IL94694A - Enantiomeric enrichment and straoselective synthesis of chiral amines - Google Patents
Enantiomeric enrichment and straoselective synthesis of chiral aminesInfo
- Publication number
- IL94694A IL94694A IL9469490A IL9469490A IL94694A IL 94694 A IL94694 A IL 94694A IL 9469490 A IL9469490 A IL 9469490A IL 9469490 A IL9469490 A IL 9469490A IL 94694 A IL94694 A IL 94694A
- Authority
- IL
- Israel
- Prior art keywords
- amino
- chiral
- process according
- omega
- ketone
- Prior art date
Links
- 150000001412 amines Chemical class 0.000 title claims abstract description 89
- 230000015572 biosynthetic process Effects 0.000 title claims description 15
- 230000000707 stereoselective effect Effects 0.000 title claims description 14
- 238000003786 synthesis reaction Methods 0.000 title claims description 14
- 238000000034 method Methods 0.000 claims abstract description 69
- 108090000340 Transaminases Proteins 0.000 claims abstract description 58
- 150000002576 ketones Chemical class 0.000 claims abstract description 32
- 102000003929 Transaminases Human genes 0.000 claims abstract description 19
- 125000003277 amino group Chemical group 0.000 claims abstract description 13
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 8
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 44
- 239000000203 mixture Substances 0.000 claims description 22
- 238000002360 preparation method Methods 0.000 claims description 17
- 244000005700 microbiome Species 0.000 claims description 15
- 125000000217 alkyl group Chemical group 0.000 claims description 13
- 150000003839 salts Chemical class 0.000 claims description 11
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 10
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
- 230000002401 inhibitory effect Effects 0.000 claims description 7
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 claims description 6
- BHRZNVHARXXAHW-UHFFFAOYSA-N sec-butylamine Chemical group CCC(C)N BHRZNVHARXXAHW-UHFFFAOYSA-N 0.000 claims description 6
- 239000000126 substance Substances 0.000 claims description 6
- 125000003118 aryl group Chemical group 0.000 claims description 5
- 239000011541 reaction mixture Substances 0.000 claims description 5
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims description 4
- LCTONWCANYUPML-UHFFFAOYSA-N Pyruvic acid Chemical compound CC(=O)C(O)=O LCTONWCANYUPML-UHFFFAOYSA-N 0.000 claims description 4
- 239000012736 aqueous medium Substances 0.000 claims description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
- HHLFWLYXYJOTON-UHFFFAOYSA-N glyoxylic acid Chemical group OC(=O)C=O HHLFWLYXYJOTON-UHFFFAOYSA-N 0.000 claims description 4
- KHPXUQMNIQBQEV-UHFFFAOYSA-N oxaloacetic acid Chemical compound OC(=O)CC(=O)C(O)=O KHPXUQMNIQBQEV-UHFFFAOYSA-N 0.000 claims description 4
- 239000004471 Glycine Substances 0.000 claims description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 3
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 3
- 125000001624 naphthyl group Chemical group 0.000 claims description 3
- 125000003884 phenylalkyl group Chemical group 0.000 claims description 3
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 3
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 claims description 2
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 claims description 2
- 150000001299 aldehydes Chemical class 0.000 claims description 2
