Determine the necessary mass, volume, or concentration for preparing a solution.
This is a demo store. No orders will be fulfilled.
| SKU | Size | Availability |
Price | Qty |
|---|---|---|---|---|
|
P101874-1g
|
1g |
3
|
$82.90
|
|
|
P101874-5g
|
5g |
3
|
$373.90
|
|
|
P101874-10g
|
10g |
3
|
$672.90
|
|
|
P101874-25g
|
25g |
3
|
$1,512.90
|
|
|
P101874-100g
|
100g |
3
|
$5,445.90
|
|
|
P101874-500g
|
500g |
2
|
$24,505.90
|
|
| Synonyms | PLP | Vitazechs | FT-0631236 | P5P | P-5'-P | Pyromijin | 3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde 5-phosphate | CCG-266929 | EX-A980 | MC-1 | Pyridoxal 5/'-phosphate (hydrate) | SGCUT00188 | VITAMIN B6 (PYRIDOXAL 5-PHOSPHATE) | 3-hydroxy-2- |
|---|---|
| Specifications & Purity | Moligand™, ≥98% |
| Biochemical and Physiological Mechanisms | Pyridoxal 5′-phosphate (PLP) aids in carbohydrate and fat metabolism by serving as a cofactor. It is majorly responsible for catalyzing the enzymatic reactions involved in sphingolipid synthesis and neurotransmitter (dopamine and serotonin) synthesis. PLP |
| Storage Temp | Store at -20°C |
| Shipped In |
Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available. |
| Grade | Moligand™ |
| Product Description |
Pyridoxal 5′-phosphate (PLP) is synthesized in a multiple-step process. The two pathways inlcude pyridoxal phosphate biosynthetic protein (PdxA)- pyridoxine-5′-phosphate synthase (PdxJ) pathway and the pyridoxal 5′-phosphate synthase subunit PDX1/PDX2 pathway. It is the active form of pyridoxine.
Pyridoxal 5′-phosphate hydrate has also been used:
• as a reference standard to quantify vitamin B6 in feed and digesta samples using high performance liquid chromatography (HPLC)
• in D-amino acid transaminase reaction(10)
• as a cofactor for L-glutamic acid decarboxylase |
Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Class | Pyridines and derivatives |
| Subclass | Pyridine carboxaldehydes |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Pyridoxals and derivatives |
| Alternative Parents | Monoalkyl phosphates Methylpyridines Hydroxypyridines Aryl-aldehydes Vinylogous acids Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | Pyridoxal - Aryl-aldehyde - Monoalkyl phosphate - Hydroxypyridine - Methylpyridine - Organic phosphoric acid derivative - Phosphoric acid ester - Alkyl phosphate - Vinylogous acid - Heteroaromatic compound - Azacycle - Organopnictogen compound - Aldehyde - Organic oxygen compound - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Aromatic heteromonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as pyridoxals and derivatives. These are compounds containing a pyridoxal moiety, which consists of a pyridine ring substituted at positions 2,3,4, and 5 by a methyl group, a hydroxyl group, a carbaldehyde group, and a hydroxymethyl group, respectively. |
| External Descriptors | monohydroxypyridine - pyridinecarbaldehyde - methylpyridines - vitamin B6 phosphate |
|
|
|
| Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
|---|
| IUPAC Name | (4-formyl-5-hydroxy-6-methylpyridin-3-yl)methyl dihydrogen phosphate |
|---|---|
| INCHI | InChI=1S/C8H10NO6P/c1-5-8(11)7(3-10)6(2-9-5)4-15-16(12,13)14/h2-3,11H,4H2,1H3,(H2,12,13,14) |
| InChIKey | NGVDGCNFYWLIFO-UHFFFAOYSA-N |
| Smiles | CC1=NC=C(C(=C1O)C=O)COP(=O)(O)O |
| Isomeric SMILES | CC1=NC=C(C(=C1O)C=O)COP(=O)(O)O |
