D-Phenylalanine - Moligand™, ≥98% , Agonist of HCA 3 receptor, CAS No.673-06-3, Agonist of HCA 3 receptor

CAS: 673-06-3 Cat. No.: P109094 Peso molecular: 165.19 Beilstein Registry Number: 2804068 Número EC: 211-603-5
Disponible para pedir
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥98%
Synonyms
D-.beta.-Phenyl-.alpha.-alanine | EN300-60166 | NSC 25005 | Phenylalanine,d- | Spectrum2_001558 | 4C53B247-2FE4-4464-92C0-9F3782A08966 | BDBM36161 | Dichloromethylmethane | DB02556 | KBio2_007341 | C02265 | IDI1_000453 | KBio1_000453 | D-PHENYLALANINE [WH
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5g
P109094-5g
≥10
11,90US$
25g
P109094-25g
9
18,90US$
100g
P109094-100g
10
54,90US$
500g
P109094-500g
2
151,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

Moligand™, ≥98% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 56 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

It is an essential amino acid with anti-depressant and analgesic activities. pharmaceutical intermediates, mainly used to treat, prevent osteoporosis, cardiovascular, diabetes, arterioscleros.

Specifications

Sinónimos
D-.beta.-Phenyl-.alpha.-alanine | EN300-60166 | NSC 25005 | Phenylalanine, d- | Spectrum2_001558 | 4C53B247-2FE4-4464-92C0-9F3782A08966 | BDBM36161 | Dichloromethylmethane | DB02556 | KBio2_007341 | C02265 | IDI1_000453 | KBio1_000453 | D-PHENYLALANINE [WH
Especificaciones y pureza
Moligand™, ≥98%
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Grado
Moligand™
Tipo de acción
AGONIST
Mecanismo de acción
Agonist of HCA 3 receptor
Pureza
≥98%
Nombres e identificadores
Pubchem Sid488184663
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488184663
Sonrisas canónicasC1=CC=C(C=C1)CC(C(=O)O)N
IUPAC Name(2R)-2-amino-3-phenylpropanoic acid
InChIKeyCOLNVLDHVKWLRT-MRVPVSSYSA-N
INCHI1S/C9H11NO2/c10-8(9(11)12)6-7-4-2-1-3-5-7/h1-5,8H,6,10H2,(H,11,12)/t8-/m1/s1
Isómeros SMILES C1=CC=C(C=C1)C[C@H](C(=O)O)N
WGK Alemania 3
RTECS AY7533000
Peso molecular 165.19
Beilstein 2804068
Reaxy-Rn 1910407
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1910407&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClaseCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives
Direct ParentPhenylalanine and derivatives
Alternative Parents Phenylpropanoic acids  D-alpha-amino acids  Amphetamines and derivatives  Aralkylamines  Amino acids  Monocarboxylic acids and derivatives  Carboxylic acids  Organopnictogen compounds  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Phenylalanine or derivatives - 3-phenylpropanoic-acid - Alpha-amino acid - Amphetamine or derivatives - D-alpha-amino acid - Aralkylamine - Monocyclic benzene moiety - Benzenoid - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Organic nitrogen compound - Primary amine - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Primary aliphatic amine - Organic oxide - Carbonyl group - Organopnictogen compound - Organic oxygen compound - Amine - Aromatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as phenylalanine and derivatives. These are compounds containing phenylalanine or a derivative thereof resulting from reaction of phenylalanine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
External Descriptors Other amino acids
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
