Malotilate - ≥99% , CAS No.59937-28-9

CAS: 59937-28-9 Cat. No.: M126891 Peso molecular: 288.38
Disponible para pedir
GRADE & PURITY ≥99%
Synonyms
MT | M2674 | SW219173-1 | Diisopropyl-1,3-dithiol-2-ylidenemalonate | DA-3857 | MALONIC ACID, (1,3-DITHIOL-2-YLIDENE)-, DIISOPROPYL ESTER | Malotilato [INN-Spanish] | CL-1500 | NCGC00164588-02 | AS-11770 | BCP01805 | BM164653 | Kantec | (1,3-Dithiol-2-yli
Storage
Store at 2-8°C
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1g
M126891-1g
3

31,90US$

47,90US$
Guardar 16,00 US$ (33.40%)
5g
M126891-5g
1

155,90US$

233,90US$
Guardar 78,00 US$ (33.35%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C Ships Wet ice 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 24 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Malotilate, diisopropyl 1,3-dithiol-2-ylidenemalonate, is a drug used for the treatment of liver cirrhosis.
A hepatoprotective agent.

Specifications

Sinónimos
MT | M2674 | SW219173-1 | Diisopropyl-1, 3-dithiol-2-ylidenemalonate | DA-3857 | MALONIC ACID, (1, 3-DITHIOL-2-YLIDENE)-, DIISOPROPYL ESTER | Malotilato [INN-Spanish] | CL-1500 | NCGC00164588-02 | AS-11770 | BCP01805 | BM164653 | Kantec | (1, 3-Dithiol-2-yli
Especificaciones y pureza
≥99%
Nombres e identificadores
Pubchem Sid504750736
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504750736
Sonrisas canónicasCC(C)OC(=O)C(=C1SC=CS1)C(=O)OC(C)C
IUPAC Namedipropan-2-yl 2-(1,3-dithiol-2-ylidene)propanedioate
InChIKeyYPIQVCUJEKAZCP-UHFFFAOYSA-N
INCHI1S/C12H16O4S2/c1-7(2)15-10(13)9(11(14)16-8(3)4)12-17-5-6-18-12/h5-8H,1-4H3
Isómeros SMILES CC(C)OC(=O)C(=C1SC=CS1)C(=O)OC(C)C
RTECS OO0970000
Peso molecular 288.38
Reaxy-Rn 7481938
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=7481938&ln=

Documentation

✅ 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
SubclassDicarboxylic acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentDicarboxylic acids and derivatives
Alternative Parents Vinylogous thioesters  Enoate esters  1,3-dithioles  Thioenol ethers  Ketene acetals  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic heteromonocyclic compounds
Substituents Dicarboxylic acid or derivatives - Vinylogous thioester - 1,3-dithiole - Dithiole - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Carboxylic acid ester - Thioenolether - Ketene acetal or derivatives - Organoheterocyclic compound - Carbonyl group - Organooxygen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Aliphatic heteromonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as dicarboxylic acids and derivatives. These are organic compounds containing exactly two carboxylic acid groups.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NR3C1 Tclin Glucocorticoid receptor (14987 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
DRD2 Tclin Dopamine D2 receptor (23596 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GABRA1 Tclin GABA receptor alpha-1 subunit (399 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
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
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
AVPR2 Tclin Vasopressin V2 receptor (2912 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADORA1 Tclin Adenosine A1 receptor (17603 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AGTR1 Tclin Type-1 angiotensin II receptor (5176 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
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
HTR3A Tclin Serotonin 3a (5-HT3a) receptor (3366 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A3 Tclin Dopamine transporter (10535 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GRIN1 Tclin Glutamate (NMDA) receptor subunit zeta 1 (122 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCNH2 Tclin HERG (29587 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CACNA1C Tclin Voltage-gated L-type calcium channel alpha-1C subunit (766 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PDE3A Tclin Phosphodiesterase 3A (3309 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC29A1 Tclin Equilibrative nucleoside transporter 1 (1711 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA2B Tclin Alpha-2b adrenergic receptor (4412 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA2C Tclin Alpha-2c adrenergic receptor (4876 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM3 Tclin Muscarinic acetylcholine receptor M3 (7750 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR2B Tclin Serotonin 2b (5-HT2b) receptor (10323 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TBXA2R Tclin Thromboxane A2 receptor (5717 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EDNRA Tclin Endothelin receptor ET-A (5008 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADORA2A Tclin Adenosine A2a receptor (16305 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADORA3 Tchem Adenosine A3 receptor (15931 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BDKRB2 Tclin Bradykinin B2 receptor (3970 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HRH3 Tclin Histamine H3 receptor (10389 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRNA4 Tclin Neuronal acetylcholine receptor protein alpha-4 subunit (1265 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
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
Pde4d Phosphodiesterase 4D (4 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 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.

