“ab fubinaca”的搜索结果

产品 1 到 50 共 76个

每页
页面:
  1. 1
  2. 2

设置降序顺序
  1. Goserelin

    Catalog No. A21197
    Quick View
    GnRH agonist
    Goserelin(ICI 118630) is an injectable gonadotropin releasing hormone superagonist (GnRH agonist). 了解更多
  2. Aripiprazole (D8)

    Catalog No. A22004
    Quick View
    human 5-HT1A receptor partial agonist
    Aripiprazole D8 (OPC-14597 D8) is the deuterium labeled Aripiprazole, which is a human 5-HT1A receptor partial agonist with a Ki of 4.2 nM. 了解更多
  3. Bambuterol

    Catalog No. A21955
    Quick View
    beta-adrenoceptor agonist
    Bambuterol ((??)-Bambuterol; KWD-2183) is a long acting beta-adrenoceptor agonist (LABA) used in the treatment of asthma; it also is a prodrug of terbutaline. 了解更多
  4. MT-7716 free base

    Catalog No. A21928
    Quick View
    non-peptide nociceptin receptor (NOP) agonist
    MT-7716 free base (W-212393) is a selective non-peptide nociceptin receptor (NOP) agonist and promising potential treatment drug for alcohol abuse and relapse prevention. 了解更多
  5. Vilazodone D8

    Catalog No. A21876
    Quick View
    SSR inhibitor / 5-HT1A receptor partial agonist
    Vilazodone D8 is the a deuterium labeled vilazodone, which is a combined serotonin specific reuptake inhibitor (SSRI) and 5-HT1A receptor partial agonist. 了解更多
  6. AM-4668

    Catalog No. A21778
    Quick View
    GPR40 agonist
    AM-4668 is a GPR40 agonist for type 2 diabetes. EC50s of 3.6 nM and 36 nM for GPR40 in A9 cells (GPR40 IP3 assay) and CHO cells (GPR40 aequorin assay), respectively. 了解更多
  7. THIP

    Catalog No. A21738
    Quick View
    δ-GABAAR agonist
    THIP (Gaboxadol) is a selective δ-aminobutyric acid type A receptor (δ-GABAAR) agonist. 了解更多
  8. Gaboxadol hydrochloride

    Catalog No. A21730
    Quick View
    GABAA receptors agonist
    Gaboxadol hydrochloride (Lu 02-030 hydrochloride) is a selective agonist at GABAA receptors that contain α4-δ subunits, and has anxiolytic and sedative effects. 了解更多
  9. Taranabant ((1R,2R)stereoisomer)

    Catalog No. A21705
    Quick View
    CB1 receptor inverse agonist
    Taranabant (1R,2R)stereoisomer is the R-enantiomer of Taranabant. Taranabant is a highly potent and selective cannabinoid 1 (CB1) receptor inverse agonist. 了解更多
  10. diABZI STING agonist-1 trihydrochloride

    Catalog No. A21694
    Quick View
    STING receptor agonist
    diABZI STING agonist-1 (trihydrochloride) is a selective stimulator of interferon genes (STING) receptor agonist, with an EC50s of 130 for human PBMCs. 了解更多
  11. diABZI STING agonist-1

    Catalog No. A21688
    Quick View
    STING receptor agonist
    diABZI STING agonist-1 is a selective stimulator of interferon genes (STING) receptor agonist, with an EC50s of 130 nM for human PBMCs. 了解更多
  12. RGX-104 free Acid

    Catalog No. A21513
    Quick View
    LXR agonist
    RGX-104 free Acid is an orally bioavailable and potent liver-X nuclear hormone receptor (LXR) agonist that modulates innate immunity via transcriptional activation of the ApoE gene. 了解更多
  13. AM-1638

    Catalog No. A21505
    Quick View
    GPR40/FFA1 full agonist
    AM-1638 is a potent and orally bioavailable GPR40/FFA1 full agonist with an EC50 of 0.16 μM. 了解更多
  14. CP-409092 hydrochloride

    Catalog No. A21397
    Quick View
    GABAA receptor partial agonist
    CP-409092 hydrochloride is a partial agonist of GABAA receptor, with anti-anxiety activity. 了解更多
  15. SR 146131

    Catalog No. A21391
    Quick View
    nonpeptide cholecystokinin 1 receptor agonist
    SR 146131 is a potent, orally available, and selective nonpeptide (cholecystokinin 1) receptor agonist. 了解更多
  16. Prinaberel

    Catalog No. A21255
    Quick View
    ERbeta agonist
    Prinaberel(ERB-041) is a potent and selective ERbeta agonist; being >200-fold selective for ERbeta. 了解更多
  17. L-655708

    Catalog No. A21181
    Quick View
    GABAA receptor inverse agonist
    L-655708 is a potent α5 subunit-selective GABAA receptor inverse agonist (Ki = 0.45 nM). 了解更多
  18. Cutamesine