- 238000011065 in-situ storage Methods 0.000 claims description 2
- 229940107700 pyruvic acid Drugs 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 claims 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 2
- 235000004279 alanine Nutrition 0.000 claims 1
- 235000003704 aspartic acid Nutrition 0.000 claims 1
- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 claims 1
- FXHGMKSSBGDXIY-UHFFFAOYSA-N heptanal Chemical compound CCCCCCC=O FXHGMKSSBGDXIY-UHFFFAOYSA-N 0.000 claims 1
- 239000012429 reaction media Substances 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 abstract description 14
- 230000007717 exclusion Effects 0.000 abstract 1
- 229940024606 amino acid Drugs 0.000 description 49
- 102000014898 transaminase activity proteins Human genes 0.000 description 39
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 32
- 102000004190 Enzymes Human genes 0.000 description 23
- 108090000790 Enzymes Proteins 0.000 description 23
- 230000000694 effects Effects 0.000 description 22
- NGVDGCNFYWLIFO-UHFFFAOYSA-N pyridoxal 5'-phosphate Chemical compound CC1=NC=C(COP(O)(O)=O)C(C=O)=C1O NGVDGCNFYWLIFO-UHFFFAOYSA-N 0.000 description 22
- 239000000370 acceptor Substances 0.000 description 21
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 18
- 238000006243 chemical reaction Methods 0.000 description 16
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 14
- -1 A-butyl Chemical group 0.000 description 11
- 241000193830 Bacillus <bacterium> Species 0.000 description 11
- 235000007682 pyridoxal 5'-phosphate Nutrition 0.000 description 11
- 239000011589 pyridoxal 5'-phosphate Substances 0.000 description 11
- 229960001327 pyridoxal phosphate Drugs 0.000 description 11
- WECUIGDEWBNQJJ-SECBINFHSA-N (2r)-4-phenylbutan-2-amine Chemical compound C[C@@H](N)CCC1=CC=CC=C1 WECUIGDEWBNQJJ-SECBINFHSA-N 0.000 description 10
- 230000002255 enzymatic effect Effects 0.000 description 10
- 239000000047 product Substances 0.000 description 10
- DAEPDZWVDSPTHF-UHFFFAOYSA-M sodium pyruvate Chemical compound [Na+].CC(=O)C([O-])=O DAEPDZWVDSPTHF-UHFFFAOYSA-M 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 239000000284 extract Substances 0.000 description 9
- 239000008363 phosphate buffer Substances 0.000 description 9
- 239000000243 solution Substances 0.000 description 9
- RQEUFEKYXDPUSK-SSDOTTSWSA-N (1R)-1-phenylethanamine Chemical compound C[C@@H](N)C1=CC=CC=C1 RQEUFEKYXDPUSK-SSDOTTSWSA-N 0.000 description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 8
- LCTONWCANYUPML-UHFFFAOYSA-M Pyruvate Chemical compound CC(=O)C([O-])=O LCTONWCANYUPML-UHFFFAOYSA-M 0.000 description 8
- 235000001014 amino acid Nutrition 0.000 description 8
- 150000001413 amino acids Chemical class 0.000 description 8
- 238000003556 assay Methods 0.000 description 8
- 239000002609 medium Substances 0.000 description 8
- 229940076788 pyruvate Drugs 0.000 description 8
- 229910052757 nitrogen Inorganic materials 0.000 description 7
- RQEUFEKYXDPUSK-UHFFFAOYSA-N 1-phenylethylamine Chemical compound CC(N)C1=CC=CC=C1 RQEUFEKYXDPUSK-UHFFFAOYSA-N 0.000 description 6
- 229960003767 alanine Drugs 0.000 description 6
- 229940067621 aminobutyrate Drugs 0.000 description 6
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 6
- UCMIRNVEIXFBKS-UHFFFAOYSA-N beta-alanine Chemical compound NCCC(O)=O UCMIRNVEIXFBKS-UHFFFAOYSA-N 0.000 description 6
