Cell Cycle/Checkpoint(细胞周期/检查点)

Cell Cycle
Cells undergo a complex cycle of growth and division that is referred to as the cell cycle. The cell cycle consists of four phases, G1 (GAP 1), S (synthesis), G2 (GAP 2) and M (mitosis). DNA replication occurs during S phase. When cells stop dividing temporarily or indefinitely, they enter a quiescent state called G0. read more
Products for Cell Cycle/Checkpoint
- ATM/ATR(29)
- Aurora Kinase(57)
- Cdc42(4)
- Cdc7(3)
- Chk(13)
- c-Myc(27)
- CRM1(8)
- Cyclin-Dependent Kinases(69)
- E1 enzyme(1)
- G-quadruplex(12)
- Haspin(5)
- HMTase(1)
- Kinesin(27)
- Ksp(4)
- Microtubule/Tubulin(248)
- Mps1(13)
- Mitotic(7)
- RAD51(13)
- ROCK(69)
- Rho(13)
- PERK(11)
- PLK(42)
- PTEN(6)
- Wee1(8)
- PAK(24)
- Arp2/3 Complex(8)
- Dynamin(14)
- ECM & Adhesion Molecules(52)
- Cytoskeleton & Motor Proteins(63)
- Endomembrane System & Vesicular Trafficking(35)
- G1(48)
- Genotoxic Stress(22)
- G2/M(35)
- G2/S(16)
- Inositol Phosphates(67)
- Proteolysis(179)
- Cellular Chaperones(14)
- Cyclin G-associated Kinase (GAK)(1)
- MARK(3)
- NEKs(1)
- Cat.No. 产品名称 Information
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GC10008
GSK1070916
GSK-1070916A
A potent inhibitor of Aurora B and C kinases -
GC13332
Aurora A Inhibitor I
A potent and selective inhibitor of Aurora A kinase
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GC15106
CYC116
A potent Aurora kinase inhibitor
-
GC11085
TAK-901
5-[3-(乙基磺酰基)苯基]-3,8-二甲基-N-(1-甲基-4-哌啶基)-9H-吡啶并[2,3-B]吲哚-7-甲酰胺
A non-selective inhibitor of Aurora kinases -
GC14592
KW 2449
[4-[2-(1H-吲唑-3-基)乙烯基]苯基]-1-哌嗪基甲酮
A multi-kinase inhibitor -
GC10479
PHA-680632
Pha 680632
An Aurora kinase inhibitor -
GC13837
SNS-314 Mesylate
N-(3-氯苯基)-N'-[5-[2-(噻吩并3,2-D]嘧啶-4-基氨基)乙基]-2-噻唑基]脲甲磺酸盐(1:1)
A pan-Aurora kinase inhibitor -
GC17162
MK-5108 (VX-689)
VX-689
A potent inhibitor of Aurora kinases -
GC13198
AMG-900
A selective pan-Aurora kinase inhibitor
-
GC17196
Hesperadin
A multi-kinase inhibitor
-
GC10638
AT9283
A broad spectrum kinase inhibitor
-
GC15217
Danusertib (PHA-739358)
达鲁舍替,5-Amido-pyrrolopyrazole 9d
A pan-Aurora kinase and Abl inhibitor -
GC12612
JNJ-7706621
JNJ7706621, JNJ 7706621
A dual inhibitor of CDKs and Aurora kinases -
