PT77636B - Modulation of animal cellular responses with compositions containing 8-substituted guanine derivatives - Google Patents
Modulation of animal cellular responses with compositions containing 8-substituted guanine derivatives Download PDFInfo
- Publication number
- PT77636B PT77636B PT77636A PT7763683A PT77636B PT 77636 B PT77636 B PT 77636B PT 77636 A PT77636 A PT 77636A PT 7763683 A PT7763683 A PT 7763683A PT 77636 B PT77636 B PT 77636B
- Authority
- PT
- Portugal
- Prior art keywords
- cells
- mguo
- cell
- response
- antigen
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract 128
- 241001465754 Metazoa Species 0.000 title claims abstract 30
- 230000036755 cellular response Effects 0.000 title claims abstract 12
- UYTPUPDQBNUYGX-UHFFFAOYSA-N guanine Chemical class O=C1NC(N)=NC2=C1N=CN2 UYTPUPDQBNUYGX-UHFFFAOYSA-N 0.000 title claims 31
- 238000000034 method Methods 0.000 claims abstract 52
- WJSVJNDMOQTICG-UHFFFAOYSA-N 2-amino-1-[(2-methyl-4-methylidene-5-oxooxolan-2-yl)methyl]-7h-purin-6-one Chemical group NC1=NC=2N=CNC=2C(=O)N1CC1(C)CC(=C)C(=O)O1 WJSVJNDMOQTICG-UHFFFAOYSA-N 0.000 claims abstract 26
- 230000001939 inductive effect Effects 0.000 claims abstract 23
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract 20
- 239000001257 hydrogen Substances 0.000 claims abstract 20
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract 15
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract 13
- 150000001323 aldoses Chemical group 0.000 claims abstract 13
- 125000004429 atom Chemical group 0.000 claims abstract 11
- 239000003085 diluting agent Substances 0.000 claims abstract 10
- MNQZXJOMYWMBOU-UHFFFAOYSA-N glyceraldehyde Chemical compound OCC(O)C=O MNQZXJOMYWMBOU-UHFFFAOYSA-N 0.000 claims abstract 5
- 239000013543 active substance Substances 0.000 claims abstract 2
- 210000004027 cell Anatomy 0.000 claims 189
- 102000036639 antigens Human genes 0.000 claims 116
- 239000000427 antigen Substances 0.000 claims 115
- 108091007433 antigens Proteins 0.000 claims 115
- 230000004044 response Effects 0.000 claims 113
- 210000001744 T-lymphocyte Anatomy 0.000 claims 75
- 230000000694 effects Effects 0.000 claims 64
- 210000003719 b-lymphocyte Anatomy 0.000 claims 61
- ASUCSHXLTWZYBA-UMMCILCDSA-N 8-Bromoguanosine Chemical compound C1=2NC(N)=NC(=O)C=2N=C(Br)N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O ASUCSHXLTWZYBA-UMMCILCDSA-N 0.000 claims 60
- 230000003393 splenic effect Effects 0.000 claims 60
- 241000699670 Mus sp. Species 0.000 claims 56
- 230000001965 increasing effect Effects 0.000 claims 50
- 241000700159 Rattus Species 0.000 claims 42
- 239000006228 supernatant Substances 0.000 claims 34
- 125000001424 substituent group Chemical group 0.000 claims 31
- 108010002350 Interleukin-2 Proteins 0.000 claims 25
- 102000000588 Interleukin-2 Human genes 0.000 claims 25
- 210000004698 lymphocyte Anatomy 0.000 claims 25
- 230000005875 antibody response Effects 0.000 claims 22
- 239000002609 medium Substances 0.000 claims 22
- 238000001727 in vivo Methods 0.000 claims 20
- 238000004113 cell culture Methods 0.000 claims 18
- -1 N- (2-aminoethyl) carbamylmethyl Chemical group 0.000 claims 17
- 239000004480 active ingredient Substances 0.000 claims 17
- 238000002360 preparation method Methods 0.000 claims 17
- 102000014150 Interferons Human genes 0.000 claims 16
- 108010050904 Interferons Proteins 0.000 claims 16
- 239000002671 adjuvant Substances 0.000 claims 16
- 238000004519 manufacturing process Methods 0.000 claims 16
- 210000004989 spleen cell Anatomy 0.000 claims 16
- 229920002134 Carboxymethyl cellulose Polymers 0.000 claims 15
- 230000001419 dependent effect Effects 0.000 claims 15
- 229940079322 interferon Drugs 0.000 claims 15
- 210000002966 serum Anatomy 0.000 claims 15
- 210000000952 spleen Anatomy 0.000 claims 15
- 239000001768 carboxy methyl cellulose Substances 0.000 claims 14
- 235000010948 carboxy methyl cellulose Nutrition 0.000 claims 14
- 239000008112 carboxymethyl-cellulose Substances 0.000 claims 14
- 230000028993 immune response Effects 0.000 claims 14
- 239000007924 injection Substances 0.000 claims 14
- 238000002347 injection Methods 0.000 claims 14
- 241000282414 Homo sapiens Species 0.000 claims 13
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims 13
- 230000028327 secretion Effects 0.000 claims 13
- 239000000725 suspension Substances 0.000 claims 13
- NYHBQMYGNKIUIF-UUOKFMHZSA-N Guanosine Chemical compound C1=NC=2C(=O)NC(N)=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O NYHBQMYGNKIUIF-UUOKFMHZSA-N 0.000 claims 12
- 108060003951 Immunoglobulin Proteins 0.000 claims 12
- 230000000240 adjuvant effect Effects 0.000 claims 12
- 102000018358 immunoglobulin Human genes 0.000 claims 12
- 102000003996 Interferon-beta Human genes 0.000 claims 11
- 108090000467 Interferon-beta Proteins 0.000 claims 11
- 239000003795 chemical substances by application Substances 0.000 claims 11
- 230000000295 complement effect Effects 0.000 claims 11
- 238000000338 in vitro Methods 0.000 claims 11
- 102000008072 Lymphokines Human genes 0.000 claims 10
- 108010074338 Lymphokines Proteins 0.000 claims 10
- 241000699666 Mus <mouse, genus> Species 0.000 claims 10
- 230000004913 activation Effects 0.000 claims 10
- 239000000463 material Substances 0.000 claims 10
- 150000003833 nucleoside derivatives Chemical class 0.000 claims 10
- 239000000243 solution Substances 0.000 claims 10
- 239000003826 tablet Substances 0.000 claims 10
- 102000000589 Interleukin-1 Human genes 0.000 claims 9
- 108010002352 Interleukin-1 Proteins 0.000 claims 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 9
- 229930105110 Cyclosporin A Natural products 0.000 claims 8
- 108010036949 Cyclosporine Proteins 0.000 claims 8
- 229920002472 Starch Polymers 0.000 claims 8
- 230000001464 adherent effect Effects 0.000 claims 8
- 210000004102 animal cell Anatomy 0.000 claims 8
- 229960001265 ciclosporin Drugs 0.000 claims 8
- 231100000673 dose–response relationship Toxicity 0.000 claims 8
- 210000003743 erythrocyte Anatomy 0.000 claims 8
- 125000000524 functional group Chemical group 0.000 claims 8
- 238000011534 incubation Methods 0.000 claims 8
- 238000007912 intraperitoneal administration Methods 0.000 claims 8
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 claims 8
- 108010062580 Concanavalin A Proteins 0.000 claims 7
- PMATZTZNYRCHOR-CGLBZJNRSA-N Cyclosporin A Chemical compound CC[C@@H]1NC(=O)[C@H]([C@H](O)[C@H](C)C\C=C\C)N(C)C(=O)[C@H](C(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](C(C)C)NC(=O)[C@H](CC(C)C)N(C)C(=O)CN(C)C1=O PMATZTZNYRCHOR-CGLBZJNRSA-N 0.000 claims 7
