Estriol - Moligand™, analytical standard , Estrogen receptor modulator, CAS No.50-27-1, Estrogen receptor modulator

CAS: 50-27-1 Cat. No.: E105514 Peso molecular: 288.38 Beilstein Registry Number: 2508172 Número EC: 200-022-2
Disponible para pedir
GRADE & PURITY Analytical standard ? Analytical standard — certified-purity material for quantitative calibration. Use to prepare calibration standards and validate analytical methods. Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools.
Synonyms
A 13610 | Chlorapatite | Estriol, unconjugated | Overstin | Tridestrin | Estriel (TN) | ESTRIOL [MART.] | Estriol [USP:INN:BAN:JAN] | Estra-1,3,5(10)-triene-3,16alpha,17beta-triol | 16a-Hydroxyestradiol | 16alpha-Hydroxy-17beta-estradiol | Estratriol | Es
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
100mg
E105514-100mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

229,90US$

267,90US$
Guardar 38,00 US$ (14.18%)
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Why this grade

Moligand™, analytical standard Analytical standard,Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

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

📋

Quality documents

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

📚

Literature proof

Cited in 55 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
A 13610 | Chlorapatite | Estriol, unconjugated | Overstin | Tridestrin | Estriel (TN) | ESTRIOL [MART.] | Estriol [USP:INN:BAN:JAN] | Estra-1, 3, 5(10)-triene-3, 16alpha, 17beta-triol | 16a-Hydroxyestradiol | 16alpha-Hydroxy-17beta-estradiol | Estratriol | Es
Especificaciones y pureza
Moligand™, analytical standard
Mecanismos bioquímicos y fisiológicos
Endogenous estrogen. GPR30 antagonist. Shows weak estrogenic effects when administered acutely but strong estrogenic effects when administered chronically. Shows antagonistic effects when combined with estradiol (IC 50 = 2 nM, ERα). Shows antiproliferativ
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Grado
Analytical standard, Moligand™
Tipo de acción
AGONIST, MODULATOR
Mecanismo de acción
Estrogen receptor modulator
Nota
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.
Nombres e identificadores
Sonrisas canónicasCC12CCC3C(C1CC(C2O)O)CCC4=C3C=CC(=C4)O
IUPAC Name(8R,9S,13S,14S,16R,17R)-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthrene-3,16,17-triol
InChIKeyPROQIPRRNZUXQM-ZXXIGWHRSA-N
INCHI1S/C18H24O3/c1-18-7-6-13-12-5-3-11(19)8-10(12)2-4-14(13)15(18)9-16(20)17(18)21/h3,5,8,13-17,19-21H,2,4,6-7,9H2,1H3/t13-,14-,15+,16-,17+,18+/m1/s1
Isómeros SMILES C[C@]12CC[C@H]3[C@H]([C@@H]1C[C@H]([C@@H]2O)O)CCC4=C3C=CC(=C4)O
WGK Alemania 3
RTECS KG8225000
Peso molecular 288.38
Beilstein 2508172
Reaxy-Rn 2057375
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2057375&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
SuperclassLipids and lipid-like molecules
ClaseSteroids and steroid derivatives
SubclassEstrane steroids
Intermediate Tree Nodes Not available
Direct ParentEstrogens and derivatives
Alternative Parents 3-hydroxysteroids  17-hydroxysteroids  16-alpha-hydroxysteroids  Phenanthrenes and derivatives  Tetralins  1-hydroxy-2-unsubstituted benzenoids  Secondary alcohols  Cyclic alcohols and derivatives  1,2-diols  Hydrocarbon derivatives  
Molecular FrameworkAromatic homopolycyclic compounds
Substituents Estrogen-skeleton - 3-hydroxysteroid - 17-hydroxysteroid - 16-hydroxysteroid - 16-alpha-hydroxysteroid - Hydroxysteroid - Phenanthrene - Tetralin - 1-hydroxy-2-unsubstituted benzenoid - Benzenoid - Cyclic alcohol - Secondary alcohol - 1,2-diol - Polyol - Organooxygen compound - Hydrocarbon derivative - Alcohol - Organic oxygen compound - Aromatic homopolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as estrogens and derivatives. These are steroids with a structure containing a 3-hydroxylated estrane.
External Descriptors C18 steroids (estrogens) and derivatives
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
ESR1 Tclin Estrogen receptor (4 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ESR2 Tclin Estrogen receptor beta (2 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
SHBG Tchem Sex hormone-binding globulin (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
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
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
CHRM4 Tclin Muscarinic acetylcholine receptor M4 (6041 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Agtr2 Angiotensin II type 2 (AT-2) receptor (803 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
Abcb1b P-glycoprotein 1 (174 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
Shbg Testis-specific androgen-binding protein (10 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mmp9 Matrix metalloproteinase 9 (38 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
cyp51 Lanosterol 14-alpha demethylase (36 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slco1a1 Solute carrier organic anion transporter family member 1A1 (265 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ESR1 Estrogen receptor (4 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slco1a3 Solute carrier organic anion transporter family member 1A3 (65 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Liver microsome (341 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
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.