GC12208
MLN8054
4-[[9-氯-7-(2,6-二氟苯基)-5H-嘧啶并[5,4-D][2]苯并氮杂卓-2-基]氨基]苯甲酸
An inhibitor of Aurora A kinase -
GC14566
CCT137690
甲磺酸阿贝西尼
An inhibitor of Aurora kinases and FLT3 -
GC11310
CCT129202
2-[4-[6-氯-2-(4-二甲基氨基苯基)-3H-咪唑并[4,5-B]吡啶-7-基]哌嗪-1-基]-N-(噻唑-2-基)乙酰胺,CCT-129202, CCT 129202
An Aurora kinase inhibitor -
GC16519
ENMD-2076
6-(4-甲基-1-哌嗪基)-N-(5-甲基-1H-吡唑-3-基)-2-[(1E)-2-苯乙烯基]-4-嘧啶胺
A multi-kinase inhibitor -
GC12145
ENMD-2076 L-(+)-Tartaric acid
ENMD-2076 L-(+)-Tartaric acid 是一种多靶点激酶抑制剂,对 Aurora A、Flt3、KDR/VEGFR2、Flt4/VEGFR3、FGFR1 的 IC50 为 1.86、14、58.2、15.9、92.7、70.8、56.4 nM , FGFR2, Src, PDGFRα, 分别。
-
GC14409
ZM 447439
Selective inhibitor of Aurora B kinase
-
GC14955
Barasertib (AZD1152-HQPA)
5-[[7-[3-[乙基(2-羟基乙基)氨基]丙氧基]-4-喹唑啉]氨基]-N-(3-氟苯基)-1H-吡唑-3-乙酰胺,AZD1152-HQPA,AZD-1152HQPA, AZD1152 HPQA,INH 34
A selective Aurora kinase B inhibitor -
GC11549
VX-680 (MK-0457,Tozasertib)
陶扎色替,VX 680; MK-0457
An Aurora kinase inhibitor that regulates mitosis -
GC12690
MLN8237 (Alisertib)
阿立塞替,MLN 8237
Alisertib (MLN8237) 作为一种在研、可口服的选择性极光 A 激酶抑制剂,通常用于治疗实体瘤和血液系统恶性肿瘤。 -
GC15084
2-Methoxyestradiol (2-MeOE2)
二甲氧基雌二醇; 2-ME2; NSC-659853
2-Methoxyestradiol (2-MeOE2/2-Me)是一种HIF-1α抑制剂。 -
GC10512
Y-27632 dihydrochloride
y-27632, Y27632, Y-27632 dihydrochloride, Y 27632
Y-27632 dihydrochloride 作为一种选择性 Rho 激酶抑制剂,是一种新型支气管扩张剂。 -
GN10696
Garcinone C
伽升沃 C
Garcinone C 是一种黄酮衍生物,是一种从 Garcinia oblongifolia Champ 中提取的天然化合物,用作抗炎、收敛和促进肉芽的药物,对某些癌症具有潜在的细胞毒性作用。 Garcinone C 刺激 ATR 和 4E-BP1 的表达水平,同时有效抑制 cyclin B1、cyclin D1、cyclin E2、cdc2、Stat3 和 CDK7 的表达水平。 Garcinone C 以时间和剂量依赖性方式显着抑制人鼻咽癌 (NPC) 细胞系 CNE1、CNE2、HK1 和 HONE1 的细胞活力。 -
GN10426
Deacetyltaxol
10-去乙酰紫杉醇; 10-Deacetylpaclitaxel
An anticancer taxane -
GN10780
Cephalomannine
三尖杉宁碱
A taxane diterpenoid -
GN10625
7-Epitaxol
7-表紫杉醇; 7-epi-Paclitaxel
An active metabolite of paclitaxel -
GN10299
Vinorelbine
长春瑞宾
An inhibitor of microtubule polymerization -
GN10732
Oroxin B
木蝴蝶苷B
Oroxin B (OB) 是从中草药 Oroxylum indicum (L.) Vent 中分离得到的黄酮类化合物。Oroxin B (OB) 具有明显的抑制作用,通过上调 PTEN、下调 PTEN 诱导肝癌细胞早期凋亡而不是晚期凋亡COX-2、VEGF、PI3K 和 p-AKT.Oroxin B (OB) 在恶性淋巴瘤细胞中选择性诱导肿瘤抑制性 ER 应激。 -
GN10091
Schaftoside
夏佛塔苷
A flavonoid C-glycoside with diverse biological activities