CymitQuimica logo
GPCR/G-Protein

GPCR/G-Protein

GPCR/G-Protein inhibitors are compounds that target G-protein coupled receptors (GPCRs) and associated G-proteins, which play critical roles in transmitting signals from the outside to the inside of cells. These inhibitors are essential for studying the signaling pathways mediated by GPCRs, which are involved in numerous physiological processes, including sensory perception, immune response, and neurotransmission. GPCR inhibitors are also important in drug development, as many therapeutic agents target these receptors. At CymitQuimica, we offer a wide range of high-quality GPCR/G-Protein inhibitors to support your research in pharmacology, cell biology, and related fields.

Subcategories of "GPCR/G-Protein"

Show 19 more subcategories

Found 5963 products of "GPCR/G-Protein"

Sort by

Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
products per page.
  • Zovaglutide

    CAS:
    Zovaglutide is a GLP-1 receptor agonist that is utilized in diabetes research.
    Color and Shape:Solid

    Ref: TM-TP3799

    10mg
    To inquire
    50mg
    To inquire
  • 9-deoxy-9-methylene-16,16-dimethyl Prostaglandin E2

    CAS:
    Meteneprost is a strong, long-lasting Prostaglandin E2 analog effective in ending early monkey pregnancies without causing fever or GI issues.
    Formula:C23H38O4
    Color and Shape:Solid
    Molecular weight:378.553

    Ref: TM-T36829

    500µg
    172.00€
  • Methimepip dihydrobromide

    CAS:
    Methimepip dihydrobromide is a selective H3R agonist.
    Formula:C10H19Br2N3
    Color and Shape:Solid
    Molecular weight:341.091

    Ref: TM-T37727

    200mg
    1,304.00€
  • Urocortin II, human acetate


    Urocortin II, human acetate, is a selective endogenous peptide agonist of type 2 corticotropin-releasing factor (CRF2) receptors, used to study the role of CRF2 receptors in feeding behavior.
    Color and Shape:Odour Solid

    Ref: TM-TP3688

    10mg
    To inquire
    50mg
    To inquire
  • Navafenterol saccharinate

    CAS:
    AZD-8871 saccharinate is a dual-acting bronchodilator which may be useful in the treatment of Chronic Obstructive Pulmonary Disease (COPD).
    Formula:C45H47N7O9S3
    Color and Shape:Solid
    Molecular weight:926.09

    Ref: TM-T30265

    25mg
    1,444.00€
  • N-0500 HCl

    CAS:
    N-0500 HCl, a potent DA receptor agonist, displaces [3H]DP_x005f_x0002_5,6-ADTN with an IC50 of 3nM.
    Formula:C15H22ClNO2
    Purity:98.85% - 99.54%
    Color and Shape:Solid
    Molecular weight:283.79

    Ref: TM-T60107

    5mg
    35.00€
    10mg
    55.00€
    1mL*10mM (DMSO)
    To inquire
  • [Gly8]-GLP-1(7-37) acetate


    [Gly8]-GLP-1(7-37) acetate is a derivative of GLP-1, where glycine at position 8 is replaced with alanine. [Gly8]-GLP-1(7-37) acetate is also a peptide fragment of the GLP-1 receptor (GLP-1R) agonist, Dulaglutide.
    Color and Shape:Odour Solid

    Ref: TM-TP3691

    10mg
    To inquire
    50mg
    To inquire
  • SSTR4 agonist-1

    CAS:
    SSTR4agonist-1 (Compound 47) is a selective agonist of the somatostatin receptor 4 (SSTR4), with an EC50 of 4.7 nM. It has a half-life of over 130 minutes in human liver microsomes.
    Formula:C16H23N3O2
    Color and Shape:Solid
    Molecular weight:289.37

    Ref: TM-T203033

    10mg
    To inquire
    50mg
    To inquire
  • Urocortin, rat

    CAS:
    Endogenous CRF agonist. Ki values are 13, 1.5 and 0.97 nM for hCRF1, rCRF2α and mCRF2β respectively.
    Formula:C206H338N62O64
    Purity:98%
    Color and Shape:Solid
    Molecular weight:4707.26

    Ref: TM-TP1020

    1mg
    1,161.00€
  • Human follicular gonadotropin releasing peptide

    CAS:
    Human Follicular Gonadotropin Releasing Peptide (hF-GRP) is a hormonal peptide that, in vitro, can induce the secretion of pituitary luteinizing hormone (LH)
    Formula:C68H94N22O27
    Color and Shape:Solid
    Molecular weight:1651.61

    Ref: TM-T82162

    5mg
    To inquire
    50mg
    To inquire
  • mPGES-1/sEH-IN-1


    mPGES-1/sEH-IN-1 (compound 1f) is an sEH inhibitor with an IC50 value of 5 μM. It also exhibits antitumor activity by inhibiting mPGES-1, with an IC50 value of 25 µM.
    Formula:C20H16F3N3O2
    Color and Shape:Solid
    Molecular weight:387.355

