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(56 products)
- GPR(1 products)
- Glucocorticoid Receptor(167 products)
- LHRH(1 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(46 products)
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Found 3370 products of "Endocrinology/Hormones"
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Akuammicine
CAS:Akuammicine, as an indole alkaloid from Catharanthus roseus, can be used in cancer cell eradication.Formula:C20H22N2O2Color and Shape:SolidMolecular weight:322.408Glucocorticoids receptor agonist 1
CAS:<p>GRA-1, an arylpyrazole, is a potent glucocorticoid receptor agonist with robust anti-inflammatory effects and preserves insulin secretion.</p>Formula:C20H23FN2OColor and Shape:SolidMolecular weight:326.41GPCR agonist-2
CAS:GPCR agonist-2 (4-(Cyclopropylamino)-3-nitrobenzoic acid) is an agonist of the orphan human GPCR GPR109B.Formula:C10H10N2O4Purity:99.96%Color and Shape:SolidMolecular weight:222.2ALR2-IN-1
CAS:ALR2-IN-1: potent, selective inhibitor of ALR2 (IC50=1.42 μM), antiglycemic, antioxidant; for diabetes research.Formula:C16H17N3O2SPurity:99.41%Color and Shape:SoildMolecular weight:315.39Methylpiperidino pyrazole
CAS:Methylpiperidino pyrazole is an ERα inhibitor and can prevent the BPS-induced Rb phosphorylation and cell cycle progression.Formula:C29H31N3O3Purity:98.84%Color and Shape:SolidMolecular weight:469.57(Rac)-Finerenone
CAS:Rac-Finerenone, or (Rac)-BAY 94-8862, is an oral nonsteroidal MR antagonist with high selectivity and an IC50 of 18 nM.Formula:C21H22N4O3Color and Shape:SolidMolecular weight:378.432Montirelin
CAS:Montirelin is an analog of thyrotropin-releasing hormone.Formula:C17H24N6O4SColor and Shape:SolidMolecular weight:408.48D3R/MOR antagonist 2
<p>Compound 121, a D3R/MOR antagonist with K i values of 361 nM and 85.2 nM for D3R and MOR respectively, has the potential for analgesic effects through MOR</p>Formula:C25H31ClN2OPurity:98%Color and Shape:SolidMolecular weight:410.98β-Endorphin (1-27) (human) acetate
<p>β-Endorphin (1-27) (human) acetate, existing in the hypophysis cerebri and hypothalamus, exhibits antinociception activity.</p>Formula:C141H221N33O42SPurity:96.52%Color and Shape:SolidMolecular weight:3082.5221-hydroxy Eplerenone
CAS:21-hydroxy Eplerenone, a key eplerenone metabolite, is produced via CYP3A4.Formula:C24H30O7Color and Shape:SolidMolecular weight:430.497[(pF)Phe4]Nociceptin(1-13)NH2
CAS:<p>Potent, selective OP4 agonist; pKi=10.68, pEC50=9.80. >8000x selectivity vs other opioid receptors; long-lasting in vivo effects.</p>Formula:C61H99FN22O15Purity:98%Color and Shape:SolidMolecular weight:1399.6Dermorphin Analog
Dermorphin Analog, a heptapeptide from amphibian skin, binds μ-opioid receptors selectively and strongly.Formula:C44H59N11O10Purity:98%Color and Shape:SolidMolecular weight:901.43[Orn5]-URP acetate
[Orn5]-URP acetate is an effective and selective Urotensin-II receptor (UT) antagonist (pEC50 = 7.24). [Orn5]-URP exhibits no agonist activity.Formula:C50H66N10O12S2Purity:98.4300%Color and Shape:SolidMolecular weight:1063.25OT-R antagonist 1
CAS:OT-R antagonist 1: Nonpeptide, selective, low-weight blocker of oxytocin; IC50 = 8 nM for Ca2+ disruption.Formula:C28H29N3O4Purity:98%Color and Shape:SolidMolecular weight:471.55[Orn5]-URP
CAS:Urotensin-II receptor antagonist, no agonist effect, pEC50 7.24, blocks U-II in rat aorta assay.Formula:C48H62N10O10S2Purity:98%Color and Shape:SolidMolecular weight:1003.2Olmesartan impurity
CAS:Olmesartan impurity, related to parent RNH-6270, is an AT1R antagonist used for hypertension research.Formula:C33H26N4OColor and Shape:SolidMolecular weight:494.598Tetrahydro Aldosterone
CAS:<p>Tetrahydro Aldosterone is a steroidal compound that inhibits the adrenal angiotensin II receptor, with an IC50 of 10 μM.</p>Formula:C21H32O5Color and Shape:SolidMolecular weight:364.48ER ligand-9
CAS:<p>ER ligand-9 is a conjugate of an estrogen receptor (Estrogen Receptor/ERR) ligand and a linker, utilized in the synthesis of PROTACs ERD-1233.</p>Formula:C31H33NO3Color and Shape:SolidMolecular weight:467.599Cgp 44099
CAS:Cgp 44099 is a potent plasma renin inhibitor from all subprimate species.Formula:C69H104N14O13Purity:98%Color and Shape:SolidMolecular weight:1337.676PRL 2915
CAS:<p>PRL 2915 is a potent antagonist of the human somatostatin subtype 2 receptor (hsst 2), exhibiting a binding affinity (K_i) of 12 nM [1].</p>Formula:C59H71ClN12O8S2Color and Shape:SolidMolecular weight:1175.85
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