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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GC15571
SU 9516
A pro-apoptotic Cdk2/cyclin A inhibitor
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GC11089
SU11274
N-(3-氯苯基)-N-甲基-3-[[3,5-二甲基-4-[(4-甲基哌嗪-1-基)羰基-1H-吡咯-2-基]亚甲基]-2-氧代-2,3-二氢-1H-吲哚-5-磺酰胺,PKI-SU11274
A potent, selective inhibitor of c-Met -
GC33529
Sulfabenzamide (N-Sulfanilylbenzamide)
苯甲酰磺胺; N-Sulfanilylbenzamide
Sulfabenzamide (Sultrin, N-Sulfanilylbenzamide) is an antibacterial/antimicrobial which also exhibit their antitumor effects through multiple mechanisms including inhibition of membrane bound carbonic anhydrases, prevention of microtubule assembly, cell cycle arrest, and inhibition of angiogenesis. -
GC14577
Sulfacetamide Sodium
磺胺醋酰钠
A sulfonamide antibiotic -
GC16868
Sulfasalazine
柳氮磺吡啶; NSC 667219
Sulfasalazine是一种磺胺类药物。 -
GC16716
Sulindac
舒林酸; MK-231
A non-selective COX inhibitor -
GC17651
Sunitinib
舒尼替尼; SU 11248
舒尼替尼Sunitinib(SU 11248)是一种具口服活性的多靶点受体酪氨酸激酶抑制剂,对血管内皮生长因子受体(VEGFR2)和血小板衍生生长因子受体(PDGFRβ)的IC50分别为80nM和2nM。
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GC14683
Sunitinib malate
苹果酸舒尼替尼,SU 11248,SU11248,SU-11248,Sunitinib
A multi-kinase inhibitor -
GC48118
Sunitinib-d10
舒尼替尼-D10,SU 11248-d10
An internal standard for the quantification of sunitinib -
GC33732
Syntide 2
A protein kinase substrate
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GC10596
T0901317
N-(2,2,2-三氟乙基)-N-[4-[2,2,2-三氟-1-羟基-1-(三氟甲基)乙基]苯基]苯磺酰胺
T0901317是一种口服活性高选择性LXR激动剂,对LXRα的EC50为15nM,并能激活异生物质受体孕烷X受体(PXR),EC50为23nM。 -
GC13825
TA 01
An inducer of cardiomyocyte differentiation
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GC11635
TA 02
An inducer of cardiomyocyte differentiation
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GC16233
Tacrolimus (FK506)
他克莫司; FK506; Fujimycin; FR900506
他克莫司 (FK506) 是一种具有强效免疫抑制作用的大环内酯类抗生素,从筑波链霉菌中分离出来,以前曾用于预防人类同种异体移植和治疗自身免疫性疾病。 -
GC17995
Tacrolimus monohydrate
他克莫司一水合物; FK506 monohydrate; Fujimycin monohydrate; FR900506 monohydrate
他克莫司一水合物 (FK506 monohydrate) 是一种大环内酯,与 FK506 结合蛋白 (FKBP) 结合形成复合物并抑制钙调神经磷酸酶,从而抑制 T 淋巴细胞信号转导和 IL-2 转录。 -
GC16148
TAK-242
瑞沙托维; TAK-242; CLI-095
TAK 242 是一种 Toll 样受体 4 (TLR4) 信号转导抑制剂。 -
GC16543
TAK-715
N-(4-(2-乙基-4-(3-甲基苯基)噻唑-5-基)吡啶-2-基)苯甲酰胺
An inhibitor of p38α MAPK -
GC17063
Talarozole
他拉罗唑; R115866
Talarozole (R115866) 是一种口服全身性全反式维甲酸代谢阻断剂 (RAMBA),可增加内源性全反式维甲酸 (RA) 的细胞内水平。 -
GC34072
Talmapimod (SCIO-469)
他匹莫德; SCIO-469
A p38 MAPK inhibitor -
GC13984
Tamibarotene
他米巴罗汀; Am 80
A selective RARα agonist -
GC17901
Tamoxifen
他莫昔芬; ICI 47699; (Z)-Tamoxifen; trans-Tamoxifen
Tamoxifen(他莫西芬)是一种选择性雌激素受体调节剂 (SERM),可阻断乳腺细胞中的雌激素作用,并可激活不同组织细胞中的雌激素活性;Tamoxifen 还可以作为 Hsp90 激活剂,增强 Hsp90 分子伴侣 ATPase 的活性;Tamoxifen 还可以诱导 CreER(T2) 小鼠的基因敲除。 -
GC11669
Tamoxifen Citrate
他莫昔芬柠檬酸盐; ICI 46474; (Z)-Tamoxifen Citrate; trans-Tamoxifen Citrate
A selective estrogen receptor modulator -
GC48124
Tamoxifen-d5
ICI 47699-?d5; (Z)-Tamoxifen-?d5; trans-Tamoxifen-?d5
An internal standard for the quantification of tamoxifen -
GC62630
TAS-117 hydrochloride
TAS-117 hydrochloride