HCAR3 Tchem Hydroxycarboxylic acid receptor 3 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA2 Tclin Carbonic anhydrase II (17698 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA3 Tclin Carbonic anhydrase III (753 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA6 Tclin Carbonic anhydrase VI (993 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA1 Tclin Carbonic anhydrase I (13240 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA5B Tclin Carbonic anhydrase VB (957 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA5A Tclin Carbonic anhydrase VA (1168 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA14 Tclin Carbonic anhydrase XIV (1305 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA12 Tclin Carbonic anhydrase XII (6231 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA9 Tclin Carbonic anhydrase IX (8255 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC7A5 Tchem L-type amino acid transporter 1 (388 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RGS4 Tchem Regulator of G-protein signaling 4 (13867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC16A10 SLC16A10 protein (28 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Ca7 Carbonic anhydrase VII (3 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ca13 Carbonic anhydrase XIII (322 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA4 Carbonic anhydrase IV (1713 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Carbonic anhydrase (69 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ca15 Carbonic anhydrase 15 (173 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CAN2 Carbonic anhydrase 2 (140 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slc16a10 Monocarboxylate transporter 10 (73 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Carbonic anhydrase-like protein, putative (25 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

23 results found

Lot NumberCertificate TypeFechaArticulo
G2227444Certificate of AnalysisMay 19, 2026 P109094
G2227443Certificate of AnalysisMay 19, 2026 P109094
A2621150Certificate of AnalysisJan 27, 2026 P109094
B2225670Certificate of AnalysisDec 12, 2025 P109094
D2508756Certificate of AnalysisJul 09, 2024 P109094
D2508728Certificate of AnalysisJul 09, 2024 P109094
D2508727Certificate of AnalysisJul 09, 2024 P109094
B2320551Certificate of AnalysisJan 09, 2023 P109094
B2320554Certificate of AnalysisJan 09, 2023 P109094
B2320553Certificate of AnalysisJan 09, 2023 P109094
B2320552Certificate of AnalysisJan 09, 2023 P109094
B2320474Certificate of AnalysisJan 09, 2023 P109094
B2320468Certificate of AnalysisJan 09, 2023 P109094
B2320461Certificate of AnalysisJan 09, 2023 P109094
G2227445Certificate of AnalysisJun 09, 2022 P109094
G2227441Certificate of AnalysisJun 09, 2022 P109094
G2227442Certificate of AnalysisJun 09, 2022 P109094
C1810011Certificate of AnalysisJan 25, 2022 P109094
I2519040Certificate of AnalysisDec 08, 2021 P109094
B2225730Certificate of AnalysisDec 08, 2021 P109094
B2225666Certificate of AnalysisDec 08, 2021 P109094
B2225665Certificate of AnalysisDec 08, 2021 P109094
B2225664Certificate of AnalysisDec 08, 2021 P109094

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Propiedades químicas y físicas
SolubilidadSoluble in water (30 mg/ml), methanol (slightly), 1 M HCl (50 mg/ml), ethanol (<1 mg/ml at 25 °C), and DMSO (<1 mg/ml at 25 °C).
Rotación específica [α]34 ° (C=2, H2O)
Punto de fusión (°C)273-276°C
Peso molecular165.190 g/mol
XLogP3-1.500
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count3
Exact Mass165.079 Da
Monoisotopic Mass165.079 Da
Topological Polar Surface Area63.300 Ų
Heavy Atom Count12
Formal Charge0
Complexity153.000
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Jingzhi Yang, Yami Ran, Shaopeng Liu, Chenhao Ren, Yuntian Lou, Pengfei Ju, Guoliang Li, Xiaogang Li, Dawei Zhang.  (2023)  Synergistic D-Amino Acids Based Antimicrobial Cocktails Formulated via High-Throughput Screening and Machine Learning.  Advanced Science,  11  (9): (2307173).  [PMID:38126652] [10.1002/advs.202307173]
2. Zhiyang Xu, Yinzhou Yan, Xingyuan Wang, Xiaolei Wang, Zhixiang Zhou, Xi Yang, Tianrui Zhai.  (2023)  Determination of Enantiomeric Excess by Optofluidic Microlaser near Exceptional Point.  Advanced Science,      [PMID:38072636] [10.1002/advs.202308362]