- 238000006911 enzymatic reaction Methods 0.000 description 6
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 6
- DZGWFCGJZKJUFP-UHFFFAOYSA-N tyramine Chemical compound NCCC1=CC=C(O)C=C1 DZGWFCGJZKJUFP-UHFFFAOYSA-N 0.000 description 6
- 238000000605 extraction Methods 0.000 description 5
- BTCSSZJGUNDROE-UHFFFAOYSA-N gamma-aminobutyric acid Chemical compound NCCCC(O)=O BTCSSZJGUNDROE-UHFFFAOYSA-N 0.000 description 5
- 229940054269 sodium pyruvate Drugs 0.000 description 5
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 4
- JCBPETKZIGVZRE-UHFFFAOYSA-N 2-aminobutan-1-ol Chemical compound CCC(N)CO JCBPETKZIGVZRE-UHFFFAOYSA-N 0.000 description 4
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 4
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 4
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 239000008346 aqueous phase Substances 0.000 description 4
- 150000001721 carbon Chemical group 0.000 description 4
- 238000005119 centrifugation Methods 0.000 description 4
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 4
- 239000011159 matrix material Substances 0.000 description 4
- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 4
- 239000001632 sodium acetate Substances 0.000 description 4
- 235000017281 sodium acetate Nutrition 0.000 description 4
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 4
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 4
- KPGXRSRHYNQIFN-UHFFFAOYSA-N 2-oxoglutaric acid Chemical compound OC(=O)CCC(=O)C(O)=O KPGXRSRHYNQIFN-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 229940000635 beta-alanine Drugs 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 150000002430 hydrocarbons Chemical group 0.000 description 3
- 230000000937 inactivator Effects 0.000 description 3
- 238000011534 incubation Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 150000003141 primary amines Chemical class 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 241000894007 species Species 0.000 description 3
- 229960003732 tyramine Drugs 0.000 description 3
- SOZMSEPDYJGBEK-ZCFIWIBFSA-N (1r)-1-(4-bromophenyl)ethanamine Chemical compound C[C@@H](N)C1=CC=C(Br)C=C1 SOZMSEPDYJGBEK-ZCFIWIBFSA-N 0.000 description 2
- BHRZNVHARXXAHW-SCSAIBSYSA-N (2r)-butan-2-amine Chemical compound CC[C@@H](C)N BHRZNVHARXXAHW-SCSAIBSYSA-N 0.000 description 2
- SYTBZMRGLBWNTM-SNVBAGLBSA-N (R)-flurbiprofen Chemical compound FC1=CC([C@H](C(O)=O)C)=CC=C1C1=CC=CC=C1 SYTBZMRGLBWNTM-SNVBAGLBSA-N 0.000 description 2
- WFWKNGZODAOLEO-UHFFFAOYSA-N 1-(4-Methoxyphenyl)-2-propanone Chemical compound COC1=CC=C(CC(C)=O)C=C1 WFWKNGZODAOLEO-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- 108030000921 4-aminobutyrate-2-oxoglutarate transaminases Proteins 0.000 description 2
- WECUIGDEWBNQJJ-UHFFFAOYSA-N 4-phenylbutan-2-amine Chemical compound CC(N)CCC1=CC=CC=C1 WECUIGDEWBNQJJ-UHFFFAOYSA-N 0.000 description 2
- SLXKOJJOQWFEFD-UHFFFAOYSA-N 6-aminohexanoic acid Chemical compound NCCCCCC(O)=O SLXKOJJOQWFEFD-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- 241000194107 Bacillus megaterium Species 0.000 description 2
- 108010010560 Beta-alanine-pyruvate transaminase Proteins 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 2
- 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 description 2
