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Phenothiazine - 98%, high purity , CAS No.92-84-2

    Grade & Purity:
  • ≥98%
In stock
Item Number
P108681
Grouped product items
SKU Size
Availability
Price Qty
P108681-100g
100g
5
$9.90
P108681-500g
500g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$32.90

Basic Description

Synonyms PTZ | ENT-38 | phenothiazin | Souframine | Fenotiazina [Italian] | Dibenzothiazine | ALIMEMAZINE HEMITARTRATE IMPURITY C (EP IMPURITY) | Phenthiazine | Opera_ID_1719 | Contaverm | Phenegic | Phenothiazine (INN) | CAS-92-84-2 | HMS1607G06 | Phenothiazine [
Specifications & Purity ≥98%
Storage Temp Argon charged
Shipped In Normal
Product Description

A rigid, tricyclic thiazine useful as an electron donor.

The structure of phenothiazine is rigid, being tricyclic. It is known to alter dopamine (3,4-dihydroxyphenethylamine).Its use as an electron donor is based on its unique hole transporting ability, electron releasing nitrogen and sulfur heteroatoms and its non-planar structure leading to lower molecular aggregation.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organoheterocyclic compounds
Class Benzothiazines
Subclass Phenothiazines
Intermediate Tree Nodes Not available
Direct Parent Phenothiazines
Alternative Parents Diarylthioethers  Benzenoids  1,4-thiazines  Secondary amines  Azacyclic compounds  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular Framework Aromatic heteropolycyclic compounds
Substituents Phenothiazine - Diarylthioether - Aryl thioether - Benzenoid - Para-thiazine - Azacycle - Thioether - Secondary amine - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Amine - Aromatic heteropolycyclic compound
Description This compound belongs to the class of organic compounds known as phenothiazines. These are polycyclic aromatic compounds containing a phenothiazine moiety, which is a linear tricyclic system that consists of a two benzene rings joined by a para-thiazine ring.
External Descriptors phenothiazine

Associated Targets(Human)

CYP1A2 Tchem Cytochrome P450 1A2 (1 Activities)
Activity Type Activity Value -log(M) Mechanism of Action Activity Reference Publications (PubMed IDs)
SLC6A2 Tclin Sodium-dependent noradrenaline transporter (2 Activities)
Activity Type Activity Value -log(M) Mechanism of Action Activity Reference Publications (PubMed IDs)
PTGS1 Tclin Prostaglandin G/H synthase 1 (1 Activities)
Activity Type Activity Value -log(M) Mechanism of Action Activity Reference Publications (PubMed IDs)
PTGS2 Tclin Prostaglandin G/H synthase 2 (1 Activities)
Activity Type Activity Value -log(M) Mechanism of Action Activity Reference Publications (PubMed IDs)
MAOA Tclin Amine oxidase [flavin-containing] A (1 Activities)
Activity Type Activity Value -log(M) Mechanism of Action Activity Reference Publications (PubMed IDs)
NOX1 Tchem NADPH oxidase 1 (2 Activities)
Activity Type Activity Value -log(M) Mechanism of Action Activity Reference Publications (PubMed IDs)
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
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
ADORA1 Tclin Adenosine A1 receptor (17603 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
PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 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
PTH1R Tclin Parathyroid hormone receptor (47172 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
HTR4 Tclin Serotonin 4 (5-HT4) receptor (2068 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ESR2 Tclin Estrogen receptor beta (9272 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CYSLTR1 Tclin Cysteinyl leukotriene receptor 1 (2118 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

TPR Trypanothione reductase (189 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
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
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
Hdac6 Histone deacetylase 6 (222 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
Staphylococcus aureus (210822 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Acinetobacter baumannii (41033 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
Bacillus subtilis (32866 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
Mycolicibacterium smegmatis (8003 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
Cryptococcus neoformans (21258 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Candida albicans (78123 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
Oryctolagus cuniculus (11301 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
lef Anthrax lethal factor (7585 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
BCHE Cholinesterase (8742 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Nox1 NADPH oxidase 1 (5 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
Mdr1a Multidrug resistance protein 1a (106 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Rorc Nuclear receptor ROR-gamma (89407 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PDR5 Pleiotropic ABC efflux transporter of multiple drugs (46 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Snq2p (23 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TUBB2B Tubulin (2175 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Chrna3 Nicotinic acetylcholine receptor alpha6/alpha3/beta4 (315 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
Chikungunya virus (1339 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 488180292
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488180292
IUPAC Name 10H-phenothiazine
INCHI InChI=1S/C12H9NS/c1-3-7-11-9(5-1)13-10-6-2-4-8-12(10)14-11/h1-8,13H
InChIKey WJFKNYWRSNBZNX-UHFFFAOYSA-N
Smiles C1=CC=C2C(=C1)NC3=CC=CC=C3S2
Isomeric SMILES C1=CC=C2C(=C1)NC3=CC=CC=C3S2
WGK Germany 1
RTECS SN5075000
Molecular Weight 199.27
Beilstein 143237
Reaxy-Rn 143237
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=143237&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.

