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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GC64866
PERK-IN-5
PERK-IN-5 是一种高效、高选择性且口服生物可利用的蛋白激酶 R 样内质网 (ER) 激酶 (PERK) 抑制剂,PERK 与 p-eIF2α 的 IC50 为 2 nM 和 9 nM。PERK-IN-5 在 786-O 肾细胞癌异种移植瘤模型中,能显著抑制肿瘤生长。
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GC69688
PERK-IN-6
PERK-IN-6 (Compound 5) 是一种 PERK 抑制剂,IC50 为 2.5 nM。
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GC50314
PF 3758309 dihydrochloride
PF-03758309 dihydrochloride
An inhibitor of PAK4 -
GC11944
PF 4800567 hydrochloride
A selective CK1ε inhibitor
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GC18074
PF-03814735
N-[2-[(1S,4R)-6-[[4-(环丁基氨基)-5-(三氟甲基)-2-嘧啶基]氨基]-1,2,3,4-四氢萘-1,4-亚氨-9-基]-2-氧代乙基]乙酰胺
PF-03814735 是一种有效的、具有口服生物利用度的 Aurora1 和 Aurora2 激酶的可逆抑制剂,IC50 值分别为 0.8nM 和 5nM 。 -
GC33136
PF-06380101
Aur0101; Auristatin-0101
PF-06380101是Dolastatin10新型类似物,具有强细胞毒性,AMDE特性与其他auristatin类似物不同,ADCs中毒素分子。 -
GC63740
PF-06380101-d8
Aur0101-d8; Auristatin-0101-d8
PF-06380101 D8 (Aur0101 D8) 是 PF-06380101 的氘代物。PF-06380101 是一种 Auristatin 微管抑制剂,是一种细胞毒性 Dolastatin 10 类似物。 -
GC34297
PF-2771
PF-2771是一种选择性的着丝粒蛋白E(CENP-E)抑制剂,IC50值为16.1nM,具有抗肿瘤活性。
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GC17214
PF-3758309
PF 3758309; PF3758309
An inhibitor of PAK4 -
GC14234
PF-477736
PF 00477736
A selective inhibitor of checkpoint kinase 1 -
GC10479
PHA-680632
Pha 680632
An Aurora kinase inhibitor -
GC11324
PHA-767491
CAY10572;PHA767491;PHA 767491;CAY-10572;CAY 10572
A potent Cdc7 kinase inhibitor -
GC15047
PHA-793887
3-甲基-N-[1,4,5,6-四氢-6,6-二甲基-5-[(1-甲基-4-哌啶基)甲酰基]吡咯并[3,4-C]吡唑-3-基]丁酰胺
A CDK inhibitor -
GC15588
PHA-848125
PHA-848125
An inhibitor of Cdks -
GC44618
Phalloidin-AMCA Conjugate
Phalloidin-Aminomethylcoumarin Conjugate
A blue fluorophore that labels F-actin -
GC44619
Phalloidin-Fluorescein Conjugate
A green fluorophore that labels F-actin
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GC44620
Phalloidin-Tetramethylrhodamine Conjugate
An orange fluorophore that labels F-actin
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GC40265
Pheleuin
A pyrazinone
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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. -
GC49015
Phenethyl isothiocyanate
2-苯基乙基异硫代氰酸酯
An isothiocyanate with anticancer activity -
GC49128
Phenylbutazone-d9
保泰松 d9
An internal standard for the quantification of phenylbutazone -
GC15514
Phomopsin A
促微管解聚 A
A β-tubulin inhibitor -
GC48394
Phomopsinamine
Phomopsinamine A
An inhibitor of microtubule polymerization -
GC44633
Phosphatidylserines (bovine)
PtdSers (bovine)
A glycerophospholipid -
GC18522
Phosphatidylserines (sodium salt)
L-α-磷脂酰丝氨酸(钠盐),L-α-Phosphatidylserine
A mixture of phosphatidylserines isolated from soy -
GC38456
Pironetin
