关于 "c-RET" 的结果44 个结果

筛选:Proteases×
  • GC36513 structure
    LY-411575 isomer 2

    LY-411575 isomer 2 是 LY411575 的一个异构体,LY411575 为 γ-secretase 高效抑制剂。

  • GC36514 structure
    LY-411575 isomer 3

    LY-411575 isomer 3 是 LY411575 的一个异构体,LY411575 为 γ-secretase 高效抑制剂。

  • GC60377 structure
    Urolithin C
    CAS: 165393-06-6

    UrolithinC,是鞣花酸的多酚类肠道微生物代谢产物,是胰岛素分泌(insulinsecretion)的葡萄糖依赖性激活剂。UrolithinC是一种L型Ca2+通道开放剂,可增强Ca2+的流入。UrolithinC通过线粒体介导的途径诱导细胞凋亡(apoptosis),并刺激活性氧(ROS)的形成。

  • GC61107 structure
    N-Acetyl-L-glutamic acid
    CAS: 1188-37-0

    N-Acetylglutamic acid (N-Acetylglutamate) is the first intermediate involved in the biosynthesis of arginine in prokaryotes and simple eukaryotes and a regulator in the process known as the urea cycle that converts toxic ammonia to urea for excretion from the body in vertebrates.

  • GC19290 structure
    PF-3084014
    CAS: 1290543-63-3

    An inhibitor of γ-secretase

  • GC38300 structure
    Phytic acid potassium
    CAS: 129832-03-7

    Phytic acid dipotassium salt (Phytic acid potassium, IP6 (PS)), an endogenous metabolite in rice grain extract and digest, inhibits β-secretase 1 (BACE1) with IC50 of approximately 0.25 μM.

  • GC38768 structure
    Deserpidine
    CAS: 131-01-1

    Deserpidine (Harmonyl), an alkaloid isolated from the roots of Rauwolfia canescens, is a competitive angiotensin converting enzyme (ACE) inhibitor, also decreases angiotensin II-induced aldosterone secretion by the adrenal cortex.

  • GC30427 structure
    ELN 318463 racemate
    CAS: 851599-82-1

    ELN318463racemate是ELN318463的外消旋体。ELN318463是一种选择性的gamma-secretase抑制剂。

  • GC30472 structure
    Dehydrocholate sodium (Sodium dehydrocholate)
    CAS: 145-41-5

    Sodium Dehydrocholate is a semisynthetic bile acid made from cholic acid. It has been used for stimulation of biliary lipid secretion.

  • GC30887 structure
    NGP555
    CAS: 1304630-27-0

    A γ-secretase modulator

  • GC30954 structure
    Itanapraced (CHF5074)
    CAS: 749269-83-8

    A modulator of γ-secretase

  • GC31625 structure
    3-(3-Methoxyphenyl)propionic acid
    CAS: 10516-71-9

    3-(3-Methoxyphenyl)propionic acid is a naturally occurring human metabolite, It is an organic acid and excreted in human urine.

  • GC32456 structure
    R-IMPP
    CAS: 2133832-83-2

    A cell-permeable inhibitor of PCSK9 secretion

  • GC62388 structure
    YUM70
    CAS: 423145-35-1

    YUM70 is a potent inhibitor of glucose-regulated protein 78 (GRP78) inhibitor with an IC50 of 1.5 μM. YUM70 induces endoplasmic reticulum (ER) stress-mediated apoptosis in pancreatic cancer.Although YUM70 inhibits GRP78 enzymatic activity, it increases the expression of GRP78 by increasing the chaperone translation mechanism.

  • GC62859 structure
    Aβ42-IN-2
    CAS: 1914989-80-2

    Aβ42-IN-2 是一种 γ-secretase 调节剂,详细信息请参考专利文献 WO2016070107 中 的化合物 36。Aβ42-IN-2 对 αβ42 作用的 IC50 值为 6.5 nM 。Aβ42-IN-2 可用于阿尔茨海默症的研究。

  • GC62998 structure
    GSM-1
    CAS: 884600-68-4

    GSM-1 是有效的 γ-secretase 调节剂。GSM-1 直接靶向早衰蛋白 1 (PS1) 的跨膜结构域。

  • GC63235 structure
    Trans-2-butene-1,4-dicarboxylic acid
    CAS: 4436-74-2

    trans-β-Hydromuconic acid (trans-2-Butene-1,4-dicarboxylic Acid, 3-hexenediodicacid, β-Hydromuconic acid) is a normal human unsaturated dicarboxylic acid metabolite with increased excretion in patients with Dicarboxylic aciduria caused by fatty acid metabolism disorders.

  • GC63366 structure
    Fosciclopirox
    CAS: 1380539-06-9

    Fosciclopirox(CPX-POM) selectively delivers the active metabolite, Ciclopirox (CPX) that targets γ-secretase complex (Presenilin 1 and Nicastrin)2. It is used in the treatment of urothelial cancer and a number of solid and hematologic malignancies.

  • GC63407 structure
    PF-06648671
    CAS: 1587727-31-8

    PF-06648671 是一种新型的,可通透血脑屏障的,具有口服活性的 γ 分泌酶 (γ‐Secretase) 调节剂 (GSM)。PF-06648671 减少 Aβ42 和 Aβ40,并且伴随 Aβ37 和 Aβ38 的增加。PF-06648671 用于阿尔茨海默病的研究。

  • GC67476 structure
    (E/Z)-Sulindac sulfide
    CAS: 32004-67-4

    (E/Z)-Sulindac sulfide 是一种有效的 γ-secretase 调节剂。(E/Z)-Sulindac sulfide 可选择性地减少 Aβ42 产生,有利于更短的 Aβ 类型的产生。(E/Z)-Sulindac sulfide 可用于阿尔兹海默症的研究。