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
- Cat.No. 产品名称 Information
-
GC31705
Sofalcone
索法酮
Gastroprotective chalcone derivative -
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. -
GC31665
(R)-BPO-27
(R)-BPO-27是有效的CFTR抑制剂,IC50值为4nM。
-
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。 -
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。 -
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。 -
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. -
GC31239
SA72
SA72是高度选择性的脂肪酸酰胺水解酶(FAAH)抑制剂。
-
GC31170
Calmodulin-Dependent Protein Kinase II 290-309
A CaMKII inhibitor
-
GC31058
FR 167653 free base
FR-167653是一种选择性的p38MAPK抑制剂。
-
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. -
GC30990
Calcineurin substrate
钙调神经磷酸酶底物
A synthetic peptide substrate -
GC30884
LX2343
An inhibitor of BACE1 and PI3K
-
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。 -
GC30842
Androsterone (5α-Androstan-3α-ol-17-one)
雄酮; 5α-Androstan-3α-ol-17-one
An androgenic steroid
-
GC30790
Triflupromazine hydrochloride
盐酸三氟丙嗪
A phenothiazine with diverse biological activities -
GC30787
Sertindole (Lu 23-174)
舍吲哚; Lu 23-174
An atypical antipsychotic -
GC30785
4E2RCat
4E2RCat是eIF4E-eIF4G相互作用的抑制剂,IC50值为13.5μM。
-
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. -
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。
-
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.
-
GC30676
MAPK13-IN-1
MPAK13-IN-1是MAPK13(p38δ)的一个抑制剂,其IC50值为620nM。
-
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. -
GC30609
p38 MAPK-IN-2
p38MAPK-IN-2是一种p38kinase的抑制剂。
-
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。
-
GC30565
BAR502
A dual agonist of GP-BAR1 and FXR
-
GC30537
BPO-27 racemate
BPO-27racemate是有效的CFTR抑制剂,IC50值为8nM。
-
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。 -
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。
-
GC30356
Metofenazate (Methophenazine)
美托奋乃酯,Methophenazine
Metofenazate (Methophenazine) 是一种选择性钙调蛋白抑制剂。 -
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。
-
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. -
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.
-
GC30072
Dansylcadaverine (Monodansyl cadaverine)
丹酰尸胺; Monodansyl cadaverine
A fluorescent marker for autophagic vacuoles
-
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. -
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. -
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 -
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。
-
GC19453
Autophinib
A VPS34 inhibitor
-
GC19451
SBI-0640756
SBI-756
SBI-0640756 (SBI-756) 是 eIF4G1 的抑制剂,可破坏 eIF4F 复合物。 -
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。
-
GC19421
LY2562175
An FXR agonist
-
GC19400
JPH203 Dihydrochloride
KYT-0353
An inhibitor of LAT1 -
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
-
GC19366
UM-164
DAS-DFGO-II
An inhibitor of Src and p38 MAPK kinases -
GC19363
Tropifexor
LJN452
An FXR agonist -
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 -
GC19304
R1487 Hydrochloride
An inhibitor of p38α MAPK
-
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。
-
GC19279
PD-166866
A potent inhibitor of FGFR1