- 230000002950 deficient Effects 0.000 claims 7
- 238000002474 experimental method Methods 0.000 claims 7
- 230000006698 induction Effects 0.000 claims 7
- 210000002540 macrophage Anatomy 0.000 claims 7
- 239000003226 mitogen Substances 0.000 claims 7
- 230000002297 mitogenic effect Effects 0.000 claims 7
- 239000002777 nucleoside Substances 0.000 claims 7
- 238000006467 substitution reaction Methods 0.000 claims 7
- 230000001413 cellular effect Effects 0.000 claims 6
- 238000010790 dilution Methods 0.000 claims 6
- 239000012895 dilution Substances 0.000 claims 6
- 238000011156 evaluation Methods 0.000 claims 6
- 239000004615 ingredient Substances 0.000 claims 6
- 230000002401 inhibitory effect Effects 0.000 claims 6
- 210000005170 neoplastic cell Anatomy 0.000 claims 6
- 230000008569 process Effects 0.000 claims 6
- 230000009469 supplementation Effects 0.000 claims 6
- 238000011282 treatment Methods 0.000 claims 6
- 102100039897 Interleukin-5 Human genes 0.000 claims 5
- 108010002616 Interleukin-5 Proteins 0.000 claims 5
- 241000283973 Oryctolagus cuniculus Species 0.000 claims 5
- 239000002775 capsule Substances 0.000 claims 5
- ZOOGRGPOEVQQDX-UHFFFAOYSA-N cyclic GMP Natural products O1C2COP(O)(=O)OC2C(O)C1N1C=NC2=C1NC(N)=NC2=O ZOOGRGPOEVQQDX-UHFFFAOYSA-N 0.000 claims 5
- 239000001963 growth medium Substances 0.000 claims 5
- 230000028996 humoral immune response Effects 0.000 claims 5
- 150000002431 hydrogen Chemical class 0.000 claims 5
- 230000005764 inhibitory process Effects 0.000 claims 5
- 210000000265 leukocyte Anatomy 0.000 claims 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 5
- 230000004048 modification Effects 0.000 claims 5
- 238000012986 modification Methods 0.000 claims 5
- 239000011780 sodium chloride Substances 0.000 claims 5
- 210000001541 thymus gland Anatomy 0.000 claims 5
- 229940100445 wheat starch Drugs 0.000 claims 5
- WFIYPADYPQQLNN-UHFFFAOYSA-N 2-[2-(4-bromopyrazol-1-yl)ethyl]isoindole-1,3-dione Chemical compound C1=C(Br)C=NN1CCN1C(=O)C2=CC=CC=C2C1=O WFIYPADYPQQLNN-UHFFFAOYSA-N 0.000 claims 4
- ZOOGRGPOEVQQDX-UUOKFMHZSA-N 3',5'-cyclic GMP Chemical compound C([C@H]1O2)OP(O)(=O)O[C@H]1[C@@H](O)[C@@H]2N1C(N=C(NC2=O)N)=C2N=C1 ZOOGRGPOEVQQDX-UUOKFMHZSA-N 0.000 claims 4
- 102000004127 Cytokines Human genes 0.000 claims 4
- 108090000695 Cytokines Proteins 0.000 claims 4
- 102000004190 Enzymes Human genes 0.000 claims 4
- 108090000790 Enzymes Proteins 0.000 claims 4
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 claims 4
- 238000003556 assay Methods 0.000 claims 4
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims 4
- 230000015572 biosynthetic process Effects 0.000 claims 4
- 230000037396 body weight Effects 0.000 claims 4
- 238000009395 breeding Methods 0.000 claims 4
- 230000001488 breeding effect Effects 0.000 claims 4
- 108010074605 gamma-Globulins Proteins 0.000 claims 4
- 230000002949 hemolytic effect Effects 0.000 claims 4
- 230000006872 improvement Effects 0.000 claims 4
- 235000019359 magnesium stearate Nutrition 0.000 claims 4
- 230000007246 mechanism Effects 0.000 claims 4
- 239000012528 membrane Substances 0.000 claims 4
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 claims 4
- 125000004043 oxo group Chemical group O=* 0.000 claims 4
- 239000008188 pellet Substances 0.000 claims 4
- 239000002504 physiological saline solution Substances 0.000 claims 4
- 239000004033 plastic Substances 0.000 claims 4
- 229920003023 plastic Polymers 0.000 claims 4
- 239000000843 powder Substances 0.000 claims 4
- 239000002243 precursor Substances 0.000 claims 4
- 230000035755 proliferation Effects 0.000 claims 4
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 claims 4
- 238000011160 research Methods 0.000 claims 4
- 238000012360 testing method Methods 0.000 claims 4
- 210000001519 tissue Anatomy 0.000 claims 4
- HPKQEMIXSLRGJU-UUOKFMHZSA-N 2-amino-9-[(2r,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-7-methyl-3h-purine-6,8-dione Chemical compound O=C1N(C)C(C(NC(N)=N2)=O)=C2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O HPKQEMIXSLRGJU-UUOKFMHZSA-N 0.000 claims 3
- MWVSREMEETTXDC-UUOKFMHZSA-N 2-amino-9-[(2r,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-8-methoxy-3h-purin-6-one Chemical compound COC1=NC(C(N=C(N)N2)=O)=C2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O MWVSREMEETTXDC-UUOKFMHZSA-N 0.000 claims 3
- KZELNMSPWPFAEB-UMMCILCDSA-N 2-amino-9-[(2r,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-8-sulfanylidene-3,7-dihydropurin-6-one Chemical compound C1=2NC(N)=NC(=O)C=2NC(=S)N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O KZELNMSPWPFAEB-UMMCILCDSA-N 0.000 claims 3
- 102000004008 5'-Nucleotidase Human genes 0.000 claims 3
- HCAJQHYUCKICQH-VPENINKCSA-N 8-Oxo-7,8-dihydro-2'-deoxyguanosine Chemical compound C1=2NC(N)=NC(=O)C=2NC(=O)N1[C@H]1C[C@H](O)[C@@H](CO)O1 HCAJQHYUCKICQH-VPENINKCSA-N 0.000 claims 3
- 206010010356 Congenital anomaly Diseases 0.000 claims 3
- WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 claims 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 3
- 229920001917 Ficoll Polymers 0.000 claims 3
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 claims 3
- 241001494479 Pecora Species 0.000 claims 3
- 239000012980 RPMI-1640 medium Substances 0.000 claims 3
- 230000009471 action Effects 0.000 claims 3
- 239000012190 activator Substances 0.000 claims 3
- 125000002252 acyl group Chemical group 0.000 claims 3
- 239000006285 cell suspension Substances 0.000 claims 3
- 238000005119 centrifugation Methods 0.000 claims 3
- 230000003247 decreasing effect Effects 0.000 claims 3
- 239000002552 dosage form Substances 0.000 claims 3
- 239000002158 endotoxin Substances 0.000 claims 3
- 239000008187 granular material Substances 0.000 claims 3
- 210000002443 helper t lymphocyte Anatomy 0.000 claims 3
- 210000005104 human peripheral blood lymphocyte Anatomy 0.000 claims 3
- 230000004727 humoral immunity Effects 0.000 claims 3
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 3
- 230000000977 initiatory effect Effects 0.000 claims 3
- 239000008101 lactose Substances 0.000 claims 3
- 229920006008 lipopolysaccharide Polymers 0.000 claims 3
- 239000007788 liquid Substances 0.000 claims 3
- 230000002906 microbiologic effect Effects 0.000 claims 3
- 230000003389 potentiating effect Effects 0.000 claims 3
- 108010043671 prostatic acid phosphatase Proteins 0.000 claims 3
