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Targets Recommended: CDK

122

抑制剂 & 化合物

3

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TargetMol 试剂盒

9

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Cat. No. Product Name Form Specificity Of Inhibition
CL0136 ATM/ATR inhibitor kit

ATM/ATR inhibitor kit

TargetMol 试剂盒

ATM/ATR inhibitor kit
Cat.No: CL0136
Cat. No. Product Name Target Signaling Pathways
T64373 CDK1-IN-2

cdk1 inhibitor 2

CDK Cell Cycle/Checkpoint
CDK1-IN-2 (cdk1 inhibitor 2)是一种CDK1抑制剂,IC50为5.8μM。CDK1-IN-2的激酶谱显示了多种激酶的非选择性抑制。
T14914 Cdk1/2 Inhibitor III

CDK Cell Cycle/Checkpoint
Cdk1/2 Inhibitor III 是一种具有选择性的 Cdk1/2抑制剂,对 CDK1/cyclin B 的 IC50值为2.1μM。
T63437 CDK1-IN-5

CDK1-IN-5 (10h) 是一种选择性的 CDK1 抑制剂,能够作用于 CDK1 (IC50: 42.19 nM),CDK2 (IC50: 188.71 nM) 和 CDK5 (IC50: 354.15 nM)。CDK1-IN-5 能够影响细胞周期并抑制癌细胞生长,能够用于研究癌症。
T62970 CDK1-IN-1

CDK1-IN-7 是一种 CDK1 的有效抑制剂,对 CDK1/CycB 的 IC50 值为 161.2 nM。CDK1-IN-7 通过凋亡内在途径以 p53 依赖的方式诱导细胞凋亡。CDK1-IN-7 能够选择性作用于肿瘤组织,并具有潜在的抗增殖作用。CDK1-IN-7 是一种潜在的靶向抗肿瘤药物。
T63080 CDK1-IN-4

CDK1-IN-4 (10d) 是一种选择性的 CDK1 抑制剂,能够作用于 CDK1 (IC50: 44.52 nM)、CDK2 (IC50: 624.93 nM) 和 CDK5 (IC50: 135.22 nM)。CDK1-IN-4 能够影响细胞周期,进而对癌细胞的生长表现出抑制作用。CDK1-IN-4 能够用于研究癌症。
T60583 CDK1/2/4-IN-1

CDK1/2/4-IN-1 (compound 3a) 是 CDK 的有效抑制剂, 其对于 CDK1CDK2 和 CDK4 的 IC50值分别为 1.47、0.78 和 0.87 μM。CDK1/2/4-IN-1 可用于癌症研究。CDK1/2/4-IN-1 可将细胞周期阻滞在 G2/M 期并诱导细胞凋亡。CDK1/2/4-IN-1 提高 Bax、caspase-3和 P53 的水平并降低 Bcl-2 水平。
T63933 CDK1-IN-3

CDK1-IN-3 (8g) 是一种选择性的 CDK1 抑制剂,能够作用于 CDK1 (IC50: 36.8 nM),CDK2 (IC50: 305.17 nM) 和 CDK5 (IC50: 369.37 nM)。CDK1-IN-3 能够影响细胞周期,进而抑制癌细胞的生长,能够用于研究癌症。
T61254 CDK1/Cyc B-IN-1

CDK1/Cyc B-IN-1 (Compound 5) is a potent inhibitor of the CDK1/Cyc B complex, demonstrating selectivity with an IC50 value of 97 nM. This compound induces apoptosis and G2/M cell cycle arrest, effectively halting cancer cell proliferation. Additionally, CDK1/Cyc B-IN-1 exhibits a wide-ranging cytotoxic effect on various cancer cell lines [1].
T62405 KDM1/CDK1-IN-1

KDM1/CDK1-IN-1 (compound 4) 是一种有效的 KDM1 (IC50: 0.096 μM) 和 CDK1 (IC50: 0.078 μM) 抑制剂。KDM1/CDK1-IN-1 能够将 HOP-92 细胞的细胞周期阻滞在 G2/M 期,并诱导其凋亡 (apoptosis)。KDM1/CDK1-IN-1 对 CCRF-CEM 细胞 (IC50: 16.34 μM)、HOP-92 细胞 (IC50: 3.45 μM) 和 Hep-G2 细胞 (IC50: 7.79 μM) 具有较强的细胞毒性。
T6612 NU6027

