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GPCR/G protein

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Products Related to GPCR/G protein(3726)

  • GC79316 structure
    GC79316L-797591 hydrochloride
    CAS: 3026641-74-4
    Purity: >99.50%

    L-797591 hydrochloride is a selective sst 1 agonist.

  • GC79317 structure
    GC79317SSTR3 Agonist-1
    CAS: 3086695-73-7
    Purity: >98.00%

    SSTR3 Agonist-1 (Compound EX 38) is an orally active SSTR3 agonist, with an EC 50 of 0.14 nM.

  • GC79318 structure
    GC79318NOTA-TATE
    CAS: 709043-21-0
    Purity: >98.50%

    NOTA-TATE is a somatostatin receptor 2 ( SSTR2 ) binder.

  • GC79319 structure
    GC79319R06039-641
    CAS: 2138444-75-2
    Purity: >98.50%

    R06039-641 is a neuropeptide S receptor ( NPSR ) agonist with an EC 50 of 169 nM.

  • GC79320 structure
    GC79320R06039-691
    CAS: 2138445-51-7
    Purity: >99.50%

    R06039-691 is a neuropeptide S receptor ( NPSR ) agonist with an EC 50 of 93 nM.

  • GC79321 structure
    GC79321MRS 2179 ammonium
    Purity: >99.00%

    MRS 2179 ammonium is a selective and competitive antagonist for P2Y1 receptor, with K B of 0.177 μM [1] .

  • GC79322 structure
    GC79322TP receptor antagonist-3
    CAS: 165537-72-4
    Purity: >99.50%

    TP receptor antagonist-3 (compound 51280) is a potent thromboxane A2 prostanoid ( TP ) receptor with an IC 50 of 15.7 nM against Human TP.

  • GC79323 structure
    GC79323Terutroban sodium
    CAS: 609340-89-8
    Purity: >98.00%

    Terutroban (S-18886) sodium is a selective and orally active thromboxane-prostaglandin (TP) receptor antagonist with an IC 50 of 16.4 nM.

  • GC79324 structure
    GC79324HTL0039732
    CAS: 2639366-75-7
    Purity: >99.00%

    HTL0039732 is an orally active antagonist of the prostaglandin EP4 receptor (Prostaglandin E2 Receptor EP4).

  • GC79325 structure
    GC79325ML161 analog 1
    CAS: 423740-83-4
    Purity: >99.50%

    ML161 analog 1 (compound 38) is an analog of ML161.

  • GC79326 structure
    GC79326Tirzepatide sodium
    Purity: >98.00%

    Tirzepatide sodium (LY3298176 sodium) is a dual glucose-dependent insulinotropic polypeptide ( GIP ) and glucagon-like peptide-1 ( GLP-1 ) receptor agonist.

  • GC79327 structure
    GC79327BMS-986331
    CAS: 2375684-52-7
    Purity: >99.50%

    BMS-986331 is an orally active selective N-Formyl Peptide Receptor 2 (FPR2) agonist with an EC 50 of 0.5 nM in humans and 1 nM in rats.

  • GC79328 structure
    GC79328HDB-1
    CAS: 3021527-82-9
    Purity: >98.00%

    HDB-1 is a selective inhibitor of the P2Y14 receptor ( P2Y14R ) with an IC 50 of 26 pM.

  • GC79372 structure
    GC79372Rosnilimab (Mouse IgG2a)
    Purity: >98.00%

    Rosnilimab (Mouse IgG2a ) is a mouse-derived IgG2a antibody, Rosnilimab.

  • GC79373 structure
    GC79373FK3453
    CAS: 560111-91-3
    Purity: >99.50%

    FK3453 is a dual adenosine A1/A2 inhibitor and a TSLP inhibitor.

  • GC79374 structure
    GC79374PD-1/PD-L1-IN-63
    CAS: 2691796-92-4
    Purity: >98.00%

    PD-1/PD-L1-IN-63 is an orally active PD-1/PD-L1 inhibitor with an IC 50 of 9.1 nM.

  • GC79405 structure
    GC79405TSLP modulator-1
    Purity: >99.50%

    TSLP modulator-1 (Compound 14O) is a potent TSLP signaling modulator.

  • GC79450 structure
    GC79450Hydrocortisone-OVA
    Purity: >98.00%

    Hydrocortisone -OVA is a conjugate of Hydrocortisone and OVA peptide.

  • GC79504 structure
    GC79504(R)-Verapamil
    CAS: 38321-02-7
    Purity: >98.50%

    (R)-Verapamil (Dexverapamil) is an optically enantiomer of the oral-active Verapamil.

  • GC79505 structure
    GC79505RPI-GLYT2-82
    Purity: >99.00%

    RPI-GLYT2-82 is a reversible, blood-brain barrier-permeable allosteric inhibitor of GlyT2 with an IC 50 value of 554 nM.

  • GC79507 structure
    GC79507PSB-12054
    CAS: 1407632-07-8
    Purity: >98.50%

    PSB-12054 is a P2X4 receptor antagonist with IC 50 values of 0.19 μM, 2.10 μM and 1.77 μM against human, rat and mouse receptors, respectively, and exhibits selectivity over other human P2X receptor subtypes.

  • GC79667 structure
    GC79667AGFAGDDAPR
    CAS: 330204-04-1
    Purity: >98.00%

    AGFAGDDAPR is a bioactive peptide that is a competitive and orally effective inhibitor of dipeptidyl peptidase-IV ( DPP-IV ).

  • GC79668 structure
    GC79668RES-701-3 peptide TFA
    Purity: >98.00%

    RES-701-3 peptide TFA is a class II lasso peptide.

  • GC79675 structure
    GC79675FTO-IN-17
    CAS: 1434867-98-7
    Purity: >98.00%

    FTO-IN-17 is an orally active and brain-penetrant FTO (m 6 A RNA demethylase) inhibitor with an IC 50 of 1.1 μM.