10 Results for "

mouse leukemia systems

" in MedChemExpress (MCE) Product Catalog:
Products (10)

10 Results for "mouse leukemia systems" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-U00442
CAS No.: 501935-96-2
Research Areas:  

Cancer

CTX1 is a p53 activator that overcomes HdmX-mediated p53 repression. CTX1 exhibits potent anti-cancer activity in a mouse acute myeloid leukemia (AML) model system .
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1
1 Cited Publications
Cat. No.: HY-N1391
CAS No.: 78432-77-6
Synonyms: 10-Deacetylpaclitaxel
10-Deacetyltaxol (10-Deacetylpaclitaxel) is a taxane derivative found in Taxus wallichiana Zucc. and exhibits cytotoxicity against human neurotumor cell lines. It shows a concentration-dependent cytotoxic effect on cancer cells and demonstrates activity in the mouse leukemia system. 10-Deacetyltaxol can be used for research on neuroblastoma, glioblastoma multiforme, and lymphocytic leukemia .
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Cat. No.: HY-169093
CAS No.: 2768610-97-3
Research Areas:  

Cancer

MS41 is a ENL PROTAC degrader with a DC50 of 3.50 nM. MS41 recruits the VHL E3 ubiquitin ligase, triggers ENL degradation via the ubiquitin-proteasome system, and simultaneously induces AF9 degradation. MS41 reduces the chromatin occupancy of ENL-associated transcription elongation complexes, suppresses oncogene expression, and activates differentiation gene expression. MS41 inhibits leukemia cell growth and induces cell cycle arrest and apoptosis. MS41 inhibits leukemia progression in xenograft mouse models. MS41 can be used for research on mixed lineage leukemia-rearranged leukemia and nephroblastoma .
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Cat. No.: HY-170574
CAS No.: 3093767-34-8
Research Areas:  

Cancer

CQ627 is a molecular glue degrader of right open reading frame kinase 2 (RIOK2). CQ627 inhibits the ATPase activity of RIOK2 in MOLT-4 cells with an IC50 of 98 nM. By recruiting the E3 ubiquitin ligase RNF126, CQ627 promotes RIOK2 ubiquitination and induces its degradation via the ubiquitin-proteasome system (UPS), while inhibiting RIOK2-dependent mTOR/AKT signaling, suppressing cancer cell proliferation, and inducing G2/M cell cycle arrest and apoptosis. CQ627 can be used in studies related to RIOK2-targeted protein degradation and leukemia .
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Cat. No.: HY-N1391R
CAS No.: 78432-77-6
Synonyms: 10-Deacetylpaclitaxel (Standard)
10-Deacetyltaxol (Standard) (10-Deacetylpaclitaxel (Standard)) is the analytical standard of 10-Deacetyltaxol (HY-N1391). This product is intended for research and analytical applications. 10-Deacetyltaxol (10-Deacetylpaclitaxel) is a taxane derivative found in Taxus wallichiana Zucc. and exhibits cytotoxicity against human neurotumor cell lines. It shows a concentration-dependent cytotoxic effect on cancer cells and demonstrates activity in the mouse leukemia system. 10-Deacetyltaxol can be used for research on neuroblastoma, glioblastoma multiforme, and lymphocytic leukemia .
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Cat. No.: HY-149328
CAS No.: 3033545-34-2
phoBET1 is a photolabile PROTAC molecule that, upon photoactivation, functions as a BRD4 PROTAC degrader to trigger BRD4 degradation via the ubiquitin-proteasome system. Activated phoBET1 induces cancer cell apoptosis and inhibits tumor growth in xenograft mouse models. In its inactive caged state, phoBET1 exhibits only extremely low antiproliferative activity against cancer cells. phoBET1 can be applied in studies related to acute myeloid leukemia .
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Cat. No.: HY-181867
CAS No.: 2410947-65-6
Research Areas:  

Cancer

PROTAC BET Degrader-16 (Compound A10) is a BET PROTAC degrader with a DC50 of 0.31 nM against BRD4, and it preferentially targets BRD4 over other BET family members. PROTAC BET Degrader-16 degrades BRD2, BRD3 and BRD4 via the ubiquitin-proteasome system, a process that requires target binding and recruitment of the CRBN E3 ligase. PROTAC BET Degrader-16 induces cell cycle arrest and promotes apoptosis. PROTAC BET Degrader-16 exerts anti-tumor activity against acute myeloid leukemia .
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Cat. No.: HY-181869
CAS No.: 2409674-38-8
Research Areas:  

Cancer

PROTAC BET Degrader-17 is a potent BET protein PROTAC degrader. By recruiting the VHL E3 ligase, PROTAC BET Degrader-17 specifically degrades BRD2, BRD3 (DC50=0.09 nM) and BRD4 (IC50=4.3 nM). PROTAC BET Degrader-17 exhibits strong anti-tumor activity in acute myeloid leukemia (AML) studies; it not only inhibits cancer cell proliferation, induces cell cycle arrest and apoptosis, but also effectively suppresses tumor growth in xenograft mouse models. PROTAC BET Degrader-17 can be used to explore targeted therapies for acute myeloid leukemia .
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Cat. No.: HY-113798
CAS No.: 112887-62-4
Research Areas:  

Cancer

ICI 198583 is a thymidylate synthase (TS) inhibitor with a Ki value of 10 nM for both mouse and human TS. ICI 198583 serves as a substrate for folylpolyglutamate synthetase (FPGS) with a Km of 40 μM. ICI 198583 exerts persistent, dose-dependent inhibition on thymidylate synthase flux in mice. ICI 198583 is applicable to relevant research on leukemia .
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Cat. No.: HY-P991896
Synonyms: AT14-012
AT1412 is a CD9-binding antibody. AT1412 binds to the tetraspanin protein CD9 and modulates CD9 function by enhancing T cell adhesion to endothelial cells (HUVECs) and transendothelial migration. AT1412 binds to B-ALL cell lines but not to T-ALL. AT1412 induces antibody-dependent cellular cytotoxicity in B-ALL cell lines. AT1412 binds to melanoma cells, B-ALL, gastric cancer, colorectal cancer, and pancreatic cancer cells [1] .
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