255 Results for "

MCL

" in MedChemExpress (MCE) Product Catalog:
Products (255)

255 Results for "MCL" in MCE Product Catalog:

Cat. No.: HY-129700
CAS No.: 2163793-44-8
Purity:  99.05%
Target:  

Bcl-2 Family

Research Areas:  

Cancer

MCL-1/BCL-2-IN-2 is a Mcl-1 and Bcl-2 inhibitor with IC50 values of 5.4 and 7.66 μM. MCL-1/BCL-2-IN-2 is applicable to the research of Mcl-1-dependent cancers .
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Cat. No.: HY-176142
Research Areas:  

Cancer

YX0798 is a selective and orally active CDK9 inhibitor (Kd: 0.28 nM). YX0798 downregulates the oncoprotein c-MYC and pro-survival protein MCL-1. YX0798 disrupts the cell cycle and results in transcriptomic reprogramming, eventually leading to cell apoptosis. YX0798 has antitumor activity .
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Cat. No.: HY-122627
CAS No.: 678158-55-9
Purity:  99.14%
Target:  

Bcl-2 Family Apoptosis

Research Areas:  

Cancer

CLZ-8 (Compound 8) is an orally active Mcl-1-PUMA interface inhibitor, with a Ki of 0.3 μM. CLZ-8 exhibits dual activity on reduce PUMA-dependent apoptosis while deactivating Mcl-1-mediated anti-apoptosis in cancer cells .
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Cat. No.: HY-128360
CAS No.: 2351218-88-5
Research Areas:  

Cancer

dMCL1-2 is a potent, selective MCL1 PROTAC degrader based on a Cereblon ligand, with a KD value of 30 nM for binding to MCL1. dMCL1-2 induces ubiquitination and degradation of MCL1. dMCL1-2 degrades MCL1, cleaves Caspase-3, and induces Apoptosis. dMCL1-2 can be used in research related to multiple myeloma .
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Cat. No.: HY-129702
CAS No.: 2163793-56-2
Target:  

Bcl-2 Family

Research Areas:  

Cancer

MCL-1/BCL-2-IN-4 (Compound 7) is a potent and selective Mcl-1 and Bcl-2 dual inhibitor .
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Cat. No.: HY-129681
CAS No.: 2493256-46-3
Purity:  99.86%
Target:  

Bcl-2 Family

Research Areas:  

Cancer

MCL-1/BCL-2-IN-2 (Compound Nap-1) is a potent and selective Mcl-1 and Bcl-2 dual inhibitor with IC50s of 4.45 and 3.18 μM, respectively .
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Cat. No.: HY-16695
CAS No.: 509102-00-5
Synonyms: Inhibitor of MCL-1
Target:  

Bcl-2 Family

Research Areas:  

Cancer

MIM-1 is an inhibitor of myeloid cell factor 1 (Mcl-1).
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Cat. No.: HY-15805
CAS No.: 330786-01-1
Purity:  98.01%
Target:  

Src Btk

Research Areas:  

Cancer

KIN-8194 is an orally active dual inhibitor of HCK and BTK, with IC50 values of 0.915 and <0.495 nM, respectively. KIN-8194 impairs growth and integrin-mediated adhesion of BTKi-resistant mantle cell lymphoma (MCL). KIN-8194 overcomes ibrutinib (HY-10997) resistance with a survival benefit in TMD-8 ABC DLBCL xenografted mice .
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Cat. No.: HY-101778
CAS No.: 315698-17-0
Purity:  98.98%
Synonyms: EU-5346
Target:  

Bcl-2 Family

Research Areas:  

Cancer

ML311 is a potent and selective inhibitor of the Mcl-1/Bim interaction.
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Cat. No.: HY-16669
CAS No.: 713492-66-1
Target:  

Bcl-2 Family

Research Areas:  

Cancer

Mcl1-IN-1 is an inhibitor of myeloid cell factor 1 (Mcl-1) (IC50=2.4 µM).
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Cat. No.: HY-155472
CAS No.: 892250-00-9
Purity:  ≥98.0%
Target:  

