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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GC33464
Oxyresveratrol (trans-Oxyresveratrol)
氧化白藜芦醇; trans-Oxyresveratrol
A resveratrol analog -
GC33008
p38 MAPK-IN-1
p38MAPK-IN-1是p38MAPK新型高效选择性抑制剂,IC50值68nM。
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GC30609
p38 MAPK-IN-2
p38MAPK-IN-2是一种p38kinase的抑制剂。
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GC31988
p38α inhibitor 1
p38αinhibitor1是p38α的抑制剂,来自专利WO2008076265A1。
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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.
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GC11993
PAC-1
Procaspase activating compound 1
An in vitro procaspase-3 activator -
GC12511
Paclitaxel (Taxol)
紫杉醇
紫杉醇是从短叶红豆杉的树皮和针叶中提取出来的三环二萜化合物。 -
GN10498
Paeonol
丹皮酚
A phenol with diverse biological activities -
GC69650
Paeonol-d3
Paeonol-d3 是氘代的 Paeonol 。
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GC14304
Palovarotene
4-[(1E)-2-[5,6,7,8-四氢-5,5,8,8-四甲基-3-(1H-吡唑-1-基甲基)-2-萘基]乙烯基]苯甲酸,R 667; Ro 3300074
A RARγ agonist -
GC15814
Pamapimod (R-1503, Ro4402257)
Ro4402257; R1503
An orally bioavailable inhibitor of p38α MAP kinase -
GC12257
Panobinostat (LBH589)
帕比司他; LBH589; NVP-LBH589
A pan-HDAC inhibitor -
GC12718
Pantoprazole
泮托拉唑; BY1023; SKF96022
A proton pump inhibitor -
GC36847
Pantoprazole sodium
泮托拉唑钠; BY1023 sodium; SKF96022 sodium
A proton pump inhibitor -
GC36848
Pantoprazole sodium hydrate
泮托拉唑钠水合物; BY1023 sodium hydrate; SKF96022 sodium hydrate
A proton pump inhibitor -
GC36855
Paris saponin VII
重楼皂苷 VII; Chonglou Saponin VII
Chonglou Saponin VII (Dioscinin, Polyphyllin-VII, Paris saponin-VII), a kind of steroidal saponins from Chonglou (Rhizoma Paridis Chonglou), inhibits EMT and reduces the invasion of ovarian cancer cells via the GSK-3β/β-catenin signaling pathway. -
GC17229
Paroxetine HCl
盐酸帕罗西汀; BRL29060 hydrochloride; BRL29060A
A selective serotonin reuptake inhibitor -
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. -
GC71661
Paroxetine-d4 hydrochloride
Paroxetine-d4 hydrochloride是氘标记的盐酸帕罗西汀。
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GN10357
Parthenolide
小白菊内酯; (-)-Parthenolide
Parthenolide是一种NF-κB抑制剂,对Eca109、KYSE-510、SiHa和MCF-7细胞48h的IC50值分别约为10.3、13.3、8.42和9.54µM。 -
GC16327
Pazopanib (GW-786034)
帕唑帕尼; GW786034
A multi-kinase inhibitor -
GC12730
Pazopanib Hydrochloride
盐酸帕唑帕尼; GW786034 (Hydrochloride)
A multi-kinase inhibitor -
GC72911
Pazopanib-13C,d3 hydrochloride
GW786034-13C,d3 hydrochloride
Pazopanib-13C,d3 hydrochloride是氘和13C标记的盐酸帕唑帕尼。 -
GC12205
PD 146176
NSC168807
PD 146176 是一种有效的选择性网织红细胞 15-LOX-1 抑制剂。 -
GC17737
PD 169316
4-[4-(4-氟苯基)-2-(4-硝基苯基)-1H-咪唑-5-基]吡啶
A specific p38 MAPK inhibitor -
GC19279
PD-166866
A potent inhibitor of FGFR1
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GC10397
PD0325901
N-[(2R)-2,3-二羟基丙氧基]-3,4-二氟-2-[(2-氟-4-碘苯)氨基]苯甲酰胺,PD0325901,PD-0325901,PD 0325901,PD325901,PD 325901,PD-325901
PD0325901是一种具口服活性、选择性和非ATP竞争性的丝裂原活化蛋白激酶激酶(MEK)抑制剂,IC50值为0.33nM。 -