3 results found

Lot NumberCertificate TypeFechaArticulo
E2203254Certificate of AnalysisOct 29, 2025 E105514
D2523020Certificate of AnalysisApr 24, 2025 E105514
I1203045Certificate of AnalysisNov 10, 2022 E105514
Propiedades químicas y físicas
Rotación específica [α]58 ° (C=0.4, Dioxane)
Punto de fusión (°C)282°C
Peso molecular288.400 g/mol
XLogP32.500
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count3
Rotatable Bond Count0
Exact Mass288.173 Da
Monoisotopic Mass288.173 Da
Topological Polar Surface Area60.700 Ų
Heavy Atom Count21
Formal Charge0
Complexity411.000
Isotope Atom Count0
Defined Atom Stereocenter Count6
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. Lianxu Wang, Zhen Lei, Sining Yun, Xiaohuan Yang, Rong Chen.  (2023)  Quantitative structure-biotransformation relationships of organic micropollutants in aerobic and anaerobic wastewater treatments.  SCIENCE OF THE TOTAL ENVIRONMENT,      [PMID:38072270] [10.1016/j.scitotenv.2023.169170]
2. Cheng Yang, Zheng–Lian Mo, Qiu–Fang Zhang, Jin–Jie Xu, Xiao–Fang Shen, Yue–Hong Pang.  (2023)  Membrane–protected magnetic covalent organic framework for efficient extraction of estrogens in dairy products.  FOOD CHEMISTRY,      [PMID:37979275] [10.1016/j.foodchem.2023.137984]
3. Yue Bao, Yixin Zhai, Siyuan Di, Hailan Qin, Shukui Zhu.  (2023)  Room-temperature synthesis of magnetic thiophene-based covalent organic frameworks for derivatization-assisted GC–MS analysis of estrogens in environmental water.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2023.109524]
4. Min Jia, Fupei Xu, Fei Zhai, Xiaoying Yu, Meixia Du.  (2023)  An all-in-one portable colorimetric detection platform for sensitive detection of bisphenol A based on target-mediated CeO2@ZIF-8/Apt biocomposites.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,      [PMID:37845127] [10.1016/j.jcis.2023.10.055]
5. Tianrun Qian, Jia Bao, Xuepeng Liu, Gerile Oudeng, Weiwei Ye.  (2023)  A “turn-on” fluorescence resonance energy transfer aptasensor based on carbon dots and gold nanoparticles for 17β-estradiol detection in sea salt.  RSC Advances,  13  (40): (27772-27781).  [PMID:37731834] [10.1039/D3RA05410A]
6. Rui Zhao, Cheng Cheng, Xiurong Wu, Xueyan Bai, Fenghuan Wang.  (2023)  Post-synthetic modification of NH2-MIL-101(Al)@SiO2 with different non-polar ligands for improving HPLC separation performance of estrogens.  JOURNAL OF SOLID STATE CHEMISTRY,      [PMID:] [10.1016/j.jssc.2023.124289]
7. Lixia Lu, Bingchan Song, Jianwen Gao, Xinyu Shao.  (2023)  A ratiometric aptasensor for simultaneous determination of two estrogens based on multicolor upconversion nanoparticles.  SENSORS AND ACTUATORS B-CHEMICAL,      [PMID:] [10.1016/j.snb.2023.133842]
8. Qing Liu, Chao Yan, Yan Wang.  (2023)  Submicron Nonporous Silica Particles for Enhanced Separation Performance in pCEC.  MOLECULES,  28  (8): (3542).  [PMID:37110774] [10.3390/molecules28083542]