16 results found

Lot Number Certificate Type Date Item
E2117225 Certificate of Analysis Mar 04, 2025 P108681
E2117226 Certificate of Analysis Mar 04, 2025 P108681
J2227745 Certificate of Analysis Jul 22, 2022 P108681
J2227611 Certificate of Analysis Jul 22, 2022 P108681
J2227612 Certificate of Analysis Jul 22, 2022 P108681
J2227562 Certificate of Analysis Jul 22, 2022 P108681
C2506224 Certificate of Analysis Jul 22, 2022 P108681
B2210397 Certificate of Analysis Dec 15, 2021 P108681
B2210353 Certificate of Analysis Dec 15, 2021 P108681
L2405041 Certificate of Analysis Dec 15, 2021 P108681
J2331006 Certificate of Analysis Dec 15, 2021 P108681
B2303922 Certificate of Analysis Dec 15, 2021 P108681
B2210492 Certificate of Analysis Dec 15, 2021 P108681
B2427261 Certificate of Analysis Dec 15, 2021 P108681
B2210294 Certificate of Analysis Dec 15, 2021 P108681
E2422136 Certificate of Analysis Apr 10, 2021 P108681

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Chemical and Physical Properties

Solubility Soluble in water (0.13 mg/ml at 23 °C), ethanol, acetone (very), and ether (freely). Insoluble in chloroform.
Sensitivity Light & Air Sensitive.
Boil Point(°C) 371 °C
Melt Point(°C) 183°C
Molecular Weight 199.270 g/mol
XLogP3 4.200
Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 2
Rotatable Bond Count 0
Exact Mass 199.046 Da
Monoisotopic Mass 199.046 Da
Topological Polar Surface Area 37.300 Ų
Heavy Atom Count 14
Formal Charge 0
Complexity 186.000
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. Yonghe Zhang, Ruonan Zhou, Jie Sun, Peixuan Li, Deyi Wu, Chunyan Yang, Peng Zhang, Zhenghua Ju.  (2024)  Encapsulation of a novel D-A phenothiazine derivative in ZIF-8 for luminescent response to organic solvents vapor.  DYES AND PIGMENTS,  222  (111836). 
2. Na Qiu, Hongyu Wang, Ruihan Tang, Yi Yang, Xiangfei Kong, Zhenguang Hu, Fuxin Zhong, Haijun Tan.  (2024)  Synthesis of phenothiazine-based porous organic polymer and its application to iodine adsorption.  MICROPOROUS AND MESOPOROUS MATERIALS,  363  (112833). 
3. Yuying Li, Junle Zhang, Yaxuan Shi, Yuancheng Zhang, Ge Shi, Xiaomeng Zhang, Zhe Cui, Peng Fu, Minying Liu, Xiaoguang Qiao, Yanjie He, Yudong Wang, Haitao Zhao, Wenjie Zhang, Xinchang Pang.  (2023)  Robust Strategy to Improve the Compatibility between Incorporated Upconversion Nanoparticles and the Bulk Transparent Polymer Matrix.  ACS Omega,  (35): (32159–32167). 
4. Yanrong Wang, Shigui Qiu, Dunyong He, Jiandong Guo, Mengfan Zhao, Chenxi Zheng, Xuemei Wang, Caixing Wang.  (2023)  A High-Potential Bipolar Phenothiazine Derivative Cathode for Aqueous Zinc Batteries.  ChemSusChem,  16  (19): (e202300658). 
5. Xiaojing Lv, Xuchen Zhu, Ling Zhang, Mi Ouyang, Minao Xia, Chunyan Liu, Cheng Zhang.  (2023)  Highly transparent to red/green/blue photo-crosslinkable polymer for patterned electrochromic device.  Journal of Materials Chemistry C,  11  (16): (5490-5497). 
6. Yan Wang, Zhichao Zheng, Janak L. Pathak, Weiwei Feng, Weicong Wu, Chuangang Yang, Lihong Wu, Huade Zheng.  (2023)  Fabrication and characterization of photosensitive non-isocyanate polyurethane acrylate resin for 3D printing of customized biocompatible orthopedic surgical guides.  International Journal of Bioprinting,  (3): (684). 
