On the public citation graph

Structure−Activity Relationships of Selective Estrogen Receptor Modulators: Modifications to the 2-Arylbenzothiophene Core of Raloxifene

0 signed · 228 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/jbmr.5650110615openalex-snapshot
A controlled trial of raloxifene (LY139481) HCl: Impact on bone turnover and serum lipid profile in healthy postmenopausal women
inferredcites →https://doi.org/10.1007/978-1-4471-1799-5_15openalex-snapshot
Oestrogens and Cancer
inferredcites →https://doi.org/10.1007/978-1-4471-1799-5_17openalex-snapshot
Oestrogen Replacement Therapy and Cardiovascular Disease
inferredcites →https://doi.org/10.1007/bf00689672openalex-snapshot
Alternative mechanisms of action of anti-oestrogens
inferredcites →https://doi.org/10.1016/0022-1759(91)90094-vopenalex-snapshot
A kinetic assay for eosinophil peroxidase activity in eosinophils and eosinophil conditioned media
inferredcites →https://doi.org/10.1016/0022-4731(73)90076-9openalex-snapshot
The specificity of the estrogen receptor of human uterus
inferredcites →https://doi.org/10.1016/0022-4731(88)90004-0openalex-snapshot
A chemical classification of nonsteroidal antagonists of sex-steroid hormone action
inferredcites →https://doi.org/10.1016/0022-4731(88)90017-9openalex-snapshot
Non-genomic effects of estrogens and antiestrogens
inferredcites →https://doi.org/10.1016/0039-128x(95)00219-gopenalex-snapshot
Site-directed estrogen receptor antibodies stabilize 4-hydroxytamoxifen ligand, but not estradiol, and indicate ligand-specific differences in the recognition of estrogen response element DNA in vitro
inferredcites →https://doi.org/10.1016/0167-4889(88)90115-2openalex-snapshot
Effect of estradiol and antiestrogens on cholesterol biosynthesis in hormone-dependent and -independent breast cancer cell lines
inferredcites →https://doi.org/10.1016/0223-5234(94)90122-8openalex-snapshot
Synthesis, binding affinities and uterotrophic activity of some 2-substituted estradiol and ring-A-fused pyrone derivatives
inferredcites →https://doi.org/10.1016/0960-0760(94)90268-2openalex-snapshot
Design of novel antiestrogens
inferredcites →https://doi.org/10.1016/0960-894x(95)00575-eopenalex-snapshot
Synthesis and pharmacology of 2-alkyl raloxifene analogs
inferredcites →https://doi.org/10.1016/1040-8428(93)90044-5openalex-snapshot
The biological evaluation of novel antioestrogens for the treatment of breast cancer
inferredcites →https://doi.org/10.1016/1071-5576(96)82635-9openalex-snapshot
Selective estrogen receptor modulators: pharmacological profile in the rat uterus.
inferredcites →https://doi.org/10.1016/8756-3282(96)00085-3openalex-snapshot
Time-dependent changes in biochemical bone markers and serum cholesterol in ovariectomized rats: Effects of raloxifene HCl, tamoxifen, estrogen, and alendronate
inferredcites →https://doi.org/10.1016/s0015-0282(16)55667-2openalex-snapshot
Current concepts in estrogen replacement therapy in the menopause
inferredcites →https://doi.org/10.1016/s0022-3565(24)36384-0openalex-snapshot
Hypocholesterolemic Activity of Raloxifene (LY139481): Pharmacological Characterization as a Selective Estrogen Receptor Modulator
inferredcites →https://doi.org/10.1016/s0022-3565(25)24554-2openalex-snapshot
Longitudinal and cross-sectional analysis of raloxifene effects on tibiae from ovariectomized aged rats.
inferredcites →https://doi.org/10.1016/s0025-6196(12)62374-xopenalex-snapshot
Osteoporosis: Etiology, Diagnosis, and Management
inferredcites →https://doi.org/10.1021/ja00772a043openalex-snapshot
Protection of hydroxyl groups as tert-butyldimethylsilyl derivatives
inferredcites →https://doi.org/10.1021/ja00772a044openalex-snapshot
Direct evidence from carbon-13 nuclear magnetic resonance for intramolecular scrambling of carbonyl groups in a metal atom cluster carbonyl, tetrarhodium dodecacarbonyl
inferredcites →https://doi.org/10.1021/jm00127a040openalex-snapshot
17-Desoxy estrogen analogs
inferredcites →https://doi.org/10.1021/jm00127a041openalex-snapshot
Renin inhibitors. Synthesis of transition-state analog inhibitors containing phosphorus acid derivatives at the scissile bond
inferredcites →https://doi.org/10.1021/jm00129a024openalex-snapshot
2-Arylindenes and 2-arylindenones: molecular structures and considerations in the binding orientation of unsymmetrical nonsteroidal ligands to the estrogen receptor
inferredcites →https://doi.org/10.1021/jm00129a025openalex-snapshot
4-(Phosphonoalkyl)- and 4-(phosphonoalkenyl)-2-piperidinecarboxylic acids: synthesis, activity at N-methyl-D-aspartic acid receptors and anticonvulsant activity
inferredcites →https://doi.org/10.1021/jm00172a008openalex-snapshot
Torsionally and hydrophobically modified 2,3-diarylindenes as estrogen-receptor ligands
inferredcites →https://doi.org/10.1021/jm00172a009openalex-snapshot
