Home >> Signaling Pathways >> Ubiquitination/ Proteasome >> Autophagy

Autophagy(自噬)

Autophagy is a catabolic process which degrades and recycles long-lived proteins and cytoplasmic organelles through lysosome. It plays an important role in growth regulation and maintenance of homeostasis.

Products for  Autophagy

  1. Cat.No. 产品名称 Information
  2. GC31705 Sofalcone

    索法酮

    Gastroprotective chalcone derivative
  3. GC31697 Dilmapimod (SB-681323)

    度马莫得; SB-681323; GW 681323

    Dilmapimod (SB-681323,GW 681323) is a potent p38 MAPK inhibitor that potentially suppresses inflammation in chronic obstructive pulmonary disease.
  4. GC31665 (R)-BPO-27 (R)-BPO-27是有效的CFTR抑制剂,IC50值为4nM。
  5. GC31586 Monacolin J (Antibiotic MB 530A)

    辛伐他汀内酯二醇,Antibiotic MB 530A; Lovastatin diol lactone

    Monacolin J (Antibiotic MB 530A) 是一种胆固醇生物合成抑制剂,可抑制 HMG-CoA 还原酶的活性。
  6. GC31395 PX20606 trans racemate (PX-102 trans racemate)

    CPDD1220反式消旋体,PX-102 trans racemate

    PX20606 trans racemate (PX-102 trans racemate) (PX-102 trans racemate) 是一种 FXR 激动剂,在 FRET 和 M1H 试验中对 FXR 的 EC50 分别为 32 和 34 nM。
  7. GC31386 (-)-PX20606 trans isomer ((-)-PX-102 trans isomer)

    PX-20606手性,(-)-PX-102 trans isomer; (-)-PX-104

    (-)-PX20606 trans isomer ((-)-PX-102 trans isomer) 是一种 FXR 激动剂,在 FRET 和 M1H 试验中对 FXR 的 EC50 分别为 18 和 29 nM。
  8. GC31317 Sitagliptin (MK0431)

    西格列汀; MK-0431

    Sitagliptin (MK-0431) is an oral and highly selective DPP-4 inhibitor with an IC50 of 18 nM. It is used for the treatment of type 2 diabetes.
  9. GC31239 SA72 SA72是高度选择性的脂肪酸酰胺水解酶(FAAH)抑制剂。
  10. GC31170 Calmodulin-Dependent Protein Kinase II 290-309

    A CaMKII inhibitor

  11. GC31058 FR 167653 free base FR-167653是一种选择性的p38MAPK抑制剂。
  12. GC30992 Paroxetine hydrochloride hemihydrate (BRL29060 hydrochloride hemihydrate)

    盐酸帕罗西汀半水合物; BRL29060 hydrochloride hemihydrate; BRL29060A hemihydrate

    Paroxetine HCl (BRL-29060A, FG-7051) is an antidepressant drug of the SSRI type.
  13. GC30990 Calcineurin substrate

    钙调神经磷酸酶底物

    A synthetic peptide substrate
  14. GC30884 LX2343 An inhibitor of BACE1 and PI3K
  15. GC30871 Oxidopamine hydrochloride (6-Hydroxydopamine hydrochloride)

    6-羟基多巴胺盐酸盐; 6-Hydroxydopamine hydrochloride; 6-OHDA hydrochloride

    Oxidopamine hydrochloride (6-Hydroxydopamine hydrochloride)(6-OHDA)是神经递质多巴胺的拮抗剂。
  16. GC30842 Androsterone (5α-Androstan-3α-ol-17-one)

    雄酮; 5α-Androstan-3α-ol-17-one

    An androgenic steroid

  17. GC30790 Triflupromazine hydrochloride

    盐酸三氟丙嗪

    A phenothiazine with diverse biological activities
  18. GC30787 Sertindole (Lu 23-174)

    舍吲哚; Lu 23-174

    An atypical antipsychotic
  19. GC30785 4E2RCat 4E2RCat是eIF4E-eIF4G相互作用的抑制剂,IC50值为13.5μM。
  20. GC30761 α-Hydroxylinoleic acid

    α-羟基油酸; α-Hydroxylinoleic acid

    ABTL0812 (α-Hydroxylinoleic acid, LP-10218, SCLN-0812) inhibits Akt/mTOR axis by inducing the overexpression of TRIB3 and activating autophagy in lung squamous carcinoma cell lines. ABTL0812 also induces AMPK activation and ROS accumulation.
  21. GC30751 FAAH-IN-1 FAAH-IN-1是脂肪酸酰胺水解酶(FAAH)抑制剂,对大鼠和人FAAH的IC50值分别为145nM和650nM。
  22. GC30744 Norepinephrine (Adrenor)

    去甲肾上腺素; Levarterenol; L-Noradrenaline

    (-)-Norepinephrine (Arterenol, Levarterenol, L-Noradrenaline) is a natural neurotransmitter and hormone. It is an agonist of adrenergic receptors with Ki values of 330, 56, and 740 nM for α1, α2, and β1 adrenoceptors, respectively.