    Catalog No. A21152
    Quick View
    sigma 1 receptor agonist
    Cutamesine (SA4503; AGY-94806) is a selective sigma 1 receptor(??1R) agonist; high affinity for the sigma 1 receptor subtype labeled by (+)-[3H]pentazocine (IC50= 17.4??1.9 nM); 100-fold less affinity for the sigma 2 receptor. 了解更多
  19. Indeglitazar

    Catalog No. A21148
    Quick View
    PPAR agonist
    Indeglitazar is an orally available peroxisome proliferator-activated receptor (PPAR) pan-agonist for all three PPAR subtypes alpha (α), delta (δ) and gamma (γ). 了解更多
  20. Arhalofenate

    Catalog No. A21135
    Quick View
    PPARγ agonist
    Arhalofenate (MBX 102) is a selective partial agonist of peroxisome proliferator-activated receptor (PPAR)-γ, used for the treatment of type 2 diabetes. 了解更多
  21. Nelonicline

    Catalog No. A21079
    Quick View
    neuronal nicotinic receptor agonist
    Nelonicline (ABT-126) is a selective neuronal nicotinic receptor agonist. 了解更多
  22. Ralinepag

    Catalog No. A21073
    Quick View
    IP receptor agonist
    Ralinepag is a potent, orally bioavailable and non-prostanoid prostacyclin (IP) receptor agonist, with EC50s of 8.5 nM, 530 nM and 850 nM for human and rat IP receptor and human DP1 receptor, respectively. 了解更多
  23. Cenerimod

    Catalog No. A20913
    Quick View
    S1P1 agonist
    Cenerimod (ACT-334441) is a potent and orally available sphingosine 1-phosphate 1 receptor (S1P1) agonist extracted from patent WO 2016184939 A1 and WO 2011007324 A1, example 1, with an EC50 of 2.7 nM. 了解更多
  24. (R)-Baclofen

    Catalog No. A16680
    Quick View
    GABAB receptor agonist
    (R)-Baclofen(STX209) is a selective GABAB receptor agonist. 了解更多
  25. L-Glutamic acid monosodium salt

    Catalog No. A16591
    Quick View
    excitatory transmitter/agonist
    L-Glutamic acid monosodium salt acts as an excitatory transmitter and an agonist at all subtypes of glutamate receptors (metabotropic, kainate, NMDA, and AMPA). (S)-Glutamic acid shows a direct activating effect on the release of DA from dopaminergic terminals. 了解更多
  26. Indacaterol maleate

    Catalog No. A16585
    Quick View
    β-adrenoceptor agonist
    Indacaterol (QAB149) maleate is an ultra-long-acting β-adrenoceptor agonist. 了解更多
  27. (S)-Glutamic acid

    Catalog No. A15458
    Quick View
    glutamate receptors agonist
    (S)-Glutamic acid acts as an excitatory transmitter and an agonist at all subtypes of glutamate receptors (metabotropic, kainate, NMDA, and AMPA). 了解更多
  28. Taranabant

    Catalog No. A11578
    Quick View
    CB1 receptor inverse agonist
    Taranabant is a highly potent and selective cannabinoid 1 (CB1) receptor inverse agonist that inhibits the binding and functional activity of various agonists, with a binding Ki of 0.13 nM for the human CB1R in vitro. 了解更多
  29. Kynurenic acid sodium

    Catalog No. A20000
    Quick View
    GPR35/CXCR8 agonist
    Kynurenic acid sodium, an endogenous tryptophan metabolite, is a broad-spectrum antagonist targeting NMDA, glutamate, α7 nicotinic acetylcholine receptor. Kynurenic acid sodium is also an agonist of GPR35/CXCR8. 了解更多
  30. MT-7716 hydrochloride

    Catalog No. A20004
    Quick View
    NOP agonist
    MT-7716 hydrochloride (W-212393 hydrochloride) is a selective non-peptide nociceptin receptor (NOP) agonist and promising potential treatment drug for alcohol abuse and relapse prevention. 了解更多
  31. β3-AR agonist 1

    Catalog No. A12777
    Quick View
    β3-adrenergic receptor agonist
    β3-AR agonist 1 (compound 15) is a highly potent, selective, and orally available β3-adrenergic receptor (β3-AR) agonist (EC50=18 nM), being inactive to β1-, β2-, and α1A-AR (β1/β3, β2/β3, and α1A/β3>556-fold). 了解更多
  32. GPR35 agonist 1

    Catalog No. A12462
    Quick View
    GPR35/CXCR8 agonist
    GPR35 agonist 1 (compound 50) is a potent and specific G protein-coupled receptor-35 (GPR35)/CXCR8 agonist with an EC50 of 5.8 nM, displays good druggability. 了解更多
  33. U-101017

    Catalog No. A13357
    Quick View
    Benzodiazepine receptor/GABAA receptor agonist
    U-101017 is a partial agonist of benzodiazepine receptor and GABAA receptor, with anxiolytic effects. 了解更多
  34. LY2922470

