JPS55144000A - Preparation of 2-amino-adenosine-3',5'-cyclic phosphoric acid - Google Patents

Info

Publication number

JPS55144000A

JPS55144000A JP5142279A JP5142279A JPS55144000A JP S55144000 A JPS55144000 A JP S55144000A JP 5142279 A JP5142279 A JP 5142279A JP 5142279 A JP5142279 A JP 5142279A JP S55144000 A JPS55144000 A JP S55144000A

Authority

JP

Japan

Prior art keywords

phosphoric acid

cyclic phosphoric

adenosine

formula

amino

Prior art date

1979-04-27

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.)

Granted

Links

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• NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 title abstract 7
• 229910000147 aluminium phosphate Inorganic materials 0.000 title abstract 4
• SRBFZHDQGSBBOR-IOVATXLUSA-N D-xylopyranose Chemical compound O[C@@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-IOVATXLUSA-N 0.000 abstract 2
• GFFGJBXGBJISGV-UHFFFAOYSA-N Adenine Chemical compound NC1=NC=NC2=C1N=CN2 GFFGJBXGBJISGV-UHFFFAOYSA-N 0.000 abstract 1
• 229930024421 Adenine Natural products 0.000 abstract 1
• 241000894006 Bacteria Species 0.000 abstract 1
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
• 241001467578 Microbacterium Species 0.000 abstract 1
• KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium on carbon Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 abstract 1
• 229960000643 adenine Drugs 0.000 abstract 1
• 239000003513 alkali Substances 0.000 abstract 1
• 150000001348 alkyl chlorides Chemical class 0.000 abstract 1
• 125000000217 alkyl group Chemical group 0.000 abstract 1
• 239000000043 antiallergic agent Substances 0.000 abstract 1
• PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 abstract 1
• SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 abstract 1
• 239000003130 blood coagulation factor inhibitor Substances 0.000 abstract 1
• 210000001772 blood platelet Anatomy 0.000 abstract 1
• 230000003327 cancerostatic effect Effects 0.000 abstract 1
• 239000003054 catalyst Substances 0.000 abstract 1
• 239000003874 central nervous system depressant Substances 0.000 abstract 1
• 239000003795 chemical substances by application Substances 0.000 abstract 1
• 150000001875 compounds Chemical class 0.000 abstract 1
• 238000012258 culturing Methods 0.000 abstract 1
• 239000002934 diuretic Substances 0.000 abstract 1
• 230000001882 diuretic effect Effects 0.000 abstract 1
• NLFBCYMMUAKCPC-KQQUZDAGSA-N ethyl (e)-3-[3-amino-2-cyano-1-[(e)-3-ethoxy-3-oxoprop-1-enyl]sulfanyl-3-oxoprop-1-enyl]sulfanylprop-2-enoate Chemical compound CCOC(=O)\C=C\SC(=C(C#N)C(N)=O)S\C=C\C(=O)OCC NLFBCYMMUAKCPC-KQQUZDAGSA-N 0.000 abstract 1
• 229910052736 halogen Inorganic materials 0.000 abstract 1
• 125000005843 halogen group Chemical group 0.000 abstract 1
• 229910052739 hydrogen Inorganic materials 0.000 abstract 1
• 239000001257 hydrogen Substances 0.000 abstract 1
• 229910052816 inorganic phosphate Inorganic materials 0.000 abstract 1
• 230000001590 oxidative effect Effects 0.000 abstract 1
• 150000003212 purines Chemical class 0.000 abstract 1
• 238000006462 rearrangement reaction Methods 0.000 abstract 1
• 241000894007 species Species 0.000 abstract 1
• LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 abstract 1

Cited By (1)