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(22 products)
- Estrogen/progestogen Receptor(59 products)
- GPR(1 products)
- Glucocorticoid Receptor(166 products)
- LHRH(2 products)
- Opioid Receptor(326 products)
- Prostaglandin Receptor(122 products)
- RAAS(90 products)
- Reductase(50 products)
- Somatostatin(57 products)
- Thyroid hormone receptor(THR)(32 products)
- Vasopressin Receptor(48 products)
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Found 3373 products of "Endocrinology/Hormones"
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[Nphe1]Nociceptin(1-13)NH2
CAS:<p>Competitive nociceptin receptor antagonist with pKi=8.4; no agonist activity; blocks nociceptin effects in vitro/in vivo.</p>Formula:C61H100N22O15Purity:98%Color and Shape:SolidMolecular weight:1381.6Olmesartan medoxomil impurity C
CAS:Impurity C of Olmesartan medoxomil is a selective AT1 inhibitor with an IC50 of 66.2 μM.Formula:C29H28N6O5Color and Shape:SolidMolecular weight:540.57Oxytocin parallel dimer
CAS:Oxytocin parallel dimer is the disulfide-bridged homo peptide dimer.Formula:C86H132N24O24S4Molecular weight:2014.39Azilsartan Medoxomil Potassium
CAS:Azilsartan Medoxomil Potassium (TAK-491 Potassium) is an orally administered angiotensin II receptor type 1 antagonist with IC50 of 0.62 nM, which used in the treatment of adults with essential hypertension.Formula:C30H23N4O8·KPurity:99.99%Color and Shape:SolidMolecular weight:606.62A 779
CAS:A 779 is a potent antagonist of the G-protein-coupled receptor Mas, the Ang1-7 receptor, which is distinct from conventional AngII.Formula:C39H60N12O11Purity:98%Color and Shape:SolidMolecular weight:872.97PF-06478939
PF-06478939 is a peptide that functions as an agonist at the oxytocin (OT) receptor and vasopressin receptor without crossing the blood-brain barrier.Formula:C78H134N14O22S2Purity:98%Color and Shape:SolidMolecular weight:1684.11Hydrocortisone sodium succinate
CAS:Hydrocortisone sodium succinate is a glucocorticoid which is used to alleviate allergic reactions, particularly those of the skin and gums.Formula:C25H34NaO8Color and Shape:SolidMolecular weight:485.529L 363564
CAS:L 363564 is a kidney renin inhibitor.Formula:C54H76N12O10Color and Shape:SolidMolecular weight:1053.276ST-CY14
ST-CY14 is an inhibitor of the Nur77-PPARγ interaction with an EC50 of 3.15 μM. It binds to Nur77 (Kd=32 nM) to prevent its ubiquitination and degradation by PPARγ, reducing fatty acid uptake and mitochondrial respiration, and inhibiting the transcription of CD36 and FABP4. ST-CY14 suppresses proliferation and migration of MCF7 and MDA-MB-231 cancer cells and impedes tumor growth and bone metastasis in mouse models.Formula:C139H237N57O31S2Color and Shape:SolidMolecular weight:3266.86PTP1B/AKR1B1-IN-2
PTP1B/AKR1B1-IN-2 (Compound 7f) is a potent inhibitor targeting both PTP1B and AKR1B1 with IC50 values of 3.2 and 2.1 μM, respectively, and K i values of 4.0Formula:C23H23NO4S2Purity:98%Color and Shape:SolidMolecular weight:441.56AZ 1729
CAS:<p>FFA2 modulator; inhibits cAMP, enhances 35SGTPγS binding (pEC50: 6.9, 7.23); alters Gi/Gq signaling; affects lipolysis, neutrophil migration.</p>Formula:C18H16FN5OSColor and Shape:SolidMolecular weight:369.42Estrogen receptor modulator 6
CAS:<p>ER modulator 6 (3a) is a potent ERβ agonist with a K i of 0.44 nM; 19x more selective for ERβ than ERα.</p>Formula:C18H16F2O3Color and Shape:SolidMolecular weight:318.32Fluticasone 17β-Carboxylic Acid
CAS:Fluticasone 17β-carboxylic acid is an intermediate in the synthesis of the glucocorticosteroid fluticasone propionate .1Formula:C21H26F2O5Color and Shape:SolidMolecular weight:396.42Awl 60
CAS:Awl 60 is a substance P (6-11) non-competitive antagonist.Formula:C57H65N9O8SPurity:98%Color and Shape:SolidMolecular weight:1036.25Ro 64-6198
CAS:Ro 64-6198: Nonpeptide, selective NOP agonist, high brain uptake, EC50=25.6 nM, 100x NOP>opioid affinity.Formula:C26H31N3OPurity:98%Color and Shape:SolidMolecular weight:401.54[Orn8]-Urotensin II acetate
<p>[Orn8]-Urotensin II acetate is a Urotensin receptor ligand and a partial agonist at Urotensin receptors.</p>Formula:C65H87N13O20S2Purity:98.63%Color and Shape:SolidMolecular weight:1434.59AKR1B10-IN-1
CAS:AKR1B10-IN-1: potent AKR1B10 inhibitor, IC50 3.5 nM; hinders lung cancer cell growth, spread, and Cisplatin resistance.Formula:C19H16FNO4Color and Shape:SolidMolecular weight:341.338(-)-Vorozole
CAS:(-)-Vorozole, potent/selective oral non-steroidal aromatase inhibitor, shows antitumor activity, used in breast cancer research.Formula:C16H13ClN6Purity:99.02% - >99.99%Color and Shape:SoildMolecular weight:324.77UFP-101
CAS:<p>Strong, selective NOP receptor antagonist with pKi=10.24; >3000x selectivity over δ, μ, κ receptors; blocks nociceptin effects.</p>Formula:C82H138N32O21Purity:98%Color and Shape:SolidMolecular weight:1908.19[DPro10] Dynorphin A (1-11)acetate,porcine
[DPro10] Dynorphin A (1-11)acetate,porcine is a highly potent κ-opioid receptor agonist with a Ki value of 0.13 nM.Formula:C65H107N21O15Purity:99.59%Color and Shape:SoildMolecular weight:1422.7
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