ATM/ATR; DNA-PK; CDK Cell Cycle/Checkpoint; DNA Damage/DNA Repair; PI3K/Akt/mTOR signaling
NU6027 是一种有效的 ATR/CDK 抑制剂,抑制 CDK1/2、ATR 和 DNA-PK,Ki 为 2.5 μM/1.3 μM、0.4 μM 和 2.2 μM。它以 ATR 依赖性方式增强羟基脲和顺铂的细胞毒性。
T7426 ALSTERPAULLONE

Apoptosis; GSK-3; CDK Apoptosis; Cell Cycle/Checkpoint; PI3K/Akt/mTOR signaling; Stem Cells
Alsterpaullone 是高效的 CDK 抑制剂,是一种 ATP 竞争性的 GSK-3alpha/GSK-3beta 抑制剂,且作用的 IC50值都为 4 nM。它有用于神经退行性和增生性疾病的研究潜力,具有抗肿瘤活性,诱导白血病细胞凋亡。
T40290 CDK12-IN-5

CDK12-IN-5

CDK12-IN-5 is a pyrazolotriazine compound that effectively inhibits CDK12, with an IC50 value of 23.9 nM at a high ATP concentration of 2 mM. However, CDK12-IN-5 does not exhibit inhibitory effects on CDK2/Cyclin E (IC50 = 173 μM) and CDK9/Cyclin T1 (IC50 = 127 μM) at the same high ATP concentration of 2 mM, as stated in WO2021116178A1.
T39752 CDK12-IN-2

CDK12 inhibitor 2,CDK12-IN-2

CDK Cell Cycle/Checkpoint
CDK12-IN-2 (CDK12 inhibitor 2) 是一种有效的选择性 CDK12 抑制剂,对 CDK12、CDK2、CDK7 和 CDK9 的 IC50 为 52 nM、>100 μM、>10 μM 和 16 μM。 CDK12-IN-2可用于研究CDK12的功能。
T40289 CDK12-IN-6

CDK12-IN-6

CDK12-IN-6, a pyrazolotriazine compound, is a powerful inhibitor of CDK12. Its inhibitory activity is significant with an IC50 value of 1.19 μM when tested at high ATP concentration (2 mM). Notably, CDK12-IN-6 does not exhibit any inhibitory effect on CDK2/Cyclin E (IC50 >20 μM) and CDK9/Cyclin T1 (IC50 >20 μM) when tested under the same high ATP conditions (2 mM) (WO2021116178A1).
T14915 CDK12-IN-E9

CDK Cell Cycle/Checkpoint
CDK12-IN-E9 is a potent and selective covalent CDK12 inhibitor and non-covalent CDK9 inhibitor while avoiding ABC transporter-mediated efflux. It has a weak binding ability to CDK7/CyclinH complex (IC50> 1 μM).
T64284 PROTAC CDK12/13 Degrader-1

PROTAC CDK12/13 Degrader-1 (7f) 是一种高效的、选择性的细胞周期蛋白依赖性激酶 CDK12 (DC50: 2.2 nM) 和 CDK13 (DC50: 2.1 nM) 双重降解剂。PROTAC CDK12/13 Degrader-1 表现出抗增殖效果,能够用于研究乳腺癌。
T40288 CDK12-IN-4

CDK12-IN-4

CDK12-IN-4, a pyrazolotriazine compound, exhibits potent inhibition of CDK12 by achieving an IC50 value of 0.641 μM, utilizing high ATP levels (2 mM). Notably, CDK12-IN-4 does not impact CDK2/Cyclin E (IC50 > 20 μM) or CDK9/Cyclin T1 (IC50 > 20 μM) under the influence of high ATP (2 mM) levels (WO2021116178A1).
T14990 CDK12-IN-3

CDK Cell Cycle/Checkpoint
CDK12-IN-3 is a selective CDK12 inhibitor (IC50: 491 nM in an enzymatic assay).
T75163 GW297361

VEGFR; CDK; Src Angiogenesis; Cell Cycle/Checkpoint; Tyrosine Kinase/Adaptors
GW297361 是一种有效的依赖细胞周期蛋白的激酶 Cdk1 抑制剂,对 Pho85 信号通路也具有抑制作用。GW297361对酵母 Cdk1 和 Pho85 的 IC50 分别为 20 nM 和 400 nM。
T2506 AZD-5438

AZD5438

CDK Cell Cycle/Checkpoint
AZD-5438 有效抑制 CDK1,CDK2,CDK9,IC50值分别为 16 nM, 6 nM, 20 nM,但它对 GSK3β,CDK5,CDK6 的抑制作用较弱。
T6126 JNJ-7706621