| Molecular Weight | 247.14 |
| Reaxy-Rn | 234749 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=234749&ln= |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Jun 02, 2025 | P101874 | |
| Certificate of Analysis | Jun 02, 2025 | P101874 | |
| Certificate of Analysis | Apr 28, 2025 | P101874 | |
| Certificate of Analysis | Mar 27, 2025 | P101874 | |
| Certificate of Analysis | Mar 27, 2025 | P101874 | |
| Certificate of Analysis | Mar 27, 2025 | P101874 | |
| Certificate of Analysis | Mar 27, 2025 | P101874 | |
| Certificate of Analysis | Mar 27, 2025 | P101874 | |
| Certificate of Analysis | Mar 27, 2025 | P101874 | |
| Certificate of Analysis | Mar 27, 2025 | P101874 | |
| Certificate of Analysis | Mar 27, 2025 | P101874 | |
| Certificate of Analysis | Mar 27, 2025 | P101874 | |
| Certificate of Analysis | Mar 27, 2025 | P101874 | |
| Certificate of Analysis | Mar 27, 2025 | P101874 | |
| Certificate of Analysis | Feb 23, 2024 | P101874 | |
| Certificate of Analysis | Feb 23, 2024 | P101874 | |
| Certificate of Analysis | Feb 23, 2024 | P101874 | |
| Certificate of Analysis | Jul 10, 2023 | P101874 | |
| Certificate of Analysis | Jul 10, 2023 | P101874 | |
| Certificate of Analysis | Mar 01, 2023 | P101874 | |
| Certificate of Analysis | Mar 01, 2023 | P101874 | |
| Certificate of Analysis | Mar 01, 2023 | P101874 | |
| Certificate of Analysis | Jan 12, 2023 | P101874 | |
| Certificate of Analysis | Jan 12, 2023 | P101874 | |
| Certificate of Analysis | Nov 23, 2022 | P101874 |
| Solubility | Soluble in oxygen-free H2O. Insoluble in most organic solvents. |
|---|---|
| Sensitivity | Moisture sensitive |
| Melt Point(°C) | 140-143°C |
| Molecular Weight | 247.140 g/mol |
| XLogP3 | -1.100 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 4 |
| Exact Mass | 247.025 Da |
| Monoisotopic Mass | 247.025 Da |
| Topological Polar Surface Area | 117.000 Ų |
| Heavy Atom Count | 16 |
| Formal Charge | 0 |
| Complexity | 292.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
Starting at $69.90
Starting at $62.90
Starting at $39.90
| 1. Zixin Teng, Xuewei Pan, Yunran Liu, Jiajia You, Hengwei Zhang, Zhenqiang Zhao, Zhina Qiao, Zhiming Rao. (2024) Engineering serine hydroxymethyltransferases for efficient synthesis of L-serine in Escherichia coli. BIORESOURCE TECHNOLOGY, 393 (130153). |
| 2. Nan Jiang, Xiaotong Du, Liangyu Zheng. (2023) Highly efficient synthesis of chiral lactams by using a ω-transaminase from Bacillus megaterium and its mutant enzymes. Molecular Catalysis, 547 (113364). |
| 3. Hongpeng Wang, Mercy Vimbai Masuku, Yachen Tao, Jiayao Yang, Yi Kuang, Changjiang Lyu, Jun Huang, Shengxiang Yang. (2023) Improved Stability and Catalytic Efficiency of ω-Transaminase in Aqueous Mixture of Deep Eutectic Solvents. MOLECULES, 28 (9): (3895). |
| 4. Juanjuan Ding, Wenyan Ba, Shengping You, Wei Qi, Rongxin Su. (2023) Development of an oil-sealed anaerobic fermentation process for high production of γ-aminobutyric acid with Lactobacillus brevis isolated by directional colorimetric screening. BIOCHEMICAL ENGINEERING JOURNAL, 194 (108893). |
| 5. Xiao-Ling Tang, Ning Li, Yan-Lai Liu, Jing-Peng Li, Kai-Xuan Zhao, Zhi-Qiang Liu, Yu-Guo Zheng. (2023) Engineering O-Succinyl-L-Homoserine Mercaptotransferase for Efficient L-Methionine Biosynthesis by Fermentation-Enzymatic Coupling Route. ADVANCED SYNTHESIS & CATALYSIS, 365 (7): (1048-1057). |