Synthesis of acyclic and dehydroaspartic acid analogs of Ac-Asp-Glu-OH and their inhibition of rat brain N-acetylated .alpha.-linked acidic dipeptidase (NAALA dipeptidase)
inferredcites →https://doi.org/10.1021/jm00374a021openalex-snapshot
Antiestrogens. 2. Structure-activity studies in a series of 3-aroyl-2-arylbenzo[b]thiophene derivatives leading to [6-hydroxy-2-(4-hydroxyphenyl)benzo[b]thien-3-yl]-[4-[2-(1-piperidinyl)ethoxy]phenyl]methanone hydrochloride (LY 156758), a remarkably effective estrogen antagonist with only minimal…
inferredcites →https://doi.org/10.1021/jm9508245openalex-snapshot
2-(Hydroxyalkyl)estradiols: Synthesis and Biological Evaluation
inferredcites →https://doi.org/10.1021/jo00002a039openalex-snapshot
Mechanical activation of magnesium turnings for the preparation of reactive Grignard reagents
inferredcites →https://doi.org/10.1021/jo00002a040openalex-snapshot
Isodicyclopentadienes and related molecules. 53. Unsymmetrical oxidative cleavage of cyclic ketones. Conversion to .omega.-ethoxycarbonyl aldoximes under alkaline conditions
inferredcites →https://doi.org/10.1021/jo00399a022openalex-snapshot
Stereochemical aspects of substitution reactions of stannyl and germyl anionoids with cyclohexyl derivatives
inferredcites →https://doi.org/10.1021/jo00399a023openalex-snapshot
Use of the thallium trinitrate catalyzed rearrangement of ketones in the synthesis of an acidic morphinan derivative
inferredcites →https://doi.org/10.1021/jo01014a059openalex-snapshot
The Characterization of Complex Phenols by Nuclear Magnetic Resonance Spectra
inferredcites →https://doi.org/10.1039/p19740001168openalex-snapshot
Condensed thiophen ring systems. Part XV. Preparation and some reactions of 2- and 3-(secondary amino)benzo[b]thiophens
inferredcites →https://doi.org/10.1055/s-1993-25931openalex-snapshot
Synthetic Transformations of Vinyl and Aryl Triflates
inferredcites →https://doi.org/10.1056/nejm199410203311604openalex-snapshot
Estrogen Resistance Caused by a Mutation in the Estrogen-Receptor Gene in a Man
inferredcites →https://doi.org/10.1056/nejm199506153322401openalex-snapshot
The Use of Estrogens and Progestins and the Risk of Breast Cancer in Postmenopausal Women
inferredcites →https://doi.org/10.1073/pnas.93.12.5925openalex-snapshot
Cloning of a novel receptor expressed in rat prostate and ovary.
inferredcites →https://doi.org/10.1080/00397918208061938openalex-snapshot
An Alternative Procedure for the Aluminum-Mediated Conversion of Esters to Amides
inferredcites →https://doi.org/10.1093/clinchem/30.3.352openalex-snapshot
Influence of incomplete cholesteryl ester hydrolysis on enzymic measurements of cholesterol.
inferredcites →https://doi.org/10.1096/fasebj.10.8.8666168openalex-snapshot
Raloxifene, tamoxifen, nafoxidine, or estrogen effects on reproductive and nonreproductive tissues in ovariectomized rats
inferredcites →https://doi.org/10.1111/j.1476-5381.1993.tb13840.xopenalex-snapshot
A current view of tamoxifen for the treatment and prevention of breast cancer
inferredcites →https://doi.org/10.1111/j.1749-6632.1995.tb31374.xopenalex-snapshot
Cellular Mechanisms Which Distinguish between Hormone‐ and Antihormone‐Activated Estrogen Receptor
inferredcites →https://doi.org/10.1139/v87-302openalex-snapshot
Destabilized carbocations. Nuclear magnetic resonance detection and reactivities of aryl α-thioformamidyl cations
inferredcites →https://doi.org/10.1172/jci116985openalex-snapshot
Raloxifene (LY139481 HCI) prevents bone loss and reduces serum cholesterol without causing uterine hypertrophy in ovariectomized rats.
inferredcites →https://doi.org/10.1210/edrv-16-1-35openalex-snapshot
Estrogen Receptors in Human Nontarget Tissues: Biological and Clinical Implications*
inferredcites →https://doi.org/10.1210/en.137.5.2075openalex-snapshot
Estrogen and raloxifene stimulate transforming growth factor-beta 3 gene expression in rat bone: a potential mechanism for estrogen- or raloxifene-mediated bone maintenance
inferredcites →https://doi.org/10.1210/me.10.2.119openalex-snapshot
Tripartite steroid hormone receptor pharmacology: interaction with multiple effector sites as a basis for the cell- and promoter-specific action of these hormones
inferredcites →https://doi.org/10.1210/me.9.6.659openalex-snapshot
Analysis of estrogen receptor function in vitro reveals three distinct classes of antiestrogens
inferredcites →https://doi.org/10.1246/bcsj.62.591openalex-snapshot
A Mild Selective Monobromination Reagent System for Alkoxybenzenes; N-Bromosuccinimide–Silica Gel
inferredcites →https://doi.org/10.2174/0929867301666220210212635openalex-snapshot
The Medicinal Chemistry of Nonsteroidal Antiestrogens: A Review
inferredcites →https://doi.org/10.2174/092986730303220225103819openalex-snapshot
Antiestrogens as Calmodulin Antagonists
inferredcites →https://doi.org/10.3891/acta.chem.scand.46-0654openalex-snapshot
Pyridine-Substituted Hydroxythiophenes. I. Preparation of o-(2-, 3- and 4-pyridyl)-3-hydroxythiophenes.

