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4-Aminosalicylic acid - 98%, high purity , Dihydrofolate reductase inhibitor, CAS No.65-49-6, Dihydrofolate reductase inhibitor

    Grade & Purity:
  • ≥98%
In stock
Item Number
A105007
Grouped product items
SKU Size
Availability
Price Qty
A105007-25g
25g
4
$37.90
A105007-100g
100g
5
$133.90
A105007-250g
250g
1
$300.90
A105007-500g
500g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$540.90

Competitive pteridine synthetase inhibitor

Basic Description

Synonyms 2-Hydroxy-4-aminobenzoic acid | 4-Asa | Osacyl | PAS-C | WLN: ZR CQ DVQ | Benzoic acid, 4-aminohydroxy- | Granupas | KBioSS_000422 | BRN 0473071 | Pamisyl (TN) | Apacil | Spectrum_000042 | 4-14-00-01967 (Beilstein Handbook Reference) | MLS000069418 | p-am
Specifications & Purity ≥98%
Biochemical and Physiological Mechanisms Competitive pteridine synthetase inhibitor. Shows antituberculosis activity. Inhibits NF-κB and folic acid synthesis. Orally active.
Storage Temp Argon charged
Shipped In Normal
Action Type INHIBITOR
Mechanism of action Dihydrofolate reductase inhibitor
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.
Product Description

4-Aminosalicylic acid is an inhibitor of NF κ B.
A antibacterial capable of inhibiting the growth of Mycobacterium tuberculosis

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Benzene and substituted derivatives
Subclass Benzoic acids and derivatives
Intermediate Tree Nodes Hydroxybenzoic acid derivatives - Salicylic acid and derivatives - Aminosalicylic acids and derivatives
Direct Parent Aminosalicylic acids
Alternative Parents 4-aminosalicylic acids  Salicylic acids  Aminobenzoic acids  Benzoic acids  m-Aminophenols  Benzoyl derivatives  Aniline and substituted anilines  1-hydroxy-2-unsubstituted benzenoids  1-hydroxy-4-unsubstituted benzenoids  Vinylogous acids  Amino acids  Monocarboxylic acids and derivatives  Carboxylic acids  Hydrocarbon derivatives  Organic oxides  Organooxygen compounds  Organopnictogen compounds  Primary amines  
Molecular Framework Aromatic homomonocyclic compounds
Substituents 4-aminosalicylic acid - Aminosalicylic acid - Salicylic acid - Aminobenzoic acid or derivatives - Aminobenzoic acid - Benzoic acid - Aniline or substituted anilines - M-aminophenol - Aminophenol - Benzoyl - 1-hydroxy-2-unsubstituted benzenoid - 1-hydroxy-4-unsubstituted benzenoid - Phenol - Vinylogous acid - Amino acid - Amino acid or derivatives - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Carboxylic acid - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Primary amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Amine - Aromatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as aminosalicylic acids. These are salicylic acids carrying an amino group on the benzene ring.
External Descriptors phenols - aminobenzoic acid

Product Properties

ALogP 1.3

Associated Targets(Human)

