L(-)-Carnitine - Moligand™, ≥98% , CAS No.541-15-1

CAS: 541-15-1 Cat. No.: C105423 Molecular Weight: 161.2 Beilstein Registry Number: 4292315 EC Number: 208-768-0
AVAILABLE TO ORDER
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
L-Carnitin | LEVOCARNITINE (EP MONOGRAPH) | levocarnitine HCl | MFCD00038747 | L-(-)-Carnitine | 3-carboxy-2-hydroxy-N,N,N-trimethyl-1-propanaminium | LEVOCARNITINE (USP-RS) | (-)-L-Carnitine | 1-Propanaminium, 3-carboxy-2-hydroxy-N,N,N-trimethyl-, hydrox
Storage
Argon charged,Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
5g
C105423-5g
≥10
$9.90
10g
C105423-10g
1
$10.90
25g
C105423-25g
9

$16.90

$25.90
Save $9.00 (34.75%)
100g
C105423-100g
8

$33.90

$50.90
Save $17.00 (33.40%)
500g
C105423-500g
2

$135.90

$203.90
Save $68.00 (33.35%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

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

🌡

Storage & shipping

Argon charged,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 41 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

L-Carnitine ((R)-Carnitine), a highly polar, small zwitterion, is an essential co-factor for the mitochondrial β-oxidation pathway. L-Carnitine functions to transport long chain fatty acyl-CoAs into the mitochondria for degradation by β-oxidation. L-Carnitine is an antioxidant. L-Carnitine can ameliorate metabolic imbalances in many inborn errors of metabolism

Specifications

Synonyms
L-Carnitin | LEVOCARNITINE (EP MONOGRAPH) | levocarnitine HCl | MFCD00038747 | L-(-)-Carnitine | 3-carboxy-2-hydroxy-N, N, N-trimethyl-1-propanaminium | LEVOCARNITINE (USP-RS) | (-)-L-Carnitine | 1-Propanaminium, 3-carboxy-2-hydroxy-N, N, N-trimethyl-, hydrox
Specifications & Purity
Moligand™, ≥98%
Biochemical and Physiological Mechanisms
Carnitine biosynthesized from lysine. Carnitine facilitates fatty acid transport into the mitochondrial compartment. In skeletal and cardiac muscle tissue it acts as a metabolic cofactor. Carnitine might be associated with the energy production from branc
Storage
Argon charged, Room temperature
Shipped In
Normal
Grade
Moligand™
Note
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Purity
≥98%
Names and Identifiers
Pubchem Sid488181224
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488181224
Canonical SmilesC[N+](C)(C)C[C@H](O)CC([O-])=O
IUPAC Name(3R)-3-hydroxy-4-(trimethylazaniumyl)butanoate
InChIKeyPHIQHXFUZVPYII-ZCFIWIBFSA-N
INCHI1S/C7H15NO3/c1-8(2,3)5-6(9)4-7(10)11/h6,9H,4-5H2,1-3H3/t6-/m1/s1
Isomeric SMILES C[N+](C)(C)C[C@@H](CC(=O)[O-])O
WGK Germany 3
RTECS BP2980000
Molecular Weight 161.2
Beilstein 4292315
Reaxy-Rn 4292315
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4292315&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 nitrogen compounds
ClassOrganonitrogen compounds
SubclassQuaternary ammonium salts
Intermediate Tree Nodes Not available
Direct ParentCarnitines
Alternative Parents Short-chain hydroxy acids and derivatives  Beta hydroxy acids and derivatives  Fatty acids and conjugates  Tetraalkylammonium salts  Secondary alcohols  Carboxylic acid salts  1,2-aminoalcohols  Monocarboxylic acids and derivatives  Carboxylic acids  Organopnictogen compounds  Organic zwitterions  Organic salts  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Carnitine - Beta-hydroxy acid - Short-chain hydroxy acid - Fatty acid - Hydroxy acid - Tetraalkylammonium salt - 1,2-aminoalcohol - Carboxylic acid salt - Secondary alcohol - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Organic oxygen compound - Organooxygen compound - Organic zwitterion - Organic salt - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organopnictogen compound - Amine - Alcohol - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as carnitines. These are organic compounds containing the quaternary ammonium compound carnitine.
External Descriptors carnitine
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
PDE5A Tclin Phosphodiesterase 5A (5113 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EGFR Tclin Epidermal growth factor receptor erbB1 (33727 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
F2 Tclin Thrombin (11687 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA2 Tclin Carbonic anhydrase II (17698 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HMGCR Tclin HMG-CoA reductase (2475 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
