JP2010539952A5 - - Google Patents
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- JP2010539952A5 JP2010539952A5 JP2010527257A JP2010527257A JP2010539952A5 JP 2010539952 A5 JP2010539952 A5 JP 2010539952A5 JP 2010527257 A JP2010527257 A JP 2010527257A JP 2010527257 A JP2010527257 A JP 2010527257A JP 2010539952 A5 JP2010539952 A5 JP 2010539952A5
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- 108090000765 processed proteins & peptides Proteins 0.000 claims 17
- 229920001184 polypeptide Polymers 0.000 claims 16
- 102000004196 processed proteins & peptides Human genes 0.000 claims 16
- 239000000758 substrate Substances 0.000 claims 16
- 150000001413 amino acids Chemical group 0.000 claims 12
- 101001110310 Lentilactobacillus kefiri NADP-dependent (R)-specific alcohol dehydrogenase Proteins 0.000 claims 9
- 238000000034 method Methods 0.000 claims 8
- KZSNJWFQEVHDMF-BYPYZUCNSA-N L-valine Chemical compound CC(C)[C@H](N)C(O)=O KZSNJWFQEVHDMF-BYPYZUCNSA-N 0.000 claims 5
- KZSNJWFQEVHDMF-UHFFFAOYSA-N Valine Natural products CC(C)C(N)C(O)=O KZSNJWFQEVHDMF-UHFFFAOYSA-N 0.000 claims 5
- YZBQHRLRFGPBSL-RXMQYKEDSA-N carbapenem Chemical compound C1C=CN2C(=O)C[C@H]21 YZBQHRLRFGPBSL-RXMQYKEDSA-N 0.000 claims 5
- 239000004474 valine Substances 0.000 claims 5
- ROHFNLRQFUQHCH-YFKPBYRVSA-N L-leucine Chemical compound CC(C)C[C@H](N)C(O)=O ROHFNLRQFUQHCH-YFKPBYRVSA-N 0.000 claims 4
- ROHFNLRQFUQHCH-UHFFFAOYSA-N Leucine Natural products CC(C)CC(N)C(O)=O ROHFNLRQFUQHCH-UHFFFAOYSA-N 0.000 claims 4
- AYFVYJQAPQTCCC-UHFFFAOYSA-N Threonine Natural products CC(O)C(N)C(O)=O AYFVYJQAPQTCCC-UHFFFAOYSA-N 0.000 claims 4
- 239000004473 Threonine Substances 0.000 claims 4
- 150000001875 compounds Chemical class 0.000 claims 4
- LVJARDSTTGGMSM-UHFFFAOYSA-N methyl 2-(benzamidomethyl)-3-oxobutanoate Chemical compound COC(=O)C(C(C)=O)CNC(=O)C1=CC=CC=C1 LVJARDSTTGGMSM-UHFFFAOYSA-N 0.000 claims 4
- 102000040430 polynucleotide Human genes 0.000 claims 4
- 108091033319 polynucleotide Proteins 0.000 claims 4
- 239000002157 polynucleotide Substances 0.000 claims 4
- COLNVLDHVKWLRT-QMMMGPOBSA-N L-phenylalanine Chemical compound OC(=O)[C@@H](N)CC1=CC=CC=C1 COLNVLDHVKWLRT-QMMMGPOBSA-N 0.000 claims 3
- 235000004279 alanine Nutrition 0.000 claims 3
- HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 claims 3
- 235000014304 histidine Nutrition 0.000 claims 3
- COLNVLDHVKWLRT-UHFFFAOYSA-N phenylalanine Natural products OC(=O)C(N)CC1=CC=CC=C1 COLNVLDHVKWLRT-UHFFFAOYSA-N 0.000 claims 3
- 125000006239 protecting group Chemical group 0.000 claims 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims 2
- 239000004475 Arginine Substances 0.000 claims 2
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 claims 2
- HNDVDQJCIGZPNO-YFKPBYRVSA-N L-histidine Chemical compound OC(=O)[C@@H](N)CC1=CN=CN1 HNDVDQJCIGZPNO-YFKPBYRVSA-N 0.000 claims 2
- 125000001931 aliphatic group Chemical group 0.000 claims 2
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 claims 2
- 239000013604 expression vector Substances 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 239000000203 mixture Substances 0.000 claims 2
- MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical compound OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 claims 1
- FWMNVWWHGCHHJJ-SKKKGAJSSA-N 4-amino-1-[(2r)-6-amino-2-[[(2r)-2-[[(2r)-2-[[(2r)-2-amino-3-phenylpropanoyl]amino]-3-phenylpropanoyl]amino]-4-methylpentanoyl]amino]hexanoyl]piperidine-4-carboxylic acid Chemical compound C([C@H](C(=O)N[C@H](CC(C)C)C(=O)N[C@H](CCCCN)C(=O)N1CCC(N)(CC1)C(O)=O)NC(=O)[C@H](N)CC=1C=CC=CC=1)C1=CC=CC=C1 FWMNVWWHGCHHJJ-SKKKGAJSSA-N 0.000 claims 1
- NQUVCRCCRXRJCK-UHFFFAOYSA-N 4-methylbenzoyl chloride Chemical compound CC1=CC=C(C(Cl)=O)C=C1 NQUVCRCCRXRJCK-UHFFFAOYSA-N 0.000 claims 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims 1
- DCXYFEDJOCDNAF-UHFFFAOYSA-N Asparagine Natural products OC(=O)C(N)CC(N)=O DCXYFEDJOCDNAF-UHFFFAOYSA-N 0.000 claims 1
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 claims 1
- ONIBWKKTOPOVIA-BYPYZUCNSA-N L-Proline Chemical compound OC(=O)[C@@H]1CCCN1 ONIBWKKTOPOVIA-BYPYZUCNSA-N 0.000 claims 1
- DCXYFEDJOCDNAF-REOHCLBHSA-N L-asparagine Chemical compound OC(=O)[C@@H](N)CC(N)=O DCXYFEDJOCDNAF-REOHCLBHSA-N 0.000 claims 1
- AGPKZVBTJJNPAG-WHFBIAKZSA-N L-isoleucine Chemical compound CC[C@H](C)[C@H](N)C(O)=O AGPKZVBTJJNPAG-WHFBIAKZSA-N 0.000 claims 1
- FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 claims 1
- QIVBCDIJIAJPQS-VIFPVBQESA-N L-tryptophane Chemical compound C1=CC=C2C(C[C@H](N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-VIFPVBQESA-N 0.000 claims 1
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 claims 1
- 239000004472 Lysine Substances 0.000 claims 1
- ONIBWKKTOPOVIA-UHFFFAOYSA-N Proline Natural products OC(=O)C1CCCN1 ONIBWKKTOPOVIA-UHFFFAOYSA-N 0.000 claims 1
- MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Natural products OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 claims 1
- QIVBCDIJIAJPQS-UHFFFAOYSA-N Tryptophan Natural products C1=CC=C2C(CC(N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-UHFFFAOYSA-N 0.000 claims 1
- 125000003295 alanine group Chemical group N[C@@H](C)C(=O)* 0.000 claims 1
- 229910052783 alkali metal Inorganic materials 0.000 claims 1
- 150000001340 alkali metals Chemical class 0.000 claims 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims 1
- 150000001342 alkaline earth metals Chemical class 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 125000000539 amino acid group Chemical group 0.000 claims 1
- 229910021529 ammonia Inorganic materials 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 229960001230 asparagine Drugs 0.000 claims 1
- 235000009582 asparagine Nutrition 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 235000018417 cysteine Nutrition 0.000 claims 1
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 claims 1
- 125000000151 cysteine group Chemical group N[C@@H](CS)C(=O)* 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 125000004404 heteroalkyl group Chemical group 0.000 claims 1
- 125000004446 heteroarylalkyl group Chemical group 0.000 claims 1
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims 1