JNJ 7706621

Apoptosis; CDK; Aurora Kinase Apoptosis; Cell Cycle/Checkpoint; Chromatin/Epigenetic
JNJ-7706621 是一种aurora kinase 抑制剂,有效抑制CDK1CDK2,对CDK1CDK2,aurora-A 和aurora-B 的IC50值分别为 9 nM,3 nM,11 nM 和 15 nM。
T6167 SU9516

Apoptosis; p38 MAPK; CDK; PKC; Autophagy Apoptosis; Autophagy; Cell Cycle/Checkpoint; Chromatin/Epigenetic; Cytoskeletal Signaling; MAPK
SU9516 是一种 CDK2抑制剂,IC50值为 22 nM,对 CDK1CDK4 也有抑制作用,IC50值分别为 40 和 200 nM。
T21966 MeBIO

GSK-3; Aryl Hydrocarbon Receptor; CDK Cell Cycle/Checkpoint; Immunology/Inflammation; PI3K/Akt/mTOR signaling; Stem Cells
MeBIO 是一种芳烃受体激动剂,对 GSK-3 和 CDK1/CyclinB 的 IC50 分别为 44 和 55 μM。 MeBIO 不影响 GSK-3β。
T2356 Ro-3306

Apoptosis; ERK; SGK; PKA; CDK; PKC Apoptosis; Cell Cycle/Checkpoint; Chromatin/Epigenetic; Cytoskeletal Signaling; MAPK; Metabolism; Tyrosine Kinase/Adaptors
Ro 3306 是一种选择性 ATP 竞争性CDK1抑制剂,对 CDK1CDK1/cyclin B1CDK2/cyclin E 的Ki 值为分别为 20 nM、35 nM 和 340 nM。
T2679 BMS-265246

BMS265246

CDK Cell Cycle/Checkpoint
BMS-265246 是一种有效的选择性 CDK1/2 抑制剂,对 CDK1/cyclin B 和 CDK2/cyclin E 的 IC50分别为6 nM 和9 nM。
T6924 Riviciclib hydrochloride

P276-00

Apoptosis; CDK Apoptosis; Cell Cycle/Checkpoint
Riviciclib hydrochloride (P276-00) 是一种CDK 抑制剂,抑制CDK9-cyclinT1CDK4-cyclin D1CDK1-cyclinB 的IC50值分别为 20 nM、63 nM、79 nM。它对 Cisplatin 耐药性细胞具有抗肿瘤活性。
T6837 Flavopiridol

L868275,Alvocidib,夫拉平度,NSC 649890 HCl,HMR-1275

Apoptosis; HIV Protease; CDK; Autophagy Apoptosis; Autophagy; Cell Cycle/Checkpoint; Microbiology/Virology; Proteases/Proteasome
Flavopiridol (Alvocidib) 是一种广谱CDK 竞争型抑制剂, 抑制 CDK1CDK2,CDK4的IC50分别为30,170,100 nM。
TQ0068 NVP-LCQ195

AT9311,LCQ-195

CDK Cell Cycle/Checkpoint
NVP-LCQ195 (LCQ-195) 是CDK 杂环类抑制剂,对CDK1CDK2,CDK3和CDK5的IC50为1到42 nM 之间。
T14916 CDK2-IN-4

CDK Cell Cycle/Checkpoint
CDK2-IN-4 是选择性的CDK2抑制剂,对 CDK2/cyclin A 的IC50值为 44 nM,选择性高出 CDK1/cyclin B 的 2,000 倍 (IC50=86 μM)。
T28218 NU6102

NU-6102,NU 6102

CDK Cell Cycle/Checkpoint
NU6102 是一种具有选择性和有效性的 ATP 竞争性 CDK2 抑制剂,具有抗肿瘤活性,对 CDK1/cyclinB、CDK2/cyclinA3、CDK1/CDK2、 CDK4、DYRK1A 、PDK1、ROCKII 具有抑制作用,可用于研究直肠癌。
T12617 (R)-CR8 trihydrochloride

CR8, (R)-Isomer trihydrochloride

Apoptosis; CDK Apoptosis; Cell Cycle/Checkpoint
(R)-CR8 trihydrochloride (CR8, (R)-Isomer trihydrochloride) 是一种 CDK1/2/5/7/9 抑制剂,可作为分子胶降解剂,具有神经保护活性,可诱导细胞凋亡。
T1917 GSK 3 Inhibitor IX

