Endocrinology/Hormones
Endocrinology/hormone inhibitors are compounds that block the action of hormones or interfere with hormone signaling pathways. These inhibitors are essential for studying the regulation of endocrine systems and for developing treatments for hormone-related diseases, such as diabetes, thyroid disorders, and hormone-dependent cancers. By modulating hormone activity, these inhibitors can help elucidate the complex interactions within the endocrine system. At CymitQuimica, we offer a wide range of high-quality endocrinology/hormone inhibitors to support your research in endocrinology, pharmacology, and medical sciences.
Subcategories of "Endocrinology/Hormones"
- Androgen Receptor(229 products)
- Annexin A(16 products)
- Aromatase(23 products)
- Estrogen/progestogen Receptor(66 products)
- GPR(1 products)
- Glucocorticoid Receptor(165 products)
- LHRH(2 products)
- Opioid Receptor(327 products)
- Prostaglandin Receptor(122 products)
- RAAS(89 products)
- Reductase(51 products)
- Somatostatin(57 products)
- Thyroid hormone receptor(THR)(33 products)
- Vasopressin Receptor(48 products)
Show 6 more subcategories
Found 3420 products of "Endocrinology/Hormones"
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
EMD-66684
CAS:EMD-66684 is a non-peptide angiotensin II receptor antagonist.Formula:C28H31ClN8O2Color and Shape:SolidMolecular weight:547.06TTC-352
CAS:TTC-352 is an oral selective ERalpha partial agonist with potential anti-cancer effects, disrupting ER signaling and tumor cell growth.Formula:C20H13FO3SColor and Shape:SolidMolecular weight:352.38Risarestat
CAS:Risarestat (CT-112) is a potent aldose reductase inhibitor and thyroid hormone receptor (TR) antagonist for the treatment of hypoglycemia.Formula:C16H21NO4SPurity:98.39%Color and Shape:SolidMolecular weight:323.41Trimebutine CTB salt
CAS:Trimebutine CTB salt (GIC-1001) is an opioid receptor agonist used in the study of pain.Formula:C29H36N2O8S2Purity:99.85% - >99.99%Color and Shape:SolidMolecular weight:604.74ATC 0175
CAS:ATC 0175 hydrochloride is an orally active melanocyte concentrating hormone 1 receptor antagonist that is potent and selective.Formula:C23H26ClF2N5OPurity:99.98%Color and Shape:SolidMolecular weight:461.93Finrozole
CAS:Finrozole (MPV 2213ad) is a novel selective aromatase inhibitor that is partially reversible for breast development.Formula:C18H15FN4OPurity:99.82%Color and Shape:SolidMolecular weight:322.34Glucocorticoid receptor agonist-1
CAS:Glucocorticoid receptor agonist-1 is a potent glucocorticoid receptor agonist with an IC50 of 2.8 nM[1].