- AGPKZVBTJJNPAG-UHFFFAOYSA-N isoleucine Natural products CCC(C)C(N)C(O)=O AGPKZVBTJJNPAG-UHFFFAOYSA-N 0.000 claims 1
- 229960000310 isoleucine Drugs 0.000 claims 1
- 229930182817 methionine Natural products 0.000 claims 1
- ATBIFOORFZTUKF-UHFFFAOYSA-N methyl 2-(benzamidomethyl)-3-hydroxybutanoate Chemical compound COC(=O)C(C(C)O)CNC(=O)C1=CC=CC=C1 ATBIFOORFZTUKF-UHFFFAOYSA-N 0.000 claims 1
- 229940002612 prodrug Drugs 0.000 claims 1
- 239000000651 prodrug Substances 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 239000012453 solvate Substances 0.000 claims 1
- 230000002194 synthesizing effect Effects 0.000 claims 1
- 125000000341 threoninyl group Chemical group [H]OC([H])(C([H])([H])[H])C([H])(N([H])[H])C(*)=O 0.000 claims 1
- 0 C[C@@](*)[C@]([C@]1N2C(C(O*)=O)=C(*)[C@@]1*)C2=O Chemical compound C[C@@](*)[C@]([C@]1N2C(C(O*)=O)=C(*)[C@@]1*)C2=O 0.000 description 8
- ZSKVGTPCRGIANV-ZXFLCMHBSA-N C[C@H]([C@H]([C@@H](C1)N2C(C(O)=O)=C1SCCNC=N)C2=O)O Chemical compound C[C@H]([C@H]([C@@H](C1)N2C(C(O)=O)=C1SCCNC=N)C2=O)O ZSKVGTPCRGIANV-ZXFLCMHBSA-N 0.000 description 3
- JUZNIMUFDBIJCM-GATUNPTCSA-N C[C@H]([C@H](C([C@H]1C)N2C(C(O)=O)=C1SC(C1)CN[C@@H]1C(Nc1cc(C(O)=O)ccc1)=O)C2=O)O Chemical compound C[C@H]([C@H](C([C@H]1C)N2C(C(O)=O)=C1SC(C1)CN[C@@H]1C(Nc1cc(C(O)=O)ccc1)=O)C2=O)O JUZNIMUFDBIJCM-GATUNPTCSA-N 0.000 description 2
- XFPGUZAJZDKQEC-VFCYFNJJSA-N C[C@H]([C@H](C([C@H]1C)N2C(C(O)=O)=C1SC(C1)CN[C@@H]1NCS(C)(=O)=O)C2=O)O Chemical compound C[C@H]([C@H](C([C@H]1C)N2C(C(O)=O)=C1SC(C1)CN[C@@H]1NCS(C)(=O)=O)C2=O)O XFPGUZAJZDKQEC-VFCYFNJJSA-N 0.000 description 2
- DMJNNHOOLUXYBV-PQTSNVLCSA-N C[C@H]([C@H]([C@@H]([C@H]1C)N2C(C(O)=O)=C1S[C@@H](C1)CN[C@@H]1C(N(C)C)=O)C2=O)O Chemical compound C[C@H]([C@H]([C@@H]([C@H]1C)N2C(C(O)=O)=C1S[C@@H](C1)CN[C@@H]1C(N(C)C)=O)C2=O)O DMJNNHOOLUXYBV-PQTSNVLCSA-N 0.000 description 2
- HOYUMWJOTCLELZ-OLNVJHKFSA-N C[C@H](C(C)([C@@H](C12CC1)N1C(C(O)=O)=C2SC(C2)CN[C@@H]2NCS(C)(=O)=O)C1=O)O Chemical compound C[C@H](C(C)([C@@H](C12CC1)N1C(C(O)=O)=C2SC(C2)CN[C@@H]2NCS(C)(=O)=O)C1=O)O HOYUMWJOTCLELZ-OLNVJHKFSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US97655507P | 2007-10-01 | 2007-10-01 | |
| US60/976,555 | 2007-10-01 | ||
| PCT/US2008/078513 WO2009046153A1 (en) | 2007-10-01 | 2008-10-01 | Ketoreductase polypeptides for the production of azetidinone |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2010539952A JP2010539952A (ja) | 2010-12-24 |
| JP2010539952A5 true JP2010539952A5 (https=) | 2011-11-10 |
| JP5646328B2 JP5646328B2 (ja) | 2014-12-24 |
Family
ID=40262027
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010527257A Active JP5646328B2 (ja) | 2007-10-01 | 2008-10-01 | アゼチジノンの生産のためのケトレダクターゼポリペプチド |
Country Status (10)
| Country | Link |
|---|---|
| US (14) | US7883879B2 (https=) |
| EP (1) | EP2205727B1 (https=) |
| JP (1) | JP5646328B2 (https=) |
| KR (1) | KR20100065387A (https=) |
| CN (1) | CN101883846A (https=) |
| ES (1) | ES2547528T3 (https=) |
| HU (1) | HUE027683T2 (https=) |
| IL (2) | IL204379A (https=) |
| SI (1) | SI2205727T1 (https=) |