BIO,GSK 3 IX,6-BIO,6-Bromoindirubin-3'-oxime,MLS 2052,6-bromoindirubin-3-oxime

Apoptosis; GSK-3; Tyrosine Kinases; CDK Apoptosis; Cell Cycle/Checkpoint; PI3K/Akt/mTOR signaling; Stem Cells; Tyrosine Kinase/Adaptors
GSK 3 Inhibitor IX (6-BIO) 是一种选择性可逆的,ATP 竞争性的 GSK-3α/β和 CDK1-cyclinB 复合体抑制剂,能够抑制 (GSK-3α/β)/CDK1/CDK5 的活性,IC50值分别为 5 nM/320 nM/83 nM。
T5200 Indirubin-3'-monoxime

靛玉红-3' -单肟,Indirubin-3'-oxime

GSK-3; Lipoxygenase; CDK Cell Cycle/Checkpoint; Metabolism; PI3K/Akt/mTOR signaling; Stem Cells
Indirubin-3'-monoxime (Indirubin-3'-oxime) 是一种有效的 GSK3β 抑制剂,IC50值为 22 nM。它对 CDK5/p25、CDK1/cyclin B 和CDk2/cyclin E 也有作用,IC50值分别为 100、180 和 250 nM。
T6205 AT7519

Apoptosis; GSK-3; CDK Apoptosis; Cell Cycle/Checkpoint; PI3K/Akt/mTOR signaling; Stem Cells
AT7519 是一种CDK 抑制剂,对 CDK1CDK2,CDK4-CDK6 以及 CDK9 的IC50值分别为 210,47,100,13,170 和 <10 nM。
T1912 Dinaciclib

SCH 727965,PS-095760

Apoptosis; CDK Apoptosis; Cell Cycle/Checkpoint
Dinaciclib (SCH 727965) 是一种 CDK 抑制剂,抑制 CDK1CDK2、CDK5 和 CDK9 (IC50=3/1/1/4 nM),具有选择性。Dinaciclib 具有潜在的抗肿瘤活性,可以抑制胸甘 (dThd) DNA 的整合。
T6312 R547

Ro 4584820

Apoptosis; GSK-3; PKA; CDK Apoptosis; Cell Cycle/Checkpoint; PI3K/Akt/mTOR signaling; Stem Cells; Tyrosine Kinase/Adaptors
R547 (Ro 4584820) 是一种口服有效,选择性, ATP 竞争性CDK 抑制剂,对 CDK1/cyclin B、 CDK2/cyclin E 和 CDK4/cyclin D1 作用的Ki 值分别为 2 nM、3 nM、1 nM。
T39403 Avotaciclib

BEY1107,Avotaciclib

CDK Cell Cycle/Checkpoint
Avotaciclib (BEY1107) 是一种有效和具有口服活性的 cyclin dependent kinase 1 (CDK1) 抑制剂。Avotaciclib 可用于研究局部晚期或转移性胰腺癌。
T6358 1-Azakenpaullone

1-氮杂坎帕罗酮,azakenpaullone

GSK-3 PI3K/Akt/mTOR signaling; Stem Cells
1-Azakenpaullone (azakenpaullone) 是一种 ATP 竞争性的、具有高度选择性的糖原合成酶激酶3 β (GSK-3β)的抑制剂,其 IC50=18 nM。
T1778 AT7519 Hydrochloride

AT7519 HCl,AT 7519 hydrochloride salt

Apoptosis; GSK-3; CDK Apoptosis; Cell Cycle/Checkpoint; PI3K/Akt/mTOR signaling; Stem Cells
AT7519 Hydrochloride (AT7519 HCl) 是一种多CDK 抑制剂,对 CDK1CDK2、CDK4-CDK6 以及 CDK9 的IC50值分别为 210、47、100、13、170 和 <10 nM。
T6162 BS-181 hydrochloride

BS-181 HCl

CDK Cell Cycle/Checkpoint
BS-181 hydrochloride (BS-181 HCl) 是一种高度选择性的CDK7抑制剂,IC50值为 21 nM。它对 CDK7 的选择性是对 CDK1、2、4、5、6 和 9 的 40 倍以上。
T15732 Ribociclib succinate

LEE011 琥珀酸盐,瑞博西尼琥珀酸盐,LEE011 succinate

CDK Cell Cycle/Checkpoint
Ribociclib succinate (LEE011 succinate) 是一种高度特异性的CDK4/6抑制剂,IC50值分别为 10 nM 和 39 nM。它对细胞周期蛋白 B/CDK1 复合物的效力低 1000 倍。
T2247 KenPaullone

