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Endocrinology/Hormones

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"

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Found 3180 products of "Endocrinology/Hormones"

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  • RTI-13951-33

    CAS:
    <p>RTI-13951-33 is an effective and brain-penetrant GPR88 agonist (EC50: 25 nM, in GPR88 cAMP functional assay).</p>
    Formula:C28H33N3O3
    Purity:98%
    Color and Shape:Solid
    Molecular weight:459.58
  • ER degrader 6

    CAS:
    <p>ER degrader 6 (compound 35s) is a potent selective estrogen receptor modulator (SERM) with the capacity to degrade Estrogen Receptor (ER)α.</p>
    Formula:C33H34FN3O5SSe
    Purity:98%
    Color and Shape:Solid
    Molecular weight:682.66
  • Icalcaprant

    CAS:
    <p>Icalcaprant is a kappa-opioid receptor antagonist [1].</p>
    Formula:C23H26N4O3
    Purity:98%
    Color and Shape:Solid
    Molecular weight:406.48
  • Androgen receptor degrader-2

    CAS:
    <p>Androgen Receptor Degrader-2 (Compound 9) is a potent degrader of androgen receptors, with potential application in cancer research [1].</p>
    Formula:C16H16ClN3O4
    Purity:98%
    Color and Shape:Solid
    Molecular weight:349.77
  • N-Nitrosodicyclohexylamine

    CAS:
    <p>N-Nitrosodicyclohexylamine (NDCHA), an N-nitrosocompound, exhibits anti-androgenic activity by competitively binding to the androgen receptor (AR) in opposition</p>
    Formula:C12H22N2O
    Purity:98%
    Color and Shape:Solid
    Molecular weight:210.32
  • GLL398

    CAS:
    <p>GLL398: Oral ERα down-regulator, binds strongly (IC50=1.14nM), degrades ERα in MCF-7 cells (IC50=0.21μM).</p>
    Formula:C25H23BO4
    Color and Shape:Solid
    Molecular weight:398.26
  • Elisartan

    CAS:
    <p>Elisartan is a non-peptide pro-drug of angiotensin II AT1 receptor antagonist HN-12206. It also shows anti-hypertension activities.</p>
    Formula:C27H29ClN6O5
    Purity:98%
    Color and Shape:Solid
    Molecular weight:553.01
  • Androgen receptor degrader-1

    CAS:
    <p>Androgen Receptor Degrader-1 (Compound 18) is a potent agent for androgen receptor degradation, applicable in cancer research [1].</p>
    Formula:C15H14ClN3O4
    Purity:98%
    Color and Shape:Solid
    Molecular weight:335.74
  • Nurr1 agonist 7

    CAS:
    <p>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.</p>
    Formula:C18H20O3
    Purity:99.79%
    Color and Shape:Solid
    Molecular weight:284.35
  • Trap-101 hydrochloride

    CAS:
    <p>nociceptin/orphanin FQ (NOP) receptor antagonist</p>
    Formula:C24H36ClN3O2
    Purity:98%
    Color and Shape:Solid
    Molecular weight:434.02
  • YXG-158

    CAS:
    <p>YXG-158 (Compound 23-h), an orally active androgen receptor (AR) degrader and cytochrome P450 17A1 (CYP17A1) inhibitor, exhibits AR degradation with a DC50 of 1</p>
    Formula:C30H36FN3O
    Purity:98%
    Color and Shape:Solid
    Molecular weight:473.62
  • Androgen receptor degrader-3

    CAS:
    <p>Androgen Receptor Degrader-3 (ARD-3) is a compound that inhibits androgen receptor signaling and promotes the degradation of the receptor, with potential</p>
    Formula:C45H51ClN8O5
    Purity:98%
    Color and Shape:Solid
    Molecular weight:819.39
  • Trimegestone

    CAS:
    <p>Trimegestone, a highly effective oral progestogen, is used for endometrial protection, all doses inducing secretory endometrial transformation.</p>
    Formula:C22H30O3
    Purity:98%
    Color and Shape:Solid
    Molecular weight:342.47
  • Androgen receptor antagonist 5

    CAS:
    <p>AR antagonist 5 blocks AR (IC50: 6.17 μM), hinders LNCaP cell growth, and has anti-tumor effects in mouse models.</p>
    Formula:C21H15F4N5O3S
    Color and Shape:Solid
    Molecular weight:493.43
  • N-Demethyl Mifepristone

    CAS:
    <p>N-Demethyl Mifepristone (RU 42633), an active metabolite of Mifepristone, exhibits 61% of the affinity for the glucocorticoid receptor relative to Mifepristone'</p>
    Formula:C28H33NO2
    Purity:98%
    Color and Shape:Solid
    Molecular weight:415.57
  • Androgen receptor-IN-5

    CAS:
    <p>Androgen receptor-IN-5 is a potent inhibitor of the androgen receptor with anticancer properties.</p>
    Formula:C22H10Cl2F4N4OS
    Purity:98%
    Color and Shape:Solid
    Molecular weight:525.31
  • Taragarestrant

    CAS:
    <p>Taragarestrant (D-0502), an oral estrogen receptor degrader, combats ER+ breast cancer in research.</p>
    Formula:C25H25Cl2FN2O2
    Color and Shape:Solid
    Molecular weight:475.38
  • MB-07344

    CAS:
    <p>MB-07344 is a selective THR-β (thyroid hormone receptor β) agonist with a Ki of 2.17 nM, capable of reducing plasma total cholesterol (TPC).</p>
    Formula:C19H25O5P
    Purity:99.32%
    Color and Shape:Solid
    Molecular weight:364.37
  • GPR40 Agonist 2

    CAS:
    <p>GPR40 Agonist 2 is a GPR40 agonist. It can be used in the research of diabetes.</p>
    Formula:C24H30O3
    Purity:98%
    Color and Shape:Solid
    Molecular weight:366.49
  • MCHR1 antagonist 2

    CAS:
    <p>MCHR1 antagonist 2 is an antagonist of melanin-concentratin hormone receptor 1(MCH1-R, IC50 = 65 nM) and also inhibits hERG.</p>
    Formula:C23H21FN2O5
    Purity:98.29%
    Color and Shape:Solid
    Molecular weight:424.42