Ubiquitination/ Proteasome(泛素化/蛋白酶体)
- Autophagy(1114)
- DUB(17)
- E1 Activating(1)
- E2 conjugating(1)
- E3 Ligase(7)
- Proteasome(69)
- p97(12)
- Mitophagy(82)
- ULK(9)
- Cat.No. 产品名称 Information
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GC37669
Soyasapogenol B
大豆甾醇B
Soyasapogenol B,大豆的一种成分,具有抗增殖,抗转移活性。Soyasapogenol B 触发内质网应激反应,其介导结肠直肠癌中的细胞凋亡和自噬。 -
GC37665
Sorafenib (D4)
Bay 43-9006-d4
Sorafenib D4 (Bay 43-9006 D4) 是 Sorafenib 氘代化合物标准品。Sorafenib 是一种多激酶抑制剂,抑制 Raf-1,B-Raf 和 VEGFR-3 的 IC50 分别为6 nM,20 nM,22 nM。 -
GC37664
Sorafenib (D3)
索拉非尼-D3,Bay 43-9006-d3; Donafenib
An internal standard for the quantification of sorafenib -
GC37646
SKF-86002
6-(4-氟苯基)-5-(4-吡啶基)-2,3-二氢咪唑并[2,1-B]-噻唑
An anti-inflammatory agent -
GC37630
Sevelamer
司维拉姆
Sevelamer HCl is a phosphate binding drug used to treat hyperphosphatemia via binding to dietary phosphate and prevents its absorption. - GC37601 SBE13 A potent Plk1 inhibitor
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GC37595
SB 242235
4-[4-(4-氟苯基)-1-(4-哌啶基)-1H-咪唑-5-基]-2-甲氧基嘧啶
A p38α MAPK inhibitor -
GC37575
Ruxolitinib sulfate
(BETAR)-BETA-环戊基-4-(7H-吡咯并[2,3-D]嘧啶-4-基)-1H-吡唑-1-丙腈硫酸盐,INCB018424 sulfate
A potent, selective JAK1/JAK2 inhibitor - GC37561 Rosuvastatin D6 Sodium An internal standard for the quantification of rosuvastatin
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GC37560
Rosuvastatin D6 Calcium
瑞舒伐他汀钙 D6
Rosuvastatin D6钙盐是Rosuvastatin的氘代化合物标准品。 -
GC37559
Rosuvastatin D3 Sodium
三氘代瑞舒伐他汀
Rosuvastatin D3钠盐是Rosuvastatin氘代化合物标准品。 -
GC36963
Pregnenolone monosulfate
3β-Hydroxy-5-pregnen-20-one monosulfate
Pregnenolone monosulfate 是大麻素 CB1 受体的特异性抑制剂。 -
GC36930
Pitavastatin D4
NK-104 D4
Pitavastatin D4是Pitavastatin氘代化合物标准品。 -
GC36928
Pirarubicin Hydrochloride
盐酸吡柔比星; THP Hydrochloride
An anthracycline antitumor antibiotic -
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 -
GC36872
Pepstatin Trifluoroacetate
抑肽素三氟醋酸盐; Pepstatin A Trifluoroacetate
Pepstatin Trifluoroacetate 是由放线菌类产生的一种特异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。 -
GC36871
Pepstatin Ammonium
Pepstatin A Ammonium
Pepstatin Ammonium 是由放线菌类产生的一种特异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;同时可抑制 HIV protease 的活性。 -
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. -
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. -
GC36848
Pantoprazole sodium hydrate
泮托拉唑钠水合物; BY1023 sodium hydrate; SKF96022 sodium hydrate
A proton pump inhibitor -
GC36847
Pantoprazole sodium
泮托拉唑钠; BY1023 sodium; SKF96022 sodium
A proton pump inhibitor - GC36821 OSU-T315 OSU-T315 (ILK-IN-2) is a potent Integrin-Linked Kinase (ILK) inhibitor with IC50 of 0.6 μM. OSU-T315 induces autophagy and apoptosis, both of which are integral to its antiproliferative activity. OSU-T315 exhibits anti-tumor activity.