9-Bromopaullone,NSC-664704,9-溴-7,12-二氢吲哚并[3,2-D][1]苯并氮杂卓-6(5H)-酮

GSK-3; CDK Cell Cycle/Checkpoint; PI3K/Akt/mTOR signaling; Stem Cells
KenPaullone (9-Bromopaullone) 是一种CDK1/cyclin B 和GSK-3β抑制剂,IC50值分别为 0.4 μM 和 23 nM。它也抑制 CDK2/cyclin A、CDK2/cyclin E 和 CDK5/p25 的活性,IC50值分别为 0.68 μM、7.5 μM 和 0.85 μM。。它通过增强 TGFβ-Smad3 信号通路增加和延长 foxp3 基因的转录来促进 iTreg 细胞分化。
T72057 H1k

CDK Cell Cycle/Checkpoint
H1k 是一种 eudistomin Y 荧光衍生物和溶酶体靶向抗增殖剂。它可以剂量依赖性地增加自噬信号,下调细胞周期蛋白依赖性激酶(cyclin-dependent kinase, CDK1)和细胞周期蛋白 B1的表达。
T16363 NVP-2

Apoptosis; CDK Apoptosis; Cell Cycle/Checkpoint
NVP-2 是一种具有选择性的 ATP 竞争性细胞周期蛋白依赖性激酶 9 探针,可抑制 CDK9/CycT 活性,IC50值为 0.514 nM。它对 CDK1/CycB,CDK2/CycA 和 CDK16/CycY 激酶具有抑制作用,可诱导细胞凋亡。
T2378 RGB-286638 free base

GSK-3; MEK; JAK; CDK Angiogenesis; Cell Cycle/Checkpoint; Chromatin/Epigenetic; JAK/STAT signaling; MAPK; PI3K/Akt/mTOR signaling; Stem Cells
RGB-286638 free base 是一种新型 CDK 抑制剂,抑制cyclin T1-CDK9、cyclin B1-CDK1、cyclin E-CDK2、cyclin D1-CDK4、cyclin E-CDK3和p35-CDK5活性,IC50分别为 1、2、3、4、5 和 5 nM。它也抑制 GSK-3β、TAK1、Jak2 和 MEK1,IC50值分别为 3、5、50和 54 nM。
T6787 BIO-acetoxime

BIA,GSK-3 Inhibitor X

Apoptosis; GSK-3; HSV Apoptosis; Microbiology/Virology; PI3K/Akt/mTOR signaling; Stem Cells
BIO-acetoxime (GSK-3 Inhibitor X) 是一种 GSK3α/β 抑制剂,IC50值均为 10 nM,具有抗惊厥和抗感染作用。
T22260 Aminopurvalanol A

CDK Cell Cycle/Checkpoint
Aminopurvalanol A 是一种竞争性、选择性和细胞渗透性的Cyclins/Cdk 复合物抑制剂,优先靶向G2/M 期转变进而抑制癌细胞分化。它通过抑制生理获能依赖性肌动蛋白聚合而抑制精子受精能力。
T6525 GW 5074

GW5074,3-(3,5-二溴-4-羟基苯亚甲基)-5-碘-1,3-二氢吲哚-2-酮,Raf1 Kinase Inhibitor I

Apoptosis; Raf Apoptosis; MAPK
GW 5074 (Raf1 Kinase Inhibitor I) 是一种有效且特异性的 c-Raf 抑制剂,IC50值为 9 nM。 它对 JNK1/2/3、MEK1、MKK6/7、CDK1/2、c-Src、p38 MAP、VEGFR2 或 c-Fms 的活性没有影响。
T6081 Milciclib

PHA-848125

Trk receptor; CDK; Autophagy Autophagy; Cell Cycle/Checkpoint; Tyrosine Kinase/Adaptors
Milciclib (PHA-848125) 是一种 ATP 竞争性的 CDK 和原肌球蛋白受体激酶双重抑制剂,作用于 CDK2,IC50 为 45 nM。
T9014 SKI-178

Apoptosis; S1P Receptor Apoptosis; GPCR/G Protein
SKI-178 是一种鞘氨醇激酶-1(SphK1)和 SphK2抑制剂,以 CDK1 依赖性方式诱导人急性髓性白血病细胞凋亡。

