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(230 products)
- Annexin A(16 products)
- Aromatase(23 products)
- Estrogen/progestogen Receptor(66 products)
- GPR(1 products)
- Glucocorticoid Receptor(165 products)
- LHRH(2 products)
- Opioid Receptor(327 products)
- Prostaglandin Receptor(126 products)
- RAAS(89 products)
- Reductase(51 products)
- Somatostatin(57 products)
- Thyroid hormone receptor(THR)(34 products)
- Vasopressin Receptor(48 products)
Show 6 more subcategories
Found 3427 products of "Endocrinology/Hormones"
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Liraglutide
Liraglutide is sold under the brand name €˜Victoza' and is a medication used to treat diabetes mellitus type 2 and obesity.Liraglutide binds to and activates the GLP-1 (glucagon-like peptide-1) receptor to bring about an increase in insulin secretion and a decrease in glucagon secretion and gastric emptying.Molecular weight:3,748.9 g/molD-Kynurenine
CAS:D-Kynurenine, ZINC901103, metabolizes from D-tryptophan, activates AhR, changes epithelium to mesenchyme, and tests for D-amino acid oxidase.Formula:C10H12N2O3Purity:99.68%Color and Shape:SolidMolecular weight:208.21Tolrestat
CAS:Tolrestat (AY-27773) is a potent inhibitor of aldose reductase (IC50 = 35 nM).Formula:C16H14F3NO3SPurity:98.89% - >99.99%Color and Shape:SolidMolecular weight:357.35Lipo-Oxytocin-1
Lipidated Oxytocin analog with long-lasting activities. Product has the following disulfide bonds: Cys1-Cys6 and is available as a 0.5mg vial.Purity:Min. 95%Fluticasone furoate
CAS:Fluticasone furoate (Avamys), a potent, trifluorinated steroid with anti-inflammatory effects, treats allergic rhinitis.Formula:C27H29F3O6SPurity:99.82%Color and Shape:SolidMolecular weight:538.58Ref: TM-T21404
5mg34.00€10mg50.00€1mL*10mM (DMSO)55.00€25mg87.00€50mg130.00€100mg177.00€200mg264.00€500mg447.00€Dehydro Olmesartan
CAS:Dehydro Olmesartan, from Olmesartan, is an AT1R blocker for researching hypertension.Formula:C24H24N6O2Color and Shape:SolidMolecular weight:428.49GSK9027
CAS:GSK9027, a nonsteroidal GR agonist, is a partial 2×GRE reporter gene activator, less potent than dexamethasone.Formula:C27H19F4N3O2SPurity:99.31%Color and Shape:SolidMolecular weight:525.52Prednisolone hemisuccinate
CAS:Prednisolone hemisuccinate is a soluble glucocorticoid and cortisol exerts anti-inflammatory, immunosuppressive, and antiallergic by binding to GR receptor.Formula:C25H32O8Purity:99.96%Color and Shape:SolidMolecular weight:460.52Rentiapril
CAS:Rentiapril is an orally active inhibitor of angiotensin converting enzyme (ACE), with antihypertensive activity.Formula:C13H15NO4S2Purity:98%Color and Shape:SolidMolecular weight:313.39Omapatrilat
CAS:Omapatrilat is an orally active dual inhibitor of ACE and NEP (neprilysin), with Ki values of 0.64 and 0.45 nM, respectively, suppressing induced hypotension.Formula:C19H24N2O4S2Purity:98.87%Color and Shape:SolidMolecular weight:408.53BMS-564929
CAS:BMS-564929 is an AR agonist that upregulates the expression and activity of fat-producing enzymes, reducing VAT content and lipid levels.Formula:C14H12ClN3O3Purity:98.17%Color and Shape:SolidMolecular weight:305.72Norethisterone enanthate
CAS:Norethisterone enanthate (NSC-9564) is a long-acting parenteral progestogen with antigonadotropic effects.Formula:C27H38O3Purity:99.23%Color and Shape:SolidMolecular weight:410.59Camizestrant
CAS:Camizestrant (Estrogen receptor antagonist 2) is an antagonist of the estrogen receptor and can be used in studies about ER+ HER2-advanced breast cancer[1].Formula:C24H28F4N6Purity:97.25% - 99.57%Color and Shape:SolidMolecular weight:476.51Ref: TM-T11237
1mg140.00€5mg339.00€1mL*10mM (DMSO)354.00€10mg567.00€25mg999.00€50mg1,549.00€100mg2,160.00€MK-3984
CAS:MK-3984 is a selective androgen receptor modulator, used in the study of conditions caused by androgen deficiency.Formula:C17H12F7NO2Purity:99.91%Color and Shape:SolidMolecular weight:395.27OP-1074
CAS:OP-1074 is a pure antiestrogen and a selective degrader of ER, shows specific antiestrogenic activity for ERα and ERβ.Formula:C29H31NO4Purity:98%Color and Shape:SolidMolecular weight:457.56Capesaris
CAS:Capesaris (GTX-758) is an oral estrogen receptor α agonist, used in prostate cancer research.Formula:C19H13F2NO3Purity:99.65%Color and Shape:SolidMolecular weight:341.31PF-4455242 HCl