Formula:C35H39NO6Purity:99.68%Color and Shape:SolidMolecular weight:569.69YM 511
CAS:YM 511 is a specific non-steroidal aromatase inhibitor with IC50s of 0.4 and 0.12 nM, minimally affecting other steroids.Formula:C16H12BrN5Purity:99.965%Color and Shape:SolidMolecular weight:354.2SB-657510
CAS:SB-657510: UT antagonist, Ki (nM) - human 61, monkey 17, cat 30, rat 65, mouse 56; reduces UII-induced inflammation, aids diabetic atherosclerosis.Formula:C19H22BrClN2O5SPurity:98.06%Color and Shape:SolidMolecular weight:505.81Ref: TM-T12848
1mg50.00€5mg114.00€10mg177.00€25mg295.00€50mg399.00€100mg532.00€1mL*10mM (DMSO)128.00€FL104
CAS:FL104 is a potent agonist of small-molecule urotensin II receptor, pEC50= 7.11.Formula:C24H25ClN2OPurity:98.32%Color and Shape:SolidMolecular weight:392.92Ref: TM-T27328
1mg110.00€5mg259.00€10mg353.00€25mg533.00€50mg718.00€100mg945.00€200mg1,251.00€1mL*10mM (DMSO)315.00€GLPG0492
CAS:GLPG0492 is a novel selective androgen receptor modulator.Formula:C19H14F3N3O3Purity:99.58%Color and Shape:SolidMolecular weight:389.33Ref: TM-T11410L
1mg71.00€5mg156.00€10mg224.00€25mg358.00€50mg515.00€100mg692.00€200mg888.00€1mL*10mM (DMSO)166.00€Faxeladol
CAS:Faxeladol: adrenergic, serotonin inhibitor & opioid agonist for neurological studies.Formula:C15H23NOPurity:98.77% - 99.67%Color and Shape:SolidMolecular weight:233.35G36
CAS:G36 is a cell-permeable non-steroidal antagonist of GPER.Formula:C22H22BrNO2Purity:99.49%Color and Shape:SolidMolecular weight:412.32Ref: TM-T22794
1mg38.00€5mg84.00€10mg130.00€25mg227.00€50mg384.00€100mg568.00€500mg1,215.00€1mL*10mM (DMSO)93.00€ME-3221
CAS:Apomine inhibits HMG-CoA-reductase, induces myeloma cell apoptosis, modulates myeloma, and boosts lovastatin's antitumor effects.Formula:C22H21N5O2Purity:99.84% - 99.93%Color and Shape:SolidMolecular weight:387.43IPAG
CAS:IPAG is a potent σ-receptor antagonist (pKi=4.3). IPAG can induce cell apoptosis.Formula:C17H22IN3Purity:99.65%Color and Shape:SolidMolecular weight:395.28TC-MCH 7c
CAS:TC-MCH 7c is an oral, selectable and blood-brain barrier penetrating MCH1R antagonist with IC50 performance of 5.6 nM against hMCH1R, and TC-MCH 7c is aFormula:C24H25FN2O3Purity:99.54%Color and Shape:SolidMolecular weight:408.47Ref: TM-T13101
1mg94.00€5mg274.00€10mg394.00€25mg605.00€50mg815.00€100mg1,093.00€500mg2,195.00€1mL*10mM (DMSO)248.00€Ralaniten triacetate
CAS:Ralaniten triacetate (EPI-506) is a precursor of Ralaniten, an AR-NTD inhibitor, which can be used in the study of prostate and breast cancer.Formula:C27H33ClO8Purity:98.69%Color and Shape:SolidMolecular weight:521.00Ref: TM-T36375
1mg154.00€5mg371.00€10mg620.00€25mg1,341.00€50mg1,783.00€100mg2,250.00€1mL*10mM (DMSO)425.00€P2Y2R/GPR17 antagonist 1
CAS:P2Y2R/GPR17 antagonist 1 (Compound 14m) is a dual P2Y2R (IC50: 3.17 μM) and GPR17 (IC50: 1.67 μM) antagonist.