1 results found

Lot NumberCertificate TypeFechaArticulo
B1528011Certificate of AnalysisMar 20, 2026 M126891
Propiedades químicas y físicas
SolubilidadSoluble in DMSO (58 mg/ml at 25 °C), water (<1 mg/ml at 25 °C), and ethanol (58 mg/ml at 25 °C).
Punto de fusión (°C)61 °C
Peso molecular288.400 g/mol
XLogP33.800
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count6
Rotatable Bond Count6
Exact Mass288.049 Da
Monoisotopic Mass288.049 Da
Topological Polar Surface Area103.000 Ų
Heavy Atom Count18
Formal Charge0
Complexity363.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Referencias
1. Hui Wang, Yuhan Xiong, Yi He, Lingru Kong, Lan Ding, Rui Wu, Xin-Lei Gao, Jie Ding, Nanqi Ren.  (2023)  Photocatalytic degradation of benzotriazole through synergy of electron donor–acceptor units and Au clusters in covalent organic frameworks.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2023.148309]
2. Xi Wang, Wenjing Zhu, Miao Xing, Haiyan Zhu, Enqing Chen, Jie Zhou.  (2023)  Matrine disrupts Nrf2/GPX4 antioxidant system and promotes hepatocyte ferroptosis.  CHEMICO-BIOLOGICAL INTERACTIONS,      [PMID:37716422] [10.1016/j.cbi.2023.110713]
3. Lu-Qing Xie, Sui Peng, Ya-Nan Xin, Bo Liu, Xin-Yu Jiang, Jin-Gang Yu.  (2023)  Preparation of three-dimensional 2-mercaptothiazoline modified GO aerogel for selective adsorption of Cu2+ in aqueous solution.  Journal of Environmental Chemical Engineering,      [PMID:] [10.1016/j.jece.2023.110332]
4. Kai Zheng, Jiaxiang Bai, Wanling Chen, Yaozeng Xu, Huilin Yang, Wei Li, Penghui Li, Liping Tong, Huaiyu Wang, Paul K. Chu, Dechun Geng.  (2023)  Multifunctional BPs/MT@PLGA-ALE Nanospheres for Treatment of Osteoporotic Fracture with Near-Infrared Irradiation.  ADVANCED FUNCTIONAL MATERIALS,  33  (18): (2214126).  [PMID:] [10.1002/adfm.202214126]
5. Wang Yamei, Xiao Dongdong, Tang Yang, Xia Yezhong, Zhong Yi, Zhang Linping, Sui Xiaofeng, Wang Bijia, Feng Xueling, Xu Hong, Mao Zhiping.  (2022)  Carboxymethyl cellulose-based injectable hydrogel loaded with a composite of melatonin and γ-cyclodextrin with antioxidant property for diabetic wound repair.  CELLULOSE,  30  (3): (1791-1810).  [PMID:] [10.1007/s10570-022-04981-0]
6. Si-wei Rao, Yuan-yuan Duan, Dong-sheng Zhao, Cheng-jun Liu, Shao-hua Xu, Dong Liang, Feng-xiang Zhang, Wei Shi.  (2022)  Integrative Analysis of Transcriptomic and Metabolomic Data for Identification of Pathways Related to Matrine-Induced Hepatotoxicity.  CHEMICAL RESEARCH IN TOXICOLOGY,      [PMID:36440846] [10.1021/acs.chemrestox.2c00264]
7. Guan Huanshuai, Kong Ning, Tian Run, Cao Ruomu, Liu Guanzhi, Li Yiyang, Wei Qilu, Jiao Ming, Lei Yutian, Xing Fangze, Tian Peng, Wang Kunzheng, Yang Pei.  (2022)  Melatonin increases bone mass in normal, perimenopausal, and postmenopausal osteoporotic rats via the promotion of osteogenesis.  Journal of Translational Medicine,  20  (1): (1-15).  [PMID:35296324] [10.1186/s12967-022-03341-7]
