
Endocrinology/Hormones
Subcategories of "Endocrinology/Hormones"
- Androgen Receptor(229 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(122 products)
- RAAS(89 products)
- Reductase(51 products)
- Somatostatin(57 products)
- Thyroid hormone receptor(THR)(33 products)
- Vasopressin Receptor(48 products)
Found 3420 products of "Endocrinology/Hormones"
CAY10786
CAS:CAY10786 (GPR52 antagonist-1) is an antagonist of G protein-coupled receptor 52 (GPR52, IC50 = 0.63 μM).Formula:C15H14OSPurity:99.82%Color and Shape:SolidMolecular weight:242.34Ref: TM-T36036
2mg38.00€5mg55.00€1mL*10mM (DMSO)60.00€10mg88.00€25mg168.00€50mg268.00€100mg430.00€200mg622.00€ICI 199,441 hydrochloride
CAS:ICI 199,441 hydrochloride is a potent, selective agonist of κ-opioid receptor.Formula:C21H25Cl3N2OPurity:99.57%Color and Shape:SolidMolecular weight:427.8Ref: TM-T22849
2mg33.00€5mg52.00€1mL*10mM (DMSO)58.00€10mg75.00€25mg138.00€50mg215.00€100mg314.00€200mg442.00€L-162,313
CAS:L-162,313 is an ANG II receptor agonist, a nonpeptide that mimics the biological actions of angiotensin II and induces an increase in MAP.Formula:C30H38N4O4S2Purity:98.21%Color and Shape:SolidMolecular weight:582.78GPR35 agonist 2
CAS:GPR35 agonist 2 (TC-G 1001) is a potent GPR35 agonist.The EC50 values of GPR35 agonist 2 in the β-arrestin and Ca2+ release assays were 26 and 3.2 nM,Formula:C17H11FN2O3SPurity:99.17% - 99.53%Color and Shape:SolidMolecular weight:342.34Ref: TM-T23434
1mg52.00€5mg96.00€1mL*10mM (DMSO)114.00€10mg170.00€25mg378.00€50mg560.00€100mg800.00€500mg1,644.00€GR 89696 fumarate
CAS:GR 89696 fumarate is a highly selective κ2 opioid receptor agonist (IC50 = 0.04nM) with anti-pruritchy, anti-injury and neuroprotective effects.Formula:C23H29Cl2N3O7Purity:99.84%Color and Shape:SolidMolecular weight:530.4Bevenopran
CAS:Bevenopran (CB-5945) is a peripheral antagonist of μ-opioid receptor and can be used in studies about the treatment of opioid-induced bowel dysfunction.Formula:C20H26N4O4Purity:98.69% - 98.9%Color and Shape:SolidMolecular weight:386.44Ref: TM-T14551
1mg62.00€5mg130.00€1mL*10mM (DMSO)142.00€10mg187.00€25mg299.00€50mg408.00€100mg532.00€200mg705.00€Acifran
CAS:Acifran (AY 25712) is an HM74A/GPR109A and GPR109B agonist and displays antihyperlipidemic activity.Formula:C12H10O4Purity:99.19%Color and Shape:SolidMolecular weight:218.21Estrogen receptor antagonist 8
CAS:Estrogen Receptor Antagonist 8 is an ER antagonist with anti-uterine activity and may be used in the study of ovarian dysfunction.CASNETIN SODIUM (CasN)Formula:C25H21N3O4Purity:98.48%Color and Shape:SolidMolecular weight:427.45BMS-641988
CAS:BMS-641988 is a novel nonsteroidal androgen receptor antagonist for the treatment of prostate cancer.Formula:C20H20F3N3O5SPurity:99.3% - 99.92%Color and Shape:SoildMolecular weight:471.45Moveltipril
CAS:Moveltipril (Moveltipril calcium) is a potent angiotensin-converting enzyme (ACE) inhibitor.Moveltipril is converted to captopril in the body for action.Formula:C19H30N2O5SPurity:97.55% - 98.28%Color and Shape:SolidMolecular weight:398.52Ref: TM-T25832
1mg34.00€5mg78.00€1mL*10mM (DMSO)86.00€10mg116.00€25mg212.00€50mg338.00€100mg548.00€200mg737.00€Indazole-Cl
CAS:Indazole-Cl is a selective ERß agonist and a selective estrogen receptor modifier (SERM).