Formula:C19H13ClN2O6SPurity:98.42%Color and Shape:SolidMolecular weight:432.83CRTh2 antagonist 2
CAS:CRTh2 antagonist 2 is a selective and potent CRTH2 antagonist, IC50≤10 nM. CRTh2 antagonist 2 can be used to study the direction of androgenic alopecia.Formula:C26H23ClN4O3Purity:99.05%Color and Shape:SolidMolecular weight:474.94Ref: TM-T10889
1mg52.00€5mg94.00€10mg138.00€25mg212.00€50mg290.00€100mg371.00€200mg494.00€1mL*10mM (DMSO)112.00€Posatirelin
CAS:Posatirelin, a synthetic peptide, modulates and nourishes brain systems, aiding in vascular dementia research.Formula:C17H28N4O4Purity:99.43% - 99.95%Color and Shape:SolidMolecular weight:352.43YL-365
YL-365 is a highly potent and selective GPR34 antagonist that exhibits excellent activity in neuropathic pain models for the study of neurologic diseases.Purity:98.51%Color and Shape:Odour SolidBuloxibutid
CAS:Buloxibutid: a novel AT2 receptor agonist, Ki=0.4 nM (AT2), 10 μM (AT1).Formula:C23H29N3O4S2Purity:98.24% - 98.58%Color and Shape:SolidMolecular weight:475.62Ref: TM-T14337
1mg47.00€5mg92.00€10mg145.00€25mg260.00€50mg409.00€100mg708.00€500mg1,423.00€1mL*10mM (DMSO)92.00€ONC1-13B
CAS:ONC1-13B, an androgen receptor antagonist, is used potentially for the treatment of prostate cancer.Formula:C22H16F4N4O3SPurity:99.36% - 99.85%Color and Shape:SolidMolecular weight:492.45ICI 204,448
CAS:ICI 204,448 is a potent κ-opioid agonist with potential analgesic activity for the study of neurological diseases.Formula:C23H27Cl3N2O4Purity:>99.99%Color and Shape:SolidMolecular weight:501.83GPR40/FFAR1 modulator 1
CAS:GPR40/FFAR1 modulator 1 is a Gq-coupled free fatty acid receptor 1 (GPR40/FFAR1) agonist and allosteric modulator.Formula:C21H19N5O3Purity:99.7%Color and Shape:SolidMolecular weight:389.41Zindoxifene
CAS:Zindoxifene (D 16726) is an anti-estrogenic compound with antitumor activity that can be used in studies of breast and prostate cancer.Formula:C21H21NO4Purity:98.99%Color and Shape:SolidMolecular weight:351.4ZD-6888 Hydrochloride
CAS:ZD-6888 Hydrochloride, an angiotensin type 1 receptor antagonist, is used potentially for the treatment of hypertension.Formula:C25H26ClN5OPurity:98.61% - 99.60%Color and Shape:SolidMolecular weight:447.96NNC 63-0532
CAS:NNC 63-0532 is a potentnociceptin receptor agonist, Ki=7.3 nM, EC50=305 nM.Formula:C27H29N3O3Purity:99.53%Color and Shape:SolidMolecular weight:443.54LY2881835
CAS:LY2881835 is a potent and selective GPR40 agonist.Formula:C33H33NO3Purity:98.59% - 98.59%Color and Shape:SolidMolecular weight:491.62PSB-CB5
CAS:PSB-CB5 (GPR18-IN-32)2 is a GRP18 antagonist with anti-inflammatory activity and can be used to study obesity and metabolic disorders.Formula:C20H17ClN2O2SPurity:99.26%Color and Shape:SolidMolecular weight:384.88ADL-5747
CAS:ADL-5747 (ADL-5747 (free base)) (free base) is a delta opioid receptor agonist used in the treatment of neurological disorders, skin and musculoskeletalFormula:C24H28N2O3Purity:98.94% - 99.74%Color and Shape:SolidMolecular weight:392.49AT-121
CAS:AT-121 is a dual μ-opioid and neuropeptide receptor partial agonist (Kis 16.49 and 3.67 nM, respectively).Formula:C24H38N4O3SPurity:98.49% - 99.97%Color and Shape:SolidMolecular weight:462.65Ref: TM-T37610
1mg333.00€5mg787.00€10mg1,074.00€25mg1,510.00€50mg1,882.00€100mg2,375.00€500mg4,655.00€Endoxifen hydrochloride
CAS:Endoxifen HCl, a Tamoxifen metabolite, targets estrogen receptors more effectively and blocks aromatase, showing promise for breast cancer research.Formula:C25H28ClNO2Purity:99.95%Color and Shape:SolidMolecular weight:409.95GLPG1205
CAS:GLPG1205 is a potent, orally active GPR84 (G protein-coupled receptor) antagonist with anti-inflammatory activity.Formula:C22H22N2O4Purity:99.82% - 99.94%Color and Shape:SolidMolecular weight:378.42MK 1903
CAS:MK 1903 is a strong, selective HCA2/GPR109A agonist, reducing cAMP in CHO cells with EC50 of 12.9 nM.Formula:C8H8N2O2Purity:99.96%Color and Shape:SolidMolecular weight:164.16Lorundrostat
CAS:Lorundrostat is an aldosterone synthase inhibitor.Formula:C24H33N7O2Purity:95.47%Color and Shape:SolidMolecular weight:451.56ML-335
CAS:ML-335, a μ-δ targeted agonist and MOR/DOR ligand, may lead to isomer-biased drugs with pain-relief properties.Formula:C25H32N2O3Purity:98.58%Color and Shape:SolidMolecular weight:408.53Ref: TM-T23002
5mg44.00€10mg64.00€25mg112.00€50mg175.00€100mg253.00€200mg359.00€1mL*10mM (DMSO)33.00€Izonsteride
CAS:Izonsteride (LY320236) is a selective and potent 5alpha reductase inhibitor with dual action on the type I and type II isoforms of the enzyme.Izonsteride isFormula:C24H26N2OS2Purity:99.5%Color and Shape:SolidMolecular weight:422.61JNJ-20788560
CAS:JNJ-20788560 is a delta opioid receptor (DOR) agonist with analgesic activity. It is more selective for DOR than for mu opioid receptors (MOR).