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4588397openalex-extracted
inferred← citeshttps://doi.org/10.1001/jama.279.18.1445openalex-snapshot
Effects of Raloxifene on Serum Lipids and Coagulation Factors in Healthy Postmenopausal Women
inferred← citeshttps://doi.org/10.1002/0471266949.bmc054openalex-snapshot
Female Sex Hormones, Contraceptives, And Fertility Drugs
inferred← citeshttps://doi.org/10.1002/0471266949.bmc054.pub2openalex-snapshot
Estrogen Receptor Modulators
inferred← citeshttps://doi.org/10.1002/9780470768594.ch20openalex-snapshot
Raloxifene, Evista: A Selective Estrogen Receptor Modulator (SERM)
inferred← citeshttps://doi.org/10.1002/9781118219683.ch15openalex-snapshot
Raloxifene: A Selective Estrogen Receptor Modulator (SERM)
inferred← citeshttps://doi.org/10.1002/9783527623297.ch4openalex-snapshot
Subtype‐Selective Estrogens
inferred← citeshttps://doi.org/10.1002/chem.201904761openalex-snapshot
Transition‐Metal‐Free Synthesis of Heterobiaryls through 1,2‐Migration of Boronate Complex
inferred← citeshttps://doi.org/10.1002/cmdc.200700104openalex-snapshot
Structure–Activity Relationships for a Family of Benzothiophene Selective Estrogen Receptor Modulators Including Raloxifene and Arzoxifene
inferred← citeshttps://doi.org/10.1002/ejoc.201700963openalex-snapshot
One‐Pot Synthesis of 2‐(Aryl/Alkyl)amino‐3‐cyanobenzo[b]thiophenes and Their Hetero‐Fused Analogues by Pd‐Catalyzed Intramolecular Oxidative C–H Functionalization/Arylthiolation
inferred← citeshttps://doi.org/10.1002/med.1024openalex-snapshot
Different ligands–different receptor conformations: Modeling of the hERα LBD in complex with agonists and antagonists
inferred← citeshttps://doi.org/10.1002/med.21510openalex-snapshot
Small‐molecule inhibitors of multidrug resistance‐associated protein 1 and related processes: A historic approach and recent advances
inferred← citeshttps://doi.org/10.1007/978-1-59259-152-7_6openalex-snapshot
Preclinical Studies of Raloxifene and Related Compounds
inferred← citeshttps://doi.org/10.1007/978-1-59259-223-4_6openalex-snapshot
Tamoxifen and Other Antiestrogens in Prevention and Therapy of Breast Cancer
inferred← citeshttps://doi.org/10.1007/978-1-59259-375-0_19openalex-snapshot
Androgen Replacement Therapy of Male Hypogonadism
inferred← citeshttps://doi.org/10.1007/978-1-59259-700-0_16openalex-snapshot
Androgen Replacement Therapy of Male Hypogonadism
inferred← citeshttps://doi.org/10.1007/978-3-030-78315-0_4openalex-snapshot
Chemical Considerations in Discovery of Receptor Modulators
inferred← citeshttps://doi.org/10.1007/978-3-319-99350-8_10openalex-snapshot
Structural Insights into Estrogen Receptors and Antiestrogen Therapies
inferred← citeshttps://doi.org/10.1007/978-3-642-58616-3_4openalex-snapshot
Antiestrogens and Partial Agonists
inferred← citeshttps://doi.org/10.1007/978-3-642-58616-3_5openalex-snapshot
Structure-Activity Relationships
inferred← citeshttps://doi.org/10.1007/978-981-16-5613-2_26openalex-snapshot
Selective Estrogen Receptor Modulators (SERMs)
inferred← citeshttps://doi.org/10.1007/s00894-004-0198-5openalex-snapshot
LIV-3D-QSAR model for estrogen receptor ligands
inferred← citeshttps://doi.org/10.1007/s10593-011-0737-9openalex-snapshot
Acylation of 3-acyl-2-methylbenzo[b]thiophene
inferred← citeshttps://doi.org/10.1007/s10593-013-1310-5openalex-snapshot
Synthesis of substituted benzo[b]selenophenes
inferred← citeshttps://doi.org/10.1007/s11164-016-2763-9openalex-snapshot
Synthesis and biological evaluation of novel active arylidene derivatives of 5,6-dihydro-4H-cyclopenta[b]- and 4,5,6,7-tetrahydrobenzo[b]-thiophene-2-carboxylic acid
inferred← citeshttps://doi.org/10.1016/b0-08-045044-x/00294-7openalex-snapshot
Raloxifene
inferred← citeshttps://doi.org/10.1016/j.bmc.2004.05.015openalex-snapshot
Synthesis, pharmacological evaluation, and structure–activity relationships of benzopyran derivatives with potent SERM activity
inferred← citeshttps://doi.org/10.1016/j.bmc.2004.11.051openalex-snapshot
In vitro evaluation of the anti-estrogenic activity of hydroxyl substituted diphenylnaphthyl alkene ligands for the estrogen receptor
inferred← citeshttps://doi.org/10.1016/j.bmc.2008.09.035openalex-snapshot
Synthesis, biological evaluation, structural–activity relationship, and docking study for a series of benzoxepin-derived estrogen receptor modulators
inferred← citeshttps://doi.org/10.1016/j.bmc.2010.06.016openalex-snapshot
2-Phenyl-1-[4-(2-piperidine-1-yl-ethoxy)benzyl]-1H-benzimidazoles as ligands for the estrogen receptor: Synthesis and pharmacological evaluation
inferred← citeshttps://doi.org/10.1016/j.bmc.2011.07.056openalex-snapshot
Design and synthesis of 1,3-biarylsulfanyl derivatives as new anti-breast cancer agents
inferred← citeshttps://doi.org/10.1016/j.bmc.2013.03.083openalex-snapshot
Discovery of 3-phenyl-1H-5-pyrazolylamine derivatives containing a urea pharmacophore as potent and efficacious inhibitors of FMS-like tyrosine kinase-3 (FLT3)
