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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(±)-AC 7954 hydrochloride
CAS:<p>(±)-AC 7954 hydrochloride is a urotensin-II (UT) receptor activator.</p>Formula:C19H21Cl2NO2Purity:99.42%Color and Shape:White SolidMolecular weight:366.28DK3
CAS:<p>DK3 is a potent and selective agonist of estrogen-related receptor alpha (ERRα). ERRα is a potential drug target for cancer and metabolic diseases [1].</p>Formula:C16H14N2O2Color and Shape:SolidMolecular weight:266.29SHR1653
CAS:<p>SHR1653 is a highly potent, selective and brain penetrated antagonist of oxytocin receptor (OTR)(IC50 of 15 nM for hOTR).</p>Formula:C21H21ClFN5O2Purity:98%Color and Shape:SolidMolecular weight:429.88Capesaris
CAS:<p>Capesaris (GTX-758) is an oral estrogen receptor α agonist, used in prostate cancer research.</p>Formula:C19H13F2NO3Purity:99.65%Color and Shape:SolidMolecular weight:341.31Androgen receptor antagonist 1
CAS:<p>Androgen receptor antagonist 1, an oral full AR antagonist (IC50 59 nM), for PROTAC synthesis, reducing AR protein by 24–47% in LNCaP cells at 1–10 μM.</p>Formula:C21H25ClN4O3Purity:99.054%Color and Shape:SolidMolecular weight:416.9PF-4455242 HCl
CAS:<p>PF-4455242 HCl is a selective and orally available κ-opioid receptor antagonist that exhibiting antidepressant effects.</p>Formula:C21H29ClN2O2SPurity:99.59%Color and Shape:SolidMolecular weight:408.99SB-568849
CAS:<p>SB-568849 is a melanin-concentrating hormone receptor 1 antagonist (pKi: 7.7).</p>Formula:C28H31F3N2O3Purity:98%Color and Shape:SolidMolecular weight:500.55Dimethomorph
CAS:<p>Dimethomorph is a fungicide and sterol biosynthesis inhibitor that inhibits fungal cell wall formation,. inhibits androgen receptor (AR) .</p>Formula:C21H22ClNO4Purity:99.2%Color and Shape:Solid CrystallineMolecular weight:387.86FSHR agonist 1
CAS:<p>FSHR agonist 1: high-affinity, allosteric FSHR activator, pEC50 of 7.72, interacts with TMD.</p>Formula:C26H33N3O3SColor and Shape:SolidMolecular weight:467.62MCH-1 antagonist 1
CAS:<p>MCH-1 antagonist 1 also inhibits CYP3A4 (IC50: 10μM).MCH-1 antagonist 1 is a potent melanin concentrating hormone (MCH-1) antagonist (Ki: 2.6 nM).</p>Formula:C25H26N4O2Purity:98%Color and Shape:SolidMolecular weight:414.5CP-866087
CAS:<p>CP-866087 is a novel, potent and selective mu-opioid receptor antagonist for the study of female sexual dysfunction.</p>Formula:C24H28N2O2Purity:99.56% - >99.99%Color and Shape:SoildMolecular weight:376.49SB 706375
CAS:<p>urotensin-II (UT) receptor antagonist</p>Formula:C20H22BrF3N2O5SPurity:98%Color and Shape:SolidMolecular weight:539.36ATC0065 HCl
CAS:<p>ATC0065 dihydrochloride is a novel nonpeptidic and potent melanin-concentrating hormone receptor 1 (MCHR1) selective antagonist.</p>Formula:C25H31BrCl2F3N5OColor and Shape:SolidMolecular weight:625.35GPR84 antagonist 8
CAS:<p>GPR84 antagonist 8 is a selective GPR84 antagonist applicable for investigating inflammatory and fibrotic diseases.</p>Formula:C23H23N3O5Purity:99.45%Color and Shape:SolidMolecular weight:421.45VPC-3033
CAS:<p>VPC-3033 is an antagonist of the androgen receptor. It acts by inhibiting the LNCaP cell line as well as cell lines with the wild-type androgen receptor.</p>Formula:C21H14O2Purity:98%Color and Shape:SolidMolecular weight:298.33Camizestrant