CAS:PF-4455242 HCl is a selective and orally available κ-opioid receptor antagonist that exhibiting antidepressant effects.Formula:C21H29ClN2O2SPurity:99.59%Color and Shape:SolidMolecular weight:408.99Dimethomorph
CAS:Dimethomorph is a fungicide and sterol biosynthesis inhibitor that inhibits fungal cell wall formation,. inhibits androgen receptor (AR) .Formula:C21H22ClNO4Purity:99.20%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:670.75Vorozole
CAS:Vorozole (R83842) is an orally active, potent, and selective nonsteroidal aromatase inhibitor.Vorozole exhibits antitumor activity in vivo and may be used inFormula:C16H13ClN6Purity:99.65% - 99.94%Color and Shape:SolidMolecular weight:324.77AZ12216052
CAS:AZ12216052 is a GRP8 antagonist with anxiolytic and anti-inflammatory activity and can be used to study obesity and metabolic disorders.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:455.53Ref: TM-T10084
1mg109.00€5mg241.00€1mL*10mM (DMSO)268.00€10mg354.00€25mg532.00€50mg745.00€100mg1,018.00€500mg2,035.00€CAY10595
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:GPR35 agonist 3 is a synthetic GPR35 agonist used in the study of cancer, type 2 diabetes and cardiovascular disease.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:367.88Ref: TM-T12320
1mg50.00€5mg105.00€1mL*10mM (DMSO)108.00€10mg155.00€25mg224.00€50mg315.00€100mg424.00€200mg560.00€SCH 221510
CAS:SCH 221510: oral NOP agonist, EC50=12 nM, Ki=0.3 nM, anxiolytic, for neurological research.Formula:C28H31NOPurity:99.74%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:Org30958 is a potent inhibitor of aromatase in vivo.
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:GSK1521498 free base is an effective and selective μ-opioid receptor antagonist with potential applications in obesity, alcoholism, and drug addiction.Formula:C24H20F2N4Purity:99.85%Color and Shape:SolidMolecular weight:402.44Ref: TM-T11478L
1mg118.00€5mg282.00€1mL*10mM (DMSO)310.00€10mg516.00€25mg1,007.00€50mg1,583.00€100mg2,322.00€GPR81 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:431.62Acolbifene
CAS:Acolbifene (SCH 57068) is a selective antagonist of estrogen receptors with IC50s of 2 nM and 0.4 nM for estradiol-induced transcriptional activity of ERα andFormula:C29H31NO4Purity:98.17%Color and Shape:SolidMolecular weight:457.56T-10418
CAS:T-10418 is a selective G2A/GPR132 agonist that enhances TRPV1 responses in mouse primary sensory neurons, neuropathic pain and inflammation.Formula:C22H20N2O4Purity:98.95%Color and Shape:SolidMolecular weight:376.41Ref: TM-T88533
1mg143.00€5mg346.00€1mL*10mM (DMSO)380.00€10mg546.00€25mg1,132.00€50mg1,554.00€100mg2,025.00€200mg2,721.00€Anrikefon
CAS:Anrikefon (HSK21542) is a kappa opioid receptor agonist with analgesic effect .Formula:C39H57N7O5Molecular weight:703.91AZ11657312 Free Base
CAS:AZ11657312 is a P2X7 receptor antagonist.Formula:C26H35N3O3Color and Shape:SolidMolecular weight:437.57ZK 164015
CAS:estrogen receptor silent antagonistFormula:C30H43NO4SPurity:98%Color and Shape:SolidMolecular weight:513.73LY 99335
CAS:LY 99335 is a narcotic antagonist in the class of phenylpiperidine.Formula:C14H22ClNOColor and Shape:SolidMolecular weight:255.79S07-2008
CAS:S07-2008 is a selective inhibitor of aldo-keto reductase family 1 member C3 (AKR1C3) (IC50: 0.16 μM) and has anticancer effects.Formula:C21H23N3O5SColor and Shape:SolidMolecular weight:429.496-Hydroxyluteolin
CAS:6-Hydroxyluteolin, a flavonoid compound extracted from Salvia amarissima Ortega, inhibits aldose reductase (AR) and has antimicrobial activity.Formula:C15H10O7Purity:99.67%Color and Shape:SolidMolecular weight:302.24MK771
CAS:MK771, a TRH analog, potentially eases opiate withdrawal symptoms.Formula:C16H22N6O4SColor and Shape:SolidMolecular weight:394.45S07-2001
CAS:S07-2001 boosts Doxorubicin's effect on cancer, targeting AKR1C3 with IC50 of 2.08 μM, may overcome drug resistance.Formula:C15H17N3O4SColor and Shape:SolidMolecular weight:335.38NO-Losartan A
CAS:Angiotensin II affects blood pressure and atherosclerosis via AT1; losartan blocks AT1. NO-losartan adds vasodilation.Formula:C30H28ClN7O5Color and Shape:SolidMolecular weight:602.04BRF110
CAS:BRF110: brain-penetrant Nurr1:RXRα agonist, neuroprotective against PD, boosts dopamine, no dyskinesia in mice.Formula:C22H18F3N3O2Color and Shape:SolidMolecular weight:413.39
