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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 3183 products of "Endocrinology/Hormones"

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  • Inocoterone acetate
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    Inocoterone acetate

    CAS:
    <p>Inocoterone acetate is a nonsteroidal antiandrogen that binds to the androgen receptor and possesses antiandrogenic activity in animal models.</p>
    Formula:C18H26O3
    Color and Shape:Solid
    Molecular weight:290.40

    Ref: TM-T25536

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    TRIP13-IN-1

    TRIP13-IN-1 (compound 20) is a potent ligand and inhibitor of TRIP13, demonstrating anticancer effects both in vivo and in vitro.
    Formula:C24H25NO9S
    Color and Shape:Solid
    Molecular weight:503.52

    Ref: TM-T201292

  • Angiotensin II 5-valine
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    Angiotensin II 5-valine

    CAS:
    <p>ngiotensin II 5-valine is an angiotensin II analog which is an agonist at angiotensin receptors.</p>
    Formula:C49H69N13O12
    Purity:98%
    Color and Shape:Solid
    Molecular weight:N/A

    Ref: TM-TP1017

  • N-Desmethyl Loperamide
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    N-Desmethyl Loperamide

    CAS:
    <p>N-Desmethyl Loperamide is the major metabolite of loperamide. It is also used as the precusor for radiolabelled loperamide.</p>
    Formula:C28H31ClN2O2
    Color and Shape:Solid
    Molecular weight:463.01

    Ref: TM-T33615

  • BPR1M97
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    BPR1M97

    CAS:
    <p>BPR1M97 is a mu opioid receptor (MOP) and neuropeptide-orphin FQ (NOP) receptor agonist with blood-brain barrier permeability and potency, with Kis values of 1.</p>
    Formula:C18H18Cl2N2O
    Purity:98.78% - 99.95%
    Color and Shape:Solid
    Molecular weight:349.25

    Ref: TM-T10593

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    PRO20

    <p>PRO20 is a specific and competitive antagonist of the (pro)renin receptor (PRR). It inhibits the calcium influx induced by Proproin with an IC50 value of 81 nmol/L. By blocking the binding of Prorenin to PRR, PRO20 inhibits the activation of the renin-angiotensin system (RAS), reducing the production of angiotensin II (Ang II) and exerting antihypertensive effects. PRO20 holds promise for research in antihypertensive agents.</p>
    Color and Shape:Odour Solid

    Ref: TM-TP3239

  • [Arg14,Lys15]Nociceptin
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    [Arg14,Lys15]Nociceptin

    CAS:
    <p>Potent NOP agonist (EC50 = 1 nM), &gt;875x selective vs opioid receptors; outperforms nociceptin in vivo, increases pain perception, reduces movement.</p>
    Formula:C82H137N31O22
    Purity:98%
    Color and Shape:Solid
    Molecular weight:1909.18

    Ref: TM-TP1986

  • CP-472555
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    CP-472555

    CAS:
    <p>CP-472555 is a selective nonsteroidal glucocorticoid receptor antagonist with anti-GR and anti-obesity activity in animal models.</p>
    Formula:C31H32N2O2
    Color and Shape:Solid
    Molecular weight:464.60

    Ref: TM-T31060

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    Pro8-Oxytocin TFA

    <p>Pro8-Oxytocin TFA, a modified oxytocin (OXT) ligand, exhibits greater potency and efficacy than the standard mammalian OXT ligand, Leu8-Oxytocin, at primate</p>
    Formula:C42H62N12O12S2·xC2HF3O2
    Purity:98%
    Color and Shape:Solid

    Ref: TM-T80134

  • PRL 2915
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    PRL 2915

    CAS:
    <p>PRL 2915 is a potent antagonist of the human somatostatin subtype 2 receptor (hsst 2), exhibiting a binding affinity (K_i) of 12 nM [1].</p>
    Formula:C59H71ClN12O8S2
    Color and Shape:Solid
    Molecular weight:1175.85