| 6. Xingchang Cha, Juanjuan Ding, Wenyan Ba, Shengping You, Wei Qi, Rongxin Su. (2023) High Production of γ-Aminobutyric Acid by Activating the xyl Operon of Lactobacillus brevis. ACS Omega, 8 (8): (8101–8109). |
| 7. Shiyi Wang, Yiwen Zhao, Shufen Mao, Jiang Zhu, Yangyang Zhan, Dongbo Cai, Xin Ma, Dong Wang, Shouwen Chen. (2023) Enhancing the activity of disulfide-bond-containing proteins via promoting disulfide bond formation in Bacillus licheniformis. INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 233 (123468). |
| 8. Lian Xu, Dan Nie, Bing-Mei Su, Xin-Qi Xu, Juan Lin. (2023) A chemoenzymatic strategy for the efficient synthesis of amphenicol antibiotic chloramphenicol mediated by an engineered L-threonine transaldolase with high activity and stereoselectivity. Catalysis Science & Technology, 13 (3): (684-693). |
| 9. Sai Fang, Haoran Yu, Lanxin Xiao, Zhe Wang, Yixuan Lei, Gang Xu, Lirong Yang, Wenlong Zheng, Jianping Wu. (2022) Counteracting the Activity-Diastereoselectivity Trade-Off of l-Threonine Aldolase by Regulating the Proton Transfer Microenvironment. ADVANCED SYNTHESIS & CATALYSIS, 364 (24): (4363-4370). |
| 10. Kai Yuan, Kai Huang, Yiqi Yang, Yixuan Lin, Yihao Liu, Fupeng Li, Yakun Liang, Haishuang Chang, Yuhui Chen, Tingting Tang, Shengbing Yang. (2022) Multi-roles of nanoscale bismuth metal-organic frameworks: Infectious photoacoustic probe and inhibitor of antibiotics tolerant bacteria via targeting endogenous H2S. Nano Today, 47 (101683). |
| 11. Guozeng Wang, Zhihao Jiang, Qing Xiao, Chang Jiang, Xian'ai Shi. (2022) Visible spectrophotometric assay for characterization of ω-transaminases. ANALYTICAL BIOCHEMISTRY, 658 (114933). |
| 12. Deng Hao-Hua, Yang Hui-Jing, Huang Kai-Yuan, Zheng Yi-Jing, Xu Ying-Ying, Peng Hua-Ping, Liu Yin-Huan, Chen Wei, Hong Guo-Lin. (2022) Antenna effect of pyridoxal phosphate on the fluorescence of mitoxantrone-silicon nanoparticles and its application in alkaline phosphatase assay. ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 414 (17): (4877-4884). |
| 13. Li-Chao Wang, Lian Xu, Bing-Mei Su, Xin-Qi Xu, Juan Lin. (2022) An Effective Chemo-Enzymatic method with An Evolved L-Threonine Aldolase for Preparing L-threo-4-Methylsulfonylphenylserine Ethyl Ester of High Optical Purity. Molecular Catalysis, 525 (112355). |
| 14. Wang Dong-En, You Shangqi, Huo Wenjing, Han Xiang, Xu Huiyun. (2022) Colorimetric detection of alkaline phosphatase activity based on pyridoxal phosphate–induced chromatic switch of polydiacetylene nano-liposomes. MICROCHIMICA ACTA, 189 (2): (1-12). |
| 15. Hang-Qin Zhu, Wen-Ye Hu, Xiao-Ling Tang, Ren-Chao Zheng, Yu-Guo Zheng. (2022) High-throughput assay of tyrosine phenol-lyase activity using a cascade of enzymatic reactions. ANALYTICAL BIOCHEMISTRY, 640 (114547). |
| 16. Jiahao Yao, Zhuang Li, Xiuling Ji, Yaju Xue, Baozeng Ren, Hai Zhao, Yuhong Huang. (2021) Novel enzyme-metal-organic framework composite for efficient cadaverine production. BIOCHEMICAL ENGINEERING JOURNAL, 176 (108222). |
| 17. Hu Jiawei, Li Wei, Liu Zhan, Zhang Guolin, Luo Yinggang. (2021) Molecular cloning and functional characterization of tyrosine decarboxylases from galanthamine-producing Lycoris radiata. ACTA PHYSIOLOGIAE PLANTARUM, 43 (6): (1-12). |