7. Ting Lian, Wei Liu, Yi Li, Yonggang Yang.  (2023)  Molecular packing structural transition driven handedness inversion of circularly polarized luminescence of phenothiazine substituted Phe–Phe dipeptides.  NEW JOURNAL OF CHEMISTRY,  47  (2): (653-659). 
8. Jianwen Tian, Muzhou Teng, Mu Song, Zhijia Li, Xiaoyong Zhang, Youqin Xu.  (2021)  A feasible molecular engineering for bright Π-conjugation free radical photosensitizers with aggregation-induced emission.  DYES AND PIGMENTS,  194  (109651). 
9. Yun Zhao, Yuanyuan Xue, Juanjuan Sun, Hongli Xuan, Yunli Xu, Yapeng Cui, Jinlong Dong.  (2020)  A new red fluorescent probe based on rosamine–phenothiazine for the highly selective and rapid detection of hypochlorite and its bioimaging in live cells.  NEW JOURNAL OF CHEMISTRY,  44  (29): (12674-12679). 
10. Yukun Wu, Yue He, Shiqi Li, Xiaoyan Li, Yifan Liu, Qinjun Sun, Yanxia Cui, Yuying Hao, Yucheng Wu.  (2020)  Efficient inverted perovskite solar cells with preferential orientation and suppressed defects of methylammonium lead iodide by introduction of phenothiazine as additive.  JOURNAL OF ALLOYS AND COMPOUNDS,  823  (153717). 
11. Huan Feng, Yue Wang, Jianping Liu, Zhiqiang Zhang, Xinyi Yang, Rong Chen, Qingtao Meng, Run Zhang.  (2019)  A highly specific fluorescent probe for rapid detection of hypochlorous acid in vivo and in water samples.  Journal of Materials Chemistry B,  (24): (3909-3916). 
12. S. B. Tan, Y. F. Zhao, W. W. Zhang, P. Gao, W. W. Zhu, Z. C. Zhang.  (2017)  A light-mediated metal-free atom transfer radical chain transfer reaction for the controlled hydrogenation of poly(vinylidene fluoride-chlorotrifluoroethylene).  Polymer Chemistry,  (2): (221-227). 
13. Ruming Jiang, Meiying Liu, Hongye Huang, Long Huang, Qiang Huang, Yuanqing Wen, Qian-yong Cao, Jianwen Tian, Xiaoyong Zhang, Yen Wei.  (2018)  A novel self-catalyzed photoATRP strategy for preparation of fluorescent hydroxyapatite nanoparticles and their biological imaging.  APPLIED SURFACE SCIENCE,  434  (1129). 
14. Dan Wei, Yun Xue, Hongye Huang, Meiying Liu, Guangjian Zeng, Qing Wan, Liangji Liu, Jun Yu, Xiaoyong Zhang, Yen Wei.  (2017)  Fabrication, self-assembly and biomedical applications of luminescent sodium hyaluronate with aggregation-induced emission feature.  Materials Science & Engineering C-Materials for Biological Applications,  81  (120). 
15. An Wu, Xia Ye, Qiang Huang, Wei-Min Dai, Jian-Min Zhang.  (2017)  Anti-epileptic Effects of Valepotriate Isolated from Valeriana jatamansi Jones and Its Possible Mechanisms.  Pharmacognosy Magazine,  13  (51): ( 512–516). 
16. Guangjian Zeng, Meiying Liu, Ruming Jiang, Qiang Huang, Long Huang, Qing Wan, Yanfeng Dai, Yuanqing Wen, Xiaoyong Zhang, Yen Wei.  (2017)  Fabrication of water dispersible and biocompatible AIE-active fluorescent polymeric nanoparticles through a “one-pot” Mannich reaction.  Polymer Chemistry,  (32): (4746-4751). 
17. Qian-yong Cao, Ruming Jiang, Meiying Liu, Qing Wan, Dazhuang Xu, Jianwen Tian, Hongye Huang, Yuanqing Wen, Xiaoyong Zhang, Yen Wei.  (2017)  Preparation of AIE-active fluorescent polymeric nanoparticles through a catalyst-free thiol-yne click reaction for bioimaging applications.  Materials Science & Engineering C-Materials for Biological Applications,  80  (411). 
