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)

  • GC60615 structure
    GC60615AZD2423
    CAS: 1229603-37-5
    纯度: >98.50%

    AZD2423是一种有效的、选择性的、口服生物利用的、非竞争性的CCR2趋化因子受体负向变构调节剂。AZD2423对CCR2Ca2+通量的IC50为1.2nM。

  • GC60619 structure
    GC60619BA 1 TFA
    纯度: >99.50%

    BA 1 TFA 是铃蟾肽 (BB) 受体家族的有效激动剂。

  • GC60630 structure
    GC60630Befiradol hydrochloride
    CAS: 2436760-81-3
    纯度: >99.50%

    Befiradolhydrochloride(NLX-112hydrochloride)是选择性的5-羟色胺1A(5-HT)1A受体激动剂。

  • GC60662 structure
    GC60662Brexpiprazole S-oxide
    CAS: 1191900-51-2

    BrexpiprazoleS-oxide(DM-3411)是Brexpiprazole的主要代谢产物,并通过细胞色素P4503A4(CYP3A4)代谢。Brexpiprazole是一种非典型抗精神病药,是人5-HT1A和多巴胺受体的部分激动剂,Ki分别为0.12nM和0.3nM。Brexpiprazole也是5-HT2A受体的拮抗剂,Ki为0.47nM。

  • GC60679 structure
    GC60679CCR2 antagonist 4
    CAS: 226226-39-7
    纯度: >99.50%

    CCR2antagonist4(Teijincompound1)是一种高效、特异的CCR2拮抗剂,对CCR2b的IC50值为180nM。CCR2antagonist4对MCP-1诱导的趋化作用有较强的抑制作用,其IC50为24nM。

  • GC60717 structure
    GC60717Clonidine
    CAS: 4205-90-7
    纯度: >98.50% / >99.50%

    Clonidine HCl(Kapvay) is a direct-acting α2 adrenergic agonist with an ED50 of 0.02±0.01 mg/kg.

  • GC60724 structure
    GC60724Corticotropin-releasing factor (human) (acetate)
    纯度: >98.50%

    Corticotropin-releasingfactorhumanacetate(HumanCRFacetate)能够刺激垂体前叶的促肾上腺皮质激素的合成和分泌。

  • GC60748 structure
    GC60748Dehydro Olmesartan
    CAS: 172875-98-8

    DehydroOlmesartan是Olmesartan的衍生物。Olmesartan是血管紧张素II受体(AT1R)拮抗剂,可用于高血压的研究。

  • GC60758 structure
    GC60758Deschloroclozapine
    CAS: 1977-07-7
    纯度: >98.00%

    Deschloroclozapine是一种高亲和力、选择性且代谢稳定的毒蕈碱DREADD激动剂,Deschloroclozapine能快速穿透血脑屏障,有效激活兴奋性hM3Dq和抑制性hM4Di DREADD受体。

  • GC60764 structure
    GC60764Diacetolol D7
    CAS: 1346604-19-0

    DiacetololD7是Diacetolol的氘代物。Diacetolol是Acebutolol的主要代谢产物。Diacetolol是一种β-肾上腺素受体(β-adrenoceptor)阻断剂和抗心律失常药。

  • GC60767 structure
    GC60767Dibenamine hydrochloride
    CAS: 55-43-6
    纯度: >98.00%

    Dibenamine (N-(2-Chloroethyl)dibenzylamine, Sympatholytin, Dibenzylchlorethamine) is an irreversible blocker of α1 adrenoceptors.