    Ref: TM-T204923

    10mg
    To inquire
    50mg
    To inquire
  • AKP-11

    CAS:
    AKP-11 is a sphingosine-1-phosphate receptor 1 (S1P1) agonist with an EC50 of 0.047 μM for [35S]GTPγS binding to CHO-K1 cell membranes expressing human S1P1. It reduces S1P1 surface expression and enhances Akt and ERK phosphorylation in CHO cells with S1P1-HA at a 100 nM concentration. At doses of 1.3 and 3 mg/kg, AKP-11 lowers IFN-γ and IL-17 protein levels in the spinal cord and mitigates disease severity in a rat experimental autoimmune encephalomyelitis (EAE) model. Additionally, it decreases peripheral total lymphocyte and specific T cell subsets (CD4+, CD8+, and CD26L+ T cells) counts in both EAE rats and healthy controls at a 1.3 mg/kg dosage.
    Formula:C22H22ClN3O5
    Color and Shape:Solid
    Molecular weight:443.88

    Ref: TM-T85077

    10mg
    To inquire
  • Nastorazepide hemicalcium

    CAS:
    Nastorazepide (Z-360) hemicalcium is a selective, orally-administered 1,5-benzodiazepine derivative that functions as a receptor antagonist for gastrin/cholecystokinin 2 (CCK-2), exhibiting potential antitumor activity.
    Formula:C29H36N4O5Ca
    Color and Shape:Solid
    Molecular weight:540.66

    Ref: TM-T201854

    10mg
    To inquire
    50mg
    To inquire
  • 5-HT1AR agonist 2


    5-HT1AR Agonist 2 (Compound 4f) is a potent agonist of the 5-HT1A receptor with a Ki value of 10.0 nM. It also binds to SERT, D2, and 5-HT6 receptors with Ki values of 2.8 nM, 23 nM, and 192 nM, respectively. Furthermore, this compound demonstrates stability in microsomes and induces hypothermia in mice.
    Formula:C31H31N5O3
    Color and Shape:Solid
    Molecular weight:521.61

    Ref: TM-T201624

    10mg
    To inquire
    50mg
    To inquire
  • CB1R antagonist 2


    CB1R antagonist 2 (Compound 11g) functions as an antagonist of the cannabinoid receptor 1 (CB1R), inhibiting the MAPK/NF-κB signaling pathway and exhibiting anti-inflammatory properties. In RAW264.7 cells, it suppresses LPS-induced expression of IL-6, IL-1β, and TNF-α. In murine models, it improves OVA-induced allergic rhinitis.
    Formula:C24H26N4O
    Color and Shape:Solid
    Molecular weight:386.49

    Ref: TM-T205110

    10mg
    To inquire
    50mg
    To inquire
  • CCR6 antagonist 2


    CCR6 antagonist2 (Compound 20c) acts as a CCR6 antagonist with a Ki of 1.1 nM. It inhibits CCL20-induced calcium influx with an IC50 of 4.9 nM and suppresses the chemotactic migration of CCR6+ T cells with an IC50 of 190 nM.
    Formula:C19H24N4O4
    Color and Shape:Solid
    Molecular weight:372.42

    Ref: TM-T205072

    10mg
    To inquire
    50mg
    To inquire
  • Luprostiol

    CAS:
    Luprostiol is a prostaglandin analog.
    Formula:C21H29ClO6S
    Color and Shape:Solid
    Molecular weight:444.97

    Ref: TM-T32978

    25mg
    1,369.00€
  • PACAP (1-27), human, ovine, rat

    CAS:
    PACAP (1-27) (the N-terminal fragment of PACAP-38) is a novel neuropeptides originally isolated from bovine hypothalamus, also found in humans and rats.
    Formula:C142H224N40O39S
    Purity:98%
    Color and Shape:Solid
    Molecular weight:3147.66

    Ref: TM-TP1070

    100µg
    642.00€
  • BAY-747

    CAS:
    BAY-747: oral, brain-penetrant sGC stimulator; improves rat memory, cognition, lowers blood pressure, aids Duchenne muscular dystrophy.
    Formula:C22H26F2N4O2
    Color and Shape:Solid
    Molecular weight:416.46

    Ref: TM-T75137

    25mg
    To inquire
    50mg
    To inquire
    100mg
    To inquire
  • Neuropeptide Y (22-36)

    CAS:
    Neuropeptide Y (22-36) is a 15-amino acid fragment of NPY, which is abundant in the mammalian brain and involved in multiple physiological functions.
    Formula:C85H139N29O21
    Purity:98%
    Color and Shape:Solid
    Molecular weight:1903.19

    Ref: TM-TP1681

    100mg
    To inquire
    500mg
    To inquire