9. Chengjiang Zhang, Yuhuang Li, Hongmei Yuan, Zeyi Lu, Qi Zhang, Lirong Zhao.  (2023)  Methacrylate bonded covalent organic framework monolithic column online coupling with high-performance liquid chromatography for analysis of trace estrogens in food.  JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES,      [PMID:37059013] [10.1016/j.jchromb.2023.123697]
10. Haojie Zeng, Feiyun Sun, Jianjun Zhang, Ying Wang, Songwen Yang, Dingyu Xing.  (2023)  Gradient crosslinking optimization for the selective layer to prepare polyvinyl alcohol (PVA) nanofiltration (NF) membrane: The enhanced filtration performance and potential rejection for EDCs.  JOURNAL OF MEMBRANE SCIENCE,      [PMID:] [10.1016/j.memsci.2023.121548]
11. Xuhong Cai, Junbo Liu, Dadong Liang, Shanshan Tang, Bao Xu.  (2023)  Construction of a QCM sensor for detecting diethylstilbestrol in water based on the computational design of molecularly imprinted polymers.  Arabian Journal of Chemistry,      [PMID:] [10.1016/j.arabjc.2023.104601]
12. Tiansheng Chou, Xiaosheng Huang, Jiawei Liu, Xinhua Liu, Kun Zeng, Zonghui Yan, Shaoyi Mei, Liangnan Sun, Wenqun Xi, Jinglan Ni, Jin Zi, Jun Zhao, Siqi Liu.  (2022)  First Evidence Indicates the Physiology- and Axial-Myopia-Dependent Profiles of Steroid Hormones in Aqueous Humor.  Metabolites,  12  (12): (1220).  [PMID:36557258] [10.3390/metabo12121220]
13. Lanbo Bi, Jimin Shen, Zhuoran Yao, Jing Kang, Shengxin Zhao, Pengwei Yan, Binyuan Wang, Zhonglin Chen.  (2022)  Preparation and Adsorption Properties of Magnetic Molecularly Imprinted Polymers for Selective Recognition of 17β-Estradiol.  Separations,  (11): (381).  [PMID:] [10.3390/separations9110381]
14. Liangliang He, Chanjuan Chen, Shuyi Duan, Yang Li, Chuan Li, Xinsheng Yao, Frank J. Gonzalez, Zifei Qin, Zhihong Yao.  (2022)  Inhibition of estrogen sulfation by Xian-Ling-Gu-Bao capsule.  JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY,      [PMID:36152789] [10.1016/j.jsbmb.2022.106182]
15. Wenjing Wang, Fei Zhai, Fupei Xu, Min Jia.  (2022)  Enzyme-free amplified and one-step rapid detection of bisphenol A using dual-terminal labeled split aptamer probes.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2022.107977]
16. Yanqun Yang, Yipeng Huang, Zhuqiang Wu, Rui Shi, Zhengyi Chen, Guihua Ruan.  (2022)  Porous capillary monolithic column coupled with ultrahigh performance liquid chromatography-tandem mass spectrometry for fast and effective separation and determination of estrogens.  ANALYTICA CHIMICA ACTA,      [PMID:36089309] [10.1016/j.aca.2022.340270]
17. Jin Liu, Xuhong Cai, Junbo Liu, Dadong Liang, Kaiyin Chen, Shanshan Tang, Bao Xu.  (2022)  Study on the Preparation of Estrone Molecularly Imprinted Polymers and Their Application in a Quartz Crystal Microbalance Sensor via a Computer-Assisted Design.  INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES,  23  (10): (5758).  [PMID:35628568] [10.3390/ijms23105758]