- 108020003175 receptors Proteins 0.000 claims 3
- 102000005962 receptors Human genes 0.000 claims 3
- 239000012679 serum free medium Substances 0.000 claims 3
- 210000004988 splenocyte Anatomy 0.000 claims 3
- 239000008107 starch Substances 0.000 claims 3
- 235000019698 starch Nutrition 0.000 claims 3
- 230000000638 stimulation Effects 0.000 claims 3
- 230000002195 synergetic effect Effects 0.000 claims 3
- 230000001225 therapeutic effect Effects 0.000 claims 3
- 230000009466 transformation Effects 0.000 claims 3
- JKMHFZQWWAIEOD-UHFFFAOYSA-N 2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanesulfonic acid Chemical compound OCC[NH+]1CCN(CCS([O-])(=O)=O)CC1 JKMHFZQWWAIEOD-UHFFFAOYSA-N 0.000 claims 2
- RNSGUQLXDMZREX-SDBHATRESA-N 2-amino-9-[(2r,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-8-phenylmethoxy-3h-purin-6-one Chemical compound C=1C=CC=CC=1COC1=NC=2C(=O)NC(N)=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O RNSGUQLXDMZREX-SDBHATRESA-N 0.000 claims 2
- MYDFOUUSSBDTNG-UMMCILCDSA-N 2-amino-9-[(2r,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]purine-6,8-dione Chemical class C12=NC(N)=NC(=O)C2=NC(=O)N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O MYDFOUUSSBDTNG-UMMCILCDSA-N 0.000 claims 2
- ASJSAQIRZKANQN-CRCLSJGQSA-N 2-deoxy-D-ribose Chemical compound OC[C@@H](O)[C@@H](O)CC=O ASJSAQIRZKANQN-CRCLSJGQSA-N 0.000 claims 2
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 claims 2
- FPGSEBKFEJEOSA-UMMCILCDSA-N 8-Hydroxyguanosine Chemical compound C1=2NC(N)=NC(=O)C=2NC(=O)N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O FPGSEBKFEJEOSA-UMMCILCDSA-N 0.000 claims 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims 2
- 239000005711 Benzoic acid Substances 0.000 claims 2
- 108091003079 Bovine Serum Albumin Proteins 0.000 claims 2
- HDUVDVCCDTUKCH-KQYNXXCUSA-N CC=1N([C@H]2[C@H](S)[C@H](O)[C@@H](CO)O2)C=2N=C(NC(C2N1)=O)N Chemical compound CC=1N([C@H]2[C@H](S)[C@H](O)[C@@H](CO)O2)C=2N=C(NC(C2N1)=O)N HDUVDVCCDTUKCH-KQYNXXCUSA-N 0.000 claims 2
- MIKUYHXYGGJMLM-GIMIYPNGSA-N Crotonoside Natural products C1=NC2=C(N)NC(=O)N=C2N1[C@H]1O[C@@H](CO)[C@H](O)[C@@H]1O MIKUYHXYGGJMLM-GIMIYPNGSA-N 0.000 claims 2
- WQZGKKKJIJFFOK-IVMDWMLBSA-N D-allopyranose Chemical compound OC[C@H]1OC(O)[C@H](O)[C@H](O)[C@@H]1O WQZGKKKJIJFFOK-IVMDWMLBSA-N 0.000 claims 2
- NYHBQMYGNKIUIF-UHFFFAOYSA-N D-guanosine Natural products C1=2NC(N)=NC(=O)C=2N=CN1C1OC(CO)C(O)C1O NYHBQMYGNKIUIF-UHFFFAOYSA-N 0.000 claims 2
- HMFHBZSHGGEWLO-SOOFDHNKSA-N D-ribofuranose Chemical compound OC[C@H]1OC(O)[C@H](O)[C@@H]1O HMFHBZSHGGEWLO-SOOFDHNKSA-N 0.000 claims 2
- 230000006820 DNA synthesis Effects 0.000 claims 2
- 235000019739 Dicalciumphosphate Nutrition 0.000 claims 2
- 239000007995 HEPES buffer Substances 0.000 claims 2
- NTYJJOPFIAHURM-UHFFFAOYSA-N Histamine Chemical compound NCCC1=CN=CN1 NTYJJOPFIAHURM-UHFFFAOYSA-N 0.000 claims 2
- 241000282412 Homo Species 0.000 claims 2
- 206010061598 Immunodeficiency Diseases 0.000 claims 2
- 208000029462 Immunodeficiency disease Diseases 0.000 claims 2
- 206010025323 Lymphomas Diseases 0.000 claims 2
- 229910017917 NH4 Cl Inorganic materials 0.000 claims 2
- JGSARLDLIJGVTE-MBNYWOFBSA-N Penicillin G Chemical compound N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 JGSARLDLIJGVTE-MBNYWOFBSA-N 0.000 claims 2
- 229920002873 Polyethylenimine Polymers 0.000 claims 2
- PYMYPHUHKUWMLA-LMVFSUKVSA-N Ribose Natural products OC[C@@H](O)[C@@H](O)[C@@H](O)C=O PYMYPHUHKUWMLA-LMVFSUKVSA-N 0.000 claims 2
- 229910004298 SiO 2 Inorganic materials 0.000 claims 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims 2
- 101000874347 Streptococcus agalactiae IgA FC receptor Proteins 0.000 claims 2
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 claims 2
- IQFYYKKMVGJFEH-XLPZGREQSA-N Thymidine Chemical compound O=C1NC(=O)C(C)=CN1[C@@H]1O[C@H](CO)[C@@H](O)C1 IQFYYKKMVGJFEH-XLPZGREQSA-N 0.000 claims 2
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 claims 2
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 claims 2
- 230000000996 additive effect Effects 0.000 claims 2
- 125000003525 allosyl group Chemical group 0.000 claims 2
- HMFHBZSHGGEWLO-UHFFFAOYSA-N alpha-D-Furanose-Ribose Natural products OCC1OC(O)C(O)C1O HMFHBZSHGGEWLO-UHFFFAOYSA-N 0.000 claims 2
- 125000003277 amino group Chemical group 0.000 claims 2
- 210000000628 antibody-producing cell Anatomy 0.000 claims 2
- 239000003146 anticoagulant agent Substances 0.000 claims 2
- 229940127219 anticoagulant drug Drugs 0.000 claims 2
- 235000010233 benzoic acid Nutrition 0.000 claims 2
- SESFRYSPDFLNCH-UHFFFAOYSA-N benzyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCC1=CC=CC=C1 SESFRYSPDFLNCH-UHFFFAOYSA-N 0.000 claims 2
- 230000035584 blastogenesis Effects 0.000 claims 2
- 230000031709 bromination Effects 0.000 claims 2
- 238000005893 bromination reaction Methods 0.000 claims 2
- 125000001246 bromo group Chemical group Br* 0.000 claims 2
- 239000001506 calcium phosphate Substances 0.000 claims 2
- 150000001720 carbohydrates Chemical class 0.000 claims 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 2
- 230000024245 cell differentiation Effects 0.000 claims 2
- 102000006834 complement receptors Human genes 0.000 claims 2
- 108010047295 complement receptors Proteins 0.000 claims 2
- 150000001875 compounds Chemical class 0.000 claims 2
- 238000011109 contamination Methods 0.000 claims 2
- 230000007423 decrease Effects 0.000 claims 2
- 230000007547 defect Effects 0.000 claims 2
- 230000003111 delayed effect Effects 0.000 claims 2
- NEFBYIFKOOEVPA-UHFFFAOYSA-K dicalcium phosphate Chemical compound [Ca+2].[Ca+2].[O-]P([O-])([O-])=O NEFBYIFKOOEVPA-UHFFFAOYSA-K 0.000 claims 2
- 229940038472 dicalcium phosphate Drugs 0.000 claims 2
- 229910000390 dicalcium phosphate Inorganic materials 0.000 claims 2
- 230000004069 differentiation Effects 0.000 claims 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 2
- 208000035475 disorder Diseases 0.000 claims 2
- 230000002708 enhancing effect Effects 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 239000012894 fetal calf serum Substances 0.000 claims 2
- 230000012010 growth Effects 0.000 claims 2
- 239000003102 growth factor Substances 0.000 claims 2
- 229940029575 guanosine Drugs 0.000 claims 2
- 235000013928 guanylic acid Nutrition 0.000 claims 2
- 125000005843 halogen group Chemical group 0.000 claims 2
- 230000036541 health Effects 0.000 claims 2