3. Jianrong Wang, Sha Han, Hongfang Zhao, Hongxia Li, Xiaohui Niu, Yi Wang, Kunjie Wang.  (2023)  Electrochemical enantioselective recognition by defined chiral linkers in polysaccharides modified with carbon quantum dots.  ELECTROANALYSIS,      [PMID:] [10.1002/elan.202300301]
4. Li Yuchen, Xu Guangfu, Chen Jiaquan, Yu Tao, Miao Pandeng, Du Yingxiang.  (2023)  One-step synthesis of chiral molecularly imprinted polymer TiO2 nanoparticles for enantioseparation of phenylalanine in coated capillary electrochromatography.  MICROCHIMICA ACTA,  190  (7): (1-11).  [PMID:37391671] [10.1007/s00604-023-05854-4]
5. Niu Xiaohui, Zhao Rui, Yan Simeng, Li Hongxia, Yang Jing, Cao Kunjie, Liu Xiaoyu, Wang Kunjie.  (2023)  Chiral MOFs encapsulated by polymers with poly-metallic coordination as chiral biosensors.  MICROCHIMICA ACTA,  190  (6): (1-12).  [PMID:37208529] [10.1007/s00604-023-05807-x]
6. Hou Huipeng, Tang Shanshan, Wang Wei, Liu Miao, Liang Axin, Xie Bingteng, Yi Yue, Luo Aiqin.  (2023)  Electrochemical Chiral Recognizing Tryptophan Enantiomers Based on Chiral Metal-Organic Framework D-MOF.  CHEMICAL RESEARCH IN CHINESE UNIVERSITIES,  39  (6): (976-984).  [PMID:] [10.1007/s40242-023-3004-6]
7. Qian Ye, Jin Li, Yinyin Huang, Hanbin Wu, Yilin Li, Bin Yan.  (2022)  Preparation of a cyclodextrin metal-organic framework (CD-MOF) membrane for chiral separation.  Journal of Environmental Chemical Engineering,      [PMID:] [10.1016/j.jece.2022.109250]
8. Jinglei Liu, Tianfei Chu, Mengmeng Cheng, Yan Su, Guizheng Zou, Shifeng Hou.  (2022)  Bovine serum albumin functional graphene oxide membrane for effective chiral separation.  JOURNAL OF MEMBRANE SCIENCE,      [PMID:] [10.1016/j.memsci.2022.121198]
9. Yiyi Liu, Fangling Wu, Jiabin Wang, Ling Pu, Chuan-Fan Ding.  (2022)  Simultaneous chirality separation of amino acids and their derivative by natamycin based on mobility measurements.  ANALYTICA CHIMICA ACTA,      [PMID:36089312] [10.1016/j.aca.2022.340298]
10. Hai-Bin Qin, Jun-Ping Zhou, Bo Zhang, Zhi-Qiang Liu, Yu-Guo Zheng.  (2022)  Combing with redox regulation via quorum-sensing system and fermentation strategies for improving D-pantothenic acid production.  PROCESS BIOCHEMISTRY,      [PMID:] [10.1016/j.procbio.2022.08.012]
11. Wancheng Qin, Peng Zhou, Xinyu Xu, Chuanwei Huang, Gopalan Srinivasan, Yajun Qi, Tianjin Zhang.  (2022)  High-Performance Piezoelectric Nanogenerator Based on Low-Entropy Structured Nanofibers for a Multi-Mode Energy Harvesting and Self-Powered Ultraviolet Photodetector.  ACS Applied Electronic Materials,      [PMID:] [10.1021/acsaelm.2c00411]
12. Yi Wu, Keren Lu, Fubin Pei, Yanghao Yan, Shasha Feng, Qingli Hao, Mingzhu Xia, Wu Lei.  (2022)  Construction of g-C3N4/Au/NH2-UiO-66 Z-scheme heterojunction for label-free photoelectrochemical recognition of D-penicillamine.  TALANTA,      [PMID:35687949] [10.1016/j.talanta.2022.123617]
13. Hongxia Li, Letong Wang, Simeng Yan, Jinliang Chen, Mengmeng Zhang, Rui Zhao, Xiaohui Niu, Kunjie Wang.  (2022)  Fusiform-like metal-organic framework for enantioselective discrimination of tryptophan enantiomers.  ELECTROCHIMICA ACTA,      [PMID:] [10.1016/j.electacta.2022.140409]
14. Shutong Yang, Liancheng Gu, Fangling Wu, Xinhua Dai, Fuxing Xu, Qiaoyu Li, Xiang Fang, Shaoning Yu, Chuan-Fan Ding.  (2022)  The chirality determination of amino acids by forming complexes with cyclodextrins and metal ions using ion mobility spectrometry, and a DFT calculation.  TALANTA,      [PMID:35272154] [10.1016/j.talanta.2022.123363]
15. Xiaohui Niu, Simeng Yan, Letong Wang, Jinliang Chen, Rui Zhao, Hongxia Li, Jian Liu, Kunjie Wang.  (2022)  Induction of chiral polymers from metal-organic framework for stereoselective recognition.  ANALYTICA CHIMICA ACTA,      [PMID:35151404] [10.1016/j.aca.2022.339546]
16. Xiaohui Niu, Simeng Yan, Jinliang Chen, Hongxia Li, Kunjie Wang.  (2022)  Enantioselective recognition of L/D-amino acids in the chiral nanochannels of a metal-organic framework.  ELECTROCHIMICA ACTA,      [PMID:] [10.1016/j.electacta.2021.139809]