Formula:C13H9ClN2O2Purity:99.02% - 99.86%Color and Shape:SolidMolecular weight:260.68Ref: TM-T25534
1mg115.00€2mg164.00€5mg255.00€10mg375.00€25mg562.00€50mg787.00€100mg1,074.00€200mg1,454.00€Ripisartan
CAS:Ripisartan (UP-269-6) is a potent and specific angiotensin II receptor antagonist that inhibits angiotensin II-mediated sympathetic tachycardia responses.Formula:C23H22N8OPurity:98.52%Color and Shape:SolidMolecular weight:426.47SSR126768A
CAS:SSR126768A is an oxytocin receptor antagonist that inhibits uterine contractions and may be used to prevent preterm labor.Formula:C33H31Cl2N3O4Purity:97.06%Color and Shape:SolidMolecular weight:604.52Ref: TM-T28855
1mg315.00€5mg873.00€10mg1,080.00€25mg1,431.00€50mg1,783.00€100mg2,250.00€500mg6,264.00€FPL-62129
CAS:FPL-62129 is a calcium channel antagonist and a novel angiotensin-converting enzyme inhibitor with vasodilator activity for the study of cardiovascular disease.Formula:C20H19ClF5NO4Purity:98.27% - 99.34%Color and Shape:SolidMolecular weight:467.81Terlakiren
CAS:Terlakiren (CP-80,794) is a renin inhibitor that inhibits the potency of human renin and can be used to study neurological disorders of the hypertensive type.Formula:C31H48N4O7SPurity:99.38%Color and Shape:SolidMolecular weight:620.8Y134
CAS:Y134, an oral estrogen receptor inhibitor, is 121x more selective for ERα (Ki=0.09 nM) over ERβ (Ki=11.31 nM), and blocks ER+ breast cancer cell growth.Formula:C28H28N2O3SPurity:99.98%Color and Shape:SolidMolecular weight:472.6Tirzepatide acetate
CAS:Cymit Quimica provides this product solely for uses within the scope of any statute or law providing for an immunity, exemption, or exception to patent infringement (“Exempted Uses”), including but not limited to 35 U.S.C. § 271(e)(1) in the United States, the Bolar type exemption in Europe, and any corresponding exception to patent infringement in any other country. It is the sole responsibility of the purchaser or user of this product, and the purchaser or user of this product agrees to engage only in such Exempted Uses, and to comply with all applicable intellectual property laws and/or regulations. The purchaser of this product agrees to indemnify Cymit Quimica against all claims in connection with the performance of the respective commercial agreement (e.g. supply agreement) and possible infringements of intellectual property rights.
