
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(207 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(296 products)
- Prostaglandin Receptor(119 products)
- RAAS(86 products)
- Reductase(52 products)
- Somatostatin(46 products)
- Thyroid hormone receptor(THR)(26 products)
- Vasopressin Receptor(44 products)
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Found 3178 products of "Endocrinology/Hormones"
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AM-5262
CAS:<p>AM-5262 is a potent GPR40 Full Agonist with improved rat PK profile and general selectivity profile.</p>Formula:C33H35FO4Color and Shape:SolidMolecular weight:514.63Zankiren
CAS:<p>Zankiren is a renin inhibitor. Zankiren can reduce blood pressure, plasma renin activity, and angiotension II.</p>Formula:C35H55N5O6S2Color and Shape:SolidMolecular weight:705.97NR-V04
CAS:<p>NR-V04 is a PROTAC degrader targeting NR4A1.</p>Formula:C62H87N5O11SColor and Shape:SolidMolecular weight:1110.45[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:1434.59(rel)-PROTAC ERRα Degrader-1
<p>(rel)-PROTAC ERRα Degrader-1 is a relative configuration of PROTAC ERRα Degrader-1, which is an estrogen-related receptor alpha (ERRa) degrader.</p>Formula:C54H49Cl2F6N7O8Purity:98%Color and Shape:SolidMolecular weight:1108.91Raloxifene 6-Monomethyl Ether
CAS:<p>Compound 7, Raloxifene 6-Monomethyl Ether, blocks estrogen receptor α, inhibits MCF-7 cells; IC50=250 nM, pIC50=6.6.</p>Formula:C29H29NO4SColor and Shape:SolidMolecular weight:487.61DPP-4/GPR119 modulator 1
CAS:<p>Orally active DPP-4 inhibitor/GPR119 agonist, Compound 22 lowers glucose, moderate hERG inhibition, IC50 4.9 µM, for diabetes research.</p>Formula:C30H39ClN10O3Color and Shape:SolidMolecular weight:623.15Prednicarbate
CAS:<p>Prednicarbate (Hoe 777), a corticosteroid, has antipruritic, anti-inflammatory effects, reduces lymphocytes, and inhibits vasodilators.</p>Formula:C27H36O8Purity:99.88%Color and Shape:SolidMolecular weight:488.57β-Endorphin, equine
CAS:<p>Endorphin Beta is A substance produced in the brain, especially in the pituitary gland, Endorphin Beta blocks the sensation of pain.</p>Formula:C154H248N42O44SPurity:98%Color and Shape:SolidMolecular weight:3423.94Enalapril
CAS:<p>Enalapril is a dicarbocyl-containing peptide and angiotensin-converting enzyme (ACE) inhibitor with antihypertensive activity.</p>Formula:C20H28N2O5Purity:99.47%Color and Shape:SolidMolecular weight:376.45PROTAC ERα Y537S degrader-1
CAS:<p>PROTAC ERα Y537S degrader-1 comprises a ubiquitin E3 ligase binding group, a linker and a protein binding group.</p>Formula:C46H49N5O6Color and Shape:SolidMolecular weight:767.91LY255582
CAS:<p>LY255582 is a selective centrally active opioid receptor antagonist with high affinity for mu, delta and kappa receptors with Ki of 0.4 nM, 5.2, 2.0 nM,</p>Formula:C22H35NO2Purity:98%Color and Shape:SolidMolecular weight:345.52Ethamoxytriphetol
CAS:<p>Ethamoxytriphetol is a non-steroidal estrogen antagonist.</p>Formula:C27H33NO3Color and Shape:SolidMolecular weight:419.56SNIPER(ER)-87
CAS:<p>SNIPER(ER)-87 is a chemical compound composed of a derivative of the inhibitor of apoptosis protein (IAP) ligand LCL161 conjugated to the estrogen receptor α (</p>Formula:C59H73N5O10SPurity:98%Color and Shape:SolidMolecular weight:1044.32Bexirestrant
CAS:<p>Bexirestrant is an orally active ER-α degrader commonly employed in the research of antiestrogen and antineoplastic therapies.</p>Formula:C29H26F3NO2Color and Shape:SolidMolecular weight:477.527N-Desmethyl Loperamide
CAS:<p>N-Desmethyl Loperamide is the major metabolite of loperamide. It is also used as the precusor for radiolabelled loperamide.</p>Formula:C28H31ClN2O2Color and Shape:SolidMolecular weight:463.01ERα degrader 12
<p>ERα degrader12 (Compound RA3) is an estrogen receptor alpha (ERα) degrader with antitumor properties. It significantly suppresses tumor growth in a xenograft mouse model of breast cancer.</p>Formula:C39H41NO9SColor and Shape:SolidMolecular weight:699.81PROTAC ER Degrader-15
<p>PROTAC ER Degrader-15 (Compound 40) is an orally active estrogen receptor (ER) degrader with anticancer properties, suitable for breast cancer research.</p>Formula:C47H47F4N5O5Color and Shape:SolidMolecular weight:837.9CJ-15208
CAS:<p>CJ-15208: κ-opioid antagonist, IC50: 47 nM kappa, 260 nM mu, 2600 nM delta, reverses asimadoline effects in rabbits (ED50 1.3 µM).</p>Formula:C34H35N5O4Color and Shape:SolidMolecular weight:577.67THR-β agonist 6
CAS:<p>THR-β Agonist 6, a selective and orally active compound targeting the thyroid hormone receptor β (THR-β), demonstrates specificity with EC50 values of 0.03 μM</p>Formula:C20H14Cl2N6O3Color and Shape:SolidMolecular weight:457.27