inferred← citeshttps://doi.org/10.1016/j.bmc.2015.12.045openalex-snapshot
Structural features underlying raloxifene’s biophysical interaction with bone matrix
inferred← citeshttps://doi.org/10.1016/j.bmc.2016.04.068openalex-snapshot
Synthesis and evaluation of raloxifene derivatives as a selective estrogen receptor down-regulator
inferred← citeshttps://doi.org/10.1016/j.bmcl.2003.09.049openalex-snapshot
4-(4-Alkylpiperazin-1-yl)phenyl group: A novel class of basic side chains for selective estrogen receptor modulators
inferred← citeshttps://doi.org/10.1016/j.bmcl.2004.07.072openalex-snapshot
Benzothiophene and naphthalene derived constrained SERMs
inferred← citeshttps://doi.org/10.1016/j.bmcl.2004.12.074openalex-snapshot
Benzothiophenes containing a piperazine side chain as selective ligands for the estrogen receptor α and their bioactivities in vivo
inferred← citeshttps://doi.org/10.1016/j.bmcl.2007.02.002openalex-snapshot
Identification of a series of tetrahydroisoquinoline derivatives as potential therapeutic agents for breast cancer
inferred← citeshttps://doi.org/10.1016/j.bmcl.2007.04.044openalex-snapshot
Structure–activity relationships of SERMs optimized for uterine antagonism and ovarian safety
inferred← citeshttps://doi.org/10.1016/j.bmcl.2007.04.051openalex-snapshot
Benzopyrans as selective estrogen receptor β agonists (SERBAs). Part 2: Structure–activity relationship studies on the benzopyran scaffold
inferred← citeshttps://doi.org/10.1016/j.bmcl.2010.06.151openalex-snapshot
A mutant selective anti-estrogen is a pure antagonist on EREs and AP-1 response elements
inferred← citeshttps://doi.org/10.1016/j.bmcl.2012.05.116openalex-snapshot
3-Phenyl-1H-5-pyrazolylamine-based derivatives as potent and efficacious inhibitors of FMS-like tyrosine kinase-3 (FLT3)
inferred← citeshttps://doi.org/10.1016/j.bone.2014.01.009openalex-snapshot
Bone cell-independent benefits of raloxifene on the skeleton: A novel mechanism for improving bone material properties
inferred← citeshttps://doi.org/10.1016/j.bonr.2020.100246openalex-snapshot
6′-Methoxy Raloxifene-analog enhances mouse bone properties with reduced estrogen receptor binding
inferred← citeshttps://doi.org/10.1016/j.cbi.2005.02.007openalex-snapshot
Effects of analogs of indole-3-carbinol cyclic trimerization product in human breast cancer cells
inferred← citeshttps://doi.org/10.1016/j.chembiol.2016.04.009openalex-snapshot
Controlling Sulfuryl-Transfer Biology
inferred← citeshttps://doi.org/10.1016/j.ejmech.2011.05.008openalex-snapshot
Synthesis, structure and cytotoxicity of 3-C, N, S, Se substituted benzo[b]selenophene derivatives
inferred← citeshttps://doi.org/10.1016/j.ejmech.2012.02.021openalex-snapshot
Recent advances in the synthesis of raloxifene: A selective estrogen receptor modulator
inferred← citeshttps://doi.org/10.1016/j.ejmech.2013.06.048openalex-snapshot
3D-QSAR using pharmacophore-based alignment and virtual screening for discovery of novel MCF-7 cell line inhibitors
inferred← citeshttps://doi.org/10.1016/j.ejmech.2015.05.008openalex-snapshot
Identification of a potent 5-phenyl-thiazol-2-ylamine-based inhibitor of FLT3 with activity against drug resistance-conferring point mutations
inferred← citeshttps://doi.org/10.1016/j.ejmech.2016.02.026openalex-snapshot
Design and synthesis of novel tamoxifen analogues that avoid CYP2D6 metabolism
inferred← citeshttps://doi.org/10.1016/j.ejmech.2017.07.038openalex-snapshot
An overview of benzo [b] thiophene-based medicinal chemistry
inferred← citeshttps://doi.org/10.1016/j.ejmech.2026.118890openalex-snapshot
Benzothiophene nucleus in target-directed anti-cancer drug discovery
inferred← citeshttps://doi.org/10.1016/j.ejphar.2006.03.033openalex-snapshot
Raloxifene promotes adipocyte differentiation of 3T3-L1 cells
inferred← citeshttps://doi.org/10.1016/j.jmgm.2007.06.003openalex-snapshot
Pharmacophore mapping of arylbenzothiophene derivatives for MCF cell inhibition using classical and 3D space modeling approaches
inferred← citeshttps://doi.org/10.1016/j.mce.2025.112569openalex-snapshot
Selective steroid receptor modulators, degraders and PROTACs: Therapeutic strategies in management of endocrine-related cancers
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2017.12.012openalex-snapshot
Selective estrogen receptor modulators (SERMs) and selective estrogen receptor degraders (SERDs) in cancer treatment
inferred← citeshttps://doi.org/10.1016/j.steroids.2004.07.005openalex-snapshot
Plant 2-arylobenzofurans demonstrate a selective estrogen receptor modulator profile
inferred← citeshttps://doi.org/10.1016/j.steroids.2006.01.001openalex-snapshot
Three-dimensional models of non-steroidal ligands: A comparative molecular field analysis
inferred← citeshttps://doi.org/10.1016/j.taap.2006.12.012openalex-snapshot
Characterization of Bizzy Nut extracts in estrogen-responsive MCF-7 breast cancer cells
inferred← citeshttps://doi.org/10.1016/j.tet.2010.01.069openalex-snapshot