Formula:C25H28N2O2Purity:98.02%Color and Shape:SolidMolecular weight:388.5AZD9567
CAS:AZD9567: potent, selective SGRM, oral, IC50=3.8nM, effective in SCW joint inflammation.Formula:C27H28F2N4O3Purity:98.4%Color and Shape:SolidMolecular weight:494.53Ref: TM-T14386
1mg190.00€5mg485.00€10mg700.00€25mg1,063.00€50mg1,431.00€100mg1,918.00€1mL*10mM (DMSO)533.00€AMG-009
CAS:AMG-009 is a prostaglandin D2 antagonist. For CRTH2 and DP receptors, the IC50s are 3 nM and 12 nM, respectively.Formula:C26H26Cl2N2O7SPurity:97.88%Color and Shape:SolidMolecular weight:581.47Palazestrant
CAS:Palazestrant, an antiestrogen and antineoplastic agent, effectively targets ER+/HER2+ cancer when used in conjunction with a HER2 inhibitor.Formula:C28H36FN3OPurity:97.55%Color and Shape:SolidMolecular weight:449.6Ref: TM-T72945
1mg93.00€5mg150.00€10mg215.00€25mg358.00€50mg517.00€100mg707.00€1mL*10mM (DMSO)166.00€MEDICA16
CAS:MEDICA16: GPR40 agonist, GPR120 partial agonist, ATP-citrate lyase inhibitor, lowers TG, boosts insulin sensitivity in muscle.Formula:C20H38O4Purity:99.62% - 99.87%Color and Shape:White SolidMolecular weight:342.51Ref: TM-T22967
5mg60.00€10mg92.00€25mg168.00€50mg289.00€100mg419.00€500mg874.00€1mL*10mM (DMSO)80.00€Lidorestat
CAS:Lidorestat (IDD-676) is an aldose reductase inhibitor (IC50: 5 nM) with effective, selective and oral activity.Formula:C18H11F3N2O2SPurity:99.98%Color and Shape:SolidMolecular weight:376.35Palatrigine
CAS:Palatrigine (BW-A 256C) is a compound with angiotensin-converting enzyme inhibitory and beta-adrenergic receptor blocking properties.Formula:C12H13Cl2N5Purity:98.87%Color and Shape:SolidMolecular weight:298.17Estredox
CAS:Estredox, an estrogen receptor agonist, is used potentially for the treatment of vasomotor symptoms.Formula:C25H31NO3Purity:98.02% - 98.39%Color and Shape:SolidMolecular weight:393.52Minalrestat
CAS:Minalrestat(ARI-509) is an orally active and potent aldose reductase inhibitor for the study of impaired microvascular reactivity in diabetic patients.Formula:C19H11BrF2N2O4Purity:98.64% - 99.88%Color and Shape:SolidMolecular weight:449.2SCH-486757
CAS:SCH-486757 is an agonist of nociceptin-1 (NOP1) and orphanin FQ peptide receptors and is used in the study of cough.Formula:C24H23Cl2N3OPurity:99.53% - >99.99%Color and Shape:SolidMolecular weight:440.37Orotirelin
CAS:Orotirelin (CG 3509), a TRH analog, counters pentobarbital sleep; may aid in cerebral ischemia.Formula:C16H19N7O5Purity:98.92%Color and Shape:SolidMolecular weight:389.37LY88074
CAS:LY88074, a raloxifene analog sans basic side chain, is an ERβ agonist (EC50 = 232 nM) that promotes uterine cell growth.