- 108010093096 Immobilized Enzymes Proteins 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- AHLPHDHHMVZTML-BYPYZUCNSA-N L-Ornithine Chemical compound NCCC[C@H](N)C(O)=O AHLPHDHHMVZTML-BYPYZUCNSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 241000589516 Pseudomonas Species 0.000 description 2
- 241000589776 Pseudomonas putida Species 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 241000187747 Streptomyces Species 0.000 description 2
- 229960002684 aminocaproic acid Drugs 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- AKGGYBADQZYZPD-UHFFFAOYSA-N benzylacetone Chemical compound CC(=O)CCC1=CC=CC=C1 AKGGYBADQZYZPD-UHFFFAOYSA-N 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 2
- 238000012258 culturing Methods 0.000 description 2
- 229960003692 gamma aminobutyric acid Drugs 0.000 description 2
- 239000008103 glucose Substances 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 230000001939 inductive effect Effects 0.000 description 2
- 230000005764 inhibitory process Effects 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical compound CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 229960003104 ornithine Drugs 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 239000001294 propane Substances 0.000 description 2
- 235000018102 proteins Nutrition 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- NHZMQXZHNVQTQA-UHFFFAOYSA-N pyridoxamine Chemical compound CC1=NC=C(CO)C(CN)=C1O NHZMQXZHNVQTQA-UHFFFAOYSA-N 0.000 description 2
- 238000009877 rendering Methods 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 239000001488 sodium phosphate Substances 0.000 description 2
- 229910000162 sodium phosphate Inorganic materials 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 239000006228 supernatant Substances 0.000 description 2
- 229960003080 taurine Drugs 0.000 description 2
- 238000005891 transamination reaction Methods 0.000 description 2
- 230000009466 transformation Effects 0.000 description 2
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 2
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 2
- KFNRJXCQEJIBER-UHFFFAOYSA-N (+-)-Gabaculin Natural products NC1CC(C(O)=O)=CC=C1 KFNRJXCQEJIBER-UHFFFAOYSA-N 0.000 description 1
- JMHAKVPFYWWNOW-SECBINFHSA-N (2r)-4-(4-methoxyphenyl)butan-2-amine Chemical compound COC1=CC=C(CC[C@@H](C)N)C=C1 JMHAKVPFYWWNOW-SECBINFHSA-N 0.000 description 1
- FVWVJTJAALVOQO-SECBINFHSA-N (2r)-5-pyridin-3-ylpentan-2-amine Chemical compound C[C@@H](N)CCCC1=CC=CN=C1 FVWVJTJAALVOQO-SECBINFHSA-N 0.000 description 1
- JCBPETKZIGVZRE-BYPYZUCNSA-N (2s)-2-aminobutan-1-ol Chemical compound CC[C@H](N)CO JCBPETKZIGVZRE-BYPYZUCNSA-N 0.000 description 1
- KWTSXDURSIMDCE-MRVPVSSYSA-N (R)-amphetamine Chemical compound C[C@@H](N)CC1=CC=CC=C1 KWTSXDURSIMDCE-MRVPVSSYSA-N 0.000 description 1
- KFNRJXCQEJIBER-ZCFIWIBFSA-N (S)-gabaculine Chemical compound N[C@H]1CC(C(O)=O)=CC=C1 KFNRJXCQEJIBER-ZCFIWIBFSA-N 0.000 description 1
- WYECURVXVYPVAT-UHFFFAOYSA-N 1-(4-bromophenyl)ethanone Chemical compound CC(=O)C1=CC=C(Br)C=C1 WYECURVXVYPVAT-UHFFFAOYSA-N 0.000 description 1
- WLNPAEJYFNAKKH-UHFFFAOYSA-N 1-(4-nitrophenyl)propan-1-amine Chemical compound CCC(N)C1=CC=C([N+]([O-])=O)C=C1 WLNPAEJYFNAKKH-UHFFFAOYSA-N 0.000 description 1
- MLBHFBKZUPLWBD-UHFFFAOYSA-N 1-[3-(trifluoromethyl)phenyl]-2-propanamine Chemical compound CC(N)CC1=CC=CC(C(F)(F)F)=C1 MLBHFBKZUPLWBD-UHFFFAOYSA-N 0.000 description 1
- XHOXKVFLASIOJD-UHFFFAOYSA-N 1-phenylbutan-1-amine Chemical compound CCCC(N)C1=CC=CC=C1 XHOXKVFLASIOJD-UHFFFAOYSA-N 0.000 description 1