化合物

CDK1-IN-2
Cat.No: T64373
Synonym: cdk1 inhibitor 2
Target: CDK
Cdk1/2 Inhibitor III
Cat.No: T14914
Synonym:
Target: CDK
CDK1-IN-5
Cat.No: T63437
Synonym:
Target:
CDK1-IN-1
Cat.No: T62970
Synonym:
Target:
CDK1-IN-4
Cat.No: T63080
Synonym:
Target:
CDK1/2/4-IN-1
Cat.No: T60583
Synonym:
Target:
CDK1-IN-3
Cat.No: T63933
Synonym:
Target:
CDK1/Cyc B-IN-1
Cat.No: T61254
Synonym:
Target:
KDM1/CDK1-IN-1
Cat.No: T62405
Synonym:
Target:
NU6027
Cat.No: T6612
Synonym:
Target: ATM/ATR, DNA-PK, CDK
ALSTERPAULLONE
Cat.No: T7426
Synonym:
Target: Apoptosis, GSK-3, CDK
CDK12-IN-5
Cat.No: T40290
Synonym: CDK12-IN-5
Target:
CDK12-IN-2
Cat.No: T39752
Synonym: CDK12 inhibitor 2,CDK12-IN-2
Target: CDK
CDK12-IN-6
Cat.No: T40289
Synonym: CDK12-IN-6
Target:
CDK12-IN-E9
Cat.No: T14915
Synonym:
Target: CDK
PROTAC CDK12/13 Degrader-1
Cat.No: T64284
Synonym:
Target:
CDK12-IN-4
Cat.No: T40288
Synonym: CDK12-IN-4
Target:
CDK12-IN-3
Cat.No: T14990
Synonym:
Target: CDK
GW297361
Cat.No: T75163
Synonym:
Target: VEGFR, CDK, Src
AZD-5438
Cat.No: T2506
Synonym: AZD5438
Target: CDK
JNJ-7706621
Cat.No: T6126
Synonym: JNJ 7706621
Target: Apoptosis, CDK, Aurora Kinase
SU9516
Cat.No: T6167
Synonym:
Target: Apoptosis, p38 MAPK, CDK, PKC, Autophagy
MeBIO
Cat.No: T21966
Synonym:
Target: GSK-3, Aryl Hydrocarbon Receptor, CDK
Ro-3306
Cat.No: T2356
Synonym:
Target: Apoptosis, ERK, SGK, PKA, CDK, PKC
BMS-265246
Cat.No: T2679
Synonym: BMS265246
Target: CDK
Riviciclib hydrochloride
Cat.No: T6924
Synonym: P276-00
Target: Apoptosis, CDK
Flavopiridol
Cat.No: T6837
Synonym: L868275,Alvocidib,夫拉平度,NSC 649890 HCl,HMR-1275
Target: Apoptosis, HIV Protease, CDK, Autophagy
NVP-LCQ195
Cat.No: TQ0068
Synonym: AT9311,LCQ-195
Target: CDK
CDK2-IN-4
Cat.No: T14916
Synonym:
Target: CDK
NU6102
Cat.No: T28218
Synonym: NU-6102,NU 6102
Target: CDK
(R)-CR8 trihydrochloride
Cat.No: T12617
Synonym: CR8, (R)-Isomer trihydrochloride
Target: Apoptosis, CDK
GSK 3 Inhibitor IX
Cat.No: T1917
Synonym: BIO,GSK 3 IX,6-BIO,6-Bromoindirubin-3'-oxime,MLS 2052,6-bromoindirubin-3-oxime
Target: Apoptosis, GSK-3, Tyrosine Kinases, CDK
Indirubin-3'-monoxime
Cat.No: T5200
Synonym: 靛玉红-3' -单肟,Indirubin-3'-oxime
Target: GSK-3, Lipoxygenase, CDK
AT7519
Cat.No: T6205
Synonym:
Target: Apoptosis, GSK-3, CDK
Dinaciclib
Cat.No: T1912
Synonym: SCH 727965,PS-095760
Target: Apoptosis, CDK
R547
Cat.No: T6312
Synonym: Ro 4584820
Target: Apoptosis, GSK-3, PKA, CDK
Avotaciclib
Cat.No: T39403
Synonym: BEY1107,Avotaciclib
Target: CDK
1-Azakenpaullone
Cat.No: T6358
Synonym: 1-氮杂坎帕罗酮,azakenpaullone
Target: GSK-3
AT7519 Hydrochloride
Cat.No: T1778
Synonym: AT7519 HCl,AT 7519 hydrochloride salt
Target: Apoptosis, GSK-3, CDK
BS-181 hydrochloride
Cat.No: T6162
Synonym: BS-181 HCl
Target: CDK
Ribociclib succinate
Cat.No: T15732
Synonym: LEE011 琥珀酸盐,瑞博西尼琥珀酸盐,LEE011 succinate
Target: CDK
KenPaullone
Cat.No: T2247
Synonym: 9-Bromopaullone,NSC-664704,9-溴-7,12-二氢吲哚并[3,2-D][1]苯并氮杂卓-6(5H)-酮
Target: GSK-3, CDK
H1k
Cat.No: T72057
Synonym:
Target: CDK
NVP-2
Cat.No: T16363
Synonym:
Target: Apoptosis, CDK
RGB-286638 free base
Cat.No: T2378
Synonym:
Target: GSK-3, MEK, JAK, CDK
BIO-acetoxime
Cat.No: T6787
Synonym: BIA,GSK-3 Inhibitor X
Target: Apoptosis, GSK-3, HSV
Aminopurvalanol A
Cat.No: T22260
Synonym:
Target: CDK
GW 5074
Cat.No: T6525
Synonym: GW5074,3-(3,5-二溴-4-羟基苯亚甲基)-5-碘-1,3-二氢吲哚-2-酮,Raf1 Kinase Inhibitor I
Target: Apoptosis, Raf
Milciclib
Cat.No: T6081
Synonym: PHA-848125
Target: Trk receptor, CDK, Autophagy
SKI-178
Cat.No: T9014
Synonym:
Target: Apoptosis, S1P Receptor
Cat. No. Product Name Target Signaling Pathways
T3S0737 Flavokawain A

