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CDK Related Products (488)
Related Products (488)
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CDK1/CycE1 Recombinant Human Active Protein Kinase
0 ImagesCat. No.: HY-E70654CDK1 is a cyclin-dependent kinase that functions as a serine/threonine protein kinase, and is a key player in cell cycle regulation. CDK1/CycA1 Recombinant Human Active Protein Kinase is an ortholog of CDK1. -
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CDK4/6-IN-22
0 ImagesCat. No.: HY-161978CAS No.: 3036014-62-4 -
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Telapristone acetate
0 ImagesCat. No.: HY-16483CAS No.: 198414-31-2Synonyms: CDB-4124Telapristone acetate (CDB-4124) is a potent progesterone receptor (PR) modulator. Telapristone acetate inhibits the proliferation of ovarian cancer cells by inducing cell cycle arrest and apoptosis. Telapristone effectively inhibits the occurrence and development of spontaneous and chemically induced mammary tumors in rats. Telapristone acetate can be used for breast and ovarian cancer research. -
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- JHD205
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Aloisine B
0 ImagesCat. No.: HY-118902CAS No.: 496864-14-3Aloisine B (compound 9) is a cyclin-dependent kinase (CDK) inhibitor. Aloisine B inhibits cell proliferation by arresting cells in both G1 and G2 via competing with ATP-binding pocket. -
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Garcinone C (Standard)
0 ImagesCat. No.: HY-N6954RCAS No.: 76996-27-5Garcinone C (Standard) is the analytical standard of Garcinone C. This product is intended for research and analytical applications. Garcinone C, a xanthone derivative, is a natural compound extracted from Garcinia oblongifolia that is used as an anti-inflammatory, astringency and granulation-promoting medicine, and has potential cytotoxic effects on certain cancers. Garcinone C stimulates the expression levels of ATR and 4E-BP1, arrests the cell cycle, inhibits cell viability of the human Nasopharyngeal carcinoma (NPC) cell lines CNE1, CNE2, HK1 and HONE1 in a time‑ and dose‑dependent manner through inhibition of Hedgehog signaling pathway. Garcinone C is orally active. -
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Cdk1 Rat Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS02350 -
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Cyclin A/B RxL-IN-1
0 ImagesCat. No.: HY-175729CAS No.: 3036231-62-3Cyclin A/B RxL-IN-1 is a inhibitor targeting the Cyclin A/B RxL interaction at the hydrophobic patch (HP). Cyclin A/B RxL-IN-1 inhibits Cyclin A with an IC50 of 0.12 μM. Cyclin A/B RxL-IN-1 demonstrates antitumor efficacy in mouse cell line-derived xenograft (CDX) models. CDK-IN-19 can be used for the study of E2F-driven cancers such as small-cell lung cancer (SCLC). -
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Cdk2 Rat Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS02376 -
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CDK3/CycE2 Recombinant Human Active Protein Kinase
0 ImagesCat. No.: HY-E70679CDK3 is a major player driving retinoblastoma (Rb) phosphorylation during the G0/G1 transition and in the early G1 phase of the cell cycle. CDK3 interacts with various transcription factors involved in cell proliferation, differentiation, and transformation driven by the EGFR/Ras signaling pathway. CDK3/CycE2 Recombinant Human Active Protein Kinase is an ortholog of CDK3. -
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EGFR/HER2/CDK9-IN-3
0 ImagesCat. No.: HY-147798CAS No.: 422276-47-9 -
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- YL-1-9
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(R)-PHA533533
0 ImagesCat. No.: HY-162683ACAS No.: 437982-90-6(R)-PHA533533 is an inactive enantiomer (S)-PHA533533 (active enantiomer) (HY-162683). (S)-PHA533533 is a CDK2 inhibitor with antitumor activity. -
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EGFR/HER2/CDK9-IN-1
0 ImagesCat. No.: HY-147796CAS No.: 879730-44-6 -
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MFDCH016
0 ImagesCat. No.: HY-178350MFDCH016 is a potent HDAC1/6 (IC50 = 38/59 nM) and CDK4/6 (IC50 = 680/720 nM) inhibitor. MFDCH016 induces apoptosis and cell cycle arrest in G2/M and G0/G1 phases in MCF-7 cells. MFDCH016 can modulate the HDAC-p21-CDK signaling pathway, increasing the levels of acetylated H3 and p21. MFDCH016 can be used for the study of breast cancer. -
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SB-1295
0 ImagesCat. No.: HY-155065SB-1295 is an orally active CDK9/T1 inhibitor (IC50=0.17 μM). SB-1295 shows antiproliferative activity in HCT 116 and MIA PaCa-2 cells. SB-1295 also induces MIA PaCa-2 cell death by inducing intracellular ROS production, reducing mitochondrial membrane potential and inducing apoptosis. SB-1295 has the potential to study cancer. -
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- Protein kinase inhibitor 11
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CDK9-IN-31 dimaleate
0 ImagesCat. No.: HY-160171ACDK9-IN-31 dimaleate (Compound Z1) is a CDK9 inhibitor that inhibits cancer cell growth. CDK9-IN-31 dimaleate has the potential to be developed as an anticancer agent. -
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Metralindole
0 ImagesCat. No.: HY-124321ACAS No.: 54188-38-4Metralindole is an inhibitor of human cyclin-dependent kinase CDK2 and human protein kinase CK2 holoenzyme. Metralindole shows good potential as a non-small cell lung cancer inhibitor. -
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Dendrobine (Standard)
0 ImagesDendrobine (Standard) is the analytical standard of Dendrobine. This product is intended for research and analytical applications. Dendrobine is an alkaloid isolated from Dendrobium nobile. Dendrobine possesses antiviral activity against influenza A viruses, with IC50s of 3.39 μM, 2.16 μM and 5.32 μM for A/FM-1/1/47 (H1N1), A/Puerto Rico/8/34 H274Y (H1N1) and A/Aichi/2/68 (H3N2), respectively. Dendrobine activates the JNK/p38/Nrf2 signaling pathway. Dendrobine exhibits antiviral, antitumor, anti-inflammatory, and neuroprotective properties. -
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