- AQFLVLHRZFLDDV-UHFFFAOYSA-N 1-phenylpropan-1-amine Chemical compound CCC(N)C1=CC=CC=C1 AQFLVLHRZFLDDV-UHFFFAOYSA-N 0.000 description 1
- BKMMTJMQCTUHRP-UHFFFAOYSA-N 2-aminopropan-1-ol Chemical compound CC(N)CO BKMMTJMQCTUHRP-UHFFFAOYSA-N 0.000 description 1
- KJJPLEZQSCZCKE-UHFFFAOYSA-N 2-aminopropane-1,3-diol Chemical compound OCC(N)CO KJJPLEZQSCZCKE-UHFFFAOYSA-N 0.000 description 1
- MWGATWIBSKHFMR-UHFFFAOYSA-N 2-anilinoethanol Chemical compound OCCNC1=CC=CC=C1 MWGATWIBSKHFMR-UHFFFAOYSA-N 0.000 description 1
- JJKWHOSQTYYFAE-UHFFFAOYSA-N 2-methoxyacetyl chloride Chemical compound COCC(Cl)=O JJKWHOSQTYYFAE-UHFFFAOYSA-N 0.000 description 1
- SNKZJIOFVMKAOJ-UHFFFAOYSA-N 3-Aminopropanesulfonate Chemical compound NCCCS(O)(=O)=O SNKZJIOFVMKAOJ-UHFFFAOYSA-N 0.000 description 1
- QCHPKSFMDHPSNR-UHFFFAOYSA-N 3-aminoisobutyric acid Chemical compound NCC(C)C(O)=O QCHPKSFMDHPSNR-UHFFFAOYSA-N 0.000 description 1
- LGSSDLSVHUCRFI-UHFFFAOYSA-N 3-methylcyclopentan-1-amine Chemical compound CC1CCC(N)C1 LGSSDLSVHUCRFI-UHFFFAOYSA-N 0.000 description 1
- 125000004800 4-bromophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Br 0.000 description 1
- ULGJWNIHLSLQPZ-UHFFFAOYSA-N 7-[(6,8-dichloro-1,2,3,4-tetrahydroacridin-9-yl)amino]-n-[2-(1h-indol-3-yl)ethyl]heptanamide Chemical compound C1CCCC2=NC3=CC(Cl)=CC(Cl)=C3C(NCCCCCCC(=O)NCCC=3C4=CC=CC=C4NC=3)=C21 ULGJWNIHLSLQPZ-UHFFFAOYSA-N 0.000 description 1
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 1
- UQXNEWQGGVUVQA-UHFFFAOYSA-N 8-aminooctanoic acid Chemical compound NCCCCCCCC(O)=O UQXNEWQGGVUVQA-UHFFFAOYSA-N 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- 229920000936 Agarose Polymers 0.000 description 1
- 108700023418 Amidases Proteins 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 241000228212 Aspergillus Species 0.000 description 1
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical class C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 1
- 241000051622 Bacillus meqaterium Species 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 241000222120 Candida <Saccharomycetales> Species 0.000 description 1
- 101150015280 Cel gene Proteins 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P41/00—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/10—Transferases (2.)
- C12N9/1096—Transferases (2.) transferring nitrogenous groups (2.6)
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P41/00—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture
- C12P41/006—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by reactions involving C-N bonds, e.g. nitriles, amides, hydantoins, carbamates, lactames, transamination reactions, or keto group formation from racemic mixtures
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/24—Preparation of oxygen-containing organic compounds containing a carbonyl group
- C12P7/26—Ketones
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Zoology (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Microbiology (AREA)
- Biotechnology (AREA)
- Biochemistry (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Analytical Chemistry (AREA)
- Biomedical Technology (AREA)
- Molecular Biology (AREA)
- Medicinal Chemistry (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
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| US07/369,723 US4950606A (en) | 1989-06-22 | 1989-06-22 | Enantiomeric enrichment and stereoselective synthesis of chiral amines |
