GPCR/G protein

GPCR/G protein(G 蛋白偶联受体/G 蛋白)

研究方向

GPCR/G protein 相关产品(3377)

  • GC25728 structure
    GC25728PF-4136309
    CAS: 857679-55-1

    PF-4136309 (INCB8761, PF-04136309) is a potent, selective, and orally bioavailable CCR2 antagonist with an IC50 of 5.2 nM for human CCR2.

  • GC25756 structure
    GC25756Pirenperone
    CAS: 75444-65-4

    Pirenperone (R-47456, R-50656), a quinazoline derivative, is a selective antagonist of SR-2A (5-HT2 serotonin receptor) when employed in low doses. Pirenperone behaves like a typical neuroleptic when used in higher doses (greater than 0.1 mg/kg).

  • GC25786 structure
    GC25786Propafenone
    CAS: 54063-53-5

    Propafenone (SA-79) is an orally active sodium channel blocking agent and a beta-adrenoceptor (β-adrenergic receptor) antagonist. Propafenone offers a broad spectrum of activity in the treatment of cardiac arrhythmias.

  • GC25898 structure
    GC25898SB 200646
    CAS: 143797-63-1

    SB 200646 (SB 200646A) is a potent, selective and oral-active antagonist of 5-HT2B/2C over 5-HT2A receptor with 50 fold selectivity. The pKi for rat 5-HT2C receptor, rat 5-HT2B receptor and rat 5-HT2A receptor are 6.9, 7.5 and 5.2, respectively. SB 200646 has electrophysiological and anxiolytic properties in vivo.

  • GC26002 structure
    GC26002Trazodone
    CAS: 19794-93-5
    纯度: >98.00%

    Trazodone (AF-1161) is a 5-HT 2A/2C receptor antagonist that is used as an antidepressant for treating major depressive disorder and anxiety disorders.

  • GC26016 structure
    GC26016TSHR antagonist S37
    CAS: 1217616-61-9

    TSHR antagonist S37 is a selective and competitive antagonist of the thyrotropin receptor (TSHR).

  • GC26027 structure
    GC26027V-0219
    CAS: 878453-71-5

    V-0219 is an orally active, positive allosteric modulator (PAM) of the glucagon-like peptide-1 receptor (GLP-1R), can be used for obesity-associated diabetes research.

  • GC26069 structure
    GC26069WAY-639889
    CAS: 432506-24-6

    WAY-639889 is a bioactive compound relative to neuropeptide Y-5.

  • GC26144 structure
    GC26144Menthol
    CAS: 1490-04-6

    Menthol 是个天然的止痛剂。Menthol 通过抑制神经元细胞膜的 Ca ++ 电流,刺激冷感受器,从而产生凉的感觉。

  • GC30008 structure
    GC30008Ceruletide (Caerulein)
    CAS: 17650-98-5
    纯度: >99.50%

    Ceruletide 作为一种十肽和一种有效的胆囊收缩剂,对人类和动物的胆囊肌肉和胆管具有直接的痉挛作用。

  • GC30058 structure
    GC30058GLP-1(7-37)
    CAS: 106612-94-6
    纯度: >99.50%

    GLP-1(7-37)是一种截短的胰高血糖素样肽,对GLP-1受体的EC 50 值为0.9 ± 0.1nM。

  • GC30068 structure
    GC30068Taprenepag (CP-544326)
    CAS: 752187-80-7
    纯度: >99.50%

    A potent EP 2 receptor agonist

  • GC30092 structure
    GC30092Salmeterol (GR33343X)
    CAS: 89365-50-4
    纯度: >99.50%

    Salmeterol (Astmerole, GR-33343X, SN408D) is a long-acting beta2-adrenergic receptor agonist with Ki value of 1.5 nM for WT β2AR and shows very high selectivity for the WT β2AR(β1Ki/β2Ki ratio of approximately 1500).

  • GC30095 structure
    GC30095SB-423562
    CAS: 351490-27-2
    纯度: >99.50%

    SB-423562是一种短效的(CaR)拮抗剂。

  • GC30104 structure
    GC30104Fezolinetant (ESN-364)
    CAS: 1629229-37-3
    纯度: >98.00%

    Fezolinetant (ESN-364) 是一种神经激肽 3 受体 (NK3R) 的拮抗剂,用于治疗更年期潮热。

  • GC30188 structure
    GC30188Dapiprazole hydrochloride
    CAS: 72822-13-0
    纯度: >99.50%

    An α-adrenergic receptor antagonist

  • GC30194 structure
    GC30194JNJ-10229570
    CAS: 524923-88-4
    纯度: >98.00%

    JNJ-10229570 (UNII-N9IX402L35) is a potent MC1R and MC5R antagonist.

  • GC30198 structure
    GC30198Dolasetron Mesylate hydrate
    CAS: 878143-33-0
    纯度: >99.00%

    A 5-HT 3 receptor antagonist

  • GC30206 structure
    GC30206Roluperidone (CYR-101)
    CAS: 359625-79-9
    纯度: >99.50%

    A dual antagonist of 5-HT 2A and σ 2 receptors

  • GC30224 structure
    GC30224FPTQ
    CAS: 864863-72-9
    纯度: >99.50%

    FPTQ是mGluR1拮抗剂,在人和老鼠上IC50是6nM和4nM

  • GC30254 structure
    GC30254HAEGTFT
    CAS: 926018-95-3
    纯度: >99.00%

    HAEGTFT是GLP-1多肽N-端的1-7残基。

  • GC30273 structure
    GC30273Tedatioxetine hydrobromide (Lu AA 24530 hydrobromide)
    CAS: 960151-65-9
    纯度: >99.50%

    Tedatioxetine (Lu AA24530) hydrobromide 可作为 5-HT2A、5-HT2C、5-HT3 和 α;1A-肾上腺素受体拮抗剂,可作为 5-羟色胺和去甲肾上腺素 (NE) 的首选三重再摄取抑制剂 (TRI)。

  • GC30280 structure
    GC30280Chlorpromazine D6 hydrochloride
    CAS: 1228182-46-4
    纯度: >99.50%

    Chlorpromazine D6 hydrochloride是 Chlorpromazine 的氘代物,可被用于 NMR、GC-MS 或 LC-MS 分析中的内标品,用于定量分析。

  • GC30299 structure
    GC30299GSK726701A
    CAS: 945721-87-9
    纯度: >98.50%

    GSK726701A是前列腺素E2受体4(EP4)的部分激动剂,pEC50为7.4。