PDE5A Tclin Phosphodiesterase 5A (5113 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
EGFR Tclin Epidermal growth factor receptor erbB1 (33727 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CA2 Tclin Carbonic anhydrase II (17698 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HMGCR Tclin HMG-CoA reductase (2475 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
INSR Tclin Insulin receptor (5558 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PGR Tclin Progesterone receptor (8562 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADRB1 Tclin Beta-1 adrenergic receptor (6630 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HTR1A Tclin Serotonin 1a (5-HT1a) receptor (14969 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ALOX5 Tclin Arachidonate 5-lipoxygenase (6568 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
AR Tclin Androgen Receptor (11781 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ACE Tclin Angiotensin-converting enzyme (1423 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
DRD2 Tclin Dopamine D2 receptor (23596 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TYR Tclin Tyrosinase (717 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
GABRA1 Tclin GABA receptor alpha-1 subunit (399 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
MAOA Tclin Monoamine oxidase A (11911 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CNR1 Tclin Cannabinoid CB1 receptor (20913 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
DRD1 Tclin Dopamine D1 receptor (9720 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
DRD4 Tchem Dopamine D4 receptor (7907 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SLC6A2 Tclin Norepinephrine transporter (10102 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HRH2 Tclin Histamine H2 receptor (5428 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADRA1D Tclin Alpha-1d adrenergic receptor (4171 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HTR1B Tclin Serotonin 1b (5-HT1b) receptor (2801 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HTR2A Tclin Serotonin 2a (5-HT2a) receptor (14758 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HTR2C Tclin Serotonin 2c (5-HT2c) receptor (11471 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
AVPR2 Tclin Vasopressin V2 receptor (2912 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADORA1 Tclin Adenosine A1 receptor (17603 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
AGTR1 Tclin Type-1 angiotensin II receptor (5176 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CALCR Tclin Calcitonin receptor (2215 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SLC6A4 Tclin Serotonin transporter (12625 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADRA1A Tclin Alpha-1a adrenergic receptor (8359 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HRH1 Tclin Histamine H1 receptor (7573 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADRA1B Tclin Alpha-1b adrenergic receptor (2912 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
OPRM1 Tclin Mu opioid receptor (19785 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
DRD3 Tclin Dopamine D3 receptor (14368 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
AVPR1A Tclin Vasopressin V1a receptor (5412 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
OPRD1 Tclin Delta opioid receptor (15096 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
OPRK1 Tclin Kappa opioid receptor (16155 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HTR3A Tclin Serotonin 3a (5-HT3a) receptor (3366 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SLC6A3 Tclin Dopamine transporter (10535 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
GRIN1 Tclin Glutamate (NMDA) receptor subunit zeta 1 (122 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
KCNH2 Tclin HERG (29587 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Agtr2 Angiotensin II type 2 (AT-2) receptor (803 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mc4r Melanocortin receptor 4 (1205 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Ltc4s Leukotriene C4 synthase (1 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Sigmar1 Sigma opioid receptor (160 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Npy1r Neuropeptide Y receptor type 1 (8 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Cckar Cholecystokinin A receptor (90 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Pde4d Phosphodiesterase 4D (4 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Nos2 Nitric oxide synthase, inducible (3573 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mapk1 MAP kinase ERK2 (650 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mmp2 Matrix metalloproteinase-2 (12 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Hdac6 Histone deacetylase 6 (222 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Ptpn1 Protein-tyrosine phosphatase 1B (270 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mmp9 Matrix metalloproteinase 9 (38 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Pseudomonas aeruginosa (123386 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Klebsiella pneumoniae (43867 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Micrococcus luteus (7463 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Escherichia coli (133304 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Corynebacterium xerosis (106 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mycobacterium avium (4587 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mycobacterium kansasii (6484 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mycobacterium tuberculosis (203094 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Pneumocystis carinii (749 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Bacillus cereus (7522 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mycolicibacterium smegmatis (8003 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Leishmania infantum (5912 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Trypanosoma brucei (78846 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Trypanosoma brucei brucei (13300 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Entamoeba histolytica (2676 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Cryptosporidium parvum (1150 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Leishmania amazonensis (3813 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Leishmania donovani (89745 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Leishmania major (2877 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Leishmania mexicana (936 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Trypanosoma cruzi (99888 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Trichomonas vaginalis (2376 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Toxoplasma gondii (4585 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mus musculus (284745 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Trypanosoma brucei rhodesiense (7991 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
lef Anthrax lethal factor (7585 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Corynebacterium pseudodiphtheriticum (105 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mycolicibacter terrae (137 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Colon (26 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Stomach (551 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TGR Thioredoxin glutathione reductase (28579 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mapt Microtubule-associated protein tau (6 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Small intestine (70 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Glra2 Glycine receptor (1745 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 488179842
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488179842
IUPAC Name 4-amino-2-hydroxybenzoic acid
INCHI InChI=1S/C7H7NO3/c8-4-1-2-5(7(10)11)6(9)3-4/h1-3,9H,8H2,(H,10,11)
InChIKey WUBBRNOQWQTFEX-UHFFFAOYSA-N
Smiles C1=CC(=C(C=C1N)O)C(=O)O
Isomeric SMILES C1=CC(=C(C=C1N)O)C(=O)O
WGK Germany 2
RTECS VO1225000
Molecular Weight 153.14
Beilstein 473071
Reaxy-Rn 473071
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=473071&ln=

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.

