7 Results for "

MLLT1

" in MedChemExpress (MCE) Product Catalog:
Products (7)

7 Results for "MLLT1" in MCE Product Catalog:

2
2 Cited Publications
Cat. No.: HY-112804
CAS No.: 2255338-25-9
Purity:  99.33%
Research Areas:  

Cancer

SGC-iMLLT is a first-in-class chemical probe and a potent, selective inhibitor of MLLT1/3-histone interactions with an IC50 of 0.26 μM. SGC-iMLLT shows high binding activity towards MLLT1 YEATS domain (YD) and MLLT3 YD (AF9/YEATS3) with Kds of 0.129 and 0.077 μM, respectively [1].
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Cat. No.: HY-160287
CAS No.: 2561471-13-2
Research Areas:  

Cancer

NVS MLLT-1 (compound 3), a chemical probe, is a potent and selective MLLT1 inhibitor with Kd values of 0.18 μM, 0.24 μM, and 0.22 μM for wild-type, T1 mutants, and T3 mutants, respectively [1] .
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Cat. No.: HY-155412
CAS No.: 2675452-91-0
Purity:  ≥99.0%
Research Areas:  

Cancer

PFI-6 is a selective MLLT1 and MLLT3 YEATS domain probe with IC50 values of 0.14 μM and 0.16 μM, respectively. PFI-6 is applicable for cancer research [1].
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Cat. No.: HY-RS08493
Research Areas:  

Others

MLLT1 Human Pre-designed siRNA Set A contains three designed siRNAs for MLLT1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-181834
CAS No.: 3111054-37-3
Research Areas:  

Cancer

PROTAC MLLT1 Degrader-1 is a PROTAC degrader targeting MLLT1. PROTAC MLLT1 Degrader-1 inhibits AML cell proliferation and viability, suppresses tumor growth in human AML xenograft models, and can block the oncogene transcriptional program. PROTAC MLLT1 Degrader-1 can be used for the research of MLL-rearranged acute myeloid leukemia (AML) [1].
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Cat. No.: HY-176821
CAS No.: 2650530-01-9
Research Areas:  

Cancer

PFI-6N is a negative control compound of PFI-6 (HY-155412). PFI-6N is completely inactive against YEATS domain (MLLT1/3 and YEATS2/4) by methylating the amide of PFI-6 [1].
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Cat. No.: HY-184342
Research Areas:  

Cancer

SYC-2863 is a CRBN-recruiting PROTAC degrader that selectively degrades ENL (MLLT1), with an ENL DC50 of 45 nM in MV4;11 cells. SYC-2863 inhibits the proliferation of MLL-rearranged leukemia and multiple myeloma cells. After degrading intracellular ENL, SYC-2863 dose-dependently downregulates the transcription levels of MYC and its downstream target genes, blocking the MYC-mediated malignant proliferation pathway. SYC-2863 can be used in studies related to MLL-rearranged leukemia and multiple myeloma [1].
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