Formula:C21H14O4SPurity:98.31%Color and Shape:SolidMolecular weight:362.4CAY10786
CAS:CAY10786 (GPR52 antagonist-1) is an antagonist of G protein-coupled receptor 52 (GPR52, IC50 = 0.63 μM).Formula:C15H14OSPurity:99.82%Color and Shape:SolidMolecular weight:242.34Ref: TM-T36036
2mg38.00€5mg55.00€10mg88.00€25mg168.00€50mg268.00€100mg430.00€200mg622.00€1mL*10mM (DMSO)60.00€ICI 199,441 hydrochloride
CAS:ICI 199,441 hydrochloride is a potent, selective agonist of κ-opioid receptor.Formula:C21H25Cl3N2OPurity:99.57%Color and Shape:SolidMolecular weight:427.8Ref: TM-T22849
2mg33.00€5mg52.00€10mg75.00€25mg138.00€50mg215.00€100mg314.00€200mg442.00€1mL*10mM (DMSO)58.00€L-162,313
CAS:L-162,313 is an ANG II receptor agonist, a nonpeptide that mimics the biological actions of angiotensin II and induces an increase in MAP.Formula:C30H38N4O4S2Purity:98.21%Color and Shape:SolidMolecular weight:582.78GPR35 agonist 2
CAS:GPR35 agonist 2 (TC-G 1001) is a potent GPR35 agonist.The EC50 values of GPR35 agonist 2 in the β-arrestin and Ca2+ release assays were 26 and 3.2 nM,Formula:C17H11FN2O3SPurity:99.17% - 99.53%Color and Shape:SolidMolecular weight:342.34Ref: TM-T23434
1mg52.00€5mg96.00€10mg170.00€25mg378.00€50mg560.00€100mg800.00€500mg1,644.00€1mL*10mM (DMSO)114.00€GR 89696 fumarate
CAS:GR 89696 fumarate is a highly selective κ2 opioid receptor agonist (IC50 = 0.04nM) with anti-pruritchy, anti-injury and neuroprotective effects.Formula:C23H29Cl2N3O7Purity:99.84%Color and Shape:SolidMolecular weight:530.4Bevenopran
CAS:Bevenopran (CB-5945) is a peripheral antagonist of μ-opioid receptor and can be used in studies about the treatment of opioid-induced bowel dysfunction.Formula:C20H26N4O4Purity:98.69% - 98.9%Color and Shape:SolidMolecular weight:386.44Ref: TM-T14551
1mg62.00€5mg130.00€10mg187.00€25mg299.00€50mg408.00€100mg532.00€200mg705.00€1mL*10mM (DMSO)142.00€Acifran
CAS:Acifran (AY 25712) is an HM74A/GPR109A and GPR109B agonist and displays antihyperlipidemic activity.Formula:C12H10O4Purity:99.19%Color and Shape:SolidMolecular weight:218.21Estrogen receptor antagonist 8
CAS:Estrogen Receptor Antagonist 8 is an ER antagonist with anti-uterine activity and may be used in the study of ovarian dysfunction.CASNETIN SODIUM (CasN)Formula:C25H21N3O4Purity:98.48%Color and Shape:SolidMolecular weight:427.45BMS-641988
CAS:BMS-641988 is a novel nonsteroidal androgen receptor antagonist for the treatment of prostate cancer.Formula:C20H20F3N3O5SPurity:99.3% - 99.92%Color and Shape:SoildMolecular weight:471.45Moveltipril
CAS:Moveltipril (Moveltipril calcium) is a potent angiotensin-converting enzyme (ACE) inhibitor.Moveltipril is converted to captopril in the body for action.Formula:C19H30N2O5SPurity:97.55% - 98.28%Color and Shape:SolidMolecular weight:398.52Ref: TM-T25832
1mg37.00€5mg82.00€10mg123.00€25mg225.00€50mg356.00€100mg578.00€200mg778.00€1mL*10mM (DMSO)90.00€Indazole-Cl
CAS:Indazole-Cl is a selective ERß agonist and a selective estrogen receptor modifier (SERM).