Purity:Min. 95%Fezagepras sodium
CAS:Fezagepras sodium (Setogepram sodium salt) is an orally active GPR40 agonist and is an antagonist or inverse agonist for GPR84, with anti-fibrotic, anti-Formula:C13H17NaO2Purity:99.49%Color and Shape:SolidMolecular weight:228.26Ref: TM-T12375
1mg40.00€1mL*10mM (DMSO)90.00€5mg92.00€10mg133.00€25mg241.00€50mg354.00€100mg513.00€500mg1,035.00€LP-471756
CAS:LP-471756 is a specific antagonist of GPR139 and inhibits LP-360924-stimulated cAMP production (IC50 = 640 nM).Formula:C19H23NO2SPurity:99.76%Color and Shape:SolidMolecular weight:329.46Nur77 modulator 2
CAS:Nur77 modulator 2: Kd of 0.35 μM, oral anti-inflammatory, affects Nur77/mitochondria localization.Formula:C26H25NO5Color and Shape:SolidMolecular weight:431.48Deltakephalin
CAS:Deltakephalin is a synthetic, potent specific opiate delta receptors agonist.Formula:C34H48N6O10Purity:98%Color and Shape:SolidMolecular weight:700.78LY2922083
CAS:LY2922083: Potent, selective GPR40 agonist; lowers glucose, boosts insulin and GLP-1.Formula:C31H33NO3SColor and Shape:SolidMolecular weight:499.66Amebucort
CAS:Amebucort is a synthetic glucocorticoid corticosteroid. It may used for the research of inflammatory disorders.Formula:C28H40O7Purity:98%Color and Shape:SolidMolecular weight:488.618,11-Eicosadiynoic acid
CAS:8,11-Eicosadiynoic acid, an unsaturated fatty acid, functions as a steroid 5α-reductase inhibitor and has applications in acne research [1].Formula:C20H32O2Color and Shape:SolidMolecular weight:304.47ADL 08-0011 HCl
CAS:ADL 08-0011, a μ-opioid antagonist with Ki 0.25 nM, is derived from alvimopan by gut microbes and counteracts loperamide effects in rats.Formula:C23H30ClNO3Color and Shape:SolidMolecular weight:403.947LY3104607
CAS:LY3104607 is an oral GPCR 40 agonist for type 2 diabetes, aimed at reducing glucose.Formula:C27H25N3O3Purity:98%Color and Shape:SolidMolecular weight:439.51ICI 204448
CAS:ICI 204448 is a potent and peripherally selective κ-opioid agonist.Formula:C23H26Cl2N2O4Color and Shape:SolidMolecular weight:465.37Estrogen receptor modulator 7
CAS:Estrogen Receptor Modulator 7 is a potent modulator of estrogen receptors, utilized in cancer research [1].Formula:C30H31BCl2FNO3Purity:98%Color and Shape:SolidMolecular weight:554.29FK 33-824
CAS:FK 33-824, a stable synthetic analog of methionine enkephalin, reversible with naloxone.Formula:C29H41N5O7SPurity:98%Color and Shape:SolidMolecular weight:603.73ER degrader 6
CAS:ER degrader 6 (compound 35s) is a potent selective estrogen receptor modulator (SERM) with the capacity to degrade Estrogen Receptor (ER)α.Formula:C33H34FN3O5SSePurity:98%Color and Shape:SolidMolecular weight:682.66Mu opioid receptor antagonist 7
CAS:Compound 24, also known as Mu opioid receptor antagonist 7, is a potent, centrally-acting µ-opioid receptor (µOR) antagonist with an inhibitory concentration (Formula:C22H27ClN2O2Purity:98%Color and Shape:SolidMolecular weight:386.91H3B-6545 Hydrochloride
CAS:H3B-6545 Hydrochloride is a selective, oral estrogen receptor covalent antagonist (SERCA).Formula:C30H30ClF4N5O2Color and Shape:SolidMolecular weight:604.04CIDD-0149897
CAS:CIDD-0149897 is a potent, selective, and brain-penetrant agonist of ERβ that exhibits antitumor activity in glioblastoma [1].Formula:C15H10FNO3Purity:98%Color and Shape:SolidMolecular weight:271.24Conjugated Estrogen sodium
CAS:Conjugated estrogens treat menopause symptoms, vaginal changes, and certain cancers.Formula:C18H19NaO5SPurity:98%Color and Shape:White Needle CrystalMolecular weight:370.39PD 125754
