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
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GC16441
Tigecycline mesylate
甲磺酸替加环素; GAR-936 mesylate
A glycylcycline antibiotic -
GC37789
Tigecycline tetramesylate
替加环素四甲磺酸盐; GAR-936 tetramesylate
A glycylcycline antibiotic -
GC13915
Tizoxanide
替唑尼特; TIZ
An active metabolite of nitazoxanide -
GC10424
Tolbutamide
甲苯磺丁脲
A SUR1/Kir6.2 channel inhibitor -
GC15575
Tolvaptan
托伐普坦; OPC-41061
A vasopressin V2 receptor antagonist -
GC45064
Tomatidine (hydrochloride)
盐酸番茄碱
A steroidal alkaloid with diverse biological activities -
GC17833
Topotecan
拓扑替康; SKF 104864A; NSC 609669
Topotecan (SKF 104864A; NSC 609669) 是一种口服有效的拓扑异构酶 I 抑制剂。 Topotecan 在 G0/G1 和 S 期诱导细胞周期停滞并促进细胞凋亡。拓扑替康显示出抗癌活性。 -
GC13359
Topotecan HCl
盐酸拓扑替康; SKF 104864A Hydrochloride; NSC 609669 Hydrochloride
A potent inhibitor of DNA topoisomerase I -
GC10131
Torin 1
1-[4-[4-(1-氧代丙基)-1-哌嗪基]-3-(三氟甲基)苯基]-9-(3-喹啉基)苯并[H]-1,6-萘啶-2(1H)-酮,Torin1;Torin-1
Torin 1是一种有效的ATP竞争性哺乳动物雷帕霉素靶蛋白(mTOR)抑制剂,IC50值为3nM。 -
GC13858
Torin 2
9-(6-氨基-3-吡啶基)-1-[3-(三氟甲基)苯基]苯并[H]-1,6-萘啶-2(1H)-酮
Selective inhibitor of mTOR -
GC12918
TPEN
TPEDA
A transition metal chelator -
GC13508
Trametinib (GSK1120212)
曲美替尼; GSK1120212; JTP-74057
Trametinib (GSK1120212, JTP-74057) 是第二代 MEK 激酶小分子抑制剂。 -
GC18147
Tretinoin (Aberela)
维生素A酸; Vitamin A acid; all-trans-Retinoic acid; ATRA
Tretinoin (Aberela) 是一种维生素 A 衍生的非肽类亲脂性小分子,可作为核 RA 受体 (RAR) 的配体,将其从转录抑制因子转化为激活因子 .在培养的人系膜细胞中,维甲酸 (Aberela) 以剂量和时间依赖性方式增加还原型谷胱甘肽含量和过氧化氢酶活性,从而阻止 H2O2 的细胞毒性。
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GC13311
Triclosan
三氯生
A broad-spectrum antibacterial agent -
GC31935
Trifarotene (CD5789)
曲法罗汀; CD5789
Trifarotene (CD5789) (CD5789) 是一种有效的选择性 RARγ;激动剂。 -
GC13031
Trifluoperazine 2HCl
盐酸三氟拉嗪;甲哌氟丙嗪;三氟吡拉嗪
An anti-adrenergic and anti-dopaminergic agent -
GC30790
Triflupromazine hydrochloride
盐酸三氟丙嗪
A phenothiazine with diverse biological activities -
GC63601
Trimetazidine
曲美他嗪
An Analytical Reference Standard -
GC34014
Trimetazidine dihydrochloride
盐酸曲美他嗪
An Analytical Reference Standard -
GC65386
Trimetazidine-d8 dihydrochloride
盐酸曲美他嗪 d8 (双盐酸盐)
Trimetazidine-d8 dihydrochloride 是 Trimetazidine dihydrochloride 的氘代物。Trimetazidine dihydrochloride 是一种选择性的长链 3-ketoyl coenzyme A thiolase 抑制剂,IC50 值为 75 nM,可抑制游离脂肪酸的 β-氧化。Trimetazidine dihydrochloride 是一种有效的抗心绞痛药和一种细胞保护药,具有抗氧化,抗炎,抗伤害和胃保护作用。Trimetazidine dihydrochloride 诱导自噬,还是一种 HADHA 抑制剂。 -
GC15272
Troglitazone
曲格列酮; CS-045
Selective PPARγ agonist -
GC19363
Tropifexor
LJN452
An FXR agonist -
GC14273
TTNPB (Arotinoid Acid)
Ro 13-7410; Arotinoid acid; AGN191183
A potent, selective RAR agonist -
GC10839
Tubastatin A
Tubastatin A 是一种有效的选择性 HDAC6 抑制剂,IC50 值为 15 nM。并且Tubastatin A也是一种新型GPX4抑制剂,Tubastatin A 直接与 GPX4 结合,诱导乳腺癌细胞铁死亡。
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GC10322
Tubastatin A HCl
TubastatinA盐酸盐,TSA HCl;Tubastatin A hydrochloride
A potent HDAC6 inhibitor -
GC17868
TWS119
A GSK3β inhibitor
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GN10075
Typhaneoside
香蒲新苷
Typhaneoside,从 Typha angustifolia L. 中提取。 -
GC45099
U-0126
1,4-二氨基-2,3-二氰基-1,4-双(邻氨基苯巯基)丁二烯
A MEK inhibitor and AMPK activator
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GC34849
UBCS039
UBCS039 is the first synthetic SIRT6 activator with EC50 of 38 μM,induces a time-dependent activation of autophagy in several human tumor cell lines.