A convenient approach towards 2- and 3-aminobenzo[b]thiophenes
inferred← citeshttps://doi.org/10.1016/j.tet.2018.03.067openalex-snapshot
Efficient synthesis of 3-benzoyl Benzo[b]thiophenes and raloxifene via Mercury(II)-Catalyzed cyclization of 2-alkynylphenyl alkyl sulfoxides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.01.141openalex-snapshot
Efficient synthesis of 3-oxygenated benzothiophene derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.05.043openalex-snapshot
Bromination of 3-substituted benzo[b]thiophenes: access to Raloxifen intermediate
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.10.096openalex-snapshot
Design and synthesis of condensed thienocoumarins by Suzuki–Miyaura reaction/lactonization tandem protocol
inferred← citeshttps://doi.org/10.1016/s0006-2952(02)00893-6openalex-snapshot
Characterization of selective estrogen receptor modulator (SERM) activity in two triarylethylene oxybutyric acids
inferred← citeshttps://doi.org/10.1016/s0031-6997(24)01358-9openalex-snapshot
Basic Guide to the Mechanisms of Antiestrogen Action
inferred← citeshttps://doi.org/10.1016/s0040-4039(98)02533-7openalex-snapshot
Nucleophilic aromatic substitution on 3-aroyl-2-arylbenzothiophenes. Rapid access to raloxifene and other selective estrogen receptor modulators
inferred← citeshttps://doi.org/10.1016/s0040-4039(99)00955-7openalex-snapshot
Synergistic methodologies for the synthesis of 3-aroyl-2-arylbenzo[b]thiophene-based selective estrogen receptor modulators. Two concise syntheses of raloxifene
inferred← citeshttps://doi.org/10.1016/s0065-7743(01)36055-4openalex-snapshot
Chapter 15. Targeting the estrogen receptor with SERMs
inferred← citeshttps://doi.org/10.1016/s0166-1280(02)00623-1openalex-snapshot
QSAR models in receptor-mediated effects: the nuclear receptor superfamily
inferred← citeshttps://doi.org/10.1016/s0889-8588(05)70281-1openalex-snapshot
CHEMOPREVENTION OF BREAST CANCER IN THE OLDER PATIENT
inferred← citeshttps://doi.org/10.1016/s0889-8588(05)70305-1openalex-snapshot
BREAST CANCER CHEMOPREVENTION
inferred← citeshttps://doi.org/10.1016/s0950-3552(98)80064-3openalex-snapshot
7 Other medical management of uterine fibroids
inferred← citeshttps://doi.org/10.1016/s0960-0760(03)00385-6openalex-snapshot
Structure activity relationship studies on C2 side chain substituted 1,1-bis(4-methoxyphenyl)-2-phenylalkenes and 1,1,2-tris(4-methoxyphenyl)alkenes
inferred← citeshttps://doi.org/10.1016/s0960-894x(02)00613-3openalex-snapshot
Solid-Phase synthesis and investigation of benzofurans as selective estrogen receptor modulators
inferred← citeshttps://doi.org/10.1016/s0960-894x(99)00050-5openalex-snapshot
Novel nonsteroidal selective estrogen receptor modulators. Carbon and heteroatom replacement of oxygen in the ethoxypiperidine region of raloxifene
inferred← citeshttps://doi.org/10.1016/s0960-894x(99)00076-1openalex-snapshot
Dibasic benzo[b]thiophene derivatives as a novel class of active site directed thrombin inhibitors: 4. SAR studies on the conformationally restricted C3-side chain of hydroxybenzo[b]thiophenes
inferred← citeshttps://doi.org/10.1016/s0960-894x(99)00143-2openalex-snapshot
A new anti-tubulin agent containing the benzo[b]thiophene ring system
inferred← citeshttps://doi.org/10.1016/s0960-894x(99)00145-6openalex-snapshot
Synthesis and biological activity of trans-2,3-dihydroraloxifene
inferred← citeshttps://doi.org/10.1016/s0960-894x(99)00610-1openalex-snapshot
Reversal of resistance in multidrug resistance protein (MRP1)-overexpressing cells by LY329146
inferred← citeshttps://doi.org/10.1016/s0968-0896(02)00329-2openalex-snapshot
Synthesis and estrogen receptor affinity of a 4-hydroxytamoxifen-Labeled ligand for diagnostic imaging
inferred← citeshttps://doi.org/10.1016/s0968-0896(03)00362-6openalex-snapshot
Synthesis and binding affinities of fluoroalkylated raloxifenes
inferred← citeshttps://doi.org/10.1016/s1387-1609(00)00118-3openalex-snapshot
The first organometallic antioestrogens and their antiproliferative effects
inferred← citeshttps://doi.org/10.1021/ac991413popenalex-snapshot
Bioanalytical High-Throughput Selected Reaction Monitoring-LC/MS Determination of Selected Estrogen Receptor Modulators in Human Plasma: 2000 Samples/Day
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.4c03065openalex-snapshot
From Bones to Bugs: Structure-Based Development of Raloxifene-Derived Pathoblockers That Inhibit Pyocyanin Production in Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.5b00054openalex-snapshot
Identification of GDC-0810 (ARN-810), an Orally Bioavailable Selective Estrogen Receptor Degrader (SERD) that Demonstrates Robust Activity in Tamoxifen-Resistant Breast Cancer Xenografts
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.5b01276openalex-snapshot
Selective Human Estrogen Receptor Partial Agonists (ShERPAs) for Tamoxifen-Resistant Breast Cancer