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GC36806
Omeprazole D3
奥美拉挫 D3; H 16868-d3
An internal standard for the quantification of omeprazole -
GC36758
Norepinephrine hydrochloride
去甲肾上腺素盐酸盐; Levarterenol hydrochloride; L-Noradrenaline hydrochloride
A racemic mixture of of L-norepinephrine and D-norepinephrine
- GC36736 Nicodicosapent Nicodicosapent 是一种脂肪酸烟酸共轭体,可以抑制固醇调节元件结合蛋白 (SREBP) 的活性,调节胆固醇代谢的蛋白质如 PCSK9,HMG-CoA reductase,ATP citrate lyase 和 NPC1L1 等的活性。
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GC36703
N-Benzyloleamide
N-苄基-9顺-油酸酰胺
N-Benzyloleamide 是从 Lepidium meyenii (Maca) 中分离出的一种 maccamide。N-Benzyloleamide 不可逆地抑制脂肪酸酰胺水解酶 (FAAH)。N-Benzyloleamide 影响能量代谢,显示抗氧化和抗疲劳活性。 - GC36690 Nampt-IN-3 Nampt-IN-3 (Compound 35) 同时抑制烟酰胺磷酸核糖转移酶 (NAMPT) 和 HDAC,IC50 分别为 31 nM 和 55 nM。Nampt-IN-3 有效诱导细胞凋亡 (apoptosis) 和自噬 (autophagy),最终导致细胞死亡。
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GC36671
N-Benzyllinolenamide
N-苄基-(9Z,12Z,15Z)-十八碳三烯酰胺
N-?Benzyllinolenamide 是从玛卡中得到的玛卡酰胺,为脂肪酰胺水解酶 (FAAH) 抑制剂,IC50 值为 41.8 μM。 - GC36654 MRT68921 dihydrochloride An inhibitor of ULK1/2
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GC36646
Momelotinib Mesylate
CYT387 Mesylate
Momelotinib Mesylate (CYT387 Mesylate) 是一种 ATP 竞争性的 JAK1/JAK2 抑制剂,IC50 值分别为 11 nM/18 nM,对其选择性约是 JAK3 的 10 倍。 - GC36517 LYN-1604 hydrochloride A ULK1 activator
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GC36479
Loperamide hydrochloride
盐酸洛哌丁胺; R-18553 hydrochloride
An Analytical Reference Standard -
GC36447
Licochalcone E
甘草查尔酮E
Licochalcone E 是可从Glycyrrhiza inflate 中提取到的黄酮类化合物,通过抑制AKT 和 MAPK 的激活来抑制NF-κB 和 AP-1 的转录活性。 -
GC36427
Lasalocid sodium
拉沙洛西钠; Lasalocid-A sodium; Ionophore X-537A sodium; Antibiotic X-537A sodium
An ionophore antibiotic -
GC36356
Ixazomib citrate
枸橼酸艾沙佐米; MLN9708
Ixazomib citrate (MLN9708, Ninlaro) is a prodrug of Ixazomib (MLN2238), which is a selective, orally bioavailable inhibitor of 20S proteasome that inhibits the chymotrypsin-like proteolytic (β5) site with IC50 of 3.4 nM and Ki of 0.93 nM, respectively. Ixazomib (MLN2238) also inhibits caspase-like (β1) and trypsin-like (β2) proteolytic sites with IC50 of 31 nM and 3500 nM, respectively. -
GC36346
Isosorbide mononitrate
单硝酸异山梨酯; Isosorbide-5-mononitrate
A nitric oxide donor with cardioprotective activity -
GC36339
Isorhapontigenin
异丹叶大黄素
Isorhapontigenin (ISOR), isolated from Belamcanda chinensis, is a derivative of stilbene. Isorhapontigenin possessed potent antioxidative activity. Isorhapontigenin suppresses interleukin-1β-induced inflammation and cartilage matrix damage in rat chondrocytes. -
GC36329
Irinotecan hydrochloride
伊立替康盐酸盐; (+)-Irinotecan hydrochloride; CPT-11 hydrochloride
A potent inhibitor of DNA topoisomerase I -
GC36215
Heparin Lithium salt
肝素锂
Heparin Lithium salt 是一种抗凝剂,可与 抗凝血酶III (ATIII) 可逆地结合 (50-400 U/Kg)。
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GC36163
Glycycoumarin
甘草香豆素
Glycycoumarin 是一种甘草中主要的生物活性香豆素。Glycycoumarin 通过激活自噬,抑制内质网应激介导的 JNK 和 GSK-3 介导的线粒体途径,来抑制肝细胞脂性凋亡。Glycycoumarin 能直接靶向 T-LAK 细胞源蛋白激酶发挥抗肝癌活性 。 - GC36149 GLPG2451 GLPG2451 是一种囊性纤维化跨膜电导调节器 (CFTR) 的增强剂,有效增强低温挽救的 F508del CFTR,EC50 为 11.1 nM。
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GC36136
Ginkgolide K
银杏内酯 K
A terpene trilactone with diverse biological activities -
GC36130
Gemcitabine elaidate
反油酸吉西他滨; CP-4126; CO-101; Gemcitabine 5'-elaidate
A prodrug form of gemcitabine - GC36063 FMK 9a FMK 9a是autophagin-1的抑制剂,在FRET和LRA试验中测定的IC50值分别为80 和73 nM。
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GC36061
Fluvastatin D6 sodium
氟伐他汀钠D6; XU 62-320 (D6)
An internal standard for the quantification of fluvastatin -
GC36023
FAAH inhibitor 1
Benzothiazole analog 3
FAAH inhibitor 1是脂肪酸酰胺水解酶(FAAH)抑制剂,IC50为18 nM。 -
GC36003
Erlotinib mesylate
埃罗替尼甲磺酸盐; CP-358774 mesylate; NSC 718781 mesylate; OSI-774 mesylate
An EGFR tyrosine kinase inhibitor - GC35998 Episilvestrol Episilvestrol 是 silvestrol 的衍生物,从 Aglaia silvestris 中分到,能够抑制 eIF4A 靶作用的转录过程。
- GC35982 EN6 An activator of autophagy
- GC35969 eIF4A3-IN-1 eIF4A3-IN-1 (compound 53a) 是一种选择性的真核起始因子 4A3 (eIF4A3) 抑制剂 (IC50=0.26 μM; Kd=0.043 μM),eIF4A3-IN-1 与 eIF4A3 的非 ATP 结合位点结合,并在 10 μM 和 3 μM 时明显抑制细胞无义介导的 RNA 衰变 (NMD), 可作为进一步研究 eIF4A3、外显子连接复合体 (EJC) 和 NMD 的探针。