18 results found

Lot Number Certificate Type Date Item
A2514001 Certificate of Analysis Jan 15, 2025 A105007
A2417112 Certificate of Analysis Oct 18, 2024 A105007
K2308218 Certificate of Analysis Aug 22, 2024 A105007
D2516015 Certificate of Analysis Jul 08, 2024 A105007
D2521563 Certificate of Analysis Jul 08, 2024 A105007
D2310208 Certificate of Analysis Jan 22, 2024 A105007
B2309077 Certificate of Analysis Dec 21, 2023 A105007
I2301214 Certificate of Analysis Jul 13, 2023 A105007
I2221106 Certificate of Analysis Jul 13, 2023 A105007
H2301214 Certificate of Analysis Jul 13, 2023 A105007
I2221069 Certificate of Analysis Jul 13, 2023 A105007
I2221067 Certificate of Analysis Jul 13, 2023 A105007
I2221068 Certificate of Analysis Jul 13, 2023 A105007
D2022075 Certificate of Analysis Jun 07, 2023 A105007
I2221065 Certificate of Analysis Sep 05, 2022 A105007
H2109067 Certificate of Analysis Jun 09, 2022 A105007
H2109041 Certificate of Analysis Jun 09, 2022 A105007
H2109042 Certificate of Analysis Jun 09, 2022 A105007

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Chemical and Physical Properties

Solubility Soluble in water (2 g/l) at 20 °C, dilute sodium hydroxide, dilute nitric acid, ether (slightly), methanol, acetone, and ethanol (1 G SOL IN 21 ML ALC). Virtually insoluble in benzene, chloroform, and carbon tetrachloride
Sensitivity Light and Air sensitive
Melt Point(°C) 150-151°C
Molecular Weight 153.140 g/mol
XLogP3 1.300
Hydrogen Bond Donor Count 3
Hydrogen Bond Acceptor Count 4
Rotatable Bond Count 1
Exact Mass 153.043 Da
Monoisotopic Mass 153.043 Da
Topological Polar Surface Area 83.600 Ų
Heavy Atom Count 11
Formal Charge 0
Complexity 160.000
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