INSR Tclin Insulin receptor (5558 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PGR Tclin Progesterone receptor (8562 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRB1 Tclin Beta-1 adrenergic receptor (6630 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR1A Tclin Serotonin 1a (5-HT1a) receptor (14969 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AR Tclin Androgen Receptor (11781 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ACE Tclin Angiotensin-converting enzyme (1423 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD2 Tclin Dopamine D2 receptor (23596 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MAOA Tclin Monoamine oxidase A (11911 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CNR1 Tclin Cannabinoid CB1 receptor (20913 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD1 Tclin Dopamine D1 receptor (9720 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD4 Tchem Dopamine D4 receptor (7907 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A2 Tclin Norepinephrine transporter (10102 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HRH2 Tclin Histamine H2 receptor (5428 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA1D Tclin Alpha-1d adrenergic receptor (4171 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR1B Tclin Serotonin 1b (5-HT1b) receptor (2801 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR2A Tclin Serotonin 2a (5-HT2a) receptor (14758 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR2C Tclin Serotonin 2c (5-HT2c) receptor (11471 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADORA1 Tclin Adenosine A1 receptor (17603 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CALCR Tclin Calcitonin receptor (2215 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A4 Tclin Serotonin transporter (12625 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA1A Tclin Alpha-1a adrenergic receptor (8359 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HRH1 Tclin Histamine H1 receptor (7573 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA1B Tclin Alpha-1b adrenergic receptor (2912 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OPRM1 Tclin Mu opioid receptor (19785 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD3 Tclin Dopamine D3 receptor (14368 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AVPR1A Tclin Vasopressin V1a receptor (5412 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OPRD1 Tclin Delta opioid receptor (15096 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OPRK1 Tclin Kappa opioid receptor (16155 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A3 Tclin Dopamine transporter (10535 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PTH1R Tclin Parathyroid hormone receptor (47172 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCNH2 Tclin HERG (29587 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR4 Tclin Serotonin 4 (5-HT4) receptor (2068 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PDE3A Tclin Phosphodiesterase 3A (3309 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ESR2 Tclin Estrogen receptor beta (9272 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYSLTR1 Tclin Cysteinyl leukotriene receptor 1 (2118 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ERBB2 Tclin Receptor protein-tyrosine kinase erbB-2 (7851 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Agtr2 Angiotensin II type 2 (AT-2) receptor (803 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ampC Beta-lactamase AmpC (62480 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mc4r Melanocortin receptor 4 (1205 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ltc4s Leukotriene C4 synthase (1 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Sigmar1 Sigma opioid receptor (160 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Npy1r Neuropeptide Y receptor type 1 (8 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cckar Cholecystokinin A receptor (90 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nos2 Nitric oxide synthase, inducible (3573 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mapk1 MAP kinase ERK2 (650 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mmp9 Matrix metalloproteinase 9 (38 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cpt1b Carnitine palmitoyltransferase 1B (51 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Glra2 Glycine receptor (1745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SARS-CoV-2 (38078 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
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.