| 18. Zhu Wen-Yuan, Niu Kun, Liu Peng, Fan Yu-Hang, Liu Zhi-Qiang, Zheng Yu-Guo. (2021) Identification and Characterization of an O-Succinyl-L-Homoserine Sulfhydrylase From Thioalkalivibrio sulfidiphilus. Frontiers in Chemistry, 9 |
| 19. Lichao Wang, Lian Xu, Bingmei Su, Wei Lin, Xinqi Xu, Juan Lin. (2021) Improving the Cβ Stereoselectivity of l-Threonine Aldolase for the Synthesis of l-threo-4-Methylsulfonylphenylserine by Modulating the Substrate-Binding Pocket To Control the Orientation of the Substrate Entrance. CHEMISTRY-A EUROPEAN JOURNAL, 27 (37): (9654-9660). |
| 20. Jingbai Wen, Jie Bao. (2021) Improved fermentative γ-aminobutyric acid production by secretory expression of glutamate decarboxylase by Corynebacterium glutamicum. JOURNAL OF BIOTECHNOLOGY, 331 (19). |
| 21. Hongjie Hui, Yajun Bai, Tai-Ping Fan, Xiaohui Zheng, Yujie Cai. (2020) Biosynthesis of Putrescine from L-arginine Using Engineered Escherichia coli Whole Cells. Catalysts, 10 (9): (947). |
| 22. Li-Chao Wang, Lian Xu, Xin-Qi Xu, Bing-Mei Su, Juan Lin. (2020) An L-threonine aldolase for asymmetric synthesis of β-hydroxy-α-amino acids. CHEMICAL ENGINEERING SCIENCE, 226 (115812). |
| 23. Zhu Hang-Qin, Tang Xiao-Ling, Zheng Ren-Chao, Zheng Yu-Guo. (2020) Purification and Biochemical Characterization of a Tyrosine Phenol-lyase from Morganella morganii. APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY, 192 (1): (71-84). |
| 24. Hao-Hua Deng, Kai-Yuan Huang, Quan-Hui Fang, Ya-Ping Lv, Shao-Bin He, Hua-Ping Peng, Xing-Hua Xia, Wei Chen. (2020) Schiff base and Lewis acid-base interaction-regulated aggregation/dispersion of gold nanoparticles for colorimetric recognition of rare-earth Sc3+ ions. SENSORS AND ACTUATORS B-CHEMICAL, 311 (127925). |
| 25. Hao-Hua Deng, Kai-Yuan Huang, Shao-Bin He, Li-Ping Xue, Hua-Ping Peng, Dai-Jun Zha, Wei-Ming Sun, Xing-Hua Xia, Wei Chen. (2020) Rational Design of High-Performance Donor–Linker–Acceptor Hybrids Using a Schiff Base for Enabling Photoinduced Electron Transfer. ANALYTICAL CHEMISTRY, 92 (2): (2019–2026). |
| 26. Lian Xu, Li-Chao Wang, Xin-Qi Xu, Juan Lin. (2019) Characteristics of L-threonine transaldolase for asymmetric synthesis of β-hydroxy-α-amino acids. Catalysis Science & Technology, 9 (21): (5943-5952). |
| 27. Xiao-Ling Tang, Nan-Nan Zhang, Guo-Yan Ye, Yu-Guo Zheng. (2019) Efficient biosynthesis of (R)-3-amino-1-butanol by a novel (R)-selective transaminase from Actinobacteria sp.. JOURNAL OF BIOTECHNOLOGY, 295 (49). |
| 28. Xiao-Ling Tang, Hui Suo, Ren-Chao Zheng, Yu-Guo Zheng. (2018) An efficient colorimetric high-throughput screening method for synthetic activity of tyrosine phenol-lyase. ANALYTICAL BIOCHEMISTRY, 560 (7). |
| 29. Zhang Zhi-Jun, Cai Rui-Feng, Xu Jian-He. (2018) Characterization of a new nitrilase from Hoeflea phototrophica DFL-43 for a two-step one-pot synthesis of (S)-β-amino acids. APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 102 (14): (6047-6056). |
| 30. Qian Wang, Xiao-Mei He, Xi Chen, Gang-Tian Zhu, Ren-Qi Wang, Yu-Qi Feng. (2017) Pyridoxal 5′-phosphate mediated preparation of immobilized metal affinity material for highly selective and sensitive enrichment of phosphopeptides. JOURNAL OF CHROMATOGRAPHY A, 1499 (30). |
| 31. Wu Hua-Lei, Zhang Jian-Dong, Zhang Chao-Feng, Fan Xiao-Jun, Chang Hong-Hong, Wei Wen-Long. (2017) Characterization of Four New Distinct ω-Transaminases from Pseudomonas putida NBRC 14164 for Kinetic Resolution of Racemic Amines and Amino Alcohols. APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY, 181 (3): (972-985). |