    Catalog No. A12181
    Quick View
    GPR40 agonist
    LY2922470 is a potent, selective and orally available agonist of the G protein-coupled receptor 40 (GPR40), with EC50s of 7 nM, 1 nM and 3 nM for human GPR40, mouse GPR40 and rat GPR40, respectively. 了解更多
  35. AB-MECA

    Catalog No. A12189
    Quick View
    A3 adenosine receptor agonist
    AB-MECA is a high affinity A3 adenosine receptor agonist, has high affinity for recombinant A1 and A3 receptors. 了解更多
  36. Radequinil

    Catalog No. A13395
    Quick View
    BzR partial inverse agonist
    Radequinil (AC-3933) is a benzodiazepine receptor (BzR) partial inverse agonist. AC-3933 binds to GABA(-) and GABA(+) ligand with Kis of 5.15 and 6.11 nM, respectively. 了解更多
  37. Acamprosate calcium

    Catalog No. A11308
    Quick View
    GABA receptor agonist
    Acamprosate calcium(Campral EC) is a GABA receptor agonist and modulator of glutamatergic systems; reduces alcohol consumption in animal models of alcohol addiction. 了解更多
  38. CB2R-IN-1

    Catalog No. A12306
    Quick View
    cannabinoid CB2 receptor inverse agonist
    CB2R-IN-1 is a potent cannabinoid CB2 receptor inverse agonist with a Ki of 0.9 nM. 了解更多
  39. SKL2001

    Catalog No. A16707
    Quick View
    Wnt/β-catenin agonist
    SKL2001 is an agonist of the Wnt/β-catenin pathway, with anti-cancer activity. SKL2001 stabilizes intracellular β-catenin via disruption of the Axin/β-catenin interaction. 了解更多
  40. MRK-016

    Catalog No. A12046
    Quick View
    GABAA α5 receptor agonist
    MRK-016 is a selective, orally bioavailable inverse agonist of GABAA α5 receptor, with an EC50 of 3 nM for GABAA α5, and Kis of 0.83, 0.85, 0.77?and 1.4?nM for human?GABAA?α1β3γ2, GABAA?α2β3γ2, GABAA?α3β3γ2, and GABAA?α5β3γ2, respectively; MRK-016 also readily penetrates the CNS. 了解更多
  41. SB756050

    Catalog No. A12759
    Quick View
    TGR5 agonist
    SB756050 is a selective TGR5 agonist currently in phase 1clinical trials for the treatment of type 2 diabetes. 了解更多
  42. RWJ-51204

    Catalog No. A12875
    Quick View
    partial agonist of GABA(A) receptor
    RWJ-51204 is a partial agonist of GABA(A) receptor, with Ki of 0.2-2 nM to the benzodiazepine site on GABA(A) receptors. 了解更多
  43. ROR agonist-1

    Catalog No. A18569
    Quick View
    ROR 激动剂
    ROR agonist-1 is a potent and orally bioavailable inverse agonist of the retinoic acid receptor-related orphan receptor C2 (RORC2), inhibition of IL-17A production from human primary TH 17 cells with a pIC50 of 7.5. 了解更多
  44. Semaglutide

    Catalog No. A18908
    Quick View
    GLP-1 receptor agonist
    Semaglutide, a long-acting GLP-1 analogue, is a glucagon-like peptide-1 (GLP-1) receptor agonist that can be used in the treatment of type 2 diabetes. 了解更多
  45. PF-05231023

    Catalog No. A18949
    Quick View
    FGF21-receptor agonist
    PF-05231023, a long-acting fibroblast growth factor 21 (FGF21) analog, is a FGF21-receptor agonist, suitable for development as a potential treatment for T2DM. 了解更多
  46. TPA 023

    Catalog No. A20140
    Quick View
    GABAA α2/α3 agonist
    TPA 023 is a GABAA α2/α3 subtype-selective agonist, with Ki of 0.19-0.41 nM. 了解更多
  47. CP-409092

    Catalog No. A20152
    Quick View
    GABAA receptor partial agonist
    CP-409092 is a partial agonist of GABAA receptor, with anti-anxiety activity. 了解更多
  48. Kynurenic acid

    Catalog No. A16581
    Quick View
    GPR35/CXCR8 拮抗剂
    Kynurenic acid, an endogenous tryptophan metabolite, is a broad-spectrum antagonist targeting NMDA, glutamate, α7 nicotinic acetylcholine receptor. Kynurenic acid is also an agonist of GPR35/CXCR8. 了解更多
  49. KAG-308

    Catalog No. A18389
    Quick View
    EP4 激动剂
    KAG-308, a newly-identified EP4-selective agonist shows efficacy for treating ulcerative colitis and can bring about lower risk of colorectal carcinogenesis by oral administration. 了解更多
  50. XY101

    Catalog No. A18437
    Quick View
    RORγ inverse 激动剂
    XY101 is a potent, selective, metabolically stable and orally available RORγ inverse agonist with an IC50 of 30 nM and a Kd of 380 nM. 了解更多

产品 1 到 50 共 76个

每页
页面:
  1. 1
  2. 2

设置降序顺序
Rewards