53 results found

Lot NumberCertificate TypeDateItem
I2215063Certificate of AnalysisJun 15, 2026 C105423
E2528348Certificate of AnalysisMar 10, 2025 C105423
E2528347Certificate of AnalysisMar 10, 2025 C105423
E2528229Certificate of AnalysisMar 10, 2025 C105423
E2528349Certificate of AnalysisMar 10, 2025 C105423
E2528350Certificate of AnalysisMar 10, 2025 C105423
E2529654Certificate of AnalysisMar 10, 2025 C105423
F2611175Certificate of AnalysisMar 10, 2025 C105423
H2511041Certificate of AnalysisMar 10, 2025 C105423
A2521097Certificate of AnalysisDec 30, 2024 C105423
D2616014Certificate of AnalysisDec 30, 2024 C105423
A2521094Certificate of AnalysisDec 30, 2024 C105423
A2521100Certificate of AnalysisDec 30, 2024 C105423
K2418089Certificate of AnalysisNov 11, 2024 C105423
K2418090Certificate of AnalysisNov 11, 2024 C105423
K2418091Certificate of AnalysisNov 11, 2024 C105423
K2420376Certificate of AnalysisNov 11, 2024 C105423
K2420377Certificate of AnalysisNov 11, 2024 C105423
K2420378Certificate of AnalysisNov 11, 2024 C105423
K2420379Certificate of AnalysisNov 11, 2024 C105423
K2420646Certificate of AnalysisNov 11, 2024 C105423
J2425374Certificate of AnalysisOct 19, 2024 C105423
J2425373Certificate of AnalysisOct 19, 2024 C105423
I2413275Certificate of AnalysisAug 31, 2024 C105423
I2413274Certificate of AnalysisAug 31, 2024 C105423
I2413273Certificate of AnalysisAug 31, 2024 C105423
I2413272Certificate of AnalysisAug 31, 2024 C105423
I2413271Certificate of AnalysisAug 31, 2024 C105423
I2413270Certificate of AnalysisAug 31, 2024 C105423
F2415199Certificate of AnalysisMay 31, 2024 C105423
F2415202Certificate of AnalysisMay 31, 2024 C105423
F2415240Certificate of AnalysisMay 31, 2024 C105423
E2408117Certificate of AnalysisApr 28, 2024 C105423
D2425238Certificate of AnalysisMar 25, 2024 C105423
I2403072Certificate of AnalysisNov 10, 2022 C105423
B2321867Certificate of AnalysisNov 10, 2022 C105423
B2321775Certificate of AnalysisNov 10, 2022 C105423
C2414040Certificate of AnalysisNov 10, 2022 C105423
B2321846Certificate of AnalysisNov 10, 2022 C105423
B2321836Certificate of AnalysisNov 10, 2022 C105423
B2321824Certificate of AnalysisNov 10, 2022 C105423
I2215145Certificate of AnalysisSep 03, 2022 C105423
I2215143Certificate of AnalysisSep 03, 2022 C105423
G2307579Certificate of AnalysisSep 03, 2022 C105423
I2215144Certificate of AnalysisSep 03, 2022 C105423
H2223246Certificate of AnalysisJul 21, 2022 C105423
H2223244Certificate of AnalysisJul 21, 2022 C105423
C1812008Certificate of AnalysisJan 21, 2022 C105423
C1812007Certificate of AnalysisJan 21, 2022 C105423
B2222401Certificate of AnalysisDec 20, 2021 C105423
B2222376Certificate of AnalysisDec 20, 2021 C105423
B2222364Certificate of AnalysisDec 20, 2021 C105423
B2222363Certificate of AnalysisDec 20, 2021 C105423

