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
-
GC15922
LEE011 hydrochloride
瑞博西尼盐酸盐; LEE011 hydrochloride
A selective cyclin D1/CDK4 and cyclin D3/CDK6 inhibitor -
GC16225
IPA-3
An allosteric inhibitor of PAK1
-
GC11785
CDK4 inhibitor
瑞博西尼
An antiproliferative cyclin D1/Cdk4 inhibitor -
GC14517
KPT-185
An inhibitor of XPO1/CRM1
-
GC16273
Dolastatin 10
DLS 10; NSC 376128
Dolastatin 10 (DLS 10) 是一种有效的抗有丝分裂肽,可抑制微管蛋白聚合。 -
GC12261
FRAX597
A PAK1, PAK2, and PAK3 inhibitor
-
GC11765
Cabazitaxel
卡巴他赛,XRP6258; RPR-116258A; taxoid XRP6258
A semisynthetic taxane -
GC13328
XL413 hydrochloride
BMS-863233 hydrochloride
A potent inhibitor of Cdc7 -
GC18117
XL413
A potent inhibitor of Cdc7
-
GC16607
Mesalamine
5-氨基水杨酸; Mesalamine; 5-ASA; Mesalazine
An NSAID and active metabolite of sulfasalazine, balsalazide, and olsalazine -
GC10235
Plinabulin (NPI-2358)
普那布林; NPI-2358
A tubulin depolymerizing agent -
GC15745
Mps1-IN-2
9-环戊基-2-[[2-乙氧基-4-(4-羟基哌啶-1-基)苯基]氨基]-5-甲基-8,9-二氢-5H-嘧啶并[4,5-B][1,4]二氮杂卓-6(7H)-酮
An inhibitor of Mps1 -
GC11648
BML-277
Chk2 Inhibitor II
A selective DNA damage control kinase inhibitor -
GC10722
SR-3677
N-[2-[2-(二甲基氨基)乙氧基]-4-(1H-吡唑-4-基)苯基]-2,3-二氢-1,4-苯并二恶烷-2-甲酰胺
A ROCK1 and ROCK2 inhibitor -
GC17801
PYZD-4409
PYZD-4409 是泛素激活酶 UBA1 的特异性抑制剂,IC50 为 20 μM(无细胞酶测定)。 PYZD-4409 在恶性细胞中诱导细胞死亡并优先抑制原发性急性髓细胞白血病细胞的克隆形成。
-
GC14600
SB743921
An Eg5 inhibitor
-
GC12415
Rigosertib
瑞格色替; ON-01910
Rigosertib (ON-01910) 是一种多激酶抑制剂和选择性抗癌剂,通过抑制 PI3 激酶/Akt 通路诱导细胞凋亡,促进组蛋白 H2AX 的磷酸化并诱导细胞周期 G2/M 停滞。 Rigosertib 是一种选择性和非 ATP 竞争性的 PLK1 抑制剂,IC50 为 9 nM。 -
GC13580
Rigosertib sodium
瑞格色替钠,ON-01910 sodium
Rigosertib sodium (ON-01910 sodium) 是一种多激酶抑制剂和选择性抗癌剂,通过抑制 PI3K/Akt 通路诱导细胞凋亡,促进组蛋白 H2AX 的磷酸化并诱导细胞周期 G2/M 停滞。 Rigosertib sodium 是一种选择性和非 ATP 竞争性的 PLK1 抑制剂,IC50 为 9 nM。 -
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 -
GC15712
Y-27632
A ROCK inhibitor
-
GC13423
Y-39983 dihydrochloride
ROCK family inhibitor
-
GC14234
PF-477736
PF 00477736
A selective inhibitor of checkpoint kinase 1 -
GC17994
Kif15-IN-2
(ALPHAS)-1,4-二氢-ALPHA-异丙基-N-[4-甲基-5-(5-甲基-1,3,4-恶二唑-2-基)-2-噻唑基]-2,4-二氧代-3(2H)-喹唑啉乙酰胺
Kif15-IN-2 是有丝分裂驱动蛋白 Kif15 的抑制剂,用于细胞增殖性疾病的研究。 -
GC16603
Kif15-IN-1
