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(209 products)
- Annexin A(11 products)
- Aromatase(20 products)
- Estrogen/progestogen Receptor(49 products)
- GPR(1 products)
- Glucocorticoid Receptor(153 products)
- LHRH(1 products)
- Opioid Receptor(298 products)
- Prostaglandin Receptor(120 products)
- RAAS(87 products)
- Reductase(52 products)
- Somatostatin(49 products)
- Thyroid hormone receptor(THR)(26 products)
- Vasopressin Receptor(44 products)
Show 6 more subcategories
Found 3184 products of "Endocrinology/Hormones"
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
LY2881835
CAS:<p>LY2881835 is a potent and selective GPR40 agonist.</p>Formula:C33H33NO3Purity:98.59% - 98.59%Color and Shape:SolidMolecular weight:491.62Y134
CAS:<p>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.</p>Formula:C28H28N2O3SPurity:99.98%Color and Shape:SolidMolecular weight:472.6CRTh2 antagonist 2
CAS:<p>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.</p>Formula:C26H23ClN4O3Purity:99.05%Color and Shape:SolidMolecular weight:474.94GR 89696 fumarate
CAS:<p>GR 89696 fumarate is a highly selective κ2 opioid receptor agonist (IC50 = 0.04nM) with anti-pruritchy, anti-injury and neuroprotective effects.</p>Formula:C23H29Cl2N3O7Purity:99.84%Color and Shape:SolidMolecular weight:530.4Fezagepras sodium
CAS:<p>Fezagepras sodium (Setogepram sodium salt) is an orally active GPR40 agonist and is an antagonist or inverse agonist for GPR84, with anti-fibrotic, anti-</p>Formula:C13H17NaO2Purity:99.49%Color and Shape:SolidMolecular weight:228.26IPAG
CAS:<p>IPAG is a potent σ-receptor antagonist (pKi=4.3). IPAG can induce cell apoptosis.</p>Formula:C17H22IN3Purity:99.65%Color and Shape:SolidMolecular weight:395.28Trimebutine CTB salt
CAS:<p>Trimebutine CTB salt (GIC-1001) is an opioid receptor agonist used in the study of pain.</p>Formula:C29H36N2O8S2Purity:99.85% - >99.99%Color and Shape:SolidMolecular weight:604.74SCH-486757
CAS:<p>SCH-486757 is an agonist of nociceptin-1 (NOP1) and orphanin FQ peptide receptors and is used in the study of cough.</p>Formula:C24H23Cl2N3OPurity:99.53% - >99.99%Color and Shape:SolidMolecular weight:440.37ICI 199,441 hydrochloride
CAS:<p>ICI 199,441 hydrochloride is a potent, selective agonist of κ-opioid receptor.</p>Formula:C21H25Cl3N2OPurity:99.57%Color and Shape:SolidMolecular weight:427.8ONC1-13B
CAS:<p>ONC1-13B, an androgen receptor antagonist, is used potentially for the treatment of prostate cancer.</p>Formula:C22H16F4N4O3SPurity:99.36% - 99.85%Color and Shape:SolidMolecular weight:492.45PSB-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:384.88Indazole-Cl
CAS:<p>Indazole-Cl is a selective ERß agonist and a selective estrogen receptor modifier (SERM).</p>Formula:C13H9ClN2O2Purity:99.02% - 99.86%Color and Shape:SolidMolecular weight:260.68Endoxifen hydrochloride
CAS:<p>Endoxifen HCl, a Tamoxifen metabolite, targets estrogen receptors more effectively and blocks aromatase, showing promise for breast cancer research.</p>Formula:C25H28ClNO2Purity:99.08%Color and Shape:SolidMolecular weight:409.95JNJ-20788560
CAS:<p>JNJ-20788560 is a delta opioid receptor (DOR) agonist with analgesic activity. It is more selective for DOR than for mu opioid receptors (MOR).</p>Formula:C25H28N2O2Purity:98.02%Color and Shape:SolidMolecular weight:388.5GPR40/FFAR1 modulator 1
CAS:<p>GPR40/FFAR1 modulator 1 is a Gq-coupled free fatty acid receptor 1 (GPR40/FFAR1) agonist and allosteric modulator.</p>Formula:C21H19N5O3Purity:99.7%Color and Shape:SolidMolecular weight:389.41Estredox
CAS:<p>Estredox, an estrogen receptor agonist, is used potentially for the treatment of vasomotor symptoms.</p>Formula:C25H31NO3Purity:98.02% - 98.39%Color and Shape:SolidMolecular weight:393.52Glucocorticoid receptor agonist-1
CAS:<p>Glucocorticoid receptor agonist-1 is a potent glucocorticoid receptor agonist with an IC50 of 2.8 nM[1].</p>Formula:C35H39NO6Purity:99.68%Color and Shape:SolidMolecular weight:569.69Finrozole
CAS:<p>Finrozole (MPV 2213ad) is a novel selective aromatase inhibitor that is partially reversible for breast development.</p>Formula:C18H15FN4OPurity:99.63%Color and Shape:SolidMolecular weight:322.34Ripisartan
CAS:<p>Ripisartan (UP-269-6) is a potent and specific angiotensin II receptor antagonist that inhibits angiotensin II-mediated sympathetic tachycardia responses.</p>Formula:C23H22N8OPurity:98.86%Color and Shape:SolidMolecular weight:426.47Faxeladol
CAS:<p>Faxeladol: adrenergic, serotonin inhibitor & opioid agonist for neurological studies.</p>Formula:C15H23NOPurity:98.09% - 98.77%Color and Shape:SolidMolecular weight:233.35