Bcl-2 Family

Research Areas:  

Cancer

Mcl-1 inhibitor 17 is a Mcl-1 protein inhibitor. Mcl-1 inhibitor 17 can be used for the research of cancer and other diseases .
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Cat. No.: HY-122830
CAS No.: 2366132-45-6
Purity:  98.72%
Target:  

PROTACs Btk NF-κB

Research Areas:  

Cardiovascular Disease Cancer

DD-03-171 is a PROTAC BTK degrader. DD-03-171 inhibits mantle cell lymphoma (MCL) cell proliferation (IC50 = 5.1 nM) and prolongs the survival of mice bearing a lymphoma PDX model by degrading BTK, IKFZ1, and IKFZ3. DD-03-171 also inhibits platelet function and thrombosis. (Pink: BTK ligand 9 (HY-168292); Black: linker (HY-28875); Blue: Thalidomide-NH-CH2-COOH (HY-131717)) .
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Cat. No.: HY-12422A
CAS No.: 1000023-05-1
Purity:  99.23%
Target:  

CDK

Research Areas:  

Cancer

Voruciclib hydrochloride is an orally active and selective CDK inhibitor with Ki values of 0.626 nM-9.1 nM. Voruciclib hydrochloride potently blocks CDK9, the transcriptional regulator of MCL-1. Voruciclib hydrochloride represses expression of MCL-1 in multiple models of diffuse large B-cell lymphoma (DLBCL) .
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Cat. No.: HY-P991225

Target:  

Fc Receptor (FcR) CD20

Research Areas:  

Inflammation/Immunology Cancer

BI-1206 is a recombinant and antagonistic human monoclonal antibody targeting FcγRIIB (CD32B). BI-1206 can block CD20 internalization induced by Rituximab (HY-P9913) itself or combined with others including Ibrutinib (HY-10997), Venetoclax (HY-15531), and CHOP. BI-1206 can enhance or recover the activity of Rituximab or other anti-CD20 monoclonal antibodies. BI-1206 has cytolytic activity against malignant B cells. BI-1206 can be studied for cancer research such as mantle cell lymphoma (MCL) .
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Cat. No.: HY-163681
CAS No.: 2388470-64-0
Target:  

Bcl-2 Family

Research Areas:  

Cancer

Zamzetoclax (compound 1) is a potential Mcl-1 inhibitor .
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Cat. No.: HY-101533A
CAS No.: 2143010-83-5
Target:  

Bcl-2 Family

Research Areas:  

Cancer

AZD-5991 Racemate is the racemate of AZD-5991. AZD-5991 Racemate is a Mcl-1 inhibitor with an IC50 of <3 nM in FRET assay.
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Cat. No.: HY-148203
CAS No.: 1883727-31-8
Target:  

Bcl-2 Family

Research Areas:  

Cancer

Mcl-1 inhibitor 9 (example 2) is a myeloid cell leukemia 1 (Mcl-1) inhibitor with IC50 value of 0.21889 nM. Mcl-1 inhibitor 9 shows anti-tumor activity .
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Cat. No.: HY-129701
CAS No.: 2163793-55-1
Purity:  99.22%
Target:  

Bcl-2 Family

Research Areas:  

Cancer

MCL-1/BCL-2-IN-3 (Compound 2) is a potent and selective Mcl-1 and Bcl-2 dual inhibitor with IC50s of 5.95 and 4.78 μM, respectively .
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Cat. No.: HY-RS08230
Research Areas:  

Others

MCL1 Human Pre-designed siRNA Set A contains three designed siRNAs for MCL1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-164466
CAS No.: 2682205-20-3
Target:  

Calcium Channel Notch

Research Areas:  

Cancer

CAD204520, a SERCA inhibitor (IC50 = 0.34 μM), targets mutated over wild type NOTCH1 proteins in T-cell acute lymphoblastic leukemia (T-ALL) and mantle cell lymphoma (MCL). CAD204520 can be used for T-ALL and MCL research .
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