CAS:PD 125754 is a Renin inhibitor, which represents a group of pharmaceutical drugs used primarily to treat essential hypertension.Formula:C42H65N5O7Purity:98%Color and Shape:SolidMolecular weight:751.99ER degrader 1
CAS:ER degrader 1 targets estrogen receptor, crucial for cell regulation; shows promise in cancer therapy. (Patent WO2021139756A1, compound 11)Formula:C26H32F4N4O3Color and Shape:SolidMolecular weight:524.55(rel)-BMS-641988
CAS:(rel)-BMS-641988, a relative configuration of the potent nonsteroidal androgen receptor antagonist BMS-641988, holds potential for prostate cancer research.Formula:C20H20F3N3O5SPurity:98%Color and Shape:SolidMolecular weight:471.45BMS-814580
CAS:BMS-814580: potent MCHR1 antagonist, Kb 117 nM, Ki 17 nM (human), 4.9/11.5 nM (monkey/rat), reduces feeding/weight in rodents.Formula:C24H19ClF2N2O4SColor and Shape:SolidMolecular weight:504.93GPR52 receptor modulator 1
CAS:GPR52 receptor modulator 1, a compound delineated as per Procedure 1, is a modulator of the GPR52 receptor, offering research potential in the investigation ofFormula:C19H14F4N4OPurity:98%Color and Shape:SolidMolecular weight:390.33N-Nitrosodicyclohexylamine
CAS:N-Nitrosodicyclohexylamine (NDCHA), an N-nitrosocompound, exhibits anti-androgenic activity by competitively binding to the androgen receptor (AR) in oppositionFormula:C12H22N2OPurity:98%Color and Shape:SolidMolecular weight:210.32Naloxonazine
CAS:Naloxonazine, a potent, selective opiate mu-1 (μ1) antagonist, also influences leishmania through the modulation of host coding function.Formula:C38H42N4O6Color and Shape:SolidMolecular weight:650.76MK-386
CAS:MK-386 is a potent and selective inhibitor of human type-1 5alpha-reductase.Formula:C28H49NOColor and Shape:SolidMolecular weight:415.69Nurr1 agonist 7
CAS: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.Formula:C18H20O3Purity:99.79%Color and Shape:SolidMolecular weight:284.35RU28362
CAS:RU28362 is an agonist of glucocorticoid receptor.Formula:C23H28O3Color and Shape:SolidMolecular weight:352.47TP-051
CAS:TP-051 is a FFAR1 agonist.Formula:C29H31FO6SPurity:99.45% - 99.96%Color and Shape:SolidMolecular weight:526.62Salvinorin A Carbamate
CAS:Salvinorin A carbamate, a potent κ-opioid receptor (KOR) full agonist, exhibits nearly the same potency as salvinorin A, with EC50 values of 6.2 and 4.5 nM, respectively, for activating the human KOR to augment the binding of [35S]GTPγS. Enhancing biological stability, the addition of a carbamate group to salvinorin A reduces deacetylation.Formula:C22H27NO8Color and Shape:SolidMolecular weight:433.457Androgen receptor degrader-1
CAS:Androgen Receptor Degrader-1 (Compound 18) is a potent agent for androgen receptor degradation, applicable in cancer research [1].Formula:C15H14ClN3O4Purity:98%Color and Shape:SolidMolecular weight:335.7411β-hydroxy Etiocholanolone
CAS:11β-Hydroxyetiocholanolone, a hydrocortisone metabolite, exhibits elevated fecal levels in giraffes (G. camelopardalis) and plains zebras (E. quagga) in response to environmental stress.Formula:C19H30O3Color and Shape:SolidMolecular weight:306.44H3B-6545
CAS:H3B-6545 is a selective and oral estrogen receptor covalent antagonist (SERCA) used in the research of metastatic ER-positive, HER2-negative breast cancer.Formula:C30H29F4N5O2Color and Shape:SolidMolecular weight:567.58CITFA
CAS:CITFA, a GPER agonist, enhances neurite outgrowth in rat embryonic (E18) hippocampal neurons [1].Formula:C25H35NO2Color and Shape:SolidMolecular weight:381.55

