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Search Results for " cyclin b1 "
Targets Recommended: Apoptosis 5-HT Receptor

13

抑制剂 & 化合物

3

天然产物

2

重组蛋白

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Cat. No. Product Name Target Signaling Pathways
T8445 PU02

PU-02,6-[(1-Naphthalenylmethyl)thio]-9H-purine

Apoptosis; 5-HT Receptor Apoptosis; GPCR/G Protein; Neuroscience
PU02 (6-[(1-Naphthalenylmethyl)thio]-9H-purine) 是5-HT3受体的负变构调节剂,是 6-MP 的一个衍生物。它在 HEK293 细胞测得的转染 5-HT3A 和 5-HT3AB 受体后的 IC50值分别为 0.36 和 0.73 μM。
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。
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。
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 CDK1 抑制剂,可以抑制 CDK1、CDK1/cyclin B1 和 CDK2/cyclin E (Ki=20/35/340 nM),具有选择性和 ATP 竞争性。Ro-3306 具有抗肿瘤活性,可以抑制细胞周期阻滞,诱导细胞凋亡。
T73196 RGB-286638

Others Others
RGB-286638 是一种有效的 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;同时可抑制GSK-3β,TAK1,Jak2和MEK1,IC50值分别为 3,5,50,和 54 nM。
T78647 PROTAC BRD4 Degrader-16

PROTACs PROTAC
PROTACBRD4Degrader-16是一种高效的PROTAC BRD4降解剂,具有对BRD4(BD1)和BRD4(BD2)分别为34.58 nM及40.23 nM的IC50值。该化合物有效抑制G2/M阶段细胞周期蛋白B1Cyclin B1)的表达,并显著诱导MV-4-11细胞的细胞凋亡(apoptosis)。
T70527 DAT-230

Others Others
DAT-230 is a promising microtubule inhibitor that has great potential for the treatment of fibrosarcoma in vitro and in vivo. DAT-230 exhibited potent anti-proliferative activity against various cancer cells. DAT-230 -treatment in HT-1080 cells resulted in microtubule de-polymerization and G2/M phase arrest preceding apoptosis. Phosphor-cdc2 (thr14/tyr15) reduction, cyclin B1 accumulation and aberrant spindles denoted the cyclin B1-cdc2 complex active and M phase arrest in HT-1080 cells treated ...
T74270 PROTAC BRD4 Degrader-17

Others Others
PROTACBRD4 Degrader-17 (compound 13i),作为一种高效的 PROTACBRD4 降解剂,其 IC50 值分别为 29.54 nM(针对 BRD4(BD1))和 3.82 nM(针对 BRD4(BD2))。该化合物有效抑制 G2/M 相的细胞周期蛋白 B1 (Cyclin B1) 的表达,并在 MV-4-11 细胞中显著诱导细胞凋亡(apoptosis)。
T28092 MPT0B206

Others Others
MPT0B206 is a novel tubulin polymerization inhibitor. MPT0B206 induced G2/M cell cycle arrest and the appearance of the mitotic marker MPM-2 in K562 and K562R cells, which is associated with the upregulation of cyclin B1 and the dephosphorylation of Cdc2.
T60737 LG308

Others Others
LG308 是一种新型合成化合物,具有抗微管活性。LG308 诱导细胞凋亡和细胞死亡,并且显著抑制肿瘤生长,具有前列腺癌的研究潜力。LG308 诱导有丝分裂阻滞并显着抑制 G2/M 的进程,这与细胞周期蛋白 B1 和有丝分裂标志物 MPM-2 的上调以及 cdc2 的去磷酸化有关。
T61369 p53 Activator 2

Others Others
p53 Activator 2 (compound 10ah) 插入DNA,导致显著的DNA双链断裂。该化合物通过增加p53、p-p53、CDK4、p21的表达,使细胞周期在G2/M期停滞,诱导细胞凋亡,并显著降低抗凋亡蛋白Bcl-2、Bcl-xL和cyclin B1的水平。此外,p53 Activator 2表现出对MGC-803细胞的抗增殖效果,其IC50为1.73 μM,且在MGC-803异种移植肿瘤模型中展示出有效的抗癌活性。
T71217 MPT0B214