17. Xin-hui Zhou, Qing Liu, Hai-shui Wang.  (2021)  Chiral resolution of DL-glutamic acid by a chiral additive.  JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY,  97  (5): (1240-1246).  [PMID:] [10.1002/jctb.7018]
18. Xiaodan Wang, Fangping Yang, Huawei Yang, Xu Zhang, Haoyu Tang, Shifang Luan.  (2021)  Preparation of antibacterial polypeptides with different topologies and their antibacterial properties.  Biomaterials Science,  10  (3): (834-845).  [PMID:35005755] [10.1039/D1BM01620B]
19. Liu Nijuan, Liu Jingjing, Niu Xiaohui, Wang Jia, Guo Ruibin, Mo Zunli.  (2021)  An electrochemical chiral sensor based on the synergy of chiral ionic liquid and 3D-NGMWCNT for tryptophan enantioselective recognition.  MICROCHIMICA ACTA,  188  (5): (1-13).  [PMID:33839948] [10.1007/s00604-021-04818-w]
20. Jia Wang, Zunli Mo, Nijuan Liu, Ruibin Guo, Chao Shuai, Fang Chen, Yongxin Du, Jingjing Liu, Guigui Liu, Qibing Dong, Qinqin Gao, Ying Chen, Wentong Liu.  (2021)  Construction of electrochemical chiral interface of C3N4/Ppy/ self-assembled polysaccharide.  JOURNAL OF ELECTROANALYTICAL CHEMISTRY,      [PMID:] [10.1016/j.jelechem.2021.115118]
21. Zou Jiao, Lan Xi-Wen, Zhao Guo-Qing, Huang Zhao-Ning, Liu Yi-Ping, Yu Jin-Gang.  (2020)  Immobilization of 6-O-α-maltosyl-β-cyclodextrin on the surface of black phosphorus nanosheets for selective chiral recognition of tyrosine enantiomers.  MICROCHIMICA ACTA,  187  (11): (1-11).  [PMID:33141322] [10.1007/s00604-020-04606-y]
22. Jiao Zou, Jin-Gang Yu.  (2020)  Nafion-stabilized black phosphorus nanosheets-maltosyl-β-cyclodextrin as a chiral sensor for tryptophan enantiomers.  Materials Science & Engineering C-Materials for Biological Applications,      [PMID:32409064] [10.1016/j.msec.2020.110910]
23. Tingting Wang, Yuhuan Cheng, Yulian Zhang, Jinyin Zha, Jiannong Ye, Qingcui Chu, Guifang Cheng.  (2019)  β-cyclodextrin modified quantum dots as pseudo-stationary phase for direct enantioseparation based on capillary electrophoresis with laser-induced fluorescence detection.  TALANTA,      [PMID:31987180] [10.1016/j.talanta.2019.120629]
24. Jiao Zou, Jin-Gang Yu.  (2019)  Chiral recognition of tyrosine enantiomers on a novel bis-aminosaccharides composite modified glassy carbon electrode.  ANALYTICA CHIMICA ACTA,      [PMID:31623714] [10.1016/j.aca.2019.08.018]
25. Chunlei Ma, Wensheng Ren, Jianke Tang, Xiaoli Wang, Dongxin Ji, Rongqian Meng, Cuihong Zhang, Qi Wang.  (2019)  Copper nanocluster-based fluorescence enhanced determination of d-penicillamine.  LUMINESCENCE,  34  (7): (767-773).  [PMID:31267664] [10.1002/bio.3672]
26. Yanhua Tu, Beixuan He, Songyan Gao, Dandan Guo, Xinlei Jia, Xin Dong, Meili Guo.  (2019)  CtACO1 Overexpression Resulted in the Alteration of the Flavonoids Profile of Safflower.  MOLECULES,  24  (6): (1128).  [PMID:30901924] [10.3390/molecules24061128]
27. Huang Lu, Li Yanxia, Lin Qi, Lou Benyong, Chen Yiting.  (2018)  Enantioselective permeations of amino acids through l-proline-modified gold nanochannel membrane: an experimental and theoretical study.  AMINO ACIDS,  50  (11): (1549-1556).  [PMID:30073606] [10.1007/s00726-018-2629-0]
28. Lili Guo, Baozhu Yang, Datong Wu, Yongxin Tao, Yong Kong.  (2018)  Chiral Sensing Platform Based on the Self-Assemblies of Diphenylalanine and Oxalic Acid.  ANALYTICAL CHEMISTRY,      [PMID:29595059] [10.1021/acs.analchem.8b00762]
29. Yanni Miao, Qi Liu, Wei Wang, Li Liu, Li Wang.  (2017)  Enantioseparation of amino acids by micellar capillary electrophoresis using binary chiral selectors and determination of D-glutamic acid and D-aspartic acid in rice wine.  JOURNAL OF LIQUID CHROMATOGRAPHY & RELATED TECHNOLOGIES,      [PMID:] [10.1080/10826076.2017.1364263]
