UA65518C2 - Peptide derivatives - Google Patents
Peptide derivatives Download PDFInfo
- Publication number
- UA65518C2 UA65518C2 UA95115078A UA95115078A UA65518C2 UA 65518 C2 UA65518 C2 UA 65518C2 UA 95115078 A UA95115078 A UA 95115078A UA 95115078 A UA95115078 A UA 95115078A UA 65518 C2 UA65518 C2 UA 65518C2
- Authority
- UA
- Ukraine
- Prior art keywords
- group
- spa
- rab
- rho
- age
- Prior art date
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- 108090000765 processed proteins & peptides Proteins 0.000 title claims description 40
- 150000001875 compounds Chemical class 0.000 claims abstract description 385
- 230000015572 biosynthetic process Effects 0.000 claims abstract description 54
- 239000012634 fragment Substances 0.000 claims abstract description 54
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- 239000003868 thrombin inhibitor Substances 0.000 claims abstract description 18
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- 239000008194 pharmaceutical composition Substances 0.000 claims abstract 6
- 239000004480 active ingredient Substances 0.000 claims abstract 2
- 239000000203 mixture Substances 0.000 claims description 305
- 125000000217 alkyl group Chemical group 0.000 claims description 179
- 125000004432 carbon atom Chemical group C* 0.000 claims description 172
- 238000000034 method Methods 0.000 claims description 127
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 100
- 238000002360 preparation method Methods 0.000 claims description 91
- 229910052799 carbon Inorganic materials 0.000 claims description 83
- 125000003739 carbamimidoyl group Chemical group C(N)(=N)* 0.000 claims description 56
- 238000006243 chemical reaction Methods 0.000 claims description 43
- -1 p-toluenesulfonyl group Chemical group 0.000 claims description 37
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 36
- UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 claims description 34
- 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 claims description 32
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- 150000001413 amino acids Chemical class 0.000 claims description 26
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 25
- 125000006239 protecting group Chemical group 0.000 claims description 25
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- HONIICLYMWZJFZ-UHFFFAOYSA-N azetidine Chemical compound C1CNC1 HONIICLYMWZJFZ-UHFFFAOYSA-N 0.000 claims description 21
- 125000002795 guanidino group Chemical group C(N)(=N)N* 0.000 claims description 21
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- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 17
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 17
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- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 9
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- 125000004429 atom Chemical group 0.000 claims description 3
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
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SE19939301916A SE9301916D0 (sv) | 1993-06-03 | 1993-06-03 | New peptides derivatives |
PCT/SE1994/000535 WO1994029336A1 (en) | 1993-06-03 | 1994-06-02 | New peptide derivatives |
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UA95115078A UA65518C2 (en) | 1993-06-03 | 1994-02-06 | Peptide derivatives |
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