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(327 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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(E)-4-Hydroxytamoxifen
CAS:(E)-4-Hydroxytamoxifen is a less active isomer of (Z)-4-hydroxytamoxifen and also is an estrogen receptor modulator.Formula:C26H29NO2Color and Shape:SolidMolecular weight:387.51MK-0773
CAS:MK-0773 (PF-05314882) is a selective androgen receptor modulator that binds to AR (IC50: 6.6 nM) for the study of diseases caused by endocrine abnormalities.Formula:C27H34FN5O2Purity:98.38% - 99.14%Color and Shape:SolidMolecular weight:479.59Dihydromunduletone
CAS:<p>Dihydromunduletone (DHM) is an adhesion G protein-coupled receptor (aGPCR) antagonist inhibits GPR56 and GPR114/ADGRG5, which have similar tethered agonists.</p>Formula:C25H28O6Purity:99.96%Color and Shape:SolidMolecular weight:424.49Vanilpyruvic acid
CAS:Vanillylpyruvic acid is a phenylpyruvic acid derivative applicable in biochemical experiments and drug synthesis research.Formula:C10H10O5Purity:98%Color and Shape:SolidMolecular weight:210.18Porcine dynorphin A(1-13)
CAS:Porcine dynorphin A (1-13) is a potent κ opioid receptor agonist; it's antinociceptive and raises [Ca2+]i in neurons like NMDA.Formula:C75H126N24O15Purity:98%Color and Shape:SolidMolecular weight:1603.95Endomorphin 2 TFA
CAS:Endomorphin 2 TFA, displays reasonable affinities for kappa3 binding sites, with Ki value between 20 and 30 nM.Formula:C34H38F3N5O7Color and Shape:SolidMolecular weight:685.69Hydrocortisone buteprate
CAS:Hydrocortisone buteprate is a medium-potent, non-halogenated double-ester of hydrocortisone with a highly favorable benefit-to-risk ratio for inflammatory skin disorders.Formula:C28H40O7Purity:99.19%Color and Shape:SolidMolecular weight:488.61ARD-1676
CAS:<p>ARD-1676 is an orally administered androgen receptor (AR) PROTAC degrader that combines an AR ligand with a cereblon ligand.</p>Formula:C44H46ClN7O5Purity:98%Color and Shape:SolidMolecular weight:788.33Dehydroepiandrosterone-d2
CAS:Dehydroepiandrosterone-d2 is a deuterated compound of Dehydroepiandrosterone.Formula:C19H26D2O2Color and Shape:SolidMolecular weight:290.44Betamethasone acetate
CAS:Betamethasone acetate, the 21-acetate ester of betamethasone, is a synthetic glucocorticoid corticosteroid and a corticosteroid ester.Formula:C24H31FO6Color and Shape:SolidMolecular weight:434.50Losartan (D4 Carboxylic Acid)
CAS:Losartan D4 Carboxylic Acid is the deuterium labeled Losartan, which is an angiotensin II receptor antagonist.Formula:C22H21ClN6O2Purity:98%Color and Shape:SolidMolecular weight:440.92Enalaprilat
CAS:Enalaprilat (Enalapril acid) is an ACE inhibitor used in the study of cardiovascular disease.Formula:C18H24N2O5Purity:97.28%Color and Shape:SolidMolecular weight:348.39BAN ORL 24 dihydrochloride
CAS:BAN ORL 24 dihydrochloride is a highly potent nociceptin/orphan FQ (N/OFQ) receptor (NOP) antagonist that can be used to study neurological diseases.Formula:C27H37Cl2N3O2Purity:95.03%Color and Shape:SolidMolecular weight:506.51DL-Cystine
CAS:DL-Cystine is a cysteine derivative that inhibits endothelial cell proliferation by regulating TGFβ1. a GPR inhibitor and nAChR agonist .Formula:C6H12N2O4S2Color and Shape:SolidMolecular weight:240.3Endoxifen Z-isomer hydrochloride
CAS:Endoxifen Z-isomer hydrochloride (Endoxifen HCl) is the active metabolite of Tamoxifen, which is an effective and selective estrogen receptor antagonist.Formula:C25H28ClNO2Color and Shape:SolidMolecular weight:409.95D4-abiraterone
CAS:D4-abiraterone is the active metabolite of abiraterone.Δ4-Abiraterone is a inhibitor of CYP17A1, 3β-HSD and SRD5A, and an antagonist of the androgen receptor.Formula:C24H29NOPurity:99.75% - 99.8%Color and Shape:SolidMolecular weight:347.49NQO1 substrate
CAS:<p>NQO1 substrate is a highly potent NQO1 substrate with potential antitumor activity for leukemia research.</p>Formula:C13H2F2N4OPurity:98.02% - 98.02%Color and Shape:SolidMolecular weight:268.18Dienestrol diacetate
CAS:Dienestrol diacetate, a derivative of the synthetic non-steroid phenolic compound, DIENESTROL, exhibits estrogenic activities.Formula:C22H22O4Purity:98%Color and Shape:SolidMolecular weight:350.41GPR40 agonist 6
CAS:GPR40 agonist 6 (Compound 7a) is a potent and selective agonist of free fatty acid receptor 1 ( FFAR1 or GPR40 ) with an EC 50 of 0.058 μM against GPR40 [1].Formula:C20H19NO4Color and Shape:SolidMolecular weight:337.37Rezvilutamide
CAS:Rezvilutamide (SHR3680) is an orally available androgen receptor inhibitor that crosses the blood-brain barrier and has antitumor activity.Formula:C22H20F3N3O4SPurity:99.96% - 99.97%Color and Shape:SolidMolecular weight:479.47