Formula:C13H9ClN2O2Purity:99.02% - 99.86%Color and Shape:SolidMolecular weight:260.68Ref: TM-T25534
1mg115.00€2mg164.00€5mg255.00€10mg375.00€25mg562.00€50mg787.00€100mg1,074.00€200mg1,454.00€Ripisartan
CAS:Ripisartan (UP-269-6) is a potent and specific angiotensin II receptor antagonist that inhibits angiotensin II-mediated sympathetic tachycardia responses.Formula:C23H22N8OPurity:98.52%Color and Shape:SolidMolecular weight:426.47SSR126768A
CAS:SSR126768A is an oxytocin receptor antagonist that inhibits uterine contractions and may be used to prevent preterm labor.Formula:C33H31Cl2N3O4Purity:97.06%Color and Shape:SolidMolecular weight:604.52Ref: TM-T28855
1mg315.00€5mg873.00€10mg1,080.00€25mg1,431.00€50mg1,783.00€100mg2,250.00€500mg6,264.00€FPL-62129
CAS:FPL-62129 is a calcium channel antagonist and a novel angiotensin-converting enzyme inhibitor with vasodilator activity for the study of cardiovascular disease.Formula:C20H19ClF5NO4Purity:98.27% - 99.34%Color and Shape:SolidMolecular weight:467.81Terlakiren
CAS:Terlakiren (CP-80,794) is a renin inhibitor that inhibits the potency of human renin and can be used to study neurological disorders of the hypertensive type.Formula:C31H48N4O7SPurity:99.38%Color and Shape:SolidMolecular weight:620.8Y134
CAS:Y134, an oral estrogen receptor inhibitor, is 121x more selective for ERα (Ki=0.09 nM) over ERβ (Ki=11.31 nM), and blocks ER+ breast cancer cell growth.Formula:C28H28N2O3SPurity:99.98%Color and Shape:SolidMolecular weight:472.6Tirzepatide acetate
CAS:Cymit Quimica provides this product solely for uses within the scope of any statute or law providing for an immunity, exemption, or exception to patent infringement (“Exempted Uses”), including but not limited to 35 U.S.C. § 271(e)(1) in the United States, the Bolar type exemption in Europe, and any corresponding exception to patent infringement in any other country. It is the sole responsibility of the purchaser or user of this product, and the purchaser or user of this product agrees to engage only in such Exempted Uses, and to comply with all applicable intellectual property laws and/or regulations. The purchaser of this product agrees to indemnify Cymit Quimica against all claims in connection with the performance of the respective commercial agreement (e.g. supply agreement) and possible infringements of intellectual property rights.
