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(297 products)
- Prostaglandin Receptor(120 products)
- RAAS(87 products)
- Reductase(52 products)
- Somatostatin(49 products)
- Thyroid hormone receptor(THR)(26 products)
- Vasopressin Receptor(44 products)
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Found 3183 products of "Endocrinology/Hormones"
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HP210
CAS:<p>HP210, a selective glucocorticoid receptor modulator (SGRM), can suppress IL-1β and IL-6 mRNA expression, suggesting its utility in investigating inflammation-</p>Formula:C22H19N3O2S2Purity:98%Color and Shape:SolidMolecular weight:421.54Fosdagrocorat
CAS:<p>Fosdagrocorat is an agonist of the dissociated glucocorticoid receptor.</p>Formula:C29H30F3N2O5PColor and Shape:SolidMolecular weight:574.53JJH260
CAS:<p>JJH260, a N-hydroxy hydantoin carbamate, inhibits AIG1 and ADTRP with IC50 values of 0.57 μM and 8.5 μM, respectively, and targets ABHD6, LYPLA1/2.</p>Formula:C29H34ClN5O5Color and Shape:SolidMolecular weight:568.06RTI-13951-33
CAS:<p>RTI-13951-33 is an effective and brain-penetrant GPR88 agonist (EC50: 25 nM, in GPR88 cAMP functional assay).</p>Formula:C28H33N3O3Purity:98%Color and Shape:SolidMolecular weight:459.58ER degrader 6
CAS:<p>ER degrader 6 (compound 35s) is a potent selective estrogen receptor modulator (SERM) with the capacity to degrade Estrogen Receptor (ER)α.</p>Formula:C33H34FN3O5SSePurity:98%Color and Shape:SolidMolecular weight:682.66Icalcaprant
CAS:<p>Icalcaprant is a kappa-opioid receptor antagonist [1].</p>Formula:C23H26N4O3Purity:98%Color and Shape:SolidMolecular weight:406.48Androgen receptor degrader-2
CAS:<p>Androgen Receptor Degrader-2 (Compound 9) is a potent degrader of androgen receptors, with potential application in cancer research [1].</p>Formula:C16H16ClN3O4Purity:98%Color and Shape:SolidMolecular weight:349.77N-Nitrosodicyclohexylamine
CAS:<p>N-Nitrosodicyclohexylamine (NDCHA), an N-nitrosocompound, exhibits anti-androgenic activity by competitively binding to the androgen receptor (AR) in opposition</p>Formula:C12H22N2OPurity:98%Color and Shape:SolidMolecular weight:210.32GLL398
CAS:<p>GLL398: Oral ERα down-regulator, binds strongly (IC50=1.14nM), degrades ERα in MCF-7 cells (IC50=0.21μM).</p>Formula:C25H23BO4Color and Shape:SolidMolecular weight:398.26Elisartan
CAS:<p>Elisartan is a non-peptide pro-drug of angiotensin II AT1 receptor antagonist HN-12206. It also shows anti-hypertension activities.</p>Formula:C27H29ClN6O5Purity:98%Color and Shape:SolidMolecular weight:553.01Androgen receptor degrader-1
CAS:<p>Androgen Receptor Degrader-1 (Compound 18) is a potent agent for androgen receptor degradation, applicable in cancer research [1].</p>Formula:C15H14ClN3O4Purity:98%Color and Shape:SolidMolecular weight:335.74UFP-512
CAS:<p>UFP-512 is a selective delta-opioid (DOP) receptor agonist.</p>Formula:C31H33N5O5Purity:98%Color and Shape:SolidMolecular weight:555.62Trap-101 hydrochloride
CAS:<p>nociceptin/orphanin FQ (NOP) receptor antagonist</p>Formula:C24H36ClN3O2Purity:98%Color and Shape:SolidMolecular weight:434.02YXG-158
CAS:<p>YXG-158 (Compound 23-h), an orally active androgen receptor (AR) degrader and cytochrome P450 17A1 (CYP17A1) inhibitor, exhibits AR degradation with a DC50 of 1</p>Formula:C30H36FN3OPurity:98%Color and Shape:SolidMolecular weight:473.62Androgen receptor degrader-3
CAS:<p>Androgen Receptor Degrader-3 (ARD-3) is a compound that inhibits androgen receptor signaling and promotes the degradation of the receptor, with potential</p>Formula:C45H51ClN8O5Purity:98%Color and Shape:SolidMolecular weight:819.39Nurr1 agonist 7
CAS:<p>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.</p>Formula:C18H20O3Purity:99.79%Color and Shape:SolidMolecular weight:284.35Androgen receptor antagonist 5
CAS:<p>AR antagonist 5 blocks AR (IC50: 6.17 μM), hinders LNCaP cell growth, and has anti-tumor effects in mouse models.</p>Formula:C21H15F4N5O3SColor and Shape:SolidMolecular weight:493.43N-Demethyl Mifepristone
CAS:<p>N-Demethyl Mifepristone (RU 42633), an active metabolite of Mifepristone, exhibits 61% of the affinity for the glucocorticoid receptor relative to Mifepristone'</p>Formula:C28H33NO2Purity:98%Color and Shape:SolidMolecular weight:415.57Androgen receptor-IN-5
CAS:<p>Androgen receptor-IN-5 is a potent inhibitor of the androgen receptor with anticancer properties.</p>Formula:C22H10Cl2F4N4OSPurity:98%Color and Shape:SolidMolecular weight:525.31Taragarestrant
CAS:<p>Taragarestrant (D-0502), an oral estrogen receptor degrader, combats ER+ breast cancer in research.</p>Formula:C25H25Cl2FN2O2Color and Shape:SolidMolecular weight:475.38