2'-羟基-4,4',6'-三甲氧基查耳酮,Flavokavain A

Apoptosis; p38 MAPK Apoptosis; MAPK
Flavokawain A (Flavokavain A) 是 kava 提取物中的查耳酮,是一种抗癌试剂,具有抗肿瘤活性。它通过 Bax 蛋白依赖和线粒体依赖的凋亡途径诱导细胞凋亡,有潜力用于膀胱癌的相关研究。
TN1299 Desmethylglycitein

4',6,7-三羟基异黄酮,4',6,7-三羟异黄酮,6-羟基大豆苷元,6,7,4'-Trihydroxyisoflavone

PI3K; CDK; PKC Cell Cycle/Checkpoint; Chromatin/Epigenetic; Cytoskeletal Signaling; PI3K/Akt/mTOR signaling
Desmethylglycitein (6,7,4'-Trihydroxyisoflavone) 是大豆中苷元的代谢产物,具有抗氧化性和抗癌活性。它是蛋白激酶 C(PKC)α 的直接抑制剂,抑制正常人皮肤成纤维细胞中的太阳紫外线诱导的基质金属蛋白酶1。它在体内直接结合CDK1CDK2,抑制 CDK1CDK2 活性。
T75602 Albanol B

Albanol B 是一种芳基苯并呋喃衍生物,可从桑葚中分离得到。Albanol B 具有抗阿尔茨海默病、抗菌和抗氧化活性。Albanol B 抑制癌细胞增殖,下调 CDK1表达。Albanol B 还会诱导细胞周期停滞在 G2/M 期,诱导细胞凋亡 (apoptosis)。Albanol B 诱导线粒体 ROS 产生并增加 AKT 和 ERK1/2的磷酸化水平。

天然产物

Flavokawain A
Cat.No: T3S0737
Synonym: 2'-羟基-4,4',6'-三甲氧基查耳酮,Flavokavain A
Target: Apoptosis, p38 MAPK
Desmethylglycitein
Cat.No: TN1299
Synonym: 4',6,7-三羟基异黄酮,4',6,7-三羟异黄酮,6-羟基大豆苷元,6,7,4'-Trihydroxyisoflavone
Target: PI3K, CDK, PKC
Albanol B
Cat.No: T75602
Synonym:
Target:
Cat. No. Product Name Species Expression System
TMPY-04450 CDK1 & CCNE1 Heterodimer Protein, Human, Recombinant (His & GST)

P34CDC2 & CCNE1,CDC2,CDKN1,CD...

Human Baculovirus Insect Cells
CDK1 & CCNE1 Heterodimer Protein, Human, Recombinant (His & GST) is expressed in Baculovirus insect cells with His and GST tag. The predicted molecular weight is 109.7 kDa and the accession number is NP_001777.1&NP_001229.1.
TMPH-01167 CDK1 Protein, Human, Recombinant (His)

p34 protein kinase,Cell division control protein 2 homolog,C...

Human E. coli
CDK1 Protein, Human, Recombinant (His) is expressed in E. coli.
TMPY-04775 CDK1 Protein, Mouse, Recombinant (His & GST)

CDC2>,Cdc2,Cdc2a,p34<,cyclin-dependent kinase 1

Mouse Baculovirus Insect Cells
CDK1 Protein, Mouse, Recombinant (His & GST) is expressed in Baculovirus insect cells with His and GST tag. The predicted molecular weight is 61.9 kDa and the accession number is P11440.
TMPY-04549 CDK1 Protein, Human, Recombinant (GST)

CDC2,P34CDC2,CDC28A,cyclin-dependent kinase 1

Human Baculovirus Insect Cells
CDK1 Protein, Human, Recombinant (GST) is expressed in Baculovirus insect cells with GST tag. The predicted molecular weight is 60 kDa and the accession number is P06493-1.
TMPH-01703 CDC25C Protein, Human, Recombinant (His)

Dual specificity phosphatase Cdc25C,M-phase inducer phosphat...