18. Lingli Zhang, Han Tao, Chun Ji, Qiaoling Wu, Xiao Wang, Yuangeng Wu.  (2022)  Sensitive and direct electrochemical detection of bisphenol S based on 1T&2H-MoS2/CNTs-NH2 nanocomposites.  NEW JOURNAL OF CHEMISTRY,  46  (17): (8203-8214).  [PMID:] [10.1039/D2NJ00866A]
19. Huizhong Si, Pingping He, Xuemei Wang, Lin Li, Xiaohong Hou.  (2021)  Metal organic framework/chitosan/polyethylene oxide composite columnar foam as a sorbent for the enrichment and determination of estrogens in environmental aqueous solutions.  NEW JOURNAL OF CHEMISTRY,  46  (2): (808-819).  [PMID:] [10.1039/D1NJ02426D]
20. Yi Zhang, Jie Zhou, Xiao-Xiao Zhang, Wen-Long Wang, Cheng Yang, Xueli Shi, Yong-Wei Feng, Renagul Abdurahman.  (2021)  NIR persistent luminescence nanoparticles based turn-on aptasensor for autofluorescence-free determination of 17β-estradiol in milk.  FOOD CHEMISTRY,      [PMID:34717086] [10.1016/j.foodchem.2021.131432]
21. Yue Wang, Wenchang Zhao, Ruixia Gao, Sameer Hussain, Yi Hao, Jiahao Tian, Shihui Chen, Yunhao Feng, Yubo Zhao, Yuyao Qu.  (2021)  Preparation of lightweight daisy-like magnetic molecularly imprinted polymers via etching synergized template immobilization for enhanced rapid detection of trace 17β-estradiol.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:34592596] [10.1016/j.jhazmat.2021.127216]
22. Yi Zhang, Lingling Wang, Wen-Long Wang, Cheng Yang, Yongwei Feng, Xueli Shi.  (2021)  Visual-afterglow dual-mode immunochromatographic strip for 17β-estradiol detection in milk.  TALANTA,      [PMID:34074413] [10.1016/j.talanta.2021.122427]
23. Huihui Zhao, Linyan Yang, Xueming Chen, Mei Sheng, Guomin Cao, Lankun Cai, Shujuan Meng, Chuyang Y. Tang.  (2021)  Degradation of Polyamide Nanofiltration Membranes by Bromine: Changes of Physiochemical Properties and Filtration Performance.  ENVIRONMENTAL SCIENCE & TECHNOLOGY,      [PMID:33848140] [10.1021/acs.est.1c00206]
24. Chaoqiang Pan, Jianmin Qiu, Lumei Wang, Zhiyu Yan, Weiwen Huang, Dongwei Zhang, Xuejia Zhan, Guoqing Shen, Chaoqiang Pan, Jianmin Qiu, Lumei Wang, Zhiyu Yan, Weiwen Huang, Dongwei Zhang, Xuejia Zhan, Guoqing Shen.  (2020)  Colorimetric Aptasensor for Testosterone Detection Based on Aggregation of Gold Nanoparticles Induced by Cationic Surfactant.  AUSTRALIAN JOURNAL OF CHEMISTRY,  74  (4): (261-267).  [PMID:] [10.1071/CH20237]
25. Xing Tian, Huijia Song, Yue Wang, Xuemeng Tian, Yuhai Tang, Ruixia Gao, Chengxiao Zhang.  (2020)  Hydrophilic magnetic molecularly imprinted nanobeads for efficient enrichment and high performance liquid chromatographic detection of 17beta-estradiol in environmental water samples.  TALANTA,      [PMID:32928396] [10.1016/j.talanta.2020.121367]
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