CAS:<p>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].</p>Formula:C24H28F4N6Purity:97.25% - 99.57%Color and Shape:SolidMolecular weight:476.51L 366682
CAS:<p>L 366682 is an oxytocin antagonist.</p>Formula:C40H53N9O6Purity:98%Color and Shape:SolidMolecular weight:755.91OT antagonist 1
CAS:<p>OT antagonist 1 is a potent and selective antagonist of Oxytocin(Ki of 50 nM)</p>Formula:C22H22N4O3Purity:98%Color and Shape:SolidMolecular weight:390.44VPC-13789
CAS:<p>VPC-13789: potent, selective oral antiandrogen for CRPC with 0.19 μM IC50 in LNCaP cells.</p>Formula:C21H16F3N3OColor and Shape:SolidMolecular weight:383.37Dup 747
CAS:<p>Dup 747 is an analgesic that binds with high affinity and selectivity to the kappa-opioid receptor.</p>Formula:C24H28Cl2N2O2Purity:98%Color and Shape:SolidMolecular weight:447.4(R,R)-THC
CAS:<p>agonist at ERα receptor and antagonist at ERβ receptor</p>Formula:C22H24O2Purity:98%Color and Shape:SolidMolecular weight:320.42LY285434
CAS:<p>LY285434 is a suitable angiotensin II receptor antagonist.</p>Formula:C23H25N5O2Purity:98%Color and Shape:SolidMolecular weight:403.48Chlorothalonil
CAS:<p>Chlorothalonil (DAC 2787): Broad-spectrum, efficient, low-toxicity fungicide for fruits, vegetables, rice, wheat, cotton.</p>Formula:C8Cl4N2Purity:98.01% - 98.71%Color and Shape:Colorless Crystals SolidMolecular weight:265.91D36
CAS:<p>D36 is an androgen receptor allosteric antagonist. It also has inverse agonist properties.</p>Formula:C21H24N2O2Purity:98%Color and Shape:SolidMolecular weight:336.43FERb 033
CAS:<p>ERβ receptor agonist</p>Formula:C13H9ClFNO3Purity:98%Color and Shape:SolidMolecular weight:281.67BTI-A-404
CAS:<p>BTI-A-404 is a potent and selective competitive inverse agonist of human GPR43.</p>Formula:C22H26N4O2Color and Shape:SolidMolecular weight:378.47MK-4541
CAS:<p>MK-4541: oral, selective AR modulator, blocks 5α-reductase, curbs AR+ prostate cancer growth, effective in mouse model.</p>Formula:C22H31F3N2O3Color and Shape:SolidMolecular weight:428.49SCH 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:397.55Fenhexamid
CAS:<p>Fenhexamid (Elevate), a sterol biosynthesis inhibitor, shows antifungal activity against the plant pathogenic fungus.</p>Formula:C14H17Cl2NO2Purity:99.56%Color and Shape:SolidMolecular weight:302.20Dehydro Olmesartan
CAS:<p>Dehydro Olmesartan, from Olmesartan, is an AT1R blocker for researching hypertension.</p>Formula:C24H24N6O2Color and Shape:SolidMolecular weight:428.49KB-130015
CAS:<p>KB-130015, a activator of hERG1 potassium channels, blocks native and recombinant hERG1 channels at high voltages.</p>Formula:C18H14I2O4Purity:98%Color and Shape:SolidMolecular weight:548.11RU 43044
CAS:<p>RU 43044 is a selective glucocorticoid receptor antagonist that has exhibited an antidepressant-like effect.</p>Formula:C29H34O2Purity:98%Color and Shape:SolidMolecular weight:414.58LY 281217
CAS:<p>LY 281217, an organic opioid agonist, can produce analgesic effects in mice.</p>Formula:C32H42N4O6Purity:98%Color and Shape:SolidMolecular weight:578.7Idoxifene
CAS:<p>Idoxifene is a tissue-specific selective estrogen receptor modulator.</p>Formula:C28H30INOColor and Shape:SolidMolecular weight:523.45L-366509