| WO (1) | WO2009046153A1 (https=) |
Families Citing this family (50)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2860192B1 (en) | 2005-10-12 | 2017-09-27 | MorphoSys AG | Generation and profiling of fully human HuCAL GOLD-derived therapeutic antibodies specific for human CD38 |
| CN101627116B (zh) | 2007-02-08 | 2013-07-10 | 科德克希思公司 | 酮还原酶及其用途 |
| CN101784669B (zh) * | 2007-08-24 | 2015-02-18 | 科德克希思公司 | 用于(r)-3-羟基四氢噻吩的立体选择性制备的改善的酮还原酶多肽 |
| KR101586503B1 (ko) * | 2007-09-13 | 2016-01-18 | 코덱시스, 인코포레이티드 | 아세토페논의 환원을 위한 케토리덕타제 폴리펩티드 |
| WO2009042984A1 (en) * | 2007-09-28 | 2009-04-02 | Codexis, Inc. | Ketoreductase polypeptides and uses thereof |
| WO2009046153A1 (en) | 2007-10-01 | 2009-04-09 | Codexis, Inc. | Ketoreductase polypeptides for the production of azetidinone |
| HUE026181T2 (en) | 2008-08-27 | 2016-05-30 | Codexis Inc | Ketoreductase polypeptide for the preparation of 3-aryl-3-hydroxypropanamine from 3-aryl-3-ketopropanamine |
| WO2010027710A2 (en) | 2008-08-27 | 2010-03-11 | Codexis, Inc. | Ketoreductase polypeptides and uses thereof |
| US8288141B2 (en) * | 2008-08-27 | 2012-10-16 | Codexis, Inc. | Ketoreductase polypeptides for the production of 3-aryl-3-hydroxypropanamine from a 3-aryl-3-ketopropanamine |
| CN102186972B (zh) | 2008-08-29 | 2014-08-20 | 科德克希思公司 | 用于立体选择性生产(4s)-3-[(5s)-5-(4-氟苯基)-5-羟基戊酰基]-4-苯基-1，3-噁唑烷-2-酮的酮还原酶多肽 |
| SG178456A1 (en) | 2009-08-19 | 2012-04-27 | Codexis Inc | Ketoreductase polypeptides for the preparation of phenylephrine |
| CN102884178B (zh) | 2009-12-08 | 2014-12-03 | 科德克希思公司 | 拉唑化合物的合成 |
| WO2011100265A2 (en) | 2010-02-10 | 2011-08-18 | Codexis, Inc. | Processes using amino acid dehydrogenases and ketoreductase-based cofactor regenerating system |
| WO2011140219A1 (en) | 2010-05-04 | 2011-11-10 | Codexis, Inc. | Biocatalysts for ezetimibe synthesis |
| HUE037616T2 (hu) | 2010-12-08 | 2018-09-28 | Codexis Inc | Biokatalizátorok és eljárások armodafinil szintéziséhez |
| US9102963B2 (en) | 2011-04-13 | 2015-08-11 | Codexis, Inc. | Biocatalytic process for preparing eslicarbazepine and analogs thereof |
| EP2780448B1 (en) | 2011-11-18 | 2019-09-11 | Codexis, Inc. | Biocatalysts for the preparation of hydroxy substituted carbamates |
| EP2847214B1 (en) | 2012-05-11 | 2017-12-27 | Codexis, Inc. | Engineered imine reductases and methods for the reductive amination of ketone and amine compounds |
| CN103045504B (zh) * | 2012-12-05 | 2014-06-04 | 浙江工业大学 | 微生物催化制备(2s, 3r)-2-苯甲酰氨甲基-3-羟基丁酸酯及菌株 |
| US10150959B2 (en) | 2013-03-15 | 2018-12-11 | Merck Sharp & Dohme Corp. | Immobilized ketoreductases and process for making and using immobilized ketoreductase |
| CN103373934A (zh) * | 2013-06-14 | 2013-10-30 | 苏州汇和药业有限公司 | 碳青霉烯和青霉烯类药物的手性中间体的催化合成方法 |
| ES2734209T3 (es) | 2013-08-06 | 2019-12-04 | Imago Biosciences Inc | Inhibidores de KDM1A para el tratamiento de enfermedades |
| CN104342412B (zh) * | 2013-08-09 | 2018-12-21 | 南京朗恩生物科技有限公司 | 用于生产(s)-4-氯-3-羟基丁酸乙酯的酮还原酶突变体 |
| US10696964B2 (en) | 2013-09-27 | 2020-06-30 | Codexis, Inc. | Automated screening of enzyme variants |