Citations of This Product

1. Yuan Gao, Yun Luo, Zhao Pan, Zhu Zeng, Wenxia Fan, Jingyu Hu, Zhong Zhang, Jinxing Ma, Yang Zhou, Jun Ma.  (2024)  Comparative study of Fe(II)/sulfite, Fe(II)/PDS and Fe(II)/PMS for p-arsanilic acid treatment: Efficient organic arsenic degradation and contrasting total arsenic removal.  WATER RESEARCH,  249  (120967). 
2. Qingxin Yang, Ying Liu, Fengniu Lu, Junqi Cheng, Siyuan Sun, Zhiqin Yuan, Chao Lu.  (2024)  Dopamine-based selective spectrophotometry p-aminosalicylic acid assay by hydrolyzate-triggered formation of azamonardine-like products.  ANALYTICA CHIMICA ACTA,  1287  (342059). 
3. Qiuyan Zhao, Mingyue Ding, Dangshuai Pei, Xiuhua Qi, Yexuan Mao, Xianqing Huang, Lianjun Song, Jingnan Zuo, Huijuan Yang, Xiya Zhang.  (2023)  Development of a monoclonal antibody-based lateral flow immunoassay for the detection of benzoic acid in liquid food.  Analytical Methods,  15  (45): (6229-6238). 
4. Zhiyong Zheng, Yuehua Deng, Weining Xie, Sirui Chen, Xiaoxiao Liang, Shiyuan Liu, Yanbin Jiang, Huaiyu Yang.  (2023)  Co-Former Screening Method for Multicomponent Crystals Based on Partial Least Squares Regression: A Case Study of Ciprofloxacin.  CRYSTAL GROWTH & DESIGN,  23  (5): (3244–3257). 
5. Yanghe Liu, Quan Li, Shenghuan Wang, Mengzhu Liang, Yanhong Ji, Zhenyu Cui, Mohammad Younas, Jianxin Li, Benqiao He.  (2023)  A nanofiltration membrane with positively and negatively charged groups by grafted p-aminosalicylic acid-Fe(III) chelation for Li+/Mg2+ efficient separation.  SEPARATION AND PURIFICATION TECHNOLOGY,  308  (122968). 
6. Wen Liu, Jinyao Li, Zicheng Wang, Yafei Tian, Guodong Ren, Xiaoyu Hou, Lixia Guo, Lihong Li, Chengwu Zhang, Zhifang Wu, Lili Yan, Sijin Li, Haipeng Diao.  (2022)  Construction of mitochondria targeted and FRET based ratiometric sensing nanoplatform for sulfur dioxide accurate detection in vitro and in vivo.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,  283  (121731). 
7. Guodong Ren, ZiCheng Wang, Yafei Tian, Jinyao Li, Yingyu Ma, Liang Zhou, Chengwu Zhang, Lixia Guo, Haipeng Diao, Lihong Li, Li Lu, Sufang Ma, Zhifang Wu, Lili Yan, Wen Liu.  (2022)  Targeted chemo-photodynamic therapy toward esophageal cancer by GSH-sensitive theranostic nanoplatform.  BIOMEDICINE & PHARMACOTHERAPY,  153  (113506). 
8. Yuehua Deng, Yuchen Chen, Fang Xie, Jingwen Tang, Rui Zhang, Huaiyu Yang, Yanbin Jiang, Shiyuan Liu.  (2022)  Minoxidil Multi-Component Crystals with Aromatic Carboxylic Acids: Theoretical Calculation and Structural Analysis.  CRYSTAL GROWTH & DESIGN,  22  (6): (3941–3953). 
9. Yuliya E. Tyutereva, Petr S. Sherin, Evgeniya V. Polyakova, Vyacheslav P. Grivin, Victor F. Plyusnin, Olga V. Shuvaeva, Jing Xu, Feng Wu, Ivan P. Pozdnyakov.  (2021)  Synergetic effect of potassium persulfate on photodegradation of para-arsanilic acid in Fe(III) oxalate system.  JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY,  420  (113507). 
10. Shaochun Su, Long Chen, Li Hao, Huayao Chen, Xinhua Zhou, Hongjun Zhou.  (2021)  Preparation of p-amino salicylic acid-modified polysuccinimide as water-based nanocarriers for enhancing pesticide stability and insecticidal activity.  COLLOIDS AND SURFACES B-BIOINTERFACES,  207  (111990). 
11. Xiong Peng, Li Chen, Shujun Liu, Lihua Hu, Jianwei Zhang, Aili Wang, Xiwen Yu, Zongcheng Yan.  (2021)  Insights into the interfacial interaction mechanisms of p-arsanilic acid adsorption on ionic liquid modified porous cellulose.  Journal of Environmental Chemical Engineering,  (105225). 