8. Yamei Wang, Dongdong Xiao, Hainan Yu, Ruiyu Ke, Songlin Shi, Yang Tang, Yi Zhong, Linping Zhang, Xiaofeng Sui, Bijia Wang, Xueling Feng, Hong Xu, Zhiping Mao.  (2022)  Asymmetric composite wound dressing with hydrophobic flexible bandage and tissue-adhesive hydrogel for joints skin wound healing.  COMPOSITES PART B-ENGINEERING,      [PMID:] [10.1016/j.compositesb.2022.109762]
9. Mengfan Cao, Yanjiao Zou, Yuanyuan Zhang, Ting Zeng, Qijin Wan, Guosong Lai, Nianjun Yang.  (2022)  Robust and selective electrochemical sensing of hazardous photographic developing agents using a MOF-derived 3D porous flower-like Co3O4@C/graphene nanoplate composite.  ELECTROCHIMICA ACTA,      [PMID:] [10.1016/j.electacta.2022.139967]
10. Chunji Jiang, Ziyue Ling, Yuanting Xu, Jianxu Bao, Lan Feng, Huitong Cheng, Weifeng Zhao, Changsheng Zhao.  (2021)  Long-term, synergistic and high-efficient antibacterial polyacrylonitrile nanofibrous membrane prepared by “one-pot” electrospinning process.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,      [PMID:34863546] [10.1016/j.jcis.2021.11.075]
11. Feifei Wang, Wenqian Cai, Wenzhuo Shi, Haiwen Wu, Qian Shen, Yanan He, Song Cui, Lihui An.  (2021)  Single molecule real-time sequencing revealing novel insights on the response to estrogen and androgen exposure in freshwater snails.  AQUATIC TOXICOLOGY,      [PMID:34521059] [10.1016/j.aquatox.2021.105953]
12. Renren Sun, Haixia He, Yameng Wan, Yueru Wang, Liyuan Li, Jiao Sha, Gaoliang Jiang, Yu Li, Tao Li, Baozeng Ren.  (2020)  Solubility of melatonin in ethyl acetate + (N, N-dimethylformamide, 2-methoxyethanol, 2-ethoxyethanol and methanol): Determination, correlation, thermodynamic properties and Hansen solubility parameter at saturation.  JOURNAL OF CHEMICAL THERMODYNAMICS,      [PMID:] [10.1016/j.jct.2020.106372]
13. Zhiya Sun, Mei Long, Xinxuan Liu, Yi Zhang, Shunxiang Li, Limei Bai, Huaming Yang.  (2020)  Investigation of natural minerals for ulcerative colitis therapy.  APPLIED CLAY SCIENCE,      [PMID:] [10.1016/j.clay.2020.105436]
14. Kong Qinghong, Zhang Yi, Zhang Xin, Xiang Bing, Yi Yanzhu, Zhu Junyu, Zhang Feng, Zhu Jia, Zhang Junhao.  (2019)  Functionalized Montmorillonite Intercalation Iron Compounds for Improving Flame Retardancy of Epoxy Resin Nanocomposites.  JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY,  19  (9): (5803-5809).  [PMID:30961742] [10.1166/jnn.2019.16540]
15. Xiang Li, Zhongzhen Liu, Lan Wei, Lianxi Huang, Qing Huang, Xiaoshan Jia.  (2019)  Comparison of Competitive and Synergistic Adsorption of Tetrabromobisphenol-A and Its Metabolites on Two Different Organic-Modified Clays.  JOURNAL OF CHEMICAL AND ENGINEERING DATA,      [PMID:] [10.1021/acs.jced.9b00164]
