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(55 products)
- GPR(1 products)
- Glucocorticoid Receptor(167 products)
- LHRH(1 products)
- Opioid Receptor(322 products)
- Prostaglandin Receptor(122 products)
- RAAS(90 products)
- Reductase(50 products)
- Somatostatin(54 products)
- Thyroid hormone receptor(THR)(30 products)
- Vasopressin Receptor(46 products)
Show 6 more subcategories
Found 3359 products of "Endocrinology/Hormones"
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Dimethomorph
CAS:Dimethomorph is a fungicide and sterol biosynthesis inhibitor that inhibits fungal cell wall formation,. inhibits androgen receptor (AR) .Formula:C21H22ClNO4Purity:99.2%Color and Shape:Solid CrystallineMolecular weight:387.86Endomorphin 1 acetate
CAS:Endomorphin 1 acetate is a μ-opioid receptor agonist with antinociceptive and analgesic effects and can be used to study neurological diseases.Formula:C36H42N6O7Purity:99.74%Color and Shape:SolidMolecular weight:670.75AZ12216052
CAS:<p>AZ12216052 is a GRP8 antagonist with anxiolytic and anti-inflammatory activity and can be used to study obesity and metabolic disorders.</p>Formula:C19H22BrNOSPurity:99.29%Color and Shape:SolidMolecular weight:392.35TUG-469
CAS:TUG-469 is an agonist of free fatty acid 1(FFA) receptor.Formula:C23H23NO2Purity:99.73%Color and Shape:SolidMolecular weight:345.43LY2444296
CAS:LY2444296 (FP3FBZ) is an orally active and selective antagonist of kappa opioid receptor(Ki = 1 nM).Formula:C24H22F2N2O2Purity:99.18%Color and Shape:SolidMolecular weight:408.44CRTh2 antagonist 1
CAS:CRTh2 antagonist 1 is a CRTh2 antagonist (IC50: 89 nM).Formula:C23H25N3O5SPurity:97.24%Color and Shape:SolidMolecular weight:455.53CAY10595
CAS:CAY10595 is an antagonist of the CRTh2 (DP2) receptor with a Ki of 10 nM.Formula:C20H13Cl2FN2O5Purity:99.95% - 99.97%Color and Shape:SolidMolecular weight:451.23GPR35 agonist 3
CAS:<p>GPR35 agonist 3 is a synthetic GPR35 agonist used in the study of cancer, type 2 diabetes and cardiovascular disease.</p>Formula:C12H9NO5SPurity:98.80%Color and Shape:SolidMolecular weight:279.27Opioid receptor modulator 1
CAS:Opioid receptor modulator 1 is a modulator of opioid receptor.Formula:C18H23NO2Purity:98%Color and Shape:SolidMolecular weight:285.38ORL1 antagonist 1
CAS:ORL1 antagonist 1 is an o antagonist of pioid receptor-like 1 (ORL1) (IC50 of 61 nM).Formula:C20H22ClN5Purity:98.92%Color and Shape:SolidMolecular weight:367.88SCH 221510
CAS:<p>SCH 221510: oral NOP agonist, EC50=12 nM, Ki=0.3 nM, anxiolytic, for neurological research.</p>Formula:C28H31NOPurity:99.54%Color and Shape:SolidMolecular weight:397.55GPR84 antagonist 8
CAS:GPR84 antagonist 8 is a selective GPR84 antagonist applicable for investigating inflammatory and fibrotic diseases.Formula:C23H23N3O5Purity:99.45%Color and Shape:SolidMolecular weight:421.45CP-866087
CAS:CP-866087 is a novel, potent and selective mu-opioid receptor antagonist for the study of female sexual dysfunction.Formula:C24H28N2O2Purity:99.56% - >99.99%Color and Shape:SoildMolecular weight:376.49Org30958
CAS:<p>Org30958 is a potent inhibitor of aromatase in vivo.</p>Formula:C21H30O2S2Purity:98%Color and Shape:SolidMolecular weight:378.59GSK1521498
CAS:GSK1521498 is a selective antagonist of the μ-opioid receptor (MOR).Formula:C24H23F2N4O4PPurity:98%Color and Shape:SolidMolecular weight:500.43TAK-875 Hemihydrate
CAS:TAK-875 Hemihydrate (Fasiglifam) is a selective GPR40 agonist with EC50 of 14 nM, 400-fold more potent than oleic acid.Formula:C29H32O7SH2OPurity:98%Color and Shape:SolidMolecular weight:533.63GSK1521498 free base (hydrochloride)
CAS:GSK1521498 free base (hydrochloride) is a selective antagonist of the μ-opioid receptor (MOR).Formula:C24H21ClF2N4Purity:98%Color and Shape:SolidMolecular weight:438.9GSK1521498 free base
CAS:<p>GSK1521498 free base is an effective and selective μ-opioid receptor antagonist with potential applications in obesity, alcoholism, and drug addiction.</p>Formula:C24H20F2N4Purity:99.85%Color and Shape:SolidMolecular weight:402.44GPR81 agonist 1
CAS:GPR81 agonist 1 is a GPR81 agonist that improves glycaemic control in insulin-resistant mouse models for the study of diabetes and obesity.Formula:C22H30N4O2S2Purity:99.68%Color and Shape:SolidMolecular weight:446.63GPR4 antagonist 1
CAS:GPR4 antagonist 1 is a GPR4 antagonist (IC50: 189 nM).Formula:C27H37N5Purity:98%Color and Shape:SolidMolecular weight:431.62