- 230000008348 humoral response Effects 0.000 claims 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
- 230000036039 immunity Effects 0.000 claims 2
- 230000003053 immunization Effects 0.000 claims 2
- 238000002649 immunization Methods 0.000 claims 2
- 230000007813 immunodeficiency Effects 0.000 claims 2
- 230000016784 immunoglobulin production Effects 0.000 claims 2
- 229940072221 immunoglobulins Drugs 0.000 claims 2
- 229940047124 interferons Drugs 0.000 claims 2
- 230000004073 interleukin-2 production Effects 0.000 claims 2
- 230000002132 lysosomal effect Effects 0.000 claims 2
- 230000035800 maturation Effects 0.000 claims 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 2
- 229920000609 methyl cellulose Polymers 0.000 claims 2
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 claims 2
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 claims 2
- 239000001923 methylcellulose Substances 0.000 claims 2
- 235000010981 methylcellulose Nutrition 0.000 claims 2
- 229960002216 methylparaben Drugs 0.000 claims 2
- 230000008747 mitogenic response Effects 0.000 claims 2
- 230000009826 neoplastic cell growth Effects 0.000 claims 2
- 230000001613 neoplastic effect Effects 0.000 claims 2
- 210000000440 neutrophil Anatomy 0.000 claims 2
- 125000003835 nucleoside group Chemical group 0.000 claims 2
- 230000005868 ontogenesis Effects 0.000 claims 2
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims 2
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims 2
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims 2
- 235000010232 propyl p-hydroxybenzoate Nutrition 0.000 claims 2
- 239000004405 propyl p-hydroxybenzoate Substances 0.000 claims 2
- 229960003415 propylparaben Drugs 0.000 claims 2
- 230000005855 radiation Effects 0.000 claims 2
- 238000003127 radioimmunoassay Methods 0.000 claims 2
- 230000003248 secreting effect Effects 0.000 claims 2
- 210000002955 secretory cell Anatomy 0.000 claims 2
- 238000000926 separation method Methods 0.000 claims 2
- DAEPDZWVDSPTHF-UHFFFAOYSA-M sodium pyruvate Chemical compound [Na+].CC(=O)C([O-])=O DAEPDZWVDSPTHF-UHFFFAOYSA-M 0.000 claims 2
- 239000008279 sol Substances 0.000 claims 2
- 210000002784 stomach Anatomy 0.000 claims 2
- UCSJYZPVAKXKNQ-HZYVHMACSA-N streptomycin Chemical compound CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](NC(N)=N)[C@H](O)[C@@H](NC(N)=N)[C@H](O)[C@H]1O UCSJYZPVAKXKNQ-HZYVHMACSA-N 0.000 claims 2
- 239000000126 substance Substances 0.000 claims 2
- 239000013589 supplement Substances 0.000 claims 2
- 125000003396 thiol group Chemical group [H]S* 0.000 claims 2
- 230000003612 virological effect Effects 0.000 claims 2
- FTLYMKDSHNWQKD-UHFFFAOYSA-N (2,4,5-trichlorophenyl)boronic acid Chemical compound OB(O)C1=CC(Cl)=C(Cl)C=C1Cl FTLYMKDSHNWQKD-UHFFFAOYSA-N 0.000 claims 1
- STGXGJRRAJKJRG-JDJSBBGDSA-N (3r,4r,5r)-5-(hydroxymethyl)-3-methoxyoxolane-2,4-diol Chemical compound CO[C@H]1C(O)O[C@H](CO)[C@H]1O STGXGJRRAJKJRG-JDJSBBGDSA-N 0.000 claims 1
- NHBKXEKEPDILRR-UHFFFAOYSA-N 2,3-bis(butanoylsulfanyl)propyl butanoate Chemical compound CCCC(=O)OCC(SC(=O)CCC)CSC(=O)CCC NHBKXEKEPDILRR-UHFFFAOYSA-N 0.000 claims 1
- 125000001894 2,4,6-trinitrophenyl group Chemical group [H]C1=C(C(*)=C(C([H])=C1[N+]([O-])=O)[N+]([O-])=O)[N+]([O-])=O 0.000 claims 1
- FNXPTCITVCRFRK-UMMCILCDSA-N 2,8-diamino-9-[(2r,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3h-purin-6-one Chemical compound NC1=NC(C(N=C(N)N2)=O)=C2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O FNXPTCITVCRFRK-UMMCILCDSA-N 0.000 claims 1
- GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 claims 1
- SMNDYUVBFMFKNZ-UHFFFAOYSA-N 2-furoic acid Chemical group OC(=O)C1=CC=CO1 SMNDYUVBFMFKNZ-UHFFFAOYSA-N 0.000 claims 1
- MKDXZFVCXWXGBQ-VPENINKCSA-N 8-bromo-2'-deoxyguanosine Chemical compound BrC1=NC=2C(=O)NC(N)=NC=2N1[C@H]1C[C@H](O)[C@@H](CO)O1 MKDXZFVCXWXGBQ-VPENINKCSA-N 0.000 claims 1
- JRLTTZUODKEYDH-UHFFFAOYSA-N 8-methylquinoline Chemical group C1=CN=C2C(C)=CC=CC2=C1 JRLTTZUODKEYDH-UHFFFAOYSA-N 0.000 claims 1
- UBKVUFQGVWHZIR-UHFFFAOYSA-N 8-oxoguanine Chemical class O=C1NC(N)=NC2=NC(=O)N=C21 UBKVUFQGVWHZIR-UHFFFAOYSA-N 0.000 claims 1
- 241000238876 Acari Species 0.000 claims 1
- 208000008190 Agammaglobulinemia Diseases 0.000 claims 1
- 241000416162 Astragalus gummifer Species 0.000 claims 1
- 208000023275 Autoimmune disease Diseases 0.000 claims 1
- 230000003844 B-cell-activation Effects 0.000 claims 1
- DWRXFEITVBNRMK-UHFFFAOYSA-N Beta-D-1-Arabinofuranosylthymine Natural products O=C1NC(=O)C(C)=CN1C1C(O)C(O)C(CO)O1 DWRXFEITVBNRMK-UHFFFAOYSA-N 0.000 claims 1
- 241000283690 Bos taurus Species 0.000 claims 1
- 238000011749 CBA mouse Methods 0.000 claims 1
- 241000700199 Cavia porcellus Species 0.000 claims 1
- 102000005575 Cellulases Human genes 0.000 claims 1
- 108010084185 Cellulases Proteins 0.000 claims 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- 241000207199 Citrus Species 0.000 claims 1
- 241000555825 Clupeidae Species 0.000 claims 1
- 108010078546 Complement C5a Proteins 0.000 claims 1
- 101150005261 Cul7 gene Proteins 0.000 claims 1
- UDIPTWFVPPPURJ-UHFFFAOYSA-M Cyclamate Chemical compound [Na+].[O-]S(=O)(=O)NC1CCCCC1 UDIPTWFVPPPURJ-UHFFFAOYSA-M 0.000 claims 1
- WQZGKKKJIJFFOK-CBPJZXOFSA-N D-Gulose Chemical compound OC[C@H]1OC(O)[C@H](O)[C@H](O)[C@H]1O WQZGKKKJIJFFOK-CBPJZXOFSA-N 0.000 claims 1
- QMMFVYPAHWMCMS-UHFFFAOYSA-N Dimethyl sulfide Chemical compound CSC QMMFVYPAHWMCMS-UHFFFAOYSA-N 0.000 claims 1
- 241000588724 Escherichia coli Species 0.000 claims 1
- 102000009109 Fc receptors Human genes 0.000 claims 1
- 108010087819 Fc receptors Proteins 0.000 claims 1
- 241000287828 Gallus gallus Species 0.000 claims 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 claims 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims 1
- 239000012981 Hank's balanced salt solution Substances 0.000 claims 1
- 101001112229 Homo sapiens Neutrophil cytosol factor 1 Proteins 0.000 claims 1
- 229930194542 Keto Natural products 0.000 claims 1
- WQZGKKKJIJFFOK-VSOAQEOCSA-N L-altropyranose Chemical compound OC[C@@H]1OC(O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-VSOAQEOCSA-N 0.000 claims 1
- 108700018351 Major Histocompatibility Complex Proteins 0.000 claims 1
- 241001529936 Murinae Species 0.000 claims 1
- 235000021360 Myristic acid Nutrition 0.000 claims 1
- 206010028980 Neoplasm Diseases 0.000 claims 1
- 102100023620 Neutrophil cytosol factor 1 Human genes 0.000 claims 1
- 239000004677 Nylon Substances 0.000 claims 1
- 235000019502 Orange oil Nutrition 0.000 claims 1