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Chemical and Physical Properties
SolubilitySoluble in water, pyridine, dimethyl sulfoxide, methanol and ethanol.
SensitivityMoisture sensitive
Specific Rotation[α]-32 ° (C=1, H2O)
Melt Point(°C)190°C
Molecular Weight161.200 g/mol
XLogP3-0.200
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count3
Exact Mass161.105 Da
Monoisotopic Mass161.105 Da
Topological Polar Surface Area60.400 Ų
Heavy Atom Count11
Formal Charge0
Complexity134.000
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
Documents & Articles
Citations of This Product
References
1. Qi Guo, Yang Feng, Hongjie Song, Mingxia Sun, Zixuan Zhan, Yi Lv.  (2023)  New Perylene-Based Chemiluminescent Polymer Nanoparticles for Highly Selective Detection of the Superoxide Anion In Vivo.  ANALYTICAL CHEMISTRY,      [PMID:37779257] [10.1021/acs.analchem.3c03233]
2. Lyu Jiaming, Shen Shengyuan, Chen Lin, Zhu Yiming, Zhuang Songlin.  (2023)  Frequency selective fingerprint sensor: the Terahertz unity platform for broadband chiral enantiomers multiplexed signals and narrowband molecular AIT enhancement.  PhotoniX,  (1): (1-14).  [PMID:] [10.1186/s43074-023-00108-1]
3. Yaodong Yi, Hengbin Zhang, Mingyang Chen, Binxin Chen, Yingchun Chen, Ping Li, Hui Zhou, Zhiyuan Ma, Huidi Jiang.  (2023)  Inhibition of multiple uptake transporters in cardiomyocytes/mitochondria alleviates doxorubicin-induced cardiotoxicity.  CHEMICO-BIOLOGICAL INTERACTIONS,      [PMID:37453608] [10.1016/j.cbi.2023.110627]
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5. Xu Zhang, Xiaotong Wang, Rui Shi, Xiaoku Ran, Xiahong He, Deqiang Dou.  (2023)  Effective substances and mechanism of red ginseng on rats with spleen-deficiency syndrome based on the substance and energy metabolism as well as the “brain-gut” axis.  JOURNAL OF ETHNOPHARMACOLOGY,      [PMID:37003398] [10.1016/j.jep.2023.116438]
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7. Chenhui Gu, Xuewen Hu, Baixi Shan, Xiaojing Wu, Jun Chen.  (2023)  Targeted and non-targeted metabolomics uncovering the effects of Er-Miao-Wan formula on rats with hyperuricemia.  JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS,      [PMID:36731256] [10.1016/j.jpba.2023.115246]
8. Jing Nie, Jiabei Zhou, Yi Shen, Ruimiao Lin, Haihong Hu, Kui Zeng, Huichang Bi, Min Huang, Lushan Yu, Su Zeng, Jing Miao.  (2023)  Studies on the interaction of five triazole fungicides with human renal transporters in cells.  TOXICOLOGY IN VITRO,      [PMID:36669674] [10.1016/j.tiv.2023.105555]
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12. Zefang Wang, Yan Peng, Chengjun Shi, Liping Wang, Xiaohong Chen, Wanwan Wu, Xu Wu, Yiming Zhu, Jingchen Zhang, Guiliang Cheng, Songlin Zhuang.  (2021)  Qualitative and quantitative recognition of chiral drugs based on terahertz spectroscopy.  ANALYST,  146  (12): (3888-3898).  [PMID:34042921] [10.1039/D1AN00500F]
13. Yingchun Chen, Cui Li, Yaodong Yi, Weijuan Du, Huidi Jiang, Su Zeng, Hui Zhou.  (2020)  Organic Cation Transporter 1 and 3 Contribute to the High Accumulation of Dehydrocorydaline in the Heart.  DRUG METABOLISM AND DISPOSITION,  48  (10): (1074-1083).  [PMID:32723846] [10.1124/dmd.120.000025]
14. Jin-Ming Wang, Run Xu, Qian-Nan Di, Hao-Wei Fu, Qian Xu.  (2020)  Determination of urinary carnitine levels as a potential indicator of uterine fibroids caused by nonylphenol exposure.  JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES,      [PMID:32590215] [10.1016/j.jchromb.2020.122248]
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16. Qingquan Zeng, Mengru Bai, Cui Li, Shuanghui Lu, Zhiyuan Ma, Yunchun Zhao, Hui Zhou, Huidi Jiang, Dongli Sun, Caihong Zheng.  (2019)  Multiple Drug Transporters Contribute to the Placental Transfer of Emtricitabine.  ANTIMICROBIAL AGENTS AND CHEMOTHERAPY,      [PMID:31160284] [10.1128/AAC.00199-19]
17. Xueying Liu, Xiaoku Ran, Muhammad Riaz, Haixue Kuang, Deqiang Dou, Decheng Cai.  (2019)  Mechanism Investigation of Tagetes patula L. against Chronic Nonbacterial Prostatitis by Metabolomics and Network Pharmacology.  MOLECULES,  24  (12): (2266).  [PMID:31216740] [10.3390/molecules24122266]
18. Dong-Liang Lu, Samwel Mchele Limbu, Hong-Bo Lv, Qiang Ma, Li-Qiao Chen, Mei-Ling Zhang, Zhen-Yu Du.  (2018)  The comparisons in protective mechanisms and efficiencies among dietary α-lipoic acid, β-glucan and l-carnitine on Nile tilapia infected by Aeromonas hydrophila.  FISH & SHELLFISH IMMUNOLOGY,      [PMID:30553889] [10.1016/j.fsi.2018.12.023]
19. Liping Li, Yayun Weng, Wei Wang, Mengru Bai, Hongmei Lei, Hui Zhou, Huidi Jiang.  (2017)  Multiple organic cation transporters contribute to the renal transport of sulpiride.  BIOPHARMACEUTICS & DRUG DISPOSITION,  38  (9): (526-534).  [PMID:28926871] [10.1002/bdd.2104]
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23. Hao Zhi, Zhongyan Wang, Xinyue Zhu, Wenhan Wu, Lu Yang, Yidong Dai, Zehua Wang, Ling Jiang, Yongmei Tan, Xiaodong Liu, Li Liu.  (2025)  Chronic liver injury decreases levels of cerebral carnitine and acetylcarnitine in rats partly due to the downregulation of OCTs and OCTN2 at the blood-brain barrier.  DRUG METABOLISM AND DISPOSITION,      [PMID:40300306] [10.1016/j.dmd.2025.100072]
24. Yamin Liu, Xunjiang Wang, Jiaojiao Wei, Kangning Fu, Yilin Chen, Linnan Li, Zhengtao Wang, Li Yang.  (2024)  Comprehensive Profiling of Amino Acids and Derivatives in Biological Samples: A Robust UHPLC-MS/MS Method for Investigating Acute Lung Injury.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:38537486] [10.1016/j.chroma.2024.464816]
25. Li Gao, Ai-ping Zhang, Lei Fu, Qian-wen Li, Xue-mei Qin, Jing Zhao.  (2024)  Huangqin decoction attenuates spared nerve injury (SNI)-induced neuropathic pain by modulating microglial M1/M2 polarization partially mediated by intestinal nicotinamide metabolism.  PHYTOMEDICINE,      [PMID:38614040] [10.1016/j.phymed.2024.155594]
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