16. Yongcun Song, Songyan Wang, Li-Ye Yang, Di Yu, Yang-Guang Wang, Xiao-kun Ouyang.  (2019)  Facile fabrication of core–shell/bead-like ethylenediamine-functionalized Al-pillared montmorillonite/calcium alginate for As(V) ion adsorption.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:30926490] [10.1016/j.ijbiomac.2019.03.172]
17. Yi Huang, Qi Tao, Dongzhi Hou, Sheng Hu, Shuangyan Tian, Yanzhong Chen, Ruyi Gui, Lingling Yang, Yao Wang.  (2017)  A novel ion-exchange carrier based upon liposome-encapsulated montmorillonite for ophthalmic delivery of betaxolol hydrochloride.  International Journal of Nanomedicine,      [PMID:28280338] [10.2147/IJN.S122747]
18. Qinhui Wang, Lei Shi, Xiuling Tang, Qingwei Wang, Xueliang Dang, Yan Zhang.  (2014)  Pharmacokinetic study of multiple active constituents from Kushen–Gancao Decoction after oral administration in rat by HPLC–MS/MS.  JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES,      [PMID:24976484] [10.1016/j.jchromb.2014.05.038]
19. Jin Wang, Xiaoting Hong, Gangming Fang, Xuegang Zhang.  (2024)  Deep purification of pesticide waste salt containing high-concentration organic pollutants by ethanol solvents washing and heating treatment.  Journal of Environmental Chemical Engineering,      [PMID:] [10.1016/j.jece.2024.112480]
20. Peng Yi, Xiao Shu, Chenhui Wang, Mingfu Li, Yu Huang, Min Wu, Lijuan Zhang, Quan Chen.  (2024)  Formation of cation bridges and its promoting mechanism for sorption of sulfamethoxazole by montmorillonite.  CHEMOSPHERE,      [PMID:38582173] [10.1016/j.chemosphere.2024.141841]
21. Xiaotian Zhang, Yuxia Wu, Yang Zhang, Jin Zhang, Kunci Chen, Haiyang Liu, Qing Luo, Shuzhan Fei, Jian Zhao, Mi Ou.  (2024)  Molecular Characteristics, Expression Patterns, and Response of Insulin-like Growth Factors Gene Induced by Sex Steroid Hormones in Blotched Snakehead (Channa maculata).  Fishes,  (4): (120).  [PMID:] [10.3390/fishes9040120]
22. Tingting Chen, Zimei Wu, Qiaodan Hou, Yixin Mei, Kunkun Yang, Jing Xu, Lin Wang.  (2024)  The Dual Angiogenesis Effects via Nrf2/HO-1 Signaling Pathway of Melatonin Nanocomposite Scaffold on Promoting Diabetic Bone Defect Repair.  International Journal of Nanomedicine,      [PMID:38510794] [10.2147/IJN.S449290]
23. Jia Jianping, Chen Zhitao, Li Qingqing, Li Feifei, Liu Siru, Bao Guoliang.  (2024)  The enhancement of astaxanthin production in Phaffia rhodozyma through a synergistic melatonin treatment and zinc finger transcription factor gene overexpression.  Frontiers in Microbiology,      [PMID:38666259] [10.3389/fmicb.2024.1367084]
24. Xiali Guan, Gang Zhou, Yubo Fan.  (2025)  Enhanced sensitivity electrochemical sensor for melatonin detection using Antibody-Anchored RGO and silver nanoparticles.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2025.113702]
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