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GC73601
UCM-1336
UCM-1336是一种有效的ICMT抑制剂,IC50为2μM。
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GC19366
UM-164
DAS-DFGO-II
An inhibitor of Src and p38 MAPK kinases -
GC17538
UNBS 5162
A antagonist of CXCL chemokine expression
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GC15610
UNC0638
A G9a and GLP histone methyltransferase inhibitor
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GC11375
UNC1999
A selective, cell-permeable EZH2 inhibitor
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GC49308
Ungeremine
石蒜碱内铵盐
A betaine-type alkaloid with diverse biological activities -
GC15951
URB597
FAAH Inhibitor II, URB-597, URB 597, KDS-4103
An inhibitor of FAAH -
GC15004
URMC-099
URMC-099作为一种基于7-氮杂吲哚的MLK3抑制剂,其IC50为14 nM,可特异性影响参与疾病病理生物学的特定aβ物种。
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GC15168
Urolithin A
尿石素A
Urolithin A是由鞣花酸和鞣花单宁代谢产生的一种活性成分,可作为酪氨酸酶(IC50值为71.44±10.07µmol/L)和单胺氧化酶A(IC50值为29.41±9.01µmol/L)的强效抑制剂。 -
GN10390
Ursolic acid
熊果酸; Prunol; Urson; Malol
A triterpenoid with diverse biological activities
-
GC13199
UVI 3003
A pan-RXR antagonist
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GC11424
Valproic acid
丙戊酸; VPA; 2-Propylpentanoic Acid
A class I HDAC inhibitor -
GC15794
Valproic acid sodium salt (Sodium valproate)
丙戊酸钠; Sodium Valproate sodium
Valproic acid sodium salt (Sodium valproate)(VPA)是一种具有口服活性的组蛋白脱乙酰酶 (HDAC)抑制剂,IC50 值为1.5mM,抑制HDAC1的IC50值为400μM,同时可诱导HDAC2的降解。 -
GC64378
Valproic acid-d6
丙戊酸-D6,VPA-d6; 2-Propylpentanoic Acid-d6
Valproic acid-d6 (VPA-d6) 是 Valproic acid 的氘代物。Valproic acid (VPA; 2-Propylpentanoic Acid) 是一种 HDAC 抑制剂,IC50 值为 0.5-2 mM,抑制 HDAC1 的活性,(IC50,400 μM),同时可诱导 HDAC2 的降解。Valproic acid 激活 Notch1 信号并抑制小细胞肺癌 (SCLC) 细胞的增殖。Valproic acid 可用于癫痫、双相情感障碍和偏头痛等的研究。
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GC37885
Vancomycin
万古霉素
万古霉素是扰乱肠道微生物群的强效抗生素之一。 -
GC12993
Vancomycin hydrochloride
盐酸万古霉素
A glycopeptide antibiotic
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GC15022
Vandetanib (ZD6474)
凡德他尼; ZD6474
A multi-kinase inhibitor -
GC11876
Vandetanib hydrochloride
Zactima hydrochloride; ZD6474 hydrochloride;ZD-6474 hydrochloride; ZD 6474 hydrochloride
A multi-kinase inhibitor -
GC37886
Vandetanib trifluoroacetate
凡德他尼,ZD6474 trifluoroacetate
A multi-kinase inhibitor -
GC17783
Veliparib dihydrochloride
维利帕尼二盐酸盐; ABT-888 dihydrochloride
An orally bioavailable inhibitor of PARP1 and PARP2 -
GC13412
Vemurafenib (PLX4032, RG7204)
维罗非尼; PLX4032; RG7204; RO5185426
Vemurafenib (PLX4032, RG7204)是一种选择性的强效B-RAF抑制剂,对BRAFV600E和c-RAF-1的IC50分别为31和48nM。