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| IL94694A0 IL94694A0 (en) | 1991-04-15 |
| IL94694A true IL94694A (en) | 1996-10-16 |
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| IL9469490A IL94694A (en) | 1989-06-22 | 1990-06-11 | Enantiomeric enrichment and straoselective synthesis of chiral amines |
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| US (1) | US4950606A (ja) |
| EP (1) | EP0404146B1 (ja) |
| JP (1) | JP2846074B2 (ja) |
| KR (1) | KR0147827B1 (ja) |
| AT (1) | ATE135744T1 (ja) |
| AU (1) | AU628183B2 (ja) |
| CA (1) | CA2018773C (ja) |
| DE (1) | DE69025988T2 (ja) |
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| ES (1) | ES2084618T3 (ja) |
| GR (1) | GR3019682T3 (ja) |
| HK (1) | HK1008052A1 (ja) |
| HU (1) | HU210967B (ja) |
| IE (1) | IE72956B1 (ja) |
| IL (1) | IL94694A (ja) |
| NZ (1) | NZ234154A (ja) |
| RU (2) | RU2087536C1 (ja) |
| ZA (1) | ZA904571B (ja) |
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| DE3842025A1 (de) * | 1988-12-14 | 1990-07-05 | Hoechst Ag | Verfahren zur herstellung von l-phosphinothricin |
| US5169780A (en) * | 1989-06-22 | 1992-12-08 | Celgene Corporation | Enantiomeric enrichment and stereoselective synthesis of chiral amines |
| US5141904A (en) * | 1991-02-15 | 1992-08-25 | Phillips Petroleum Company | Reactivation of spent cracking catalysts |
| CA2077400A1 (en) * | 1991-10-08 | 1993-04-09 | Mikhail Leyderman | Mandrel and a method of making a rigid tubular article |
| US6534446B1 (en) | 1994-02-23 | 2003-03-18 | Emerald Bioagriculture Corporation | Method to mitigate plant stress |
| US5439873A (en) * | 1994-02-23 | 1995-08-08 | Plant Growth Development Corporation | Method for stimulating plant growth using GABA |
| US5840656A (en) * | 1994-02-23 | 1998-11-24 | Auxein Corporation | Method for increasing fertilizer efficiency |
| DE69635082T2 (de) | 1995-10-23 | 2006-06-01 | Kaneka Corp. | Verfahren zur herstellung optisch aktiver aminoverbindungen |
| JPH10165194A (ja) * | 1996-12-12 | 1998-06-23 | Sumitomo Chem Co Ltd | 光学純度の向上方法 |
| WO1998048030A1 (en) * | 1997-04-23 | 1998-10-29 | Kaneka Corporation | Process for producing optically active amino compounds |
| RU2213142C2 (ru) * | 1998-03-11 | 2003-09-27 | Селгро | Способ получения хирального амина |
| EP1045025B1 (en) * | 1998-10-30 | 2008-10-22 | Kaneka Corporation | (S)-alpha-PHENETHYLAMINE : PYRUVATE TRANSAMINASE |
| US6432688B1 (en) | 1999-01-18 | 2002-08-13 | Daicel Chemical Industries, Ltd. | Amino alcohol dehydrogenase converts keto alcohol to amino alcohol and amino alcohol to keto alcohol |
| JP4496593B2 (ja) * | 1999-03-19 | 2010-07-07 | 住友化学株式会社 | 蛋白質、その遺伝子及びその利用 |
| DE60013939T2 (de) | 1999-03-19 | 2005-10-06 | Sumitomo Chemical Co. Ltd. | Stereoselektive Transaminase, deren kodierende Gen und deren Verwendungen |
| US6252114B1 (en) * | 2000-03-24 | 2001-06-26 | Council Of Scientific And Industrial Research | Process for preparing novel biologically active synthetic molecule 4-(p-methoxyphenyl)-2-amino-butane |
| RU2177114C2 (ru) * | 2000-04-03 | 2001-12-20 | ООО "Самаратрансгаз" | Устройство для крепления жаровой трубы в корпусе камеры сгорания |
| US7067291B2 (en) * | 2002-12-20 | 2006-06-27 | Pfizer Inc. | Biocatalytic preparation of enantiomerically enriched aminopentanenitrile |