TAS-117 hydrochloride 是一种有效、选择性、具有口服活性的别构 Akt 抑制剂 (对 Akt1、2 和 3 的 IC50 分别为 4.8、1.6 和 44 nM)。TAS-117 hydrochloride 激发抗骨髓瘤活性并增强蛋白酶体抑制诱导的致命内质网应激。TAS-117 hydrochloride 诱导细胞凋亡 (apoptosis) 和自噬 (autophagy)。 -
GC63840
Tat-beclin 1
自噬蛋白区域衍生肽
Tat-beclin 1 (Tat-BECN1), a peptide known to stimulate autophagy through mobilization of endogenous Beclin 1, induces autophagy in vitro and in vivo and improves clinical outcomes. -
GC90488
Tat-Beclin 1 (acetate)
Tat-BECN1
一种诱导自噬的肽。
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GC15184
Taurine
牛磺酸; 2-Aminoethanesulfonic acid
A sulfur-containing amino acid -
GN10304
Taxifolin
(-)-二氢槲皮素; (-)-Dihydroquercetin
Taxifolin是一种酪氨酸酶抑制剂,并具有显著的胶原酶抑制活性,其IC50值为193.3μM。 -
GC15459
Tazarotene
他扎罗汀; AGN 190168
A retinoid prodrug -
GC34057
TBHQ (tert-Butylhydroquinone)
特丁基对苯二酚; tert-Butylhydroquinone
TBHQ(tert-Butylhydroquinone)是一种强效的酚类抗氧化剂,能够减轻氧化应激和炎症反应。 -
GC39450
Tea polyphenol
茶多酚
Tea polyphenols are chemical compounds such as flavanoids and tannins found naturally in tea. Several biological properties have been associated to tea polyphenols (TP), including antioxidant, anti-carcinogenic and antimicrobial activities. -
GC15023
Telmisattan
替米沙坦; BIBR 277
Selective angiotensin II receptor antagonist -
GC13667
Temozolomide
替莫唑胺; NSC 362856; CCRG 81045; TMZ
替莫唑胺是一种口服活性烷化剂,可诱导 DNA 中 O6-甲基鸟嘌呤的形成,其在随后的 DNA 复制周期中与胸腺嘧啶错配,从而激活细胞凋亡途径,替莫唑胺可穿过血脑屏障并适用于恶性神经胶质瘤和转移性黑色素瘤。 -
GC17151
Tempol
阻聚剂701,4-Hydroxy-TEMPO
A nitroxide and spin label with SOD mimetic activity -
GC72755
Tempol-d17,15N
4-Hydroxy-TEMPO-d17,15N
Tempol-d17,15N是氘标记的Tempol。 -
GC12573
Temsirolimus
西罗莫司脂化物,Torisel;CCI-779;CCI 779;CCI779
A specific inhibitor of mTOR activity -
GC14165
Tenovin-1
A small molecule activator of p53
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GC16436
Tenovin-6
A small molecule activator of p53
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GC37761
Tenovin-6 Hydrochloride
A small molecule activator of p53
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GC33833
Tetrahydrocurcumin (HZIV 81-2)
四氢姜黄素; HZIV 81-2
A metabolite of curcumin with diverse biological activities -
GC73522
Tezacaftor-d4
VX-661-d4
Tezacaftor-d4 (VX-661-d4)是氘标记的Tezacaftor, F508del CFTR校正器。 -
GC39530
TFEB activator 1
(1E,4E)-1,5-二(2-甲氧基)-1,4-二烯基-3-戊酮,Curcumin analog C1
A synthetic curcuminoid and activator of TFEB -
GC10035
TG101209
N-(1,1-二甲基乙基)-3-[[5-甲基-2-[[4-(4-甲基-1-哌嗪基)苯基]氨基]-4-嘧啶基]氨基]苯磺酰胺,TG-101209
An inhibitor of JAK2, FLT3, RET, and JAK3 -
GC17054
Thalidomide
沙利度胺
An immunomodulatory compound with diverse biological activities -
GN10659
Theophylline
茶碱,Theolix
A phosphodiesterase inhibitor and adenosine receptor antagonist -
GC12736
Thiamet G
Thiamet G 是一种有效的 O-GlcNAcase 抑制剂 (Ki =21 nM),用于提高 O-GlcNAcylation 水平。
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GC14366
Thioguanine
6-硫鸟嘌呤,Thioguanine; 2-Amino-6-purinethiol
A thiopurine analog -
GC11977
Thioridazine HCl
盐酸硫利达嗪;盐酸硫代利哒;甲硫达嗪盐酸盐;甲硫哒嗪盐酸盐
A typical antipsychotic -
GC14574
Tigecycline
替加环素; GAR-936
A glycylcycline antibiotic -
GC16410
Tigecycline hydrochloride
盐酸替加环素; GAR-936 hydrochloride
A glycylcycline antibiotic