- 235000021314 Palmitic acid Nutrition 0.000 claims 1
- 108010047620 Phytohemagglutinins Proteins 0.000 claims 1
- 239000004793 Polystyrene Substances 0.000 claims 1
- 208000031951 Primary immunodeficiency Diseases 0.000 claims 1
- 108010076504 Protein Sorting Signals Proteins 0.000 claims 1
- 241000282941 Rangifer tarandus Species 0.000 claims 1
- 239000006146 Roswell Park Memorial Institute medium Substances 0.000 claims 1
- 229920005654 Sephadex Polymers 0.000 claims 1
- 239000012507 Sephadex™ Substances 0.000 claims 1
- 101100289792 Squirrel monkey polyomavirus large T gene Proteins 0.000 claims 1
- 235000021355 Stearic acid Nutrition 0.000 claims 1
- 229920001615 Tragacanth Polymers 0.000 claims 1
- YZCKVEUIGOORGS-NJFSPNSNSA-N Tritium Chemical compound [3H] YZCKVEUIGOORGS-NJFSPNSNSA-N 0.000 claims 1
- 206010052428 Wound Diseases 0.000 claims 1
- 208000027418 Wounds and injury Diseases 0.000 claims 1
- 210000001766 X chromosome Anatomy 0.000 claims 1
- JLZCAXCVNVVXJL-IDTAVKCVSA-N [(2r,3r,4r,5r)-3,4-diacetyloxy-5-(2-amino-8-bromo-6-oxo-3h-purin-9-yl)oxolan-2-yl]methyl acetate Chemical compound CC(=O)O[C@@H]1[C@H](OC(C)=O)[C@@H](COC(=O)C)O[C@H]1N1C(NC(N)=NC2=O)=C2N=C1Br JLZCAXCVNVVXJL-IDTAVKCVSA-N 0.000 claims 1
- SJLDUTNIPDQOCZ-UMMCILCDSA-N [(2r,3s,4r,5r)-5-(2-amino-8-bromo-6-oxo-3h-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl dihydrogen phosphate Chemical compound BrC1=NC=2C(=O)NC(N)=NC=2N1[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]1O SJLDUTNIPDQOCZ-UMMCILCDSA-N 0.000 claims 1
- 230000002159 abnormal effect Effects 0.000 claims 1
- 238000010521 absorption reaction Methods 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 230000002378 acidificating effect Effects 0.000 claims 1
- 230000003213 activating effect Effects 0.000 claims 1
- 238000004115 adherent culture Methods 0.000 claims 1
- 230000032683 aging Effects 0.000 claims 1
- 125000003172 aldehyde group Chemical group 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 208000026935 allergic disease Diseases 0.000 claims 1
- 230000000172 allergic effect Effects 0.000 claims 1
- WQZGKKKJIJFFOK-PHYPRBDBSA-N alpha-D-galactose Chemical compound OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-PHYPRBDBSA-N 0.000 claims 1
- 235000019270 ammonium chloride Nutrition 0.000 claims 1
- 230000003321 amplification Effects 0.000 claims 1
- 230000003698 anagen phase Effects 0.000 claims 1
- 230000001494 anti-thymocyte effect Effects 0.000 claims 1
- 230000000890 antigenic effect Effects 0.000 claims 1
- 238000013459 approach Methods 0.000 claims 1
- 239000012736 aqueous medium Substances 0.000 claims 1
- PYMYPHUHKUWMLA-WDCZJNDASA-N arabinose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)C=O PYMYPHUHKUWMLA-WDCZJNDASA-N 0.000 claims 1
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 claims 1
- YZXBAPSDXZZRGB-DOFZRALJSA-N arachidonic acid Chemical class CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O YZXBAPSDXZZRGB-DOFZRALJSA-N 0.000 claims 1
- 235000021342 arachidonic acid Nutrition 0.000 claims 1
- 238000010420 art technique Methods 0.000 claims 1
- 230000003416 augmentation Effects 0.000 claims 1
- 230000001580 bacterial effect Effects 0.000 claims 1
- 239000011324 bead Substances 0.000 claims 1
- 229960002903 benzyl benzoate Drugs 0.000 claims 1
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 claims 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 claims 1
- IQFYYKKMVGJFEH-UHFFFAOYSA-N beta-L-thymidine Natural products O=C1NC(=O)C(C)=CN1C1OC(CO)C(O)C1 IQFYYKKMVGJFEH-UHFFFAOYSA-N 0.000 claims 1
- 210000001185 bone marrow Anatomy 0.000 claims 1
- 150000001735 carboxylic acids Chemical class 0.000 claims 1
- 230000020411 cell activation Effects 0.000 claims 1
- 230000010261 cell growth Effects 0.000 claims 1
- 210000000170 cell membrane Anatomy 0.000 claims 1
- 230000019522 cellular metabolic process Effects 0.000 claims 1
- 230000008859 change Effects 0.000 claims 1
- 238000012512 characterization method Methods 0.000 claims 1
- 239000003153 chemical reaction reagent Substances 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 claims 1
- 235000020971 citrus fruits Nutrition 0.000 claims 1
- 238000003501 co-culture Methods 0.000 claims 1
- 229910052681 coesite Inorganic materials 0.000 claims 1
- 238000004891 communication Methods 0.000 claims 1
- 239000000470 constituent Substances 0.000 claims 1
- 235000012343 cottonseed oil Nutrition 0.000 claims 1
- 239000002385 cottonseed oil Substances 0.000 claims 1
- 229910052906 cristobalite Inorganic materials 0.000 claims 1
- 210000004748 cultured cell Anatomy 0.000 claims 1
- 125000004093 cyano group Chemical group *C#N 0.000 claims 1
- 239000000625 cyclamic acid and its Na and Ca salt Substances 0.000 claims 1
- 230000016396 cytokine production Effects 0.000 claims 1
- 230000009089 cytolysis Effects 0.000 claims 1
- 231100000135 cytotoxicity Toxicity 0.000 claims 1
- 230000003013 cytotoxicity Effects 0.000 claims 1
- 230000034994 death Effects 0.000 claims 1
- 230000007812 deficiency Effects 0.000 claims 1
- 239000008367 deionised water Substances 0.000 claims 1
- 229910021641 deionized water Inorganic materials 0.000 claims 1
- 238000010494 dissociation reaction Methods 0.000 claims 1
- 230000005593 dissociations Effects 0.000 claims 1
- 238000001035 drying Methods 0.000 claims 1
- 239000000839 emulsion Substances 0.000 claims 1
- 230000002255 enzymatic effect Effects 0.000 claims 1
- 239000003797 essential amino acid Substances 0.000 claims 1
- 235000020776 essential amino acid Nutrition 0.000 claims 1
- 239000000284 extract Substances 0.000 claims 1
- 238000001914 filtration Methods 0.000 claims 1
- 239000012847 fine chemical Substances 0.000 claims 1
- 239000012530 fluid Substances 0.000 claims 1
- 230000005714 functional activity Effects 0.000 claims 1
- 229930182830 galactose Natural products 0.000 claims 1
- 230000009395 genetic defect Effects 0.000 claims 1
- 239000003365 glass fiber Substances 0.000 claims 1
- 239000008103 glucose Substances 0.000 claims 1
- ZDXPYRJPNDTMRX-UHFFFAOYSA-N glutamine Natural products OC(=O)C(N)CCC(N)=O ZDXPYRJPNDTMRX-UHFFFAOYSA-N 0.000 claims 1
- 235000011187 glycerol Nutrition 0.000 claims 1
- 125000004970 halomethyl group Chemical group 0.000 claims 1
- 238000003306 harvesting Methods 0.000 claims 1
- 238000010438 heat treatment Methods 0.000 claims 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid group Chemical group C(CCCCC)(=O)O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 claims 1