NK 10958, NL 9C, PA 48153c, (-)-Pironetin
An inhibitor of microtubule assembly -
GC44652
PK7242 (maleate)
An inducer of reactivation of mutant p53
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GC61995
PKCβ inhibitor 1
3-[1-[3-(1H-咪唑-1-基)丙基]-1H-吲哚-3-基]-4-(苯氨基)-1H-吡咯-2,5-二酮
A PKCβ Inhibitor -
GC45846
PKUMDL-LC-101-D04
GPX4-Activator-1d4
An allosteric activator of GPX4 -
GC44661
PLC thio-PIP2 (sodium salt)
A novel, chromogenic substrate for PLC
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GC10235
Plinabulin (NPI-2358)
普那布林; NPI-2358
A tubulin depolymerizing agent -
GC73885
PLK1/BRD4-IN-3
PLK1/BRD4-IN-3(化合物21)是溴结构域4 (BRD4)和polo样激酶1 (PLK1)的选择性双重抑制剂。
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GC73773
PLK1/BRD4-IN-5
PLK1/BRD4-IN-5(化合物SC10)是一种口服活性PLK1和BRD4抑制剂,IC50值分别为0.3 nM和60.8 nM。
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GC65189
PLK4-IN-1
PLK4-IN-1 (Example A6) 是 PLK4 的抑制剂,其 IC50 值为 ≤ 0.1 μM。
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GC72983
PLK4-IN-4
PLK4-IN-4(化合物22)是一种强效的PLK4抑制剂,IC50值为7.9 nM。
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GC69718
Plogosertib
CYC140
Plogosertib (CYC140) 是一种选择性的、有效的、具有口服活性的 ATP 竞争性的 PLK1 抑制剂 (IC50: 3 nM)。Plogosertib 是一种有抗增殖活性的抗癌剂,可用于多种肿瘤的研究,包括食管癌、胃癌、白血病、非小细胞肺癌、卵巢癌和鳞状细胞癌。 -
GC46019
Pluviatolide
(-)-Pluviatolide
A lignan -
GC17977
PM 102
heparin antagonist
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GC10521
Podophyllotoxin
鬼臼毒素; Podophyllotoxin
A lignan with diverse biological activities -
GC49077
Podophyllotoxin-d6
PPT-d6
An internal standard for the quantification of podophyllotoxin and picropodophyllotoxin -
GC64705
Podophyllotoxone
鬼臼脂毒酮
Podophyllotoxone 是从八角莲根中分离得到的,具有抗癌活性。Podophyllotoxone 能够抑制 tubulin 微管蛋白聚合。 -
GC60294
Poloppin
Poloppin是一种有效的细胞渗透抑制剂,可抑制有丝分裂的polo样激酶(PLK)IC50=26.9μM),并可通过Polo-box结构域(PBD)阻止蛋白之间的相互作用(Kd=29.5μM)。Poloppin选择性地杀死表达突变KRAS的细胞,增强有丝分裂中的死亡。Poloppin可用作KRAS突变型癌症的研究,可作为单一试剂,或与c-MET抑制剂联合使用。
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GC14735
Poloxime
Poloxime 是 poloxin 的水解产物,是一种非 ATP 竞争性 Plk1 抑制剂,具有中等的 Plk1 抑制活性。
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GC13543
Poloxin
2-甲基-5-(1-甲基乙基)-2,5-环己二烯-1,4-二酮1-[O-(2-甲基苯甲酰)肟]
An inhibitor of the Plk1 polo-box domain -
GC91874
Polysarcosine20
pSar20
Polysarcosine20是一种胺官能化的亲水性聚合物。 -
GC45680
Prodan
N,N-二甲基-6-丙酰-2-萘胺
A solvatochromic fluorescent probe -
GC47979
Propiconazole-d7
An internal standard for the quantification of propiconazole
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GC91190
Propoxur-d3
一种用于测量丙氧乐的内部标准。
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GC18353
Prostaglandin A2
前列腺素A2,Medullin
A naturally occurring prostaglandin with antiviral/antitumor activity -
GC44730
proTAME
Pro-N-4-tosyl-L-arginine methyl ester
proTAME是一种细胞渗透性的后期促进复合物/环体(APC/C)抑制剂。