30. Xiaomei Lu, Jie Tang, Xinxin Dang, Xiaoli Jing, Kailin Xu, Hui Li, Bing Liang.  (2017)  Chiral recognition and determination of enantiomeric excess of chiral compounds by UV-visible-shortwave near infrared diffuse reflectance spectroscopy with chemometrics.  RSC Advances,  (22): (13552-13560).  [PMID:] [10.1039/C6RA24952C]
31. Yongxin Tao, Xiaogang Gu, Baozhu Yang, Linhong Deng, Liping Bao, Yong Kong, Fuqiang Chu, Yong Qin.  (2017)  Electrochemical Enantioselective Recognition in a Highly Ordered Self-Assembly Framework.  ANALYTICAL CHEMISTRY,      [PMID:28208293] [10.1021/acs.analchem.6b04377]
32. Datong Wu, Ying Zhou, Pengfei Cai, Shanshan Shen, Yuanjiang Pan.  (2015)  Specific cooperative effect for the enantiomeric separation of amino acids using aqueous two-phase systems with task-specific ionic liquids.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:25888099] [10.1016/j.chroma.2015.03.047]
33. Xiao-Yan Liu, Hong-Xun Fang, Li-Ping Yu.  (2013)  Molecularly imprinted photonic polymer based on β-cyclodextrin for amino acid sensing.  TALANTA,      [PMID:24148405] [10.1016/j.talanta.2013.05.003]
34. Jin-Wen Liu, Tingting Chen, Meiqun Cai, Yingfeng Qin, Mei Li.  (2024)  A Dual-Mode Optical Sensing Strategy for Rapid Detection of D-Penicillamine in Pharmaceutical Formulations.  ANALYTICAL LETTERS,      [PMID:] [10.1080/00032719.2024.2419533]
35. Wenrong Cai, Yanjing Shi, Ning Liu, Zheng-Zhi Yin, Junyao Li, Laidi Xu, Datong Wu, Yong Kong.  (2024)  A photothermal effect-based chiral sensor for chiral discrimination and sensitive detection.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:38788508] [10.1016/j.saa.2024.124494]
36. Jun Zhang, Kai Wu, Xiaoqing Gao, Min Zhang, Xin Zhou, Florian Bertram, Chen Shen, Yunlong Zhou.  (2024)  Achiral and chiral ligands synergistically harness chiral self-assembly of inorganics.  Science Advances,  10  (42):   [PMID:39423258] [10.1126/sciadv.ado5948]
37. Xiaohui Niu, Yongqi Liu, Rui Zhao, Mei Yuan, Hongfang Zhao, Hongxia Li, Kunjie Wang.  (2024)  Enhancing Electrochemical Signal for Efficient Chiral Recognition by Encapsulating C60 Fullerene into Chiral Lanthanum-Based MOFs.  ACS Applied Materials & Interfaces,      [PMID:38556802] [10.1021/acsami.4c03134]
38. Wen-Bo Gao, Shu-Ting Xu, Yong-Jie Yan, Cheng Yang, Xiu-Ping Yan.  (2025)  Kinetic Method Coupled with Thermal-Assisted Paper Spray Ionization Mass Spectrometry for Direct Determination of Enantiomeric Excess of Multiple d/l-Amino Acids in Functional Foods.  JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY,      [PMID:40079893] [10.1021/jasms.5c00050]
39. Shen Yan, Fang Nan, Liu Xinru, Ling Yu, Su Yuming, Tan Tian, Chen Feng, Lin He, Zhao Boxuan, Wang Jin, Si Duanhui, Xie Shunji, Wang Ye, Zhou Da, Zhang Teng, Cao Rong, Wang Cheng.  (2025)  Observation of metal-organic interphase in Cu-based electrochemical CO2-to-ethanol conversion.  Nature Communications,  16  (1): (1-18).  [PMID:40021652] [10.1038/s41467-025-57221-x]
40. Luzheng Dong, Jun Wu, Xiashi Zhu.  (2024)  Preparation of amino acid chiral ionic liquid and visual chiral recognition of glutamine and phenylalanine enantiomers.  CHIRALITY,  36  (4): (e23665).  [PMID:38570326] [10.1002/chir.23665]
41. Jinbo Hu, Wenbo Wang, Xinyan Liu, Yeqi Du, Hao Zhang, Ranlong Duan, Xinchao Bian, Yanlong Liu, Xuesi Chen.  (2024)  Synergistic enhancement of poly(lactide) melt strength via copolymerization and multi-arm branching strategy.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:39357705] [10.1016/j.ijbiomac.2024.136161]
42. Jing Zhang, Ye Yang, Yi-Ping Liu, Guo-Cong Liu, Xi Zhu, Xin-Yu Jiang, Jin-Gang Yu.  (2025)  Highly selective and efficient recognition of tyrosine enantiomers at Au NPs/D-sorbitol/GCE-based chiral sensor.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2025.115424]
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