| 32. Ailin Xiao, Jing Li, Tianjian Liu, Zhuxi Liu, Chuanfei Wei, Xiaomeng Xu, Qin Li, Jingxin Li. (2016) l-Cysteine enhances nutrient absorption via a cystathionine-β-synthase-derived H2S pathway in rodent jejunum. CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 43 (5): (562-568). |
| 33. S. Tang, D. Huang, N. An, D. Chen, D. Zhao. (2016) A novel pathway for the production of H2S by DAO in rat jejunum. NEUROGASTROENTEROLOGY AND MOTILITY, 28 (5): (687-692). |
| 34. Miao Chen, Liya Rong, Xiaoqing Chen. (2015) A simple and sensitive detection of glutamic-pyruvic transaminase activity based on fluorescence quenching of bovine serum albumin. RSC Advances, 5 (125): (103557-103562). |
| 35. Ailin Xiao,Hongjuan Wang,Xin Lu,Jianchun Zhu,Di Huang,Tonghui Xu,Jianqiang Guo,Chuanyong Liu,Jingxin Li. (2015-11-05) H2S, a novel gasotransmitter, involves in gastric accommodation.. Scientific reports, 5 (16086-16086). |
| 36. Hui-Hua Cao, Wei-Wei Kong, Xi-Ya Chen, Sadaf Ayaz, Cai-Ping Hou, Yi-Sheng Wang, Shi-Huo Liu, Jia-ping Xu. (2024) Bmo-miR-6498-5p suppresses Bombyx mori nucleopolyhedrovirus infection by down-regulating BmPLPP2 to modulate pyridoxal phosphate content in B. mori. INSECT MOLECULAR BIOLOGY, |
| 37. Binbin Chen, Jiahui Huang, Yingchun Liu, Lirong Yang, Qi Wang, Haoran Yu. (2025) Computational Study on the Catalytic Mechanism of UstD Catalyzing the Synthesis of γ-Hydroxy-α-Amino Acids. Journal of Chemical Information and Modeling, 65 (4): (2026-2037). |
| 38. Puhong Yi, Yue Xu, Hanlin Liu, Yuhua Hao, Mengdan Liu, Zhiqiang Liu, Yaping Xue, Liqun Jin, Yuguo Zheng. (2024) Efficient kinetic resolution of D,L‐phosphinothricin using an aminotransferase-mediated cascade. PROCESS BIOCHEMISTRY, |
| 39. Qian Tan, Linbo Gou, Tai-Ping Fan, Yujie Cai. (2024) Enzymatic properties of ornithine decarboxylase from Clostridium aceticum DSM1496. BIOTECHNOLOGY AND APPLIED BIOCHEMISTRY, |
| 40. Shaoyang Zhang, Guorong Zhu, Zhixiang Pan, Yi Wei, Zuoming Nie, Qing Sheng, Zhongyi Yang. (2024) Improving the production efficiency of L-threo-methylsulfonylphenylserine by removing acetaldehyde through aeration. PROCESS BIOCHEMISTRY, 144 (133). |
| 41. Bingjie Wang, Pengfei Jiang, Lihua Zhang, Zhaogai Wang, Wei Zong. (2025) Key enzymes, physicochemical properties and volatile compounds in garlic (Allium sativum L.) cloves at different storage temperatures. Food Bioscience, (105881). |
| 42. Pei-Pei Liu, Xin-Yue Yu, Qing-Qing Pan, Jia-Jun Ren, Yu-Xuan Han, Kai Zhang, Yan Wang, Yin Huang, Tao Ban. (2025) Multi-Omics and Network-Based Drug Repurposing for Septic Cardiomyopathy. Pharmaceuticals, 18 (1): (43). |
| 43. Ying-Ying Xu, Bin Zhang, Jie Bao. (2025) Production of γ-aminobutyric acid using corncob residue as carbohydrate feedstock by engineered Corynebacterium glutamicum. BIOCHEMICAL ENGINEERING JOURNAL, 215 (109629). |
| 44. Lili Zhang, Yu Hong, Jiapeng Lu, Yi Wang, Wei Luo. (2024) Semi-rational engineering of ω-transaminase for enhanced enzymatic activity to 2-ketobutyrate. ENZYME AND MICROBIAL TECHNOLOGY, 180 (110505). |
| 45. Lijun Jin, Lixia Jin, Haiyang Liu, Zhe Wang, yuguang Lv. (2024) Study on the Properties of rhodamine B fluorescent probe Y2ST. JOURNAL OF THE INDIAN CHEMICAL SOCIETY, 101 (101420). |