  • GC60790 structure
    GC60790Doxazosin D8
    CAS: 1126848-44-9

    An internal standard for the quantification of doxazosin

  • GC60829 structure
    GC60829Exendin-3/4 (59-86)
    CAS: 1263874-37-8
    纯度: >97.00%

    Exendin-3/4(59-86)是Exendin-4多肽衍生物。

  • GC60846 structure
    GC60846Flesinoxan
    CAS: 98206-10-1
    纯度: >99.00%

    Flesinoxan是一种降压剂,是一种有效的,高亲和力的选择性的5-羟色胺1A(5-HT1A)受体激动剂,EC50值为24nM。Flesinoxan还具有有效的抗焦虑/抗抑郁作用。

  • GC60876 structure
    GC60876GLP-1(7-36), amide TFA
    纯度: >99.00%

    GLP-1(7-36),amideTFA是一种主要的肠道激素,在葡萄糖的刺激下,它能促使胰岛β细胞分泌胰岛素。

  • GC60877 structure
    GC60877GLP-2(3-33)
    CAS: 275801-62-2
    纯度: >99.00%

    GLP-2(3-33)由二肽基肽酶IV(DPPIV)产生,是一种GLP-2受体部分激动剂(EC50=5.8nM)。

  • GC60899 structure
    GC60899Hibifolin
    CAS: 55366-56-8
    纯度: >98.00%

    Hibifolin (Gossypetin-8-O-β-D-glucuronide) is a flavonol glycoside and acts as a potential inhibitor of adenosine deaminase (ADA) with a Ki of 49.92 μM. Hibifolin prevents β-amyloid-induced neurotoxicity in cultured cortical neurons.

  • GC60914 structure
    GC60914Hydrocortisone hemisuccinate
    CAS: 2203-97-6
    纯度: >98.00%

    Hydrocortisone hemisuccinate (A-hydrocort, Hydrocortisone 21-hemisuccinate), a physiological glucocorticoid with anti-inflammatory properties, is an inhibitor of proinflammatory cytokine with IC50 of 6.7 μM and 21.4 μM for Interleukin-6 (IL-6) and IL-3, respectively.

  • GC60915 structure
    GC60915Hydroxy ziprasidone
    CAS: 884305-08-2

    Hydroxyziprasidone是Ziprasidone的杂质。Ziprasidone,一种抗精神药物,是5-HT和多巴胺(dopaminereceptor)受体拮抗剂。

  • GC60938 structure
    GC60938Iprindole
    CAS: 5560-72-5
    纯度: >98.00%

    Iprindole具有抗抑郁的生物活性,是一种弱的去甲肾上腺素和5-HT摄取的抑制剂。

  • GC60957 structure
    GC60957Jatrorrhizine hydroxide
    CAS: 483-43-2
    纯度: >98.00%

    Jatrorrhizine (Neprotin, Yatrorizine), one of the active constituents of Coptis chinensis Franch, has multiple bioactivities, such as hypoglycemic, antimicrobial, and antioxidant activities. It is an inhibitor of AChE with IC50 of 872 nM and demonstrates >115-fold selectivity for AChE over BuChE.

  • GC60965 structure
    GC60965Keto Ziprasidone
    CAS: 884305-07-1

    KetoZiprasidone是Ziprasidone的杂质。Ziprasidone,一种抗精神药物,是5-HT和多巴胺(dopaminereceptor)受体拮抗剂。

  • GC60969 structure
    GC60969KRAS inhibitor-9
    CAS: 300809-71-6
    纯度: >99.50%

    KRASinhibitor-9是有效的KRAS抑制剂(Kd=92μM),阻止GTP-KRAS的形成和KRAS下游激活。KRASinhibitor-9以中等的结合亲和力与KRASG12D,KRASG12C和KRASQ61H蛋白结合。KRASinhibitor-9导致G2/M细胞周期停滞并诱导凋亡(apoptosis)。KRASinhibitor-9选择性抑制具有KRAS突变的NSCLC细胞的增殖,但不抑制正常肺细胞的增殖。KRASinhibitor-9

  • GC60971 structure
    GC60971L-692429
    CAS: 145455-23-8
    纯度: >99.50%

    L-692429(MK-0751)是一种苯并内酰胺的衍生物,也是一种非肽基生长激素促分泌素(GHS)激动剂。L-692429以Ki值为63nM来结合G蛋白偶联受体(Gprotein-coupledreceptor)。