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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GC12467
KPT-330
塞利尼索
KPT-330(Selinexor)是一种具有口服活性的选择性核输出抑制剂(SINE)化合物,抑制核输出蛋白XPO1(又名CRM1)。 -
GC14615
KPT-9274
Orally acitve allosteric inhibitor of PAK4
-
GC18909
KRIBB3
An Hsp7 and inhibitor of microtubule polymerization
-
GC33377
KSI-3716
KSI-3716是c-Myc的抑制剂。
-
GC11118
KU 55933
2-吗啉-4-基-6-噻蒽-1-基吡喃-4-酮
KU 55933是一种高效且特异的ATM激酶抑制剂,能够使人类肿瘤细胞对电离辐射和化疗药物更加敏感。KU 55933在体外的IC₅₀值为13nM,Ki值为2.2nM。 -
GC33404
KU 59403
KU59403是ATM的一个有效抑制剂,其IC50值为3nM。
-
GC12054
KU-60019
KU60019;KU 60019
A potent ATM kinase inhibitor -
GC47532
KUS121
A VCP modulator
-
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 -
GC72824
KX2-361
KX-02
KX2-361(KX-02)是一种Src激酶和微管蛋白聚合抑制剂。 -
GC14288
KX2-391
5-[4-[2-(4-吗啉基)乙氧基]苯基]-N-(苯基甲基)-2-吡啶乙酰胺,KX2-391; KX-01
A Src kinase inhibitor -
GC10222
KX2-391 dihydrochloride
5-[4-[2-(4-吗啉基)乙氧基]苯基]-N-(苯基甲基)-2-吡啶乙酰胺盐酸盐,KX2-391 2HCl; KX2-391
A Src kinase inhibitor -
GC44020
L-681,217
An antibiotic
-
GC40793
L-erythro Sphinganine (d18:0)
L-苏式-二氢鞘胺醇
A bioactive sphingolipid -
GC49547
L-Glutamic Acid γ-p-Nitroanilide (hydrate)
γ-Glu-pNA, Glutamate γ-(4-Nitroanilide), L-GPNA, E-pNA
A colorimetric substrate for γ-glutamyl transpeptidase -
GC91028
L-K6L9 (trifluoroacetate salt)
一种细胞溶解肽(即能够破坏细胞的蛋白质分子)。
-
GC49205
L-Leu-AMC (hydrochloride)
L-亮氨酰7-氨基-4-甲基香豆素盐酸盐,Leu-AMC hydrochloride
A fluorogenic substrate for leucine aminopeptidase -
GC44081
L-myo-Inositol-1,4,5-triphosphate (sodium salt)
D-myo-Inositol-3,5,6-triphosphate, Ins(1,4,5)P3, 1,4,5IP3
Isomer of D-myo-inositol-1,4,5-triphosphate -
GC47577
L-Ornithine lactam (hydrochloride)
(S)-3-氨基哌啶-2-酮盐酸盐
A synthetic intermediate -
GC41520
Lachnone A
A fungal metabolite
-
GC49471
LAMP1 Monoclonal Antibody (Clone Ly1C6)
For immunochemical analysis of LAMP1
-
GC41272
Lateropyrone
Avenacein Y
A fungal metabolite -
GC15671
Latrunculin A
红海海绵素A,LAT-A
一种可逆抑制肌动蛋白聚合的药物
-
GC50052
Laulimalide
Microtubule stabilzing agent
-
GC50214
LCB 03-0110 dihydrochloride
Potent c-SRC kinase inhibitor; also inhibits DDR2, BTK and Syk
-
GC39209
LCH-7749944
GNF-PF-2356
LCH-7749944 (GNF-PF-2356) is a novel and potent p21-activated kinase 4 (PAK4) inhibitor with an IC50 of 14.93 μM and has less potently inhibitory effect against PAK1, PAK5 and PAK6. LCH-7749944 causes successful inhibition of EGFR activity due to its inhibitory effect on PAK4. -
GC17067
LDC000067
(3-(6-(2-甲氧基苯基)嘧啶-4-基氨基)苯基)甲烷磺酰胺,LDC067
A Cdk9 inhibitor -
GC33086
LDN-192960
3-[(2,7-二甲氧基吖啶-9-基)硫基]丙胺
An inhibitor of haspin and DYRK2 -
GC44047
LDN-192960 (hydrochloride)
An inhibitor of haspin and DYRK2
-
GC10842
LEE011
瑞博西尼; LEE011
A selective cyclin D1/CDK4 and cyclin D3/CDK6 inhibitor -
GC15922
LEE011 hydrochloride
瑞博西尼盐酸盐; LEE011 hydrochloride
A selective cyclin D1/CDK4 and cyclin D3/CDK6 inhibitor -
GC15377
LEE011 succinate
瑞博西尼琥珀酸盐; LEE011 succinate
A selective cyclin D1/CDK4 and cyclin D3/CDK6 inhibitor -
GC49751
Lefamulin
来法莫林,BC-3781
A pleuromutilin antibiotic -
GC18345
Leptomycin A
来普霉素A
An inhibitor of nuclear transport -
GC10954
Leptomycin B
来普霉素B; CI 940; LMB
Leptomycin B (LMB)是染色体区域维持1 (CRM1)的抑制剂,CRM1是核蛋白输出蛋白之一。 -
GC33175
Lexibulin dihydrochloride (CYT-997 dihydrochloride)
CYT-997 dihydrochloride
An inhibitor of microtubule polymerization -
GC14857
LFM-A13
A BTK inhibitor
-
GC70857
LIMK-IN-1
LIMK-IN-1(化合物14)是LIM激酶(LIMK)的抑制剂,LIMK1和LIMK2的IC50分别为0.5 nM和0.9 nM。
-
GC90981
Lipid 10
?EA-PIP
一种可离子化的阳离子脂质
-
GC69379
Lipid 8
Lipid 8 是一种可电离的氨基脂质,可用于合成脂质纳米颗粒。
-
GC91124
Lipid III-45
Cationic Lipid A
一种可离子化的阳离子脂质
-
GC74104
Lisavanbulin dihydrochloride
BAL-101553 dihydrochloride
Lisavanbulin dihydrochloride(BAL-101553)是微管靶向剂Avanbulin(BAL 27862)的前药。 -
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。 -
GC30393
Litronesib Racemate (LY-2523355 Racemate)
LY2523355 Racemate
Litronesib 消旋体 (LY-2523355 Racemate) (LY2523355 Racemate) 是 litronesib 的消旋体。 -
GC61014
Lusianthridin
4,7-二羟基-2-甲氧基-9,10-二氢菲
Lusianthridin是来自Dendrobiumvenustum的天然化合物,具有抗迁移作用。Lusianthridin通过抑制Src-STAT3信号,促进c-Myc的降解。 -
GC44094
LX7101 (hydrochloride)
A LIMK and ROCK inhibitor
-
GC12402
LX7101 HCL
A LIMK and ROCK inhibitor
-
GC15741
LY2603618
LY2603618; IC-83
A Chk1 inhibitor -
GC15663
LY2606368
5-[[5-[2-(3-氨基丙氧基)-6-甲氧基苯基]-1H-吡唑-3-基]氨基]-2-吡嗪甲腈,LY2606368
LY2606368 是一种 ATP 竞争性 CHK1 抑制剂,目前处于临床阶段,Ki 为 0.9 nM,IC50 <1 nM。 -
GC16822
LY2835219
Abemaciclib; LY2835219 methanesulfonate
LY2835219 free base是 CDK4 和 CDK6 的强效选择性抑制剂,在非细胞实验中的 IC50 分别为 2nM 和 10nM。