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.7b01682openalex-snapshot
Discovery of LSZ102, a Potent, Orally Bioavailable Selective Estrogen Receptor Degrader (SERD) for the Treatment of Estrogen Receptor Positive Breast Cancer
inferred← citeshttps://doi.org/10.1021/acsmedchemlett.4c00078openalex-snapshot
Synthesis Studies and the Evaluation of C6 Raloxifene Derivatives
inferred← citeshttps://doi.org/10.1021/bi0205092openalex-snapshot
Identification by MALDI-TOF Mass Spectrometry of 17α-Bromoacetamidopropylestradiol Covalent Attachment Sites on Estrogen Receptor α
inferred← citeshttps://doi.org/10.1021/bi9919706openalex-snapshot
The Major Cyclic Trimeric Product of Indole-3-carbinol Is a Strong Agonist of the Estrogen Receptor Signaling Pathway
inferred← citeshttps://doi.org/10.1021/ci2004779openalex-snapshot
Integrating Medicinal Chemistry, Organic/Combinatorial Chemistry, and Computational Chemistry for the Discovery of Selective Estrogen Receptor Modulators with F orecaster , a Novel Platform for Drug Discovery
inferred← citeshttps://doi.org/10.1021/ci200540yopenalex-snapshot
A Scaffold-Independent Subcellular Event-Based Analysis: Characterization of Significant Structural Modifications
inferred← citeshttps://doi.org/10.1021/ci900254bopenalex-snapshot
Pharmacophore Modeling for Qualitative Prediction of Antiestrogenic Activity
inferred← citeshttps://doi.org/10.1021/co100088qopenalex-snapshot
Highly Substituted Lactone/Ester-Containing Furan Library by the Palladium-Catalyzed Carbonylation of Hydroxyl-Substituted 3-Iodofurans
inferred← citeshttps://doi.org/10.1021/co200090popenalex-snapshot
Parallel Synthesis of a Desketoraloxifene Analogue Library via Iodocyclization/Palladium-Catalyzed Coupling
inferred← citeshttps://doi.org/10.1021/cr020101aopenalex-snapshot
Metalated Heterocycles and Their Applications in Synthetic Organic Chemistry
inferred← citeshttps://doi.org/10.1021/cr980018gopenalex-snapshot
Comparative QSAR Analysis of Estrogen Receptor Ligands
inferred← citeshttps://doi.org/10.1021/jm000170mopenalex-snapshot
Pyrazole Ligands: Structure−Affinity/Activity Relationships and Estrogen Receptor-α-Selective Agonists
inferred← citeshttps://doi.org/10.1021/jm010086mopenalex-snapshot
Design, Synthesis, and Preclinical Characterization of Novel, Highly Selective Indole Estrogens
inferred← citeshttps://doi.org/10.1021/jm0101601openalex-snapshot
Photochemical Synthesis of N-Arylbenzophenanthridine Selective Estrogen Receptor Modulators (SERMs)
inferred← citeshttps://doi.org/10.1021/jm020291hopenalex-snapshot
A New Series of Estrogen Receptor Modulators That Display Selectivity for Estrogen Receptor β
inferred← citeshttps://doi.org/10.1021/jm020450xopenalex-snapshot
Antiestrogens and Selective Estrogen Receptor Modulators as Multifunctional Medicines. 2. Clinical Considerations and New Agents
inferred← citeshttps://doi.org/10.1021/jm020536qopenalex-snapshot
De Novo Design, Synthesis, and Evaluation of Novel Nonsteroidal Phenanthrene Ligands for the Estrogen Receptor
inferred← citeshttps://doi.org/10.1021/jm0210562openalex-snapshot
Antiestrogenically Active 1,1,2-Tris(4-hydroxyphenyl)alkenes without Basic Side Chain: Synthesis and Biological Activity
inferred← citeshttps://doi.org/10.1021/jm030086hopenalex-snapshot
Estrogen Receptor Modulators: Identification and Structure−Activity Relationships of Potent ERα-Selective Tetrahydroisoquinoline Ligands
inferred← citeshttps://doi.org/10.1021/jm034243oopenalex-snapshot
Estrogen Receptor Ligands. II. Discovery of Benzoxathiins as Potent, Selective Estrogen Receptor α Modulators
inferred← citeshttps://doi.org/10.1021/jm050723zopenalex-snapshot
A Selective Estrogen Receptor Modulator Designed for the Treatment of Uterine Leiomyoma with Unique Tissue Specificity for Uterus and Ovaries in Rats
inferred← citeshttps://doi.org/10.1021/jm9705521openalex-snapshot
Three-Dimensional Quantitative Structure−Activity Relationship Study of Nonsteroidal Estrogen Receptor Ligands Using the Comparative Molecular Field Analysis/Cross-Validated r2-Guided Region Selection Approach
inferred← citeshttps://doi.org/10.1021/jm970688zopenalex-snapshot
Synthesis and Pharmacology of Conformationally Restricted Raloxifene Analogues: Highly Potent Selective Estrogen Receptor Modulators
inferred← citeshttps://doi.org/10.1021/jm990078uopenalex-snapshot
Carboxylic Acid Analogues of Tamoxifen: (Z)-2-[p-(1,2-Diphenyl-1-butenyl)phenoxy]-N,N-dimethylethylamine. Estrogen Receptor Affinity and Estrogen Antagonist Effects in MCF-7 Cells
inferred← citeshttps://doi.org/10.1021/jo034325kopenalex-snapshot
Synthesis of Constrained Raloxifene Analogues by Complementary Use of Friedel−Crafts and Directed Remote Metalation Reactions
inferred← citeshttps://doi.org/10.1021/jo062141aopenalex-snapshot
One-Pot Synthesis of Substituted 2-Aminobenzo[b]thiophenes
inferred← citeshttps://doi.org/10.1021/jo9711807openalex-snapshot
Parallel Synthesis of Tamoxifen and Derivatives on Solid Support via Resin Capture