    Ref: TM-T76594

  • TF-505
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    TF-505

    CAS:
    <p>TF-505, a steroid 5α-reductase inhibitor, is used potentially for the treatment of benign prostatic hyperplasia.</p>
    Formula:C33H37NO4
    Purity:98%
    Color and Shape:Solid
    Molecular weight:511.65

    Ref: TM-T28956

  • ERRγ agonist-2
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    ERRγ agonist-2

    CAS:
    <p>ERRγ agonist-2 is a potent and selective ERRγ inverse agonist with a K d value of 6.5 μM.</p>
    Formula:C27H21N5O2
    Color and Shape:Solid
    Molecular weight:447.49

    Ref: TM-T74840

  • Neuropeptide AF (human) acetate
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    Neuropeptide AF (human) acetate

    <p>Neuropeptide AF (human) acetate (Neuropeptide AF (human) acetate (192387-38-5 Free base)) is an anti-opioid neuropeptide, a Neuropeptide AF (human) derivative,</p>
    Purity:99.89%
    Color and Shape:Soild

    Ref: TM-TP1082L

  • A 779
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    A 779

    CAS:
    <p>A 779 is a potent antagonist of the G-protein-coupled receptor Mas, the Ang1-7 receptor, which is distinct from conventional AngII.</p>
    Formula:C39H60N12O11
    Purity:98%
    Color and Shape:Solid
    Molecular weight:872.97

    Ref: TM-T7616

  • ARCC-4
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    ARCC-4

    CAS:
    <p>ARCC-4: A VHL-recruiting, low-nanomolar (DC50=5nM) AR degrader; outshines enzalutamide; degrades AR mutants resistant to therapy.</p>
    Formula:C53H56F3N7O7S2
    Purity:98%
    Color and Shape:Solid
    Molecular weight:1024.18

    Ref: TM-T14318

  • Parathyroid hormone (1-34) (rat)
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    Parathyroid hormone (1-34) (rat)

    CAS:
    <p>Parathyroid hormone (PTH) receptor agonist. Increases serum PTH levels and bone mass in rats.</p>
    Formula:C180H291N55O48S2
    Purity:98%
    Color and Shape:Solid
    Molecular weight:4057.74

    Ref: TM-TP1964

  • THR-β agonist 6
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    THR-β agonist 6

    CAS:
    <p>THR-β Agonist 6, a selective and orally active compound targeting the thyroid hormone receptor β (THR-β), demonstrates specificity with EC50 values of 0.03 μM</p>
    Formula:C20H14Cl2N6O3
    Color and Shape:Solid
    Molecular weight:457.27

    Ref: TM-T74785

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    BWA-6047

    <p>BWA-6047 is a dual AR/AR-V7 and GSPT1 PROTAC-type degrader (AR: DC50= 3.7 nM; AR-V7: DC50= 3.0 nM; GSPT1: DC50= 1.2 nM). It facilitates the ubiquitination and degradation of AR/AR-V7 and, through molecular glue properties, induces a PPI between GSPT1 and CRBN, leading to GSPT1 degradation. BWA-6047 is applicable in prostate cancer research.</p>
    Formula:C42H46ClN5O7
    Color and Shape:Solid
    Molecular weight:767.30858

    Ref: TM-T207136

  • ARD-69
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    ARD-69

    <p>ARD-69, a potent PROTAC, degrades AR in prostate cancer, with low DC50 values in AR+ cell lines, and suppresses AR gene expression.</p>
    Formula:C62H74ClFN8O7S
    Color and Shape:Solid
    Molecular weight:1129.83

    Ref: TM-T30123

  • Lactandrate
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    Lactandrate

    CAS:
    <p>Lactandrate is a homo-aza-steroidal ester of p-bis(2-chloroethyl) amino phenyl acetic acid.</p>
    Formula:C31H44Cl2N2O3
    Color and Shape:Solid
    Molecular weight:563.6

    Ref: TM-T32526