed / Lapsed

Assigned Categories & Tags

No categories assigned to this patent yet.

Assign Category Tag