18. Zi Long, Meiying Liu, Liucheng Mao, Guangjian Zeng, Qiang Huang, Hongye Huang, Fengjie Deng, Yiqun Wan, Xiaoyong Zhang, Yen Wei.  (2017)  One-step synthesis, self-assembly and bioimaging applications of adenosine triphosphate containing amphiphilies with aggregation-induced emission feature.  Materials Science & Engineering C-Materials for Biological Applications,  73  (252). 
19. Qing Wan, Ruming Jiang, Liucheng Mao, Dazhuang Xu, Guangjian Zeng, Yingge Shi, Fengjie Deng, Meiying Liu, Xiaoyong Zhang, Yen Wei.  (2017)  A powerful “one-pot” tool for fabrication of AIE-active luminescent organic nanoparticles through the combination of RAFT polymerization and multicomponent reactions.  Materials Chemistry Frontiers,  (6): (1051-1058). 
20. Zi Long, Meiying Liu, Ruming Jiang, Guangjiang Zeng, Qing Wan, Hongye Huang, Fengjie Deng, Yiqun Wan, Xiaoyong Zhang, Yen Wei.  (2017)  Ultrasonic-assisted Kabachnik-Fields reaction for rapid fabrication of AIE-active fluorescent organic nanoparticles.  ULTRASONICS SONOCHEMISTRY,  35  (319). 
21. Guangjian Zeng, Meiying Liu, Kexin Shi, Chunning Heng, Liucheng Mao, Qing Wan, Hongye Huang, Fengjie Deng, Xiaoyong Zhang, Yen Wei.  (2016)  Surface modification of nanodiamond through metal free atom transfer radical polymerization.  APPLIED SURFACE SCIENCE,  390  (710). 
22. Yun Xue, Meiying Liu, Hongye Huang, Fengjie Deng, Guangjian Zeng, Qing Wan, Shangdong Liang, Xiaoyong Zhang, Yen Wei.  (2016)  Facile preparation, through Schiff base formation, of luminescent amphiphilic carbohydrate polymers with aggregation-induced emission characteristics for biological imaging.  RSC Advances,  (79): (76011-76016). 
23. Qing Wan, Guangjian Zeng, Ziyang He, Liucheng Mao, Meiying Liu, Hongye Huang, Fengjie Deng, Xiaoyong Zhang, Yen Wei.  (2016)  Fabrication and biomedical applications of AIE active nanotheranostics through the combination of a ring-opening reaction and formation of dynamic hydrazones.  Journal of Materials Chemistry B,  (34): (5692-5699). 
24. Junyu Chen, Songsong Luo, Dazhuang Xu, Yun Xue, Hongye Huang, Qing Wan, Meiying Liu, Xiaoyong Zhang, Yen Wei.  (2016)  Fabrication of AIE-active amphiphilic fluorescent polymeric nanoparticles through host–guest interaction.  RSC Advances,  (60): (54812-54819). 
25. Zi Long, Meiying Liu, Ke Wang, Fengjie Deng, Dazhuang Xu, Liangji Liu, Yiqun Wan, Xiaoyong Zhang, Yen Wei.  (2016)  Facile synthesis of AIE-active amphiphilic polymers: Self-assembly and biological imaging applications.  Materials Science & Engineering C-Materials for Biological Applications,  66  (215). 
26. Yahong Cheng, Yi Ding, Ziyan Tang, Xiaoyi Lei, Yufang Ma, Mengxin Xia, Jiaying Li, Gaoge Hu, Jiahui Zhang, Jing Rao.  (2025)  Polydatin mitigates seizures via mitochondrial protection: Mechanisms unraveled by network pharmacology and experimental validation.  Food Bioscience,  68  (106439). 
27. Qiaolin Zuo, Zhenzhong Fan, Qingwang Liu, Yuanfeng Fu, Luoqi Cui, Junfeng Yang.  (2024)  Preparation of Double-Networked Slow-Expanding Nanomicrospheres and Evaluation of Drive Modulation Performance.  MOLECULES,  29  (22): (5378). 
28. Li Lele, Ge Shengyu, Wang Yang, Zhu Heyun, Feng Bo.  (2025)  Untargeted metabolomics reveal the corrective effects of scorpion on epileptic mice.  Scientific Reports,  15  (1): (1-9). 

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