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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GC32853
PD0166285
6-(2,6-二氯苯基)-2-[[4-[2-(二乙基氨基)乙氧基]苯基]氨基]-8-甲基吡啶并[2,3-D]嘧啶-7(8H)-酮
PD0166285 is a potent Wee1 and Chk1 inhibitor with activity at nanomolar concentrations (IC50=24 nM for Wee1 and 72 nM for Myt1). PD0166285 is also a novel G2 checkpoint abrogator. PD0166285 induces apoptosis. -
GC32846
BOS-172722
BOS172722 is a monopolar spindle 1 (MPS1) checkpoint inhibitor with IC50 of 11 nM, Ki of 0.11 nM.
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GC32830
NVS-PAK1-1
An allosteric inhibitor of PAK1
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GC32816
Estramustine phosphate sodium
雌莫司汀磷酸钠
A derivative of estradiol that destabilizes microtubules -
GC32810
DM4
N2'-去乙酰基-N2'-(4-巯基-4-甲基-1-氧代戊基)-美登素
A derivative of maytansine -
GC32785
ML327
ML327 is an isoxazole compound that blocks MYC expression and tumor formation in neuroblastoma. ML327 also restores E-cadherin expression with In-Cell Western EC50 of 1.0 μM. ML327 induces apoptosis.
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GC32753
Taltobulin (HTI-286)
N,BETA,BETA-三甲基-L-苯基丙氨酰基-N-[(1S,2E)-3-羧基-1-(1-甲基乙基)-2-丁烯基]-N,3-二甲基-L-缬氨酰胺,HTI-286; SPA-110
An inhibitor of microtubule polymerization -
GC32751
Centrinone-B (LCR-323)
LCR-323
Centrinone-B (LCR-323) (LCR-323) 是一种有效且高度选择性的 PLK4 抑制剂,Ki 为 0.59 nM。 -
GC32743
Phen-DC3 Trifluoromethanesulfonate (Phen-DC3 Triflate)
Phen-DC3 Triflate
Phen-DC3 Trifluoromethanesulfonate is a G-quadruplex (G4) specific ligand which can inhibit FANCJ and DinG helicases with IC50s of 65 ± 6 and 50 ± 10 nM, respectively. -
GC32692
APTO-253 (LOR-253)
LOR-253; LT-253
APTO-253 是一种新型小分子,通过诱导 Kruppel 样因子 4 (KLF4) 主转录因子基因表达,从而抑制细胞周期并导致程序性细胞死亡,发挥强大的抗肿瘤活性。 -
GC32688
Centrinone (LCR-263)
LCR-263
A Plk4 inhibitor -
GC32551
Ombrabulin (AC-7700)
奥瑞布林,AVE8062; AC7700
Ombrabulin (AC-7700) (AVE8062) 是 CA-4 磷酸盐的衍生物,已知其通过选择性破坏内皮细胞的微管蛋白细胞骨架而表现出抗血管作用。 -
GC32448
Thymosin beta 4 (Thymosin β4)
胸腺素beta4
胸腺素 β4 是细胞中主要的肌动蛋白螯合蛋白,可与 G-肌动蛋白相互作用。 -
GC32186
Puromycin (CL13900)
嘌呤霉素二盐酸盐水合物
Puromycin 2HCl (CL13900) is an aminonucleoside antibiotic, which acts as a protein synthesis inhibitor.