Purity:Min. 95%Fezagepras sodium
CAS:Fezagepras sodium (Setogepram sodium salt) is an orally active GPR40 agonist and is an antagonist or inverse agonist for GPR84, with anti-fibrotic, anti-Formula:C13H17NaO2Purity:99.49%Color and Shape:SolidMolecular weight:228.26Ref: TM-T12375
1mg43.00€5mg96.00€10mg140.00€25mg255.00€50mg374.00€100mg542.00€500mg1,093.00€1mL*10mM (DMSO)96.00€LP-471756
CAS:LP-471756 is a specific antagonist of GPR139 and inhibits LP-360924-stimulated cAMP production (IC50 = 640 nM).Formula:C19H23NO2SPurity:99.76%Color and Shape:SolidMolecular weight:329.46Nur77 modulator 2
CAS:Nur77 modulator 2: Kd of 0.35 μM, oral anti-inflammatory, affects Nur77/mitochondria localization.Formula:C26H25NO5Color and Shape:SolidMolecular weight:431.48Deltakephalin
CAS:Deltakephalin is a synthetic, potent specific opiate delta receptors agonist.Formula:C34H48N6O10Purity:98%Color and Shape:SolidMolecular weight:700.78LY2922083
CAS:LY2922083: Potent, selective GPR40 agonist; lowers glucose, boosts insulin and GLP-1.Formula:C31H33NO3SColor and Shape:SolidMolecular weight:499.66Amebucort
CAS:Amebucort is a synthetic glucocorticoid corticosteroid. It may used for the research of inflammatory disorders.Formula:C28H40O7Purity:98%Color and Shape:SolidMolecular weight:488.618,11-Eicosadiynoic acid
CAS:8,11-Eicosadiynoic acid, an unsaturated fatty acid, functions as a steroid 5α-reductase inhibitor and has applications in acne research [1].Formula:C20H32O2Color and Shape:SolidMolecular weight:304.47ADL 08-0011 HCl
CAS:ADL 08-0011, a μ-opioid antagonist with Ki 0.25 nM, is derived from alvimopan by gut microbes and counteracts loperamide effects in rats.Formula:C23H30ClNO3Color and Shape:SolidMolecular weight:403.947LY3104607
CAS:LY3104607 is an oral GPCR 40 agonist for type 2 diabetes, aimed at reducing glucose.Formula:C27H25N3O3Purity:98%Color and Shape:SolidMolecular weight:439.51ICI 204448
CAS:ICI 204448 is a potent and peripherally selective κ-opioid agonist.Formula:C23H26Cl2N2O4Color and Shape:SolidMolecular weight:465.37Estrogen receptor modulator 7
CAS:Estrogen Receptor Modulator 7 is a potent modulator of estrogen receptors, utilized in cancer research [1].Formula:C30H31BCl2FNO3Purity:98%Color and Shape:SolidMolecular weight:554.29FK 33-824
CAS:FK 33-824, a stable synthetic analog of methionine enkephalin, reversible with naloxone.Formula:C29H41N5O7SPurity:98%Color and Shape:SolidMolecular weight:603.73ER degrader 6
CAS:ER degrader 6 (compound 35s) is a potent selective estrogen receptor modulator (SERM) with the capacity to degrade Estrogen Receptor (ER)α.Formula:C33H34FN3O5SSePurity:98%Color and Shape:SolidMolecular weight:682.66Mu opioid receptor antagonist 7
CAS:Compound 24, also known as Mu opioid receptor antagonist 7, is a potent, centrally-acting µ-opioid receptor (µOR) antagonist with an inhibitory concentration (Formula:C22H27ClN2O2Purity:98%Color and Shape:SolidMolecular weight:386.91H3B-6545 Hydrochloride
CAS:H3B-6545 Hydrochloride is a selective, oral estrogen receptor covalent antagonist (SERCA).Formula:C30H30ClF4N5O2Color and Shape:SolidMolecular weight:604.04CIDD-0149897
CAS:CIDD-0149897 is a potent, selective, and brain-penetrant agonist of ERβ that exhibits antitumor activity in glioblastoma [1].Formula:C15H10FNO3Purity:98%Color and Shape:SolidMolecular weight:271.24Conjugated Estrogen sodium
CAS:Conjugated estrogens treat menopause symptoms, vaginal changes, and certain cancers.Formula:C18H19NaO5SPurity:98%Color and Shape:White Needle CrystalMolecular weight:370.39PD 125754