| US20050009151A1 (en) * | 2003-07-10 | 2005-01-13 | Pharmacia Corporation | Methods for the stereospecific and enantiomeric enrichment of beta-amino acids |
| US7172885B2 (en) * | 2004-12-10 | 2007-02-06 | Cambrex North Brunswick, Inc. | Thermostable omega-transaminases |
| EP1889907B1 (en) * | 2005-05-23 | 2009-09-02 | Kaneka Corporation | Novel amino group transferase, gene encoding the same and method of using the same |
| EP1818411A1 (en) * | 2006-02-13 | 2007-08-15 | Lonza AG | Process for the preparation of optically active chiral amines |
| EP1897956A1 (en) | 2006-09-06 | 2008-03-12 | Lonza AG | Process for preparation of optically active amines by optical resolution of racemic amines employing a bacterial omega-transaminase |
| JP5253372B2 (ja) | 2007-02-27 | 2013-07-31 | マニー株式会社 | かしめ装置 |
| DE102007042600A1 (de) | 2007-09-07 | 2009-03-12 | Evonik Degussa Gmbh | Verfahren zur Herstellung von enantiomerenangereichten Aminen |
| CN102123999B (zh) * | 2008-05-22 | 2014-06-18 | 默沙东公司 | 制备食欲素受体拮抗剂的方法 |
| HUE052297T2 (hu) | 2009-01-08 | 2021-04-28 | Codexis Inc | Transzamináz polipeptidek |
| DE102009000592A1 (de) | 2009-02-04 | 2010-08-05 | Evonik Degussa Gmbh | Verfahren zur Herstellung von Aminogruppen tragenden, multizyklischen Ringsystemen |
| JP5707344B2 (ja) | 2009-02-26 | 2015-04-30 | コデクシス， インコーポレイテッド | トランスアミナーゼ生体触媒 |
| WO2011005477A1 (en) | 2009-06-22 | 2011-01-13 | Codexis, Inc. | Transaminase reactions |
| HUE038434T2 (hu) | 2010-06-17 | 2018-10-29 | Codexis Inc | Biokatalizátorok és módszerek (S)-3(1-aminoetil)-fenol szintéziséhez |
| EP2606139B1 (en) | 2010-08-16 | 2015-07-15 | Codexis, Inc. | Biocatalysts and methods for the synthesis of (1r,2r)-2-(3,4-dimethoxyphenethoxy)cyclohexanamine |
| WO2014060571A1 (en) * | 2012-10-18 | 2014-04-24 | Sandoz Ag | A process for preparing indoline derivatives |
| SG11201504752YA (en) | 2012-12-21 | 2015-07-30 | Codexis Inc | Engineered biocatalysts and methods for synthesizing chiral amines |
| US9617573B2 (en) | 2013-02-28 | 2017-04-11 | Codexis, Inc. | Engineered transaminase polypeptides for industrial biocatalysis |
| EP3638688A4 (en) | 2017-06-14 | 2021-07-07 | Codexis, Inc. | MODIFIED TRANSAMINASE POLYPEPTIDES INTENDED FOR INDUSTRIAL BIOCATALYSIS |
| KR20190109696A (ko) | 2018-03-18 | 2019-09-26 | 양만주 | 재사용이 가능한 페트병 홀더 |
| TWI851589B (zh) | 2018-07-31 | 2024-08-11 | 德商拜耳廠股份有限公司 | 編碼改良之轉胺酶蛋白質之核酸 |
| CA3126671A1 (en) | 2019-01-15 | 2020-07-23 | Codexis, Inc. | Engineered transaminase polypeptides |
| EP4133064A4 (en) | 2020-04-10 | 2024-07-24 | Codexis, Inc. | Engineered transaminase polypeptides |
| IL311268A (en) * | 2021-09-15 | 2024-05-01 | Richter Gedeon Nyrt | PROCESS TO PRODUCE (1r,4r)-4-SUBSTITUTED CYCLOHEXANE-1-AMINES |
| CN119060058A (zh) * | 2024-08-21 | 2024-12-03 | 武汉九州钰民医药科技有限公司 | 一种甲苯磺酸利特昔替尼的合成方法 |
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| US3871958A (en) * | 1972-03-04 | 1975-03-18 | Ajinomoto Kk | Biological method of producing serine and serinol derivatives |
| US3944617A (en) * | 1976-02-20 | 1976-03-16 | American Cyanamid Company | Synthesis of dl-2-amino-1-butanol |
| FI70597C (fi) * | 1979-04-06 | 1986-09-24 | Carlsberg Biotechnology Ltd | Foerfarande foer enzymatisk framstaellning av peptider |
| JPS55138389A (en) * | 1979-04-14 | 1980-10-29 | Denki Kagaku Kogyo Kk | Preparation of amino alcohols |
| JPS58198296A (ja) * | 1982-05-12 | 1983-11-18 | Chisso Corp | ｄ−２−アミノブタノ−ルの製造法 |