- 229960001340 histamine Drugs 0.000 claims 1
- 210000004408 hybridoma Anatomy 0.000 claims 1
- 125000002951 idosyl group Chemical class C1([C@@H](O)[C@H](O)[C@@H](O)[C@H](O1)CO)* 0.000 claims 1
- 230000036737 immune function Effects 0.000 claims 1
- 230000002434 immunopotentiative effect Effects 0.000 claims 1
- 230000001976 improved effect Effects 0.000 claims 1
- 239000012535 impurity Substances 0.000 claims 1
- 239000003112 inhibitor Substances 0.000 claims 1
- 239000002799 interferon inducing agent Substances 0.000 claims 1
- 229960001388 interferon-beta Drugs 0.000 claims 1
- 239000007928 intraperitoneal injection Substances 0.000 claims 1
- 238000011835 investigation Methods 0.000 claims 1
- 125000002346 iodo group Chemical group I* 0.000 claims 1
- 150000002500 ions Chemical class 0.000 claims 1
- 125000000468 ketone group Chemical group 0.000 claims 1
- WHXSMMKQMYFTQS-NJFSPNSNSA-N lithium-9 Chemical group [9Li] WHXSMMKQMYFTQS-NJFSPNSNSA-N 0.000 claims 1
- 210000001165 lymph node Anatomy 0.000 claims 1
- 210000000207 lymphocyte subset Anatomy 0.000 claims 1
- 230000000527 lymphocytic effect Effects 0.000 claims 1
- 230000002979 macrophagic effect Effects 0.000 claims 1
- 239000003550 marker Substances 0.000 claims 1
- 230000010534 mechanism of action Effects 0.000 claims 1
- 230000001404 mediated effect Effects 0.000 claims 1
- YLGXILFCIXHCMC-JHGZEJCSSA-N methyl cellulose Chemical compound COC1C(OC)C(OC)C(COC)O[C@H]1O[C@H]1C(OC)C(OC)C(OC)OC1COC YLGXILFCIXHCMC-JHGZEJCSSA-N 0.000 claims 1
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 claims 1
- 230000000813 microbial effect Effects 0.000 claims 1
- 238000001000 micrograph Methods 0.000 claims 1
- 230000007193 modulation by symbiont of host erythrocyte aggregation Effects 0.000 claims 1
- 238000010172 mouse model Methods 0.000 claims 1
- 230000001338 necrotic effect Effects 0.000 claims 1
- 230000035407 negative regulation of cell proliferation Effects 0.000 claims 1
- 230000007935 neutral effect Effects 0.000 claims 1
- 230000003448 neutrophilic effect Effects 0.000 claims 1
- 210000002445 nipple Anatomy 0.000 claims 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 1
- 238000003199 nucleic acid amplification method Methods 0.000 claims 1
- 210000004940 nucleus Anatomy 0.000 claims 1
- 235000015097 nutrients Nutrition 0.000 claims 1
- 229920001778 nylon Polymers 0.000 claims 1
- 235000021313 oleic acid Nutrition 0.000 claims 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims 1
- 239000001048 orange dye Substances 0.000 claims 1
- 239000010502 orange oil Substances 0.000 claims 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 claims 1
- 239000002245 particle Substances 0.000 claims 1
- 230000037361 pathway Effects 0.000 claims 1
- 229940056360 penicillin g Drugs 0.000 claims 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 1
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 claims 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims 1
- 230000001885 phytohemagglutinin Effects 0.000 claims 1
- 230000004983 pleiotropic effect Effects 0.000 claims 1
- 229920001155 polypropylene Polymers 0.000 claims 1
- 229920002223 polystyrene Polymers 0.000 claims 1
- 230000021625 positive regulation of cell division Effects 0.000 claims 1
- 230000032287 positive regulation of immunoglobulin secretion Effects 0.000 claims 1
- 239000000047 product Substances 0.000 claims 1
- 230000009696 proliferative response Effects 0.000 claims 1
- 230000001737 promoting effect Effects 0.000 claims 1
- 108090000623 proteins and genes Proteins 0.000 claims 1
- 230000005588 protonation Effects 0.000 claims 1
- INCIMLINXXICKS-UHFFFAOYSA-M pyronin Y Chemical compound [Cl-].C1=CC(=[N+](C)C)C=C2OC3=CC(N(C)C)=CC=C3C=C21 INCIMLINXXICKS-UHFFFAOYSA-M 0.000 claims 1
- 230000002285 radioactive effect Effects 0.000 claims 1
- 230000009257 reactivity Effects 0.000 claims 1
- 230000010076 replication Effects 0.000 claims 1
- 238000012827 research and development Methods 0.000 claims 1
- 239000011347 resin Substances 0.000 claims 1
- 229920005989 resin Polymers 0.000 claims 1
- 230000004043 responsiveness Effects 0.000 claims 1
- 230000000717 retained effect Effects 0.000 claims 1
- 229940085605 saccharin sodium Drugs 0.000 claims 1
- 230000002000 scavenging effect Effects 0.000 claims 1
- 239000013049 sediment Substances 0.000 claims 1
- 230000035945 sensitivity Effects 0.000 claims 1
- 239000000377 silicon dioxide Substances 0.000 claims 1
- 235000012239 silicon dioxide Nutrition 0.000 claims 1
- 229960001462 sodium cyclamate Drugs 0.000 claims 1
- 229940054269 sodium pyruvate Drugs 0.000 claims 1
- 229910052682 stishovite Inorganic materials 0.000 claims 1
- 229960005322 streptomycin Drugs 0.000 claims 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 claims 1
- 230000008093 supporting effect Effects 0.000 claims 1
- 230000001629 suppression Effects 0.000 claims 1
- 230000020382 suppression by virus of host antigen processing and presentation of peptide antigen via MHC class I Effects 0.000 claims 1
- 230000004083 survival effect Effects 0.000 claims 1
- 230000005737 synergistic response Effects 0.000 claims 1
- 230000009885 systemic effect Effects 0.000 claims 1
- 239000000454 talc Substances 0.000 claims 1
- 229910052623 talc Inorganic materials 0.000 claims 1
- 230000002123 temporal effect Effects 0.000 claims 1
- 150000003573 thiols Chemical group 0.000 claims 1
- 230000002992 thymic effect Effects 0.000 claims 1
- 229940104230 thymidine Drugs 0.000 claims 1
- 231100000331 toxic Toxicity 0.000 claims 1
- 230000002588 toxic effect Effects 0.000 claims 1
- 231100000419 toxicity Toxicity 0.000 claims 1
- 230000001988 toxicity Effects 0.000 claims 1
- 239000000196 tragacanth Substances 0.000 claims 1
- 235000010487 tragacanth Nutrition 0.000 claims 1
- 229940116362 tragacanth Drugs 0.000 claims 1
- 230000026683 transduction Effects 0.000 claims 1
- 238000010361 transduction Methods 0.000 claims 1
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 claims 1
- 229910052905 tridymite Inorganic materials 0.000 claims 1
- 229910052722 tritium Inorganic materials 0.000 claims 1
- 210000004881 tumor cell Anatomy 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/16—Purine radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/439,846 US4539205A (en) | 1982-11-09 | 1982-11-09 | Modulation of animal cellular responses with compositions containing 8-substituted guanine derivatives |