Human E. coli
Functions as a dosage-dependent inducer in mitotic control. Tyrosine protein phosphatase required for progression of the cell cycle. When phosphorylated, highly effective in activating G2 cells into prophase. Directly dephosphorylates CDK1 and activates its kinase activity. CDC25C Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 57.4 kDa and the accession number is P30307.
TMPY-04542 CDK2 Protein, Human, Recombinant (His)

CDKN2,cyclin-dependent kinase 2,p33(CDK2)

Human Baculovirus Insect Cells
CDK2 is a member of the Ser/Thr protein kinase family. This protein kinase is highly similar to the gene products of S. cerevisiae cdc28, and S. pombe cdc2. It is a catalytic subunit of the cyclin-dependent protein kinase complex, whose activity is restricted to the G1-S phase, and essential for cell cycle G1/S phase transition. Cdks (cyclin-dependent kinases) are heteromeric serine/threonine kinases that control progression through the cell cycle in concert with their regulatory subunits, the c...
TMPH-02884 CTDP1 Protein, Mouse, Recombinant (His & Myc)

Fcp1,Ctdp1,RNA polymerase II subunit A C-t...

Mouse E. coli
Processively dephosphorylates 'Ser-2' and 'Ser-5' of the heptad repeats YSPTSPS in the C-terminal domain of the largest RNA polymerase II subunit. This promotes the activity of RNA polymerase II. Plays a role in the exit from mitosis by dephosphorylating crucial mitotic substrates (USP44, CDC20 and WEE1) that are required for M-phase-promoting factor (MPF)/CDK1 inactivation. CTDP1 Protein, Mouse, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The p...
TMPY-01401 Cyclin A1 Protein, Human, Recombinant (His)

cyclin A1,CT146

Human Baculovirus Insect Cells
Cyclin A1 is a member of the highly conserved cyclin family that is characterized by a dramatic periodicity in protein abundance, and belongs to the A-type cyclin subfamily. The mammalian A-type cyclin family consists of two members: cyclin A1 and cyclin A2. Different cyclins exhibit distinct expression. Cyclin A1 is expressed in mice exclusively in the germ cell lineage and high rate of cyclinA1 is found in human testis and certain myeloid leukaemia cells. Cyclin A1 is primarily function in the...
TMPH-01552 IRF1 Protein, Human, Recombinant (GST & His)

Human Baculovirus Insect Cells
Transcriptional regulator which displays a remarkable functional diversity in the regulation of cellular responses. Regulates transcription of IFN and IFN-inducible genes, host response to viral and bacterial infections, regulation of many genes expressed during hematopoiesis, inflammation, immune responses and cell proliferation and differentiation, regulation of the cell cycle and induction of growth arrest and programmed cell death following DNA damage. Stimulates both innate and acquired imm...

重组蛋白

CDK1 & CCNE1 Heterodimer Protein, Human, Recombinant (His & GST)
Cat.No: TMPY-04450
Species: Human
Expression System: Baculovirus Insect Cells
CDK1 Protein, Human, Recombinant (His)
Cat.No: TMPH-01167
Species: Human
Expression System: E. coli
CDK1 Protein, Mouse, Recombinant (His & GST)
Cat.No: TMPY-04775
Species: Mouse
Expression System: Baculovirus Insect Cells
CDK1 Protein, Human, Recombinant (GST)
Cat.No: TMPY-04549
Species: Human
Expression System: Baculovirus Insect Cells
CDC25C Protein, Human, Recombinant (His)
Cat.No: TMPH-01703
Species: Human
Expression System: E. coli
CDK2 Protein, Human, Recombinant (His)
Cat.No: TMPY-04542
Species: Human
Expression System: Baculovirus Insect Cells
CTDP1 Protein, Mouse, Recombinant (His & Myc)
Cat.No: TMPH-02884
Species: Mouse
Expression System: E. coli
Cyclin A1 Protein, Human, Recombinant (His)
Cat.No: TMPY-01401
Species: Human
Expression System: Baculovirus Insect Cells
IRF1 Protein, Human, Recombinant (GST & His)
Cat.No: TMPH-01552
Species: Human
Expression System: Baculovirus Insect Cells
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