| JPS5939294A (ja) * | 1982-08-27 | 1984-03-03 | Hamari Yakuhin Kogyo Kk | 光学活性２−アミノ−１−ブタノ−ルの製造法 |
| HU193902B (en) * | 1983-09-01 | 1987-12-28 | Genetics Inst | Process for preparing l-amino acids by means of transamination |
| IT1191638B (it) * | 1985-10-31 | 1988-03-23 | Montedison Spa | Processo per la separazione enzimatica degli isomeri ottici del 2-amminobutanolo |
| US4620861A (en) * | 1985-11-04 | 1986-11-04 | Corning Glass Works | Method for making index-profiled optical device |
| IT1188641B (it) * | 1986-03-28 | 1988-01-20 | Montedison Spa | Processo per la risoluzione enzimatica di 2-ammino-1-alcanoli racemi |
| JPS63237796A (ja) * | 1987-03-25 | 1988-10-04 | Kanegafuchi Chem Ind Co Ltd | 光学活性１−メチル−３−フエニルプロピルアミンの製造法 |
| JPS63273486A (ja) * | 1987-04-30 | 1988-11-10 | Tanabe Seiyaku Co Ltd | １−（４−メトキシフェニル）−２−アミノプロパンの製法 |
| DE3818851A1 (de) * | 1988-06-03 | 1989-12-14 | Hoechst Ag | Neue transaminase, ihre herstellung und ihre verwendung |
-
1989
- 1989-06-22 US US07/369,723 patent/US4950606A/en not_active Expired - Lifetime
-
1990
- 1990-06-11 IL IL9469490A patent/IL94694A/en active IP Right Grant
- 1990-06-12 CA CA002018773A patent/CA2018773C/en not_active Expired - Lifetime
- 1990-06-13 ZA ZA904571A patent/ZA904571B/xx unknown
- 1990-06-14 IE IE215990A patent/IE72956B1/en not_active IP Right Cessation
- 1990-06-19 AU AU57541/90A patent/AU628183B2/en not_active Expired
- 1990-06-20 NZ NZ234154A patent/NZ234154A/xx unknown
- 1990-06-21 EP EP90111754A patent/EP0404146B1/en not_active Expired - Lifetime
- 1990-06-21 HU HU903945A patent/HU210967B/hu unknown
- 1990-06-21 RU SU904830607A patent/RU2087536C1/ru active
- 1990-06-21 DE DE69025988T patent/DE69025988T2/de not_active Expired - Lifetime
- 1990-06-21 DK DK90111754.9T patent/DK0404146T3/da active
- 1990-06-21 AT AT90111754T patent/ATE135744T1/de not_active IP Right Cessation
- 1990-06-21 RU RU93004462A patent/RU2116347C1/ru active
- 1990-06-21 ES ES90111754T patent/ES2084618T3/es not_active Expired - Lifetime
- 1990-06-22 JP JP2165480A patent/JP2846074B2/ja not_active Expired - Lifetime
- 1990-06-22 KR KR1019900009317A patent/KR0147827B1/ko not_active Expired - Lifetime
-
1996
- 1996-04-19 GR GR960401061T patent/GR3019682T3/el unknown
-
1998
- 1998-06-27 HK HK98107175A patent/HK1008052A1/en not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| US4950606A (en) | 1990-08-21 |
| KR0147827B1 (ko) | 1998-08-01 |
| DE69025988T2 (de) | 1996-08-14 |
| IE902159L (en) | 1990-12-22 |
| IE72956B1 (en) | 1997-05-07 |
| DK0404146T3 (da) | 1996-06-17 |
| AU628183B2 (en) | 1992-09-10 |
| DE69025988D1 (de) | 1996-04-25 |
| HK1008052A1 (en) | 1999-04-30 |
| IL94694A0 (en) | 1991-04-15 |
| ATE135744T1 (de) | 1996-04-15 |
| RU2116347C1 (ru) | 1998-07-27 |
| ES2084618T3 (es) | 1996-05-16 |
| HU210967B (en) | 1995-09-28 |
| EP0404146B1 (en) | 1996-03-20 |
| KR910000616A (ko) | 1991-01-29 |
| RU2087536C1 (ru) | 1997-08-20 |
| AU5754190A (en) | 1991-01-03 |
| HU903945D0 (en) | 1990-11-28 |
| IE902159A1 (en) | 1991-01-02 |
| EP0404146A2 (en) | 1990-12-27 |
| HUT54423A (en) | 1991-02-28 |
| NZ234154A (en) | 1991-08-27 |
| JP2846074B2 (ja) | 1999-01-13 |
| EP0404146A3 (en) | 1992-03-11 |
| CA2018773C (en) | 2000-03-21 |
| ZA904571B (en) | 1991-03-27 |
| GR3019682T3 (en) | 1996-07-31 |
| JPH03103192A (ja) | 1991-04-30 |
| CA2018773A1 (en) | 1990-12-22 |
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