| JP6643987B2 (ja) | 2013-11-13 | 2020-02-12 | コデクシス， インコーポレイテッド | ケトン化合物およびアミン化合物の還元的アミノ化のための操作されたイミンレダクターゼおよび方法 |
| EP3134519B1 (en) | 2014-04-22 | 2018-06-06 | c-LEcta GmbH | Ketoreductases |
| DK3224354T3 (da) | 2014-11-25 | 2021-03-01 | Codexis Inc | Manipulerede iminreductaser og fremgangsmåder til den reduktive aminering af keton- og aminforbindelser |
| CN104531627B (zh) * | 2014-12-23 | 2017-07-21 | 浙江大学 | 羰基还原酶、工程菌及其应用 |
| WO2016130412A1 (en) * | 2015-02-10 | 2016-08-18 | Codexis, Inc. | Ketoreductase polypeptides for the synthesis of chiral compounds |
| PL3256218T3 (pl) | 2015-02-12 | 2025-03-31 | Imago Biosciences Inc. | Inhibitor kdm1a i jego zastosowanie w terapii |
| CN104846025B (zh) * | 2015-03-31 | 2018-06-01 | 浙江大学 | 一种制备(2s，3r)-2-苯甲酰氨甲基-3-羟基丁酸甲酯的方法 |
| WO2017001907A1 (en) | 2015-06-29 | 2017-01-05 | Teva Pharmaceuticals International Gmbh | Biocatalytic processes for the preparation of vilanterol |
| CN106811491B (zh) * | 2015-12-01 | 2022-07-19 | 焦作健康元生物制品有限公司 | 光学活性的β-羟基酯类化合物的制备方法及其中间体 |
| CN107354179B (zh) * | 2016-05-09 | 2021-02-19 | 上海医药工业研究院 | 一种制备含有羟基的手性化合物的方法 |
| US20220025424A1 (en) * | 2016-08-16 | 2022-01-27 | Imago Biosciences, Inc. | Compositions and methods for producing stereoisomerically pure aminocyclopropanes |
| WO2018035259A1 (en) | 2016-08-16 | 2018-02-22 | Imago Biosciences, Inc. | Methods and processes for the preparation of kdm1a inhibitors |
| CA3061133A1 (en) | 2017-04-27 | 2018-11-01 | Codexis, Inc. | Ketoreductase polypeptides and polynucleotides |
| EP3652328A1 (en) | 2017-07-14 | 2020-05-20 | c-LEcta GmbH | Ketoreductases |
| BR112021001066A2 (pt) | 2018-05-11 | 2021-04-20 | Imago Biosciences, Inc. | composto, método de tratamento de uma doença mediada por kdm1a, método de tratamento de uma doença mediada por globina, composição farmacêutica; método de inibição de kdm1a, método para obter um efeito em um paciente, e método para inibir pelo menos uma função de kdm1a |
| CN109295019B (zh) * | 2018-10-29 | 2021-01-12 | 浙江大学 | 一种醇脱氢酶突变体及其应用 |
| EP3938394A1 (en) | 2019-03-15 | 2022-01-19 | MorphoSys AG | Anti-cd38 antibodies and pharmaceutical compositions thereof for the treatment of autoantibody-mediated autoimmune disease |
| CN111363730A (zh) * | 2020-03-23 | 2020-07-03 | 焦作健康元生物制品有限公司 | 一种用于生产4-aa的酮还原酶制备方法 |
| CN111378704A (zh) * | 2020-03-23 | 2020-07-07 | 焦作健康元生物制品有限公司 | 一种酮还原酶生产4-aa中间体的方法 |
| WO2022036662A1 (zh) * | 2020-08-21 | 2022-02-24 | 浙江华睿生物技术有限公司 | 酶法合成3-羟基丁酸酯的方法 |
| CN114634957B (zh) * | 2020-12-15 | 2024-08-16 | 苏州引航生物科技有限公司 | 一种生物催化合成4aa中间体的方法 |
| CN112941043B (zh) * | 2021-05-17 | 2021-09-10 | 中国科学院天津工业生物技术研究所 | 羰基还原酶突变体及在制备手性β’-羟基-β-氨基酸酯中的应用 |
| CN115478057B (zh) * | 2021-05-31 | 2025-04-04 | 尚科生物医药（上海）有限公司 | 一种用于制备(s)-3,4-二羟基-2’-氯苯乙醇的酮还原酶突变体 |
| IL322082A (en) * | 2023-01-12 | 2025-09-01 | Novartis Ag | Engineered ketoreductase polypeptides |
| CN119842647B (zh) * | 2024-12-29 | 2025-07-22 | 苏州诺恩斯生物科技有限公司 | 一种用于合成度洛西汀中间体的脱氢酶突变体及其应用 |
| CN119570755B (zh) * | 2025-01-07 | 2026-03-17 | 上海泓博尚奕药物技术有限公司 | 一种酮还原酶突变体及其在合成(r)-1-(2,6-二氯苯基)乙醇中的应用 |
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