inferred← citeshttps://doi.org/10.1021/ml2002532openalex-snapshot
Hydrophobic Interactions Improve Selectivity to ERα for Benzothiophene SERMs
inferred← citeshttps://doi.org/10.1021/ol061859+openalex-snapshot
Synthesis of Polycyclic Heterocycles via a One-Pot Ortho Alkylation/Direct Heteroarylation Sequence
inferred← citeshttps://doi.org/10.1021/ol502381eopenalex-snapshot
Direct Synthesis of Diverse 2-Aminobenzo[b]thiophenes via Palladium-Catalyzed Carbon–Sulfur Bond Formation Using Na2S2O3as the Sulfur Source
inferred← citeshttps://doi.org/10.1021/tx000208yopenalex-snapshot
Structure−Activity Relationships for a Large Diverse Set of Natural, Synthetic, and Environmental Estrogens
inferred← citeshttps://doi.org/10.1021/tx0342722openalex-snapshot
Oxidation of Raloxifene to Quinoids: Potential Toxic Pathways via a Diquinone Methide and o-Quinones
inferred← citeshttps://doi.org/10.1021/tx049776uopenalex-snapshot
Bioactivation of the Selective Estrogen Receptor Modulator Desmethylated Arzoxifene to Quinoids: 4‘-Fluoro Substitution Prevents Quinoid Formation
inferred← citeshttps://doi.org/10.1023/a:1010019410881openalex-snapshot
Mechanism of Action and Preclinical Profile of Raloxifene, a Selective Estrogen Receptor Modulator*
inferred← citeshttps://doi.org/10.1038/39645openalex-snapshot
Molecular basis of agonism and antagonism in the oestrogen receptor
inferred← citeshttps://doi.org/10.1039/b914424bopenalex-snapshot
As many as six tandem reactions in one step! Unprecedented formation of highly functionalized benzothiophenes
inferred← citeshttps://doi.org/10.1039/c5ra02114fopenalex-snapshot
One-pot synthesis of 2,3-substituted benzo[b]thiophenes via Cu( i ) catalysed intramolecular cyclisation from dithioesters
inferred← citeshttps://doi.org/10.1039/c6md00553eopenalex-snapshot
Design and synthesis of novel selective estrogen receptor degradation inducers based on the diphenylheptane skeleton
inferred← citeshttps://doi.org/10.1039/c6ob02461kopenalex-snapshot
A practical synthesis of benzothiophenes via visible-light-promoted cyclization of disulfides and alkynes
inferred← citeshttps://doi.org/10.1039/c7ob01747bopenalex-snapshot
Visible-light-induced tandem cyclization of 2-alkynylanilines with disulfides: a convenient method for accessing benzothiophenes under transition-metal-free and photocatalyst-free conditions
inferred← citeshttps://doi.org/10.1039/c9md00570fopenalex-snapshot
Recent progress in selective estrogen receptor downregulators (SERDs) for the treatment of breast cancer
inferred← citeshttps://doi.org/10.1039/d0gc00917bopenalex-snapshot
Nickel-catalyzed and Li-mediated regiospecific C–H arylation of benzothiophenes
inferred← citeshttps://doi.org/10.1055/a-2500-6460openalex-snapshot
Synthesis of 2-Aminobenzo[b]thiophenes via an Intramolecular Dehydrogenative C–S Bond Formation Effected by Iodine(III) Reagents
inferred← citeshttps://doi.org/10.1073/pnas.142288199openalex-snapshot
Kinetic analysis of estrogen receptor/ligand interactions
inferred← citeshttps://doi.org/10.1073/pnas.94.25.14105openalex-snapshot
Molecular determinants of tissue selectivity in estrogen receptor modulators
inferred← citeshttps://doi.org/10.1080/00397911.2014.943348openalex-snapshot
Piperidine Nucleophilic Substitution Without Solvent: An Efficient Synthesis of Raloxifene
inferred← citeshttps://doi.org/10.1080/01443610310001620305openalex-snapshot
Comparative analysis of oestrogen and raloxifene effects on the phospholipid composition of high density lipoproteins in healthy postmenopausal women
inferred← citeshttps://doi.org/10.1080/01961779908047953openalex-snapshot
Recent Advances in the Synthesis and Applications of Benzo[b]thiophenes
inferred← citeshttps://doi.org/10.1080/08927022.2012.717281openalex-snapshot
Agonist and antagonist recognition studies for oestrogen receptor by molecular dynamics simulation
inferred← citeshttps://doi.org/10.1080/1062936x.2020.1864468openalex-snapshot
Endocrine disruption: the noise in available data adversely impacts the models’ performance
inferred← citeshttps://doi.org/10.1080/14756360802469127openalex-snapshot
β-Lactam type molecular scaffolds for antiproliferative activity: Synthesis and cytotoxic effects in breast cancer cells
inferred← citeshttps://doi.org/10.1080/17415991003721266openalex-snapshot
Recent trends in the chemistry of aminobenzo[b]thiophenes
inferred← citeshttps://doi.org/10.1089/jwh.1999.8.321openalex-snapshot
Selective Estrogen Receptor Modulators: A Controversial Approach for Managing Postmenopausal Health
inferred← citeshttps://doi.org/10.1093/jnci/90.20.1514openalex-snapshot
Cancer Chemoprevention: Progress and Promise
inferred← citeshttps://doi.org/10.1111/cbdd.12239openalex-snapshot
Discovery of Synthetic Leishmania Inhibitors by Screening of a 2‐Arylbenzothiophene Library
inferred← citeshttps://doi.org/10.1111/j.1527-3466.2001.tb00183.xopenalex-snapshot
Cardiovascular Effects of Raloxifene Hydrochloride