CAS:<p>L-366,509 is an antagonist of oxytocin.</p>Formula:C25H33NO5SPurity:98%Color and Shape:SolidMolecular weight:459.6Cyprodinil
CAS:<p>Cyprodinil is a fungicide blocking methionine synthesis in fungi and hinders B. cinerea, P. herpotrichoides, H. oryzae growth; it's also an AR agonist.</p>Formula:C14H15N3Color and Shape:SolidMolecular weight:225.29DDD028
CAS:<p>DDD-028 is a potential non-opioid and non-cannabinoid analgesic. It was used for treating neuropathic and inflammatory pain.</p>Formula:C20H20N2Purity:98%Color and Shape:SolidMolecular weight:288.39Androgen receptor antagonist 3
CAS:<p>Androgen receptor antagonist 3 (Compound C18) has anticancer activities that is an antagonist of androgen receptor (AR) (IC 50 = 2.4 μM) [1].</p>Formula:C22H18ClNColor and Shape:SolidMolecular weight:331.84J9
CAS:<p>J9 is an inhibitor of Glucocorticoid resistance. J9 reverses Dexamethasone Resistance in T-cell Acute Lymphoblastic Leukemia.</p>Formula:C12H12N4Color and Shape:SolidMolecular weight:212.25Aldose reductase-IN-4
CAS:<p>Aldose reductase-IN-4 (compund IIc) is an inhibitor of aldose reductase with IC50s of 11.70 μM and 0.98 μM for ALR1 and ALR2, respectively [1].</p>Formula:C14H10FNO3SColor and Shape:SolidMolecular weight:291.3Aldose reductase-IN-6
CAS:<p>AR inhibitor Aldose reductase-IN-6: IC50 3.164 μM, Ki 0.018 μM, non-toxic to normal cells.</p>Formula:C20H16N4O2SColor and Shape:SolidMolecular weight:376.43BMS-819881
CAS:<p>BMS-819881 is a melaninconcentrating hormone receptor 1 (MCHR1) antagonist, which binds rat MCHR1 with a Ki of 7 nM and it also is selective and potent for</p>Formula:C24H21ClN2O4SPurity:98%Color and Shape:SolidMolecular weight:468.95Olmesartan methyl ester
CAS:<p>Olmesartan methyl ester: an intermediate for synthesizing Olmesartan medoxomil, a strong AT1 receptor blocker.</p>Formula:C25H28N6O3Color and Shape:SolidMolecular weight:460.53GPR40 agonist 1
CAS:<p>GPR40 agonist 1 is an effective new GPR40 agonist (EC50s: 17 nM and 2 nM for rGPR40 and hGPR40).</p>Formula:C27H30FN3O4Purity:98%Color and Shape:SolidMolecular weight:479.54Endomorphin 1 acetate
CAS:<p>Endomorphin 1 acetate is a μ-opioid receptor agonist with antinociceptive and analgesic effects and can be used to study neurological diseases.</p>Formula:C36H42N6O7Color and Shape:SolidMolecular weight:670.75SIM-688
CAS:<p>SIM-688 is a selective and orally active estrogen receptor inhibitor of NF-κB transcriptional activity (IC50 = 122 nM in HAECT-1 cells).</p>Formula:C34H31F3N2O2Purity:99.56%Color and Shape:SolidMolecular weight:556.62ORL1 antagonist 1
CAS:<p>ORL1 antagonist 1 is an o antagonist of pioid receptor-like 1 (ORL1) (IC50 of 61 nM).</p>Formula:C20H22ClN5Purity:98.92%Color and Shape:SolidMolecular weight:367.88Opioid receptor modulator 1
CAS:<p>Opioid receptor modulator 1 is a modulator of opioid receptor.</p>Formula:C18H23NO2Purity:98%Color and Shape:SolidMolecular weight:285.38BMS-986124
CAS:<p>BMS-986124 is an allosteric modulator of the μ-Opioid Receptor.</p>Formula:C16H15BrClNO3S2Color and Shape:SolidMolecular weight:448.78Estrogen receptor-IN-1
CAS:<p>Estrogen receptor-IN-1 (compound 16) is an effective estrogen receptor (ER) inhibitor with IC 50 s of 13, 5μM for ERα and Erβ, respectively [1].</p>Formula:C14H16OSiColor and Shape:SolidMolecular weight:228.36
