微信关注
China
Total item
Cart Subtotal
￥ 0.00 “glucagon receptor”的搜索结果
-
Apalutamide (ARN-509)
Catalog No. A11923 Androgen Receptor 抑制剂Apalutamide (ARN-509)是一种具有潜在抗肿瘤活性的雄激素受体拮抗剂，IC50 为 16 nM。ARN-509与靶组织中的AR结合，从而阻止了雄激素诱导的受体激活，并促进了无法转运至细胞核的无活性复合物的形成。这防止了AR应答基因的结合和转录。 了解更多 -
Laropiprant (MK0524)
Catalog No. A11483 DP1 抑制剂Laropiprant (MK0524)与烟酸合用可降低血液胆固醇。是一种有效的，选择性的 DP receptor 拮抗剂，Ki 值为 0.57 nM，对 TP 受体的 Ki 值为 2.95 nM。 了解更多 -
Orphenadrine citrate
Catalog No. A11712 -
Aniracetam
Catalog No. A10078 -
Rupatadine Fumarate
Catalog No. A12356 PAFR 抑制剂/H1 receptor 抑制剂Rupatadine Fumarate是PAFR和组胺(H1)受体的抑制剂，Ki分别为550和102 nM。 了解更多 -
Rupatadine
Catalog No. A11222 PAFR 抑制剂/H1 receptor 抑制剂Rupatadine是PAFR和组胺（H1）受体的抑制剂，Ki分别为550和102 nM。 了解更多 -
LDN-212854
Catalog No. A12821 -
LCZ696 (Valsartan)
Catalog No. A14206 angiotensin receptor-neprilysin 抑制剂LCZ696 (Valsartan)是一种生物利用型双效血管紧张素受体-中性溶血素抑制剂（ARNi），用于治疗高血压和心力衰竭。 了解更多 -
Atosiban
Catalog No. A14334 -
EGFR Inhibitor
Catalog No. A13673 EGFR 抑制剂EGFR inhibitor是一种可透过细胞的4,6-二取代嘧啶化合物，可选择性抑制EGFR激酶，在体外的IC50值为21 nM，可阻断细胞中的受体自身磷酸化。 了解更多 -
Reparixin L-lysine salt
Catalog No. A15219 CXCL8 receptor 抑制剂Reparixin L-lysine salt是CXCL8受体的抑制剂，也抑制CXCR1和CXCR2的活化，已显示在各种损伤模型中减弱了炎症反应。 了解更多 -
Antazoline HCl
Catalog No. A16411 -
LY 3200882
Catalog No. A16816 TGFβRI 抑制剂LY 3200882是有效的、高选择性TGF-β receptor type 1 (TGFβRI)抑制剂，在体外肿瘤组织和免疫细胞以及体内皮下肿瘤中，有效地以浓度依赖方式抑制TGFβ介导的SMAD磷酸化。 了解更多 -
Flopropione
Catalog No. A16550 5-HT1A receptor antagonist/COMT inhibitorFlopropione是5-HT1A受体拮抗剂，也是儿茶酚-邻甲基转移酶（COMT）抑制剂。 了解更多 -
Eucalyptol
Catalog No. A15662 -
Importazole
Catalog No. A17128 nuclear transport receptor importin-β 抑制剂Importazole是Importin-β的细胞可渗透抑制剂。它可能通过改变与RanGTP的相互作用来特异性抑制importin-β的功能。 了解更多 -
Loxapine Succinate
Catalog No. A17347 D2DR and D4DR inhibitorLoxapine Succinate is a D2DR and D4DR inhibitor and serotonergic receptor antagonist. Loxapine succinate is an antipsychotic agent used in schizophrenia. 了解更多 -
AX-024 hydrochloride
Catalog No. A18332 TNF receptor inhibitorAX-024 is an orally available inhibitor of the TCR-Nck interaction that selectively inhibits TCR-triggered T cell activation (IC50 value 1 nM). Inhibiting an immediate TCR signal has promise for treating a broad spectrum of human T cell-mediated autoimmune and inflammatory diseases. 了解更多 -
-
最新产品
AG1295
Catalog No. A17227 -
-
Benorylate
Catalog No. A17501 Prostaglandin Receptor inhibitorBenorilate, also known as Win-11450, is an ester of aspirin and paracetamol with analgesic, antipyretic, and anti-inflammatory activity used in the treatment of rheumatoid diseases. Benorilate has less severe side effects than aspirin. 了解更多 -
Dinoprost tromethamine
Catalog No. A17505 Prostaglandin Receptor inhibitorDinoprost Tromethamine, also known as Dinoprost Trometamol, is a naturally occurring prostaglandin used in medicine to induce labor and as an abortifacient. 了解更多 -