inferred← citeshttps://doi.org/10.1134/s1070363218040126openalex-snapshot
A Convenient Approach to 2-Aminobenzo[b]chalcogenophenes Based on Copper-Catalyzed Transformation of 4-(2-Bromophenyl)-1,2,3-chalcogenodiazoles in the Presence of a Base and Amines
inferred← citeshttps://doi.org/10.1134/s107036322011033xopenalex-snapshot
In Vitro Activity of Organochalcogen Compounds: II. Cytotoxic Effect of 2-Aminobenzo[b]thiophenes Against K562 and HeLa Tumor Cell Lines
inferred← citeshttps://doi.org/10.1134/s1070428013040015openalex-snapshot
4-(2-R-Aryl)-1,2,3-chalcogenadiazoles in the synthesis of fused heterocycles
inferred← citeshttps://doi.org/10.1155/2013/743139openalex-snapshot
Computational Study of Estrogen Receptor-Alpha Antagonist with Three-Dimensional Quantitative Structure-Activity Relationship, Support Vector Regression, and Linear Regression Methods
inferred← citeshttps://doi.org/10.1158/1535-7163.mct-14-0319openalex-snapshot
Novel Selective Estrogen Mimics for the Treatment of Tamoxifen-Resistant Breast Cancer
inferred← citeshttps://doi.org/10.1186/s12915-017-0449-4openalex-snapshot
Targeting protein quality control pathways in breast cancer
inferred← citeshttps://doi.org/10.1210/edrv.20.3.0368openalex-snapshot
Tamoxifen, Raloxifene, and the Prevention of Breast Cancer*
inferred← citeshttps://doi.org/10.1248/cpb.52.79openalex-snapshot
A New Series of Estrogen Receptor Modulators: Effect of Alkyl Substituents on Receptor-Binding Affinity
inferred← citeshttps://doi.org/10.1248/cpb.c19-01108openalex-snapshot
Development of Photoswitchable Estrogen Receptor Ligands
inferred← citeshttps://doi.org/10.1289/ehp.00108s5829openalex-snapshot
Influence of Exogenous Estrogen Receptor Ligands on Uterine Leiomyoma: Evidence from an in Vitro/in Vivo Animal Model for Uterine Fibroids
inferred← citeshttps://doi.org/10.1517/13543776.16.5.559openalex-snapshot
Estrogen receptor modulator review
inferred← citeshttps://doi.org/10.1517/13543784.15.3.317openalex-snapshot
Arzoxifene: the development and clinical outcome of an ideal SERM
inferred← citeshttps://doi.org/10.1530/jme-16-0024openalex-snapshot
Antiestrogens: structure-activity relationships and use in breast cancer treatment
inferred← citeshttps://doi.org/10.1586/14737140.4.4.523openalex-snapshot
Raloxifene and its role in breast cancer prevention
inferred← citeshttps://doi.org/10.1590/s0004-27301999000600008openalex-snapshot
Raloxifeno e osteoporose: revisão de um novo modulador seletivo do receptor de estrógeno
inferred← citeshttps://doi.org/10.1787/9789264078857-enopenalex-snapshot
Detailed Background Review of the Uterotrophic Bioassay
inferred← citeshttps://doi.org/10.2147/cia.s3344openalex-snapshot
Managing the risk of invasive breast cancer in women at risk for breast cancer and osteoporosis: the role of raloxifene
inferred← citeshttps://doi.org/10.2165/00002018-200124140-00003openalex-snapshot
Comparative Tolerability of First-Generation Selective Estrogen Receptor Modulators in Breast Cancer Treatment and Prevention
inferred← citeshttps://doi.org/10.2165/00002512-200724050-00002openalex-snapshot
Selective Estrogen Receptor Modulators for Postmenopausal Osteoporosis
inferred← citeshttps://doi.org/10.2165/00003495-200767160-00004openalex-snapshot
Estrogen Receptor Modulators and Down Regulators
inferred← citeshttps://doi.org/10.2174/0929867329666221006110528openalex-snapshot
Effectiveness of Selective Estrogen Receptor Modulators in Breast Cancer Therapy: An Update
inferred← citeshttps://doi.org/10.2174/1574884711308020006openalex-snapshot
The Discovery and Development of Selective Estrogen Receptor Modulators (SERMs) for Clinical Practice
inferred← citeshttps://doi.org/10.2217/17455057.3.2.139openalex-snapshot
Raloxifene: A Selective Estrogen Receptor Modulator for Reducing the Risk of Invasive Breast Cancer in Postmenopausal Women
inferred← citeshttps://doi.org/10.3109/14756366.2011.642374openalex-snapshot
N-Arylbenzamides: extremely simple scaffolds for the development of novel estrogen receptor agonists
inferred← citeshttps://doi.org/10.3390/molecules17067415openalex-snapshot
Application of 4D-QSAR Studies to a Series of Raloxifene Analogs and Design of Potential Selective Estrogen Receptor Modulators
inferred← citeshttps://doi.org/10.3816/cbc.2007.n.047openalex-snapshot
Breast Cancer Risk Management
inferred← citeshttps://doi.org/10.4155/fmc.15.181openalex-snapshot
Design and Synthesis of Novel Flexible Ester-Containing Analogs of Tamoxifen and Their Evaluation as Anticancer Agents
inferred← citeshttps://doi.org/10.70675/41b22f7az01dcz48abzaa5ez4d3ae90798c7openalex-snapshot
Comprehensive data analysis and predictive chemoinformatics models for REACH related physicochemical and (eco)toxicity properties
inferred← citeshttps://doi.org/10.7326/0003-4819-130-5-199903020-00015openalex-snapshot
Clinical Effects of Raloxifene Hydrochloride in Women
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.