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GC32134
Parbendazole (SKF 29044)
帕苯咪唑,SKF 29044
An inhibitor of microtubule assembly -
GC31952
ROCK-IN-1
ROCK-IN-1是一种有效的ROCK抑制剂,能够抑制ROCK2的活性,IC50值为1.2nM。
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GC31883
ROCK2-IN-2
ROCK2-IN-2是一种选择性ROCK2抑制剂,IC50<1μM。详细信息请参考专利文献US20180093978A1中的化合物A-30。
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GC31803
Litronesib (LY-2523355)
(-)-N-[4-(2,2-二甲基丙酰基)-5-[[2-(乙基氨基)乙磺酰胺]甲基]-5-苯基-4,5-二氢-1,3,4-噻二唑-2-基]-2,2-二甲基丙酰胺,LY2523355
Litronesib (LY-2523355) (LY2523355) 是一种选择性有丝分裂特异性驱动蛋白 Eg5 抑制剂,具有抗肿瘤活性。 -
GC30801
PE859
PE859是tau和Aβ积累的有效抑制剂,IC50值分别为0.66和1.2μM。
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GC30393
Litronesib Racemate (LY-2523355 Racemate)
LY2523355 Racemate
Litronesib 消旋体 (LY-2523355 Racemate) (LY2523355 Racemate) 是 litronesib 的消旋体。 -
GC19468
AZD1390
AZD1390 是一种强效、高选择性、口服生物可利用的脑渗透性 ATM 抑制剂,在细胞中的 IC50 为 0.78 nM。
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GC19466
Eltanexor (KPT-8602)
第二代 exportin-1 抑制剂
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GC19306
RAD51 Inhibitor B02
B02
A RAD51 inhibitor -
GC19244
Mertansine
美登素,DM1; Maytansinoid DM1
An anticancer agent -
GC19213
Eltanexor Z-isomer
KPT-8602 (Z-isomer)
Eltanexor Z-异构体(KPT-8602 Z-异构体)是 KPT-8602 活性较低的异构体。 -
GC19177
GSK180736A
A ROCK1 and GRK2 inhibitor
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GC19112
Crolibulin
EPC2407
Crolibulin (EPC2407) 是一种微管蛋白聚合抑制剂,具有有效的细胞凋亡诱导和细胞生长抑制作用。 Crolibulin 具有抗肿瘤活性。克罗利布林还具有心血管毒性和神经毒性。 -
GC19092
CCT241736
A dual inhibitor of Aurora kinases and FLT3
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GC19058
BAY1217389
An orally bioavailable inhibitor of Mps1
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GC19047
AZ32
An ATM kinase inhibitor
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GC19034
AR-13324 mesylate
奈他地尔二甲磺酸盐
AR-13324 是一种有效的 ROCK I 和 ROCK II 抑制剂,已被证明可在低浓度下诱导培养的人和猪 TM 细胞发生形态学变化。 -
GC19010
Endosidin 2
ES2
A cell-permeable inhibitor of exocytosis and endosomal recycling
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GC18956
AZ82
An inhibitor of KIFC1
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GC18909
KRIBB3
An Hsp7 and inhibitor of microtubule polymerization
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GC18852
S14161
8-乙氧基-2-(4-氟苯基)-3-硝基-2H-1-苯并吡喃
An inhibitor of cyclin D transactivation -
GC18847
RSM-932A
TCD-717
RSM-932A 是一种 ChoKα 抑制剂,对多种肿瘤来源的细胞系具有有效的体外抗增殖活性,对小鼠的人异种移植物具有体内抗肿瘤活性。
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GC18763
TN-16
NSC 239274
An inhibitor of microtubule assembly -
GC18734
JS-K
A nitric oxide donor
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GC18727
O-methyl Sterigmatocystin
O-甲基杂色曲霉素
An aflatoxin precursor -
GC18726
1-Methyl-1,4-dihydronicotinamide
A nicotinamide derivative
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GC18720
G-5555
A PAK1 inhibitor
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GC18699
JCP174
7-amino-4-chloro-3-Propoxyisocoumarin
An inhibitor of palmitoyl protein thioesterase-1 -
GC18693
Fascaplysin (chloride)
NSC 622398
A selective Cdk4 inhibitor
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GC18666
Debromohymenialdisine
DBH, SKF 108753
An inhibitor of Chk1 and Chk2 -
GC18616
MMP-8 Inhibitor I
Matrix Metalloproteinase-8 Inhibitor I
A selective inhibitor of MMP-8 -
GC18578
YK-3-237
An inhibitor of tubulin polymerization and activator of SIRT1
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GC18565
Suc-AAP-Abu-pNA
Elastase Colorimetric Substrate IV
A substrate for pancreatic elastase -
GC18539
all-trans-4-hydroxy Retinoic Acid
维甲酸杂质
A metabolite of all-trans retinoic acid
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GC18522
Phosphatidylserines (sodium salt)
L-α-磷脂酰丝氨酸(钠盐),L-α-Phosphatidylserine
A mixture of phosphatidylserines isolated from soy -
GC18452
3,4-Dichloroisocoumarin
3,4-DCI
A serine protease inhibitor