  23. GC30676 MAPK13-IN-1 MPAK13-IN-1是MAPK13(p38δ)的一个抑制剂,其IC50值为620nM。
  24. GC30646 Skatole(3-Methylindole)

    粪臭素; 3-Methylindole; 3-Methyl-1H-indole

    Skatole (3-methylindole, Scatole) is a mildly toxic white crystalline organic compound that occurs naturally in feces. It has a fairly broad bacteriostatic effect.
  25. GC30609 p38 MAPK-IN-2 p38MAPK-IN-2是一种p38kinase的抑制剂。
  26. GC30608 Ipsalazide

    伊普柳氮

    Ipsalazide是一种新的柳氮磺吡啶类似物,旨在释放胃肠道中的5-氨基水杨酸和无毒载体分子。

  27. GC30565 BAR502 A dual agonist of GP-BAR1 and FXR
  28. GC30537 BPO-27 racemate BPO-27racemate是有效的CFTR抑制剂,IC50值为8nM。
  29. GC30366 FAAH-IN-2

    4-(3-氯-4-氟苯氨基)-7-甲氧基喹唑啉-6-醇,O-Desmorpholinopropyl Gefitinib

    FAAH-IN-2是摘自专利WO/2008/100977A2中的FAAH抑制剂。
  30. GC30360 Cresol (Cresol mixture of isomers) Cresol是一种有机化合物,是芳香族有机化合物广泛存在的天然及合成基团。
  31. GC30356 Metofenazate (Methophenazine)

    美托奋乃酯,Methophenazine

    Metofenazate (Methophenazine) 是一种选择性钙调蛋白抑制剂。
  32. GC30343 Selenomethionine (Seleno-DL-methionine)

    硒代蛋氨酸; Seleno-DL-methionine; DL-Selenomethionine

    硒代蛋氨酸(Seleno-DL-methionine)是一种天然存在的含硒氨基酸,是硒的常见天然食物来源。

  33. GC30263 Glucosamine (D-Glucosamine)

    氨基葡萄糖; D-Glucosamine; Chitosamine

    Glucosamine (2-amino-2-deoxy-D-glucose) is an amino sugar and a prominent precursor in the biochemical synthesis of glycosylated proteins and lipids. It is commonly used as a treatment for osteoarthritis. Glucosamine(GS) treatment selectively downregulates HIF-1α at the protein level in YD-8 cells via interference of production of the citric acid cycle metabolites.
  34. GC30158 p38-α MAPK-IN-1

    p38-α MAPK-IN-1 is an inhibitor of p38-α, with IC50 value of 2300 nM in EFC displacement assay, and 5500 nM in HTRF assay.

  35. GC30072 Dansylcadaverine (Monodansyl cadaverine)

    丹酰尸胺; Monodansyl cadaverine

    A fluorescent marker for autophagic vacuoles

  36. GC30056 Danthron (Dantron)

    1,8-二羟基蒽醌; Dantron; Chrysazin; 1,8-Dihydroxyanthraquinone

    Danthron (Chrysazin, Antrapurol) functions in regulating glucose and lipid metabolism by activating AMPK. Danthron is a natural product extracted from the traditional Chinese medicine rhubarb. Danthron used to be a laxativa and now is currently used as an antioxidant in synthetic lubricants, in the synthesis of experimental antitumor agents, as a fungicide and as an intermediate for making dyes.
  37. GC30054 Dantrolene sodium hemiheptahydrate (Dantrolene sodium hydrate)

    丹曲林钠,Dantrolene sodium hydrate

    Dantrolene sodium hemiheptahydrate (Dantrium) ia a skeletal muscle relaxant that acts by interfering with excitation-contraction coupling in the muscle fiber.
  38. GC30011 20-Deoxyingenol

    20-去氧巨大戟醇;20-去氧巨大戟萜醇

    A diterpenoid with antioxidant and osteoprotective activities
  39. GC19479 AZ304 AZ304 是一种 ATP 竞争性双 BRAF 激酶抑制剂,有效抑制野生型 BRAF、V600E 突变型 BRAF 和野生型 CRAF,IC50 分别为 79 nM、38 nM 和 68 nM。 AZ304 对其他激酶也有显着影响,例如 p38 (IC50, 6 nM)、CSF1R (IC50, 35 nM)。抗肿瘤活性。
  40. GC19453 Autophinib A VPS34 inhibitor
  41. GC19451 SBI-0640756

    SBI-756

    SBI-0640756 (SBI-756) 是 eIF4G1 的抑制剂,可破坏 eIF4F 复合物。
  42. GC19411 IITZ-01 IITZ-01 是一种有效的溶酶体自噬抑制剂,具有单剂抗肿瘤活性,对 PI3Kγ 的 IC50 为 2.62 μM。
  43. GC19421 LY2562175 An FXR agonist
  44. GC19400 JPH203 Dihydrochloride

    KYT-0353

    An inhibitor of LAT1
  45. GC19396 H 89

    N-[2-[P-溴苯丙烯盐基氨基]乙基]-5-异喹啉磺酰胺

    A PKA inhibitor

  46. GC19366 UM-164

    DAS-DFGO-II

    An inhibitor of Src and p38 MAPK kinases
  47. GC19363 Tropifexor

    LJN452

    An FXR agonist
  48. GC19325 SD 0006

    3-[N-(2-羟基乙酰基)-4-哌啶基]-4-(4-嘧啶基)-5-(4-氯苯基)吡唑,SD-06

    An inhibitor of p38α MAPK
  49. GC19304 R1487 Hydrochloride An inhibitor of p38α MAPK
  50. GC19293 PFK-158 PFK-158 是一种有效的选择性 PFKFB3 抑制剂,通过减少癌细胞中葡萄糖的摄取、ATP 的产生、乳酸的释放以及诱导细胞凋亡和自噬,显示出广泛的抗肿瘤活性.PFK-158 在 EC 细胞中以剂量和时间依赖性方式抑制细胞活力。
  51. GC19279 PD-166866 A potent inhibitor of FGFR1

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