c171

STING-IN-3 (C-171) 是干扰素基因刺激物 (STING) 的抑制剂。 它与 STING 结合，抑制其棕榈酰化，并阻止 TBK1 的募集和磷酸化。

EN4 (EN4 MYC inhibitor) 是一种靶向 M​​YC 的半胱氨酸 171 (C171) 的共价配体。它抑制 MYC 转录活性，下调 MYC 靶标，并具有抗肿瘤作用。它对 c-MYC 的选择性高于 N-MYC 和 L-MYC。

VPC171 是一种新型腺苷 A1 受体正变构调节剂 (PAM)。

ZINC17167211 is a selective peroxisome proliferator-activated receptors-α agonist.

11-Beta-hydroxyandrostenedione (NSC-17102) 是主要存在于肾上腺的类固醇，也是 11β-羟基类固醇脱氢酶同工酶抑制剂。随着 4-androstenedione 的提高，通过测量血浆中的11-Beta-hydroxyandrostenedione，能够区分高雄激素血症的肾上腺或卵巢起源。

Azotomycin is an antagonist of L-glutamine and may be used as an immunosuppressant.

JC-171 is a selective NLRP3 inflammasome inhibitor, with an IC50 of 8.45 μM for inhibiting LPS ATP-induced interleukin-1β (IL-1β) release from J774A.1 macrophages[1]. JC-171 (0-100 μM) blocks NLRP3 inflammasome activation and IL-1β production in primary macrophages dose dependently[1]. Cell Viability Assay[1] Cell Line: J774A.1 murine macrophage cells JC-171 treatment delays the progression and reduces the severity of experimental autoimmune encephalomyelitis (EAE) in mouse[1]. Animal Model: Mice immunized subcutaneously with 200 μg Myelin oligodendrocyte glycoprotein (MOG) 35-55 peptide emulsified in Complete Freund's Adjuvant (CFA) on day 0 followed by injection of 200 ng of pertussis toxin. [1]. Chunqing Guo, et al. Development and Characterization of a Hydroxyl-Sulfonamide Analogue, 5-Chloro-N-[2-(4-hydroxysulfamoyl-phenyl)-ethyl]-2-methoxy-benzamide, as a Novel NLRP3 Inflammasome Inhibitor for Potential Treatment of Multiple Sclerosis. ACS Chem Neurosci. 2017 Oct 18;8(10):2194-2201.

Ginkgolic acid C17:1 是分离自银杏叶中，通过诱导PTEN 和SHP-1酪氨酸磷酸酶抑制组成型和诱导型 STAT3 活化。它具有抗癌活性。

Ginkgolic Acids(C13:0,C15:1,C17:2,C15:0,C17:1) 是一种天然产物，可用作天然产物对照品，用于生命科学相关领域的研究，其产品编号为 TN8870。