Molindone hydrochloride
Catalog No. A17647 MAO inhibitorMolindone HCl is a D2 dopamine receptor antagonist. It also acts as a MAO inhibitor. 了解更多 -
L-(-)-α-Methyldopa (hydrate)
Catalog No. A18111 DOPA decarboxylase inhibitorMethyldopa Sesquihydrate is a DOPA decarboxylase inhibitor and indirect α2-adrenergic receptor agonist used to treat hypertension. 了解更多 -
TGFβRI-IN-1
Catalog No. A18800 TGFβRI kinase inhibitorTGFβRI-IN-1 is an oral active and selective TGFβ receptor type I (TGFβRI) kinase inhibitor, with IC50 values of 2 nM and 7.6 μM for TGFβRI and TGFβRII, respectively. 了解更多 -
c-Fms-IN-10
Catalog No. A19017 FMS inhibitorc-Fms-IN-10 is the derivative of thieno [3,2-d] pyrimidine, an kinase inhibitor of FMS (Colony stimulating factor-1 receptor, CSF-1R) with IC50 of 2 nM. c-Fms-IN-10 has anti-tumor activity. 了解更多 -
c-Fms-IN-8
Catalog No. A18879 CSF-1R, c-FMS Type II inhibitorc-Fms-IN-8 (compound 4a) is a colony stimulating factor-1 receptor (CSF-1R, c-FMS) Type II inhibitor, with an IC50 of 9.1 nM. 了解更多 -
MD2-TLR4-IN-1
Catalog No. A18452 MD2-TLR4 inhibitorMD2-TLR4-IN-1 (compound 22m) is an inhibitor of myeloid differentiation protein 2/toll-like receptor 4 (MD2-TLR4) complex, inhibiting lipopolysaccharides (LPS)-induced expression of tumor necrosis factor alpha (TNF-α) and interleukin-6 (IL-6) in macrophages with IC50 values of 0.89 μM and 0.53 μM, respectively. 了解更多 -
TRPC6-IN-1
Catalog No. A12309 TRPC6 inhibitorTRPC6-IN-1 is a Transient Receptor Potential Canonical 6 Channel (TRPC6) inhibitor, with an EC50 of 4.66 μM. 了解更多 -
Vilazodone Hydrochloride
Catalog No. A11604 serotonin transporter (SER) inhibitorVilazodone Hydrochloride (EMD 68843 Hydrochloride) is a serotonin transporter (SER) inhibitor and 5-HT1A receptor partial agonist. 了解更多 -
CHMFL-EGFR-202
Catalog No. A12524 EGFR inhibitorCHMFL-EGFR-202 is a potent, irreversible inhibitor of epidermal growth factor receptor (EGFR) mutant kinase, with IC50s of 5.3 nM and 8.3 nM for drug-resistant mutant EGFR T790M and WT EGFR kinases, respectively. 了解更多
联系我们
United StatesAdooq Bioscience
Toll Free: (866) 930-6790
Fax: +1-323-606-8156
Email: sales@adooq.com
Not your Region? View all Distributors
FILTER BY:
Filtering:
- 作用机制: Inhibitor (抑制剂) 删除该内容
购物选项
- 分类
-
- Epigenetics (2)
- Apoptosis (8)
- Protein Tyrosine Kinases (20)
- Angiogenesis (14)
- JAK / Stat (6)
- Cell Cycle (1)
- Cytoskeleton (1)
- Cell Metabolism (4)
- Autophagy Signaling (1)
- Immunology & Inflammation (6)
- GPCR / G Protein (25)
- TGF-β / Smad (6)
- Neuronal Signaling (10)
- Proteases (1)
- Microbiology (1)
- Membrane Transporters/Ion Channels (6)
- Endocrinology / Hormones (3)
- Others (1)
- Ready to Use Solution (5)
- Products On Sale (13)
- 靶点
ADOOQ 产品质量保证
We promise all products to perform as described.