GC11015
PD168393
An irreversible EGFR kinase inhibitor
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GC12819
PD98059
2-(2-氨基-3-甲氧基苯基)-4H-1-苯并吡喃-4-酮
D98059是一种有效的选择性MEK抑制剂,IC50为2 μM。 -
GN10084
Peiminine
贝母素乙,Vertieinon
An alkaloid with diverse biological activities -
GC11610
Pemetrexed
培美曲塞二钠盐; LY231514 disodium
An antifolate with anticancer activity -
GC17694
Pemetrexed disodium hemipenta hydrate
培美曲塞二钠水合物; LY231514 disodium hemipenta hydrate
Pemetrexed disodium hemipenta hydrate 是一种新型抗叶酸剂,LY231514 的五谷氨酸的 Ki 值分别为 1.3、7.2 和 65 nM,用于抑制胸苷酸合酶 (TS)、二氢叶酸还原酶 (DHFR) 和甘氨酰胺核糖核苷酸甲酰转移酶 (GARFT)。 -
GC10458
Penfluridol
五氟利多; R-16341
A typical antipsychotic -
GC36868
Pennogenin 3-O-beta-chacotrioside
偏诺皂苷元-3-O-Α-L-吡喃鼠李糖-(1→4)[Α-L-吡喃鼠李糖基](1→2)-Β-D-葡萄糖苷
Pennogenin 3-O-beta-chacotrioside, an active component isolated from Paris polyphylla, modulates autophagy via increasing the expressions of autophagy-related proteins LC3 and Beclin-1, and posesses anti-colorectal cancer activity. -
GC40685
Pentoxifylline
NSC 637086, Oxpentifylline
Pentoxifylline is a methylxanthine derivative. -
GC11974
Pepstatin A
抑肽素; Pepstatin A
胃抑素Pepstatin A是由放线菌类产生的一种特异性的、具有口服活性的天冬氨酸蛋白酶 (aspartic proteases) 抑制剂,能够抑制 hemoglobin-pepsin、hemoglobin-proctase、casein-pepsin、casein-proctase、casein-acid protease 和 hemoglobin-acid protease 的活性,IC50 值分别为 4.5 nM、6.2 nM、150 nM、290 nM、520 nM 和 260 nM;Pepstatin A可抑制 HIV protease 的活性.Pepstatin A (0-120 µM) 抑制了受体活化因子NF-κB配体(RANKL)-诱导的破骨细胞分化。 -
GC32107
Peretinoin (NIK333)
NIK333
Peretinoin (NIK333) 是一种具有维生素 A 样结构的口服无环类维生素 A,可靶向类维生素 A 核受体,如类维生素 X 受体 (RXR) 和视黄酸受体 (RAR)。 -
GC15680
Perifosine
哌立福新; KRX-0401; NSC 639966; D21266
Perifosine 是 Akt 的抑制剂 。
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GC11857
Pexmetinib (ARRY-614)
ARRY-614
A dual inhibitor of Tie2 and p38 MAPK -
GC50253
PF 543 hydrochloride
Sphingosine Kinase 1 Inhibitor II hydrochloride
A potent inhibitor of SPHK1 -
GC15358
PF 750
N-苯基-4-(3-喹啉基甲基)-1-哌啶甲酰胺
A selective, potent FAAH inhibitor -
GC36879
PF-04457845
N-哒嗪-3-基-4-(3-{[5-(三氟甲基)吡啶-2-基]醚}苯亚甲基丙酮)哌啶-1-羧酰胺
A selective FAAH inhibitor -
GC16417
PF-04691502
2-氨基-8-[反式-4-(2-羟基乙氧基)环己基]-6-(6-甲氧基-3-吡啶基)-4-甲基吡啶并[2,3-D]嘧啶-7(8H)-酮
PF-04691502 是一种有效的选择性 PI3K 和 mTOR 抑制剂。 PF-04691502 与人 PI3Kα、β、δ、γ 和 mTOR 结合,Kis 分别为 1.8、2.1、1.6、1.9 和 16 nM。 -
GC16984
PF-3845
Inhibitor of FAAH
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GC10689
PF-4708671
PF-4708671 是一种新型的细胞渗透性 S6K1 抑制剂,特异性抑制 S6K1 亚型,Ki 为 20 nM,IC50 为 160 nM。
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GC15375
PFI-1 (PF-6405761)
PF06405761
A BET bromodomain inhibitor -
GC16993
PFK-015
A selective inhibitor of PFKFB3
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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。
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GC10261
PH-797804
PH797804;PH 797804
A selective p38 MAPK inhibitor -
GC11733
PHA-665752
(2R)-1-[[5-[(Z)-[5-[[(2,6-二氯苯基)甲基]磺酰]-1,2-二氢-2-氧代-3H-吲哚-3-亚基]甲基]-2,4-二甲基-1H-吡咯-3-基]羰基]-2-(1-吡咯烷甲基)吡咯烷
A selective c-Met inhibitor