| US06/546,679 US4643992A (en) | 1982-11-09 | 1983-11-01 | Modulation of animal cellular responses with compositions containing 8-substituted guanine derivatives |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| PT77636A PT77636A (en) | 1983-12-01 |
| PT77636B true PT77636B (en) | 1986-03-19 |
Family
ID=27032191
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PT77636A PT77636B (en) | 1982-11-09 | 1983-11-09 | Modulation of animal cellular responses with compositions containing 8-substituted guanine derivatives |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US4643992A (enExample) |
| EP (1) | EP0112632B1 (enExample) |
| AU (1) | AU568325B2 (enExample) |
| CA (1) | CA1236401A (enExample) |
| DE (1) | DE3382156D1 (enExample) |
| DK (1) | DK167898B1 (enExample) |
| ES (1) | ES8601301A1 (enExample) |
| FI (1) | FI87733C (enExample) |
| GR (1) | GR78733B (enExample) |
| IE (1) | IE56701B1 (enExample) |
| IL (1) | IL70164A (enExample) |
| NO (1) | NO174215C (enExample) |
| NZ (1) | NZ206208A (enExample) |
| PT (1) | PT77636B (enExample) |
| WO (1) | WO1984001898A1 (enExample) |
Families Citing this family (47)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4849411A (en) * | 1982-11-09 | 1989-07-18 | Scripps Clinic And Research Foundation | Modulation of animal cellular responses with compositions containing 8-substituted guanine derivatives |
| US5476659A (en) * | 1982-11-09 | 1995-12-19 | The Scripps Research Institute | Cancerous B cell treatment using substituted nucleoside derivatives |
| US4900675A (en) * | 1983-11-01 | 1990-02-13 | Scripps Clinic And Research Foundation | Modulation of animal cellular responses with compositions containing isoxanthopterin-8-(1'-β-aldoglycosidyl) derivatives |
| US5093318A (en) * | 1983-11-01 | 1992-03-03 | Scripps Clinic And Research Foundation | Immunostimulating guanosine derivatives and their pharmaceutical compositions |
| US5166141A (en) * | 1983-11-01 | 1992-11-24 | Scripps Clinic And Research Foundation | Immunostimulating 7-deaza-7-oxa- and 7-deaza-7-oxo-analogs of 8-substituted-guanine-9-(1'-beta-D-aldoglycosidyl) derivatives and methods of treating test animals |
| FR2560212B1 (fr) * | 1984-02-24 | 1989-12-29 | Unicet | Anticorps monoclonaux contre l'interferon a2 et hybridomes produisant de tels anticorps |
| US5011828A (en) * | 1985-11-15 | 1991-04-30 | Michael Goodman | Immunostimulating guanine derivatives, compositions and methods |
| ZA869297B (en) * | 1985-12-13 | 1987-11-25 | Scripps Clinic Res | Modulation of animal cellular responses with compositions containing isoxanthopterin-8-(1'-beta-aldoglycosidyl)derivatives |
| US6060459A (en) * | 1987-10-28 | 2000-05-09 | Pro-Neuron, Inc. | Enhancing blood cell count with oxypurine nucleosides |
| US4880784A (en) * | 1987-12-21 | 1989-11-14 | Brigham Young University | Antiviral methods utilizing ribofuranosylthiazolo[4,5-d]pyrimdine derivatives |
| US4902985A (en) * | 1988-02-25 | 1990-02-20 | Raytheon Company | Microwave reflectiion amplifiers having increased bandwidth |
| GB2216416B (en) * | 1988-03-11 | 1992-06-24 | Sandoz Ltd | Nucleobase source for the stimulation of the immune system |
| WO1989010158A1 (en) * | 1988-04-27 | 1989-11-02 | Immunomedics, Inc. | Improved radiotherapy |
| AU5845594A (en) * | 1992-11-13 | 1994-06-08 | Scripps Research Institute, The | Cancerous b cell treatment using substituted nucleoside derivatives |
| US5786359A (en) * | 1994-05-27 | 1998-07-28 | The Scripps Research Institute | N9 alkyl or aralkyl derivatives of 7, 8-disubstituted guanines |
| US5441942A (en) * | 1994-05-27 | 1995-08-15 | The Scripps Research Institute | 2'3'-dideoxy-2',3'-didehydro-7,8-disubstituted guanosines and their immunostimulative effect |
| US6338963B1 (en) | 1994-07-25 | 2002-01-15 | Neotherapeutics, Inc. | Use of carbon monoxide dependent guanylyl cyclase modifiers to stimulate neuritogenesis |
| US20030100520A1 (en) * | 1997-01-21 | 2003-05-29 | Philip Needleman | Immunological process and constructs for increasing the hdl cholesterol concentration by dna vaccination |
| US6303617B1 (en) | 1998-05-04 | 2001-10-16 | Neotherapeutics, Inc. | Serotonin-like 9-substituted hypoxanthine and methods of use |
| US6562801B1 (en) * | 1999-04-15 | 2003-05-13 | Board Of Regents, The University Of Texas System | PpGpp and pppGpp as immunomodulatory agents |
| US6288069B1 (en) | 1999-11-16 | 2001-09-11 | Neotherapeutics, Inc. | Use of 9-substituted hypoxanthine derivatives to stimulate regeneration of nervous tissue |
| US6407237B1 (en) | 2001-02-21 | 2002-06-18 | Neotherapeutics, Inc. | Crystal forms of 9-substituted hypoxanthine derivatives |
| US6849735B1 (en) * | 2000-06-23 | 2005-02-01 | Merck Eprova Ag | Methods of synthesis for 9-substituted hypoxanthine derivatives |
| DK1790344T3 (da) | 2000-07-07 | 2011-05-02 | Spectrum Pharmaceuticals Inc | Fremgangsmåder til behandling af sygdomsfremkaldt perifer neuropati og beslægtede tilstande |
| US20030138769A1 (en) * | 2000-08-16 | 2003-07-24 | Birkett Ashley J. | Immunogenic HBc chimer particles having enhanced stability |
| US6759427B2 (en) * | 2001-04-20 | 2004-07-06 | Spectrum Pharmaceuticals, Inc. | Synthesis and methods of use of tetrahydroindolone analogues and derivatives |
| EP1395262A4 (en) * | 2001-06-15 | 2006-04-12 | Ribapharm Corp | NUCLEOSIDE-VACCINE-ADJUVANTS |
| US20030055249A1 (en) * | 2001-07-17 | 2003-03-20 | Fick David B. | Synthesis and methods of use of pyrimidine analogues and derivatives |
| US7361352B2 (en) * | 2001-08-15 | 2008-04-22 | Acambis, Inc. | Influenza immunogen and vaccine |
| US20030175863A1 (en) * | 2001-08-15 | 2003-09-18 | Birkett Ashley J. | Influenza immunogen and vaccine |
| US7321033B2 (en) * | 2001-11-27 | 2008-01-22 | Anadys Pharmaceuticals, Inc. | 3-B-D-ribofuranosylthiazolo [4,5-d] pyrimidine nucleosides and uses thereof |
| US7351413B2 (en) * | 2002-02-21 | 2008-04-01 | Lorantis, Limited | Stabilized HBc chimer particles as immunogens for chronic hepatitis |
| ATE465742T1 (de) | 2003-09-05 | 2010-05-15 | Anadys Pharmaceuticals Inc | Tlr7-liganden zur behandlung von hepatitis c |
| NZ555723A (en) | 2004-12-17 | 2010-07-30 | Anadys Pharmaceuticals Inc | 3,5-disubstituted and 3,5,7-trisubstituted-3H-oxazolo and 3H-thiazolo[4,5-d]pyrimidin-2-one compounds and prodrugs thereof |
| BRPI0618789A2 (pt) | 2005-11-21 | 2016-08-30 | Anadys Pharmaceuticals Inc | processos de preparação de 5-amino-3h-tiazol [4,5-d] pirimidin-2-ona, de ciclocondensação de 2,4-diamino-5-halo-pirimidina e de oxidação de 5-amino-3h-tiazol [4,5-d] pirimidin-2-tiona |