2-[[(2S)-2-(1,4-二氢-2,4-二氧代-3(2H)-喹唑啉基)-3-甲基-1-氧代丁基]氨基]-4-甲基-5-噻唑羧酸乙酯
Kif15-IN-1 是有丝分裂驱动蛋白家族成员 15 (Kif15) 的抑制剂,用于细胞增殖性疾病的研究。 -
GC14974
AMG 925
A dual inhibitor of FLT3 and Cdk4
-
GC10034
MMAF
一甲基澳瑞他汀F,Monomethylauristatin F
An auristatin with anticancer activity -
GC10030
EHop-016
A Rac1 and Rac3 inhibitor
-
GC11068
GSK2656157
A PERK inhibitor
-
GC15337
VE-822
ATR抑制剂
-
GC11252
CW069
An inhibitor of KIFC/HSET
-
GC15894
CK-636
CK-0944636
An inhibitor of Arp2/3 complex action -
GC10442
MK-8745
An Aurora A kinase inhibitor
-
GC13903
Ro3280
A selective Plk1 inhibitor
-
GC10163
MLN0905
2-[[5-[3-(二甲基氨基)丙基]-2-甲基-3-吡啶基]氨基]-5,7-二氢-9-(三氟甲基)-6H-嘧啶并[5,4-D][1]苯并氮杂卓-6-硫酮,PLK1 Inhibitor
A Plk1 inhibitor -
GC16000
WHI-P180
3-[(6,7-二甲氧基-4-喹唑啉基)氨基]苯酚,Janex 3
A multi-kinase inhibitor -
GC17400
R547
[4-氨基-2-[(1-甲磺酰基哌啶-4-基)氨基]嘧啶-5-基](2,3-二氟-6-甲氧基苯基)甲酮
A selective Cdk inhibitor -
GC10842
LEE011
瑞博西尼; LEE011
A selective cyclin D1/CDK4 and cyclin D3/CDK6 inhibitor -
GC16425
Flavopiridol hydrochloride
(-)-2-(2-氯苯基)-5,7-二羟基-8-[(3S,4R)-3-羟基-1-甲基-4-哌啶基]-4H-1-苯并吡喃-4-酮盐酸盐,Alvocidib Hydrochloride; L86-8275 Hydrochloride; HMR-1275 Hydrochloride
An inhibitor of cyclin-dependent kinases -
GC11835
Deferasirox
地拉罗司; ICL 670
Deferasirox是一种具口服活性的铁螯合剂,用于治疗铁过载疾病。 -
GC15741
LY2603618
LY2603618; IC-83
A Chk1 inhibitor -
GC10196
ETP-46464
ATM Inhibitor III, ATR Inhibitor III
An ATR inhibitor -
GC16489
CP-466722
An ATM kinase inhibitor
-
GC14526
CGK733
ATM/ATR Kinase Inhibitor
An anticancer compound -
GC16268
Purvalanol B
(2R)-2-[[6-[(3-氯-4-羧基苯基)氨基]-9-(1-甲基乙基)-9H-嘌呤-2-基]氨基]-3-甲基-1-丁醇,NG 95; NG95; NG-95
A CDK inhibitor -
GC11224
BI6727(Volasertib)
伏拉塞替; BI 6727
A polo-like kinase inhibitor -
GC14807
Fingolimod (FTY720) HCl
盐酸芬戈莫德; FTY720
芬戈莫德(FTY720)是一种免疫抑制剂,通常用于治疗多发性硬化症,也有抗癌作用,可以作为HDACi(组蛋白脱乙酰酶抑制剂)。 -
GC17648
Dinaciclib(SCH727965)
(2S)-1-[3-乙基-7-[[(1-氧代-3-吡啶基)甲基]氨基]吡唑并[1,5-A]嘧啶-5-基]-2-哌啶乙醇,SCH 727965
A CDK inhibitor -
GC15739
CHIR-124
4-[((3S)-1-氮杂双环[2,2,2]辛-3-基)氨基]-3-(1H-苯并咪唑-2-基)-6-氯喹啉-2(1H)-酮
A selective Chk1 inhibitor -
GC12865
BMS265246
A cell-permeable inhibitor of Cdk1 and Cdk2
-
GC12338
Wortmannin
渥曼青霉素; SL-2052; KY-12420
渥曼青霉素是一种高效的 PI3 激酶特异性直接抑制剂,最初源自真菌 (1,2)。