CAS:PD 125754 is a Renin inhibitor, which represents a group of pharmaceutical drugs used primarily to treat essential hypertension.Formula:C42H65N5O7Purity:98%Color and Shape:SolidMolecular weight:751.99ER degrader 1
CAS:ER degrader 1 targets estrogen receptor, crucial for cell regulation; shows promise in cancer therapy. (Patent WO2021139756A1, compound 11)Formula:C26H32F4N4O3Color and Shape:SolidMolecular weight:524.55(rel)-BMS-641988
CAS:(rel)-BMS-641988, a relative configuration of the potent nonsteroidal androgen receptor antagonist BMS-641988, holds potential for prostate cancer research.Formula:C20H20F3N3O5SPurity:98%Color and Shape:SolidMolecular weight:471.45BMS-814580
CAS:BMS-814580: potent MCHR1 antagonist, Kb 117 nM, Ki 17 nM (human), 4.9/11.5 nM (monkey/rat), reduces feeding/weight in rodents.Formula:C24H19ClF2N2O4SColor and Shape:SolidMolecular weight:504.93GPR52 receptor modulator 1
CAS:GPR52 receptor modulator 1, a compound delineated as per Procedure 1, is a modulator of the GPR52 receptor, offering research potential in the investigation ofFormula:C19H14F4N4OPurity:98%Color and Shape:SolidMolecular weight:390.33N-Nitrosodicyclohexylamine
CAS:N-Nitrosodicyclohexylamine (NDCHA), an N-nitrosocompound, exhibits anti-androgenic activity by competitively binding to the androgen receptor (AR) in oppositionFormula:C12H22N2OPurity:98%Color and Shape:SolidMolecular weight:210.32Naloxonazine
CAS:Naloxonazine, a potent, selective opiate mu-1 (μ1) antagonist, also influences leishmania through the modulation of host coding function.Formula:C38H42N4O6Color and Shape:SolidMolecular weight:650.76MK-386
CAS:MK-386 is a potent and selective inhibitor of human type-1 5alpha-reductase.Formula:C28H49NOColor and Shape:SolidMolecular weight:415.69Nurr1 agonist 7
CAS:Nurr1 agonist 7 is an agonist of Nurr1 (EC50: 0.12 μM), which can be used to study neurological disorders such as Parkinson's disease.Formula:C18H20O3Purity:99.79%Color and Shape:SolidMolecular weight:284.35RU28362
CAS:RU28362 is an agonist of glucocorticoid receptor.Formula:C23H28O3Color and Shape:SolidMolecular weight:352.47TP-051
CAS:TP-051 is a FFAR1 agonist.Formula:C29H31FO6SPurity:99.45% - 99.96%Color and Shape:SolidMolecular weight:526.62Salvinorin A Carbamate
CAS:Salvinorin A carbamate, a potent κ-opioid receptor (KOR) full agonist, exhibits nearly the same potency as salvinorin A, with EC50 values of 6.2 and 4.5 nM, respectively, for activating the human KOR to augment the binding of [35S]GTPγS. Enhancing biological stability, the addition of a carbamate group to salvinorin A reduces deacetylation.Formula:C22H27NO8Color and Shape:SolidMolecular weight:433.457Androgen receptor degrader-1
CAS:Androgen Receptor Degrader-1 (Compound 18) is a potent agent for androgen receptor degradation, applicable in cancer research [1].Formula:C15H14ClN3O4Purity:98%Color and Shape:SolidMolecular weight:335.7411β-hydroxy Etiocholanolone
CAS:11β-Hydroxyetiocholanolone, a hydrocortisone metabolite, exhibits elevated fecal levels in giraffes (G. camelopardalis) and plains zebras (E. quagga) in response to environmental stress.Formula:C19H30O3Color and Shape:SolidMolecular weight:306.44H3B-6545
CAS:H3B-6545 is a selective and oral estrogen receptor covalent antagonist (SERCA) used in the research of metastatic ER-positive, HER2-negative breast cancer.Formula:C30H29F4N5O2Color and Shape:SolidMolecular weight:567.58CITFA
CAS:CITFA, a GPER agonist, enhances neurite outgrowth in rat embryonic (E18) hippocampal neurons [1].Formula:C25H35NO2Color and Shape:SolidMolecular weight:381.55