| DE602007012247D1 (de) * | 2006-06-22 | 2011-03-10 | Anadys Pharmaceuticals Inc | Prodrugs von 5-amino-3-(3'-deoxy-beta-d-ribofuranosyl)-thiazolä4,5-düpyrimidin-2,7-dion |
| DE602007012881D1 (en) | 2006-07-18 | 2011-04-14 | Anadys Pharmaceuticals Inc | Carbonat- und carbamat-prodrugs von thiazolo ä4,5-dü-pyrimidinen |
| EP2173376B1 (en) * | 2007-08-02 | 2015-03-25 | Biondvax Pharmaceuticals Ltd. | Multimeric multiepitope influenza vaccines |
| WO2009073179A2 (en) | 2007-12-03 | 2009-06-11 | President And Fellows Of Harvard College | Chlamydia antigens |
| KR20110091560A (ko) | 2008-12-03 | 2011-08-11 | 프로테아 벡신 테크놀로지스 엘티디. | 글루타밀 ｔＲＮＡ 합성효소(ＧｔＳ) 단편들 |
| SI2364314T1 (sl) | 2008-12-09 | 2014-07-31 | Gilead Sciences, Inc. | Modulatorji Tollu podobnih receptorjev |
| WO2011067758A2 (en) | 2009-12-02 | 2011-06-09 | Protea Vaccine Technologies Ltd. | Immunogenic fragments and multimers from streptococcus pneumoniae proteins |
| US9303070B2 (en) | 2011-02-22 | 2016-04-05 | Biondvax Pharmaceuticals Ltd. | Multimeric multiepitope polypeptides in improved seasonal and pandemic influenza vaccines |
| WO2013150518A1 (en) | 2012-04-01 | 2013-10-10 | Rappaport Family Institute For Research In The Medical Sciences | Extracellular matrix metalloproteinase inducer (emmprin) peptides and binding antibodies |
| AU2015242154B2 (en) | 2014-04-03 | 2019-04-04 | Biondvax Pharmaceuticals Ltd. | Compositions of multimeric-multiepitope influenza polypeptides and their production |
| PT3166607T (pt) | 2014-07-11 | 2022-12-07 | Gilead Sciences Inc | Moduladores de receptores de tipo toll para o tratamento do vih |
| SG11201701520TA (en) | 2014-09-16 | 2017-04-27 | Gilead Sciences Inc | Solid forms of a toll-like receptor modulator |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1174077A (en) * | 1967-02-18 | 1969-12-10 | Ajinomoto Kk | Process for Preparing 8-Mercaptopurine Derivatives |
-
1983
- 1983-11-01 US US06/546,679 patent/US4643992A/en not_active Expired - Lifetime
- 1983-11-07 AU AU23302/84A patent/AU568325B2/en not_active Expired
- 1983-11-07 WO PCT/US1983/001722 patent/WO1984001898A1/en not_active Ceased
- 1983-11-08 ES ES527138A patent/ES8601301A1/es not_active Expired
- 1983-11-08 EP EP83306791A patent/EP0112632B1/en not_active Expired - Lifetime
- 1983-11-08 DE DE8383306791T patent/DE3382156D1/de not_active Expired - Lifetime
- 1983-11-08 IE IE2605/83A patent/IE56701B1/en not_active IP Right Cessation
- 1983-11-08 CA CA000440679A patent/CA1236401A/en not_active Expired
- 1983-11-08 IL IL70164A patent/IL70164A/xx not_active IP Right Cessation
- 1983-11-09 PT PT77636A patent/PT77636B/pt unknown
- 1983-11-09 GR GR72936A patent/GR78733B/el unknown
- 1983-11-09 NZ NZ206208A patent/NZ206208A/en unknown
-
1984
- 1984-07-06 DK DK334884A patent/DK167898B1/da not_active IP Right Cessation
- 1984-07-06 NO NO842765A patent/NO174215C/no not_active IP Right Cessation
- 1984-07-09 FI FI842748A patent/FI87733C/fi not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| IL70164A (en) | 1988-06-30 |
| WO1984001898A1 (en) | 1984-05-24 |
| DK334884D0 (da) | 1984-07-06 |
| NZ206208A (en) | 1987-03-31 |
| US4643992A (en) | 1987-02-17 |
| PT77636A (en) | 1983-12-01 |
| AU568325B2 (en) | 1987-12-24 |
| ES527138A0 (es) | 1985-11-01 |
| EP0112632B1 (en) | 1991-02-06 |
| AU2330284A (en) | 1984-06-04 |
| NO174215B (no) | 1993-12-20 |
| FI842748A0 (fi) | 1984-07-09 |
| IE832605L (en) | 1984-05-09 |
| IL70164A0 (en) | 1984-02-29 |
| NO842765L (no) | 1984-07-06 |
| FI842748L (fi) | 1984-07-09 |
| CA1236401A (en) | 1988-05-10 |
| NO174215C (no) | 1994-03-30 |
| FI87733B (fi) | 1992-11-13 |
| DE3382156D1 (de) | 1991-03-14 |
| EP0112632A3 (en) | 1985-01-23 |
| GR78733B (enExample) | 1984-10-02 |
| DK167898B1 (da) | 1994-01-03 |
| EP0112632A2 (en) | 1984-07-04 |
| IE56701B1 (en) | 1991-11-06 |
| FI87733C (fi) | 1993-02-25 |
| DK334884A (da) | 1984-07-06 |
| ES8601301A1 (es) | 1985-11-01 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| PT77636B (en) | Modulation of animal cellular responses with compositions containing 8-substituted guanine derivatives | |
| US4539205A (en) | Modulation of animal cellular responses with compositions containing 8-substituted guanine derivatives | |
| Yoneda et al. | Prostaglandins are necessary for osteoclast-activating factor production by activated peripheral blood leukocytes. | |
| Taniguchi et al. | Antigen-specific suppressive factor produced by a transplantable IJ bearing T-cell hybridoma | |
| Allison et al. | The role of de novo purine synthesis in lymphocyte transformation | |
| DE3856279T2 (de) | 7-Thia-Guanosin-Derivate mit antiviraler, antitumoraler, antimetastatischer und immunstimulierender Wirkung | |
| AU627178B2 (en) | Immunostimulating 7-deaza-7-oxa- and 7-deaza-7-thia- analogs of 8-substituted-guanine-9-(1'beta-d-aldoglycosidyl) derivatives, compositions and methods | |
| US4950647A (en) | T cell immunopotentiator | |
| US5968912A (en) | Methods for immunosuppressing | |
| US4849411A (en) | Modulation of animal cellular responses with compositions containing 8-substituted guanine derivatives | |
| US4948730A (en) | Modulation of animal cellular responses with compositions containing 8-substituted guanine derivatives | |
| US5147636A (en) | Modulation of animal cellular responses with compositions containing 8-substituted guanine derivatives and interferons | |
| Goodman | Cellular and biochemical studies of substituted guanine ribonucleoside immunostimulants | |
| US5441942A (en) | 2'3'-dideoxy-2',3'-didehydro-7,8-disubstituted guanosines and their immunostimulative effect | |
| HEMMI et al. | Selective inhibition of nucleoside transport into mouse lymphoma L-5178Y cells by cimicifugoside | |
| US4159320A (en) | Activated MASF | |
| JP2591725B2 (ja) | ８−置換グアニン誘導体を含む免疫調節剤 | |
| US5382580A (en) | N9 morpholino derivatives of 7,8-disubstituted guanines | |
| Zegers et al. | Therapy in adenosine deaminase and purine nucleoside phosphorylase deficient patients | |
| DE3687169T2 (de) | Modulation tierischer cellularer reaktionen mittels zubereitungen, die isoxanthopterin-8-(1'-beta-aldoglykosidyl)-abkoemmlinge enthalten. | |
| US4900675A (en) | Modulation of animal cellular responses with compositions containing isoxanthopterin-8-(1'-β-aldoglycosidyl) derivatives | |
| Hoffman et al. | Studies on purine and pyrimidine requirements of a strain of Streptococcus faecalis |