12. Liu Xinning, Liu Yuanchang, Zhao Guangjian, Zhang Yidan, Liu Lu, Wang Juan, Wang Yifan, Zhang Siyu, Li Xin, Guo Dongliang, Wang Peng, Xu Ximing.  (2021)  Biochemical Characterization of Arylamine N-acetyltransferases From Vibrio vulnificus.  Frontiers in Microbiology,  11   
13. Shengnan Chen, Jing Deng, Cheng Ye, Chengcheng Xu, Lingyi Huai, Xiao Ling, Jun Li, Xueyan Li.  (2021)  Degradation of p-arsanilic acid by pre-magnetized Fe0/persulfate system: Kinetics, mechanism, degradation pathways and DBPs formation during subsequent chlorination.  CHEMICAL ENGINEERING JOURNAL,  410  (128435). 
14. Yun Wang, Bing Jiang, Linlin Wang, Zhongmin Feng, Hongtao Fan, Ting Sun.  (2021)  Hierarchically structured two-dimensional magnetic microporous biochar derived from hazelnut shell toward effective removal of p-arsanilic acid.  APPLIED SURFACE SCIENCE,  540  (148372). 
15. Yuxin Li, Li Liu, Zeming Wang, Lixiang Zhou, Yeqing Lan, Cheng Chen.  (2021)  Simultaneous oxidation of 4-aminophenylarsonic acid and adsorption of the produced inorganic arsenic by a combination of Co3O4-La2CO5@RSBC with peroxymonosulfate.  CHEMICAL ENGINEERING JOURNAL,  413  (127417). 
16. Ying Zhang, Xie-an Yu, Yiting Hu, Xuefei Bai, Ran Zhang, Mi Lu, Jianhui Sun, Jiangwei Tian, Bo-Yang Yu.  (2020)  A polydopamine-polyethyleneimine/quantum dot sensor for instantaneous readout of cell surface charge to reflect cell states.  SENSORS AND ACTUATORS B-CHEMICAL,  324  (128696). 
17. Yuliya E. Tyutereva, Petr S. Sherin, Evgeniya V. Polyakova, Olga S. Koscheeva, Vyacheslav P. Grivin, Victor F. Plyusnin, Olga V. Shuvaeva, Ivan P. Pozdnyakov.  (2020)  Photodegradation of para-arsanilic acid mediated by photolysis of iron(III) oxalate complexes.  CHEMOSPHERE,  261  (127770). 
18. Qiong Wu, Xiaoxia Ye, Yuancai Lv, Ruihan Pei, Minya Wu, Minghua Liu.  (2020)  Lignin-based magnetic activated carbon for p-arsanilic acid removal: Applications and absorption mechanisms.  CHEMOSPHERE,  258  (127276). 
19. Yunyun Xu, Jiaxin Lv, Yao Song, Xiaoyu Zhou, Chen Tian, Xujia Hong, Yuepeng Cai, Cunyuan Zhao, Zhang Lin.  (2019)  Efficient removal of low-concentration organoarsenic by Zr-based metal–organic frameworks: cooperation of defects and hydrogen bonds.  Environmental Science-Nano,  (12): (3590-3600). 
20. Yuliya E. Tyutereva, Peter S. Sherin, Zizheng Liu, Victor F. Plyusnin, Ivan P. Pozdnyakov.  (2019)  UVC-induced photodegradation of p-arsanilic acid assisted by humic substances.  MENDELEEV COMMUNICATIONS,  29  (512). 
21. Hongyu Cen, Zhenyu Chen, Xingpeng Guo.  (2019)  N, S co-doped carbon dots as effective corrosion inhibitor for carbon steel in CO2-saturated 3.5% NaCl solution.  Journal of the Taiwan Institute of Chemical Engineers,  99  (224). 
22. Jing Xu, Heng Zhang, Tao Luo, Zizheng Liu, Jun Xia, Xiang Zhang.  (2018)  Phototransformation of p-arsanilic acid in aqueous media containing nitrogen species.  CHEMOSPHERE,  212  (777). 
23. Tianyi Sun, Zhiwei Zhao, Zhijie Liang, Jie Liu, Wenxin Shi, Fuyi Cui.  (2018)  Efficient degradation of p-arsanilic acid with arsenic adsorption by magnetic CuO-Fe3O4 nanoparticles under visible light irradiation.  CHEMICAL ENGINEERING JOURNAL,  334  (1527). 
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