Others Others
MPT0B214 is a novel and potent microtubule inhibitor with potential anticancer activity. MPT0B214 inhibited tubulin polymerization through strongly binding to the tubulin's colchicine-binding site and had cytotoxic activity in a variety of human tumor cell lines. After treatment with MPT0B214, KB cells were arrested in the G2-M phase before cell death occurred, which were associated with upregulation of cyclin B1, dephosphorylation of Cdc2, phosphorylation of Cdc25C and elevated expression of th...
T35696 Olomoucine II

Others Others
Olomoucine II is an inhibitor of cyclin-dependent kinases (CDKs; IC50s = 7.6, 0.1, 19.8, 0.45, and 0.06 μM for Cdk1, -2, -4, -7, and -9, respectively).1It is selective for CDKs over 10 additional kinases (IC50s = >100 μM for all) but does inhibit ERK2 (IC50= 32 μM) and the ATP-binding cassette transporter B1 (ABCB1; IC50= 6.4 μM).1,2Olomoucine II inhibits proliferation of a variety of cancer cells, including those expressing wild-type p53 or mutant p53 (mean IC50s = 7.4 and 10.1 μM, respectively...

化合物

PU02
Cat.No: T8445
Synonym: PU-02,6-[(1-Naphthalenylmethyl)thio]-9H-purine
Target: Apoptosis, 5-HT Receptor
RGB-286638 free base
Cat.No: T2378
Synonym:
Target: GSK-3, MEK, JAK, CDK
H1k
Cat.No: T72057
Synonym:
Target: CDK
Ro-3306
Cat.No: T2356
Synonym:
Target: Apoptosis, ERK, SGK, PKA, CDK, PKC
RGB-286638
Cat.No: T73196
Synonym:
Target: Others
PROTAC BRD4 Degrader-16
Cat.No: T78647
Synonym:
Target: PROTACs
DAT-230
Cat.No: T70527
Synonym:
Target: Others
PROTAC BRD4 Degrader-17
Cat.No: T74270
Synonym:
Target: Others
MPT0B206
Cat.No: T28092
Synonym:
Target: Others
LG308
Cat.No: T60737
Synonym:
Target: Others
p53 Activator 2
Cat.No: T61369
Synonym:
Target: Others
MPT0B214
Cat.No: T71217
Synonym:
Target: Others
Olomoucine II
Cat.No: T35696
Synonym:
Target: Others
Cat. No. Product Name Target Signaling Pathways
T5S1467 Cucurbitacin E

CDK; Autophagy Autophagy; Cell Cycle/Checkpoint
Cucurbitacin E 是从黄瓜的攀缘茎中分离得到的一种天然产物。它显着抑制细胞周期蛋白B1/CDC2复合物的活性,具有预防神经变性,具有强效的抗增殖、抗肿瘤、抗炎和镇痛作用行动。
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。
T3824 Jaceosidin

Apoptosis; BCL; COX; UGT Apoptosis; Immunology/Inflammation; Metabolism; Neuroscience
Jaceosidin 是从毛莲蒿中得到的一种黄酮类天然产物,可激活Bax,下调 Mcl-1 和 c-FLIP 的表达,诱导癌细胞凋亡。它能够降低炎性因子水平,激活 NF-κB,抑制COX-2的表达,具有抗癌和抗炎作用。

天然产物

Cucurbitacin E
Cat.No: T5S1467
Synonym:
Target: CDK, Autophagy
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
Jaceosidin
Cat.No: T3824
Synonym:
Target: Apoptosis, BCL, COX, UGT
Cat. No. Product Name Species Expression System
TMPH-00081 CDKB1-2 Protein, Arabidopsis thaliana, Recombinant (His)

CDKB1-2,CDKB1;2,Cyclin-dependent ...

Arabidopsis thaliana P. pastoris (Yeast)
Together with CDKB1-1, promotes both the last division in the stomatal cell lineage as well as the number of stomata. In collaboration with MYB124 and MYB88, restrict the G1/S transition and chloroplast and nuclear number during stomatal formation, and normally maintain fate and developmental progression throughout the stomatal cell lineage. CDKB1-2 Protein, Arabidopsis thaliana, Recombinant (His) is expressed in yeast with N-6xHis tag. The predicted molecular weight is 37.6 kDa and the accessio...
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...

重组蛋白

CDKB1-2 Protein, Arabidopsis thaliana, Recombinant (His)
Cat.No: TMPH-00081
Species: Arabidopsis thaliana
Expression System: P. pastoris (Yeast)
CDK2 Protein, Human, Recombinant (His)
Cat.No: TMPY-04542
Species: Human
Expression System: Baculovirus Insect Cells
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