97 Results for "

GSPT

" in MedChemExpress (MCE) Product Catalog:
Products (97)

97 Results for "GSPT" in MCE Product Catalog:

Cat. No.: HY-RS05868
Research Areas:  

Others

GSPT1 Human Pre-designed siRNA Set A contains three designed siRNAs for GSPT1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS05869
Research Areas:  

Others

GSPT2 Human Pre-designed siRNA Set A contains three designed siRNAs for GSPT2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-143435
CAS No.: 329706-62-9
AG6033 is a CRBN-dependent molecular glue degrader targeting GSPT1 (DC50 of 2.5 μM) and IKZF1. AG6033 induces degradation of GSPT1 via π-π stacking and hydrogen bonding with CRBN in a partially CRBN-dependent manner, decreases IKZF1 levels, and promotes degradation of CRBN substrates. AG6033 induces apoptosis in lung adenocarcinoma cells. AG6033 can be used for the research of lung cancer .
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Cat. No.: HY-159622
CAS No.: 3024909-51-8
Target:  

Drug Intermediate

Research Areas:  

Cancer

Boc-Pip-C-oxotetrahydropyrimidin-bromophenyl is a synthetic intermediate for molecular glue. Boc-Pip-C-oxotetrahydropyrimidin-bromophenyl can be used in synthesis GSPT1 degrader-9 (HY-159610) .
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Cat. No.: HY-163938A
CAS No.: 3033871-15-4
Research Areas:  

Cancer

PROTAC erf3a Degrader-2 (Compound C59) is an orally active PROTAC erf3a Degrader. PROTAC erf3a Degrader-2 inhibits protein expression of SRD5A3 and GSPT1(eRF3a). PROTAC erf3a Degrader-2 inhibits cancer cell proliferation (eg: 22Rv1). PROTAC erf3a Degrader-2 can be used for research of prostate cancer, ovarian cancer, liver cancer, cervical cancer, leukemia, breast cancer .
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Cat. No.: HY-159623
CAS No.: 3024909-50-7
Target:  

Drug Intermediate

Research Areas:  

Cancer

Thalidomide 5-Pip-C-oxotetrahydropyrimidin-bromophenyl is a synthetic intermediate for molecular glues. Thalidomide 5-Pip-C-oxotetrahydropyrimidin-bromophenyl can be used to synthesize GSPT1 degrader-9 (HY-159610) .
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Cat. No.: HY-159619
CAS No.: 3034310-18-1
Target:  

PROTAC Linkers

Research Areas:  

Cancer

Boc-azetidine-2C-oxotetrahydropyrimidin-bromophenyl is a PROTAC Linker. Boc-azetidine-2C-oxotetrahydropyrimidin-bromophenyl can be used in the synthesis of PROTAC GSPT1 degrader-1 (HY-159609) .
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Cat. No.: HY-W599025
CAS No.: 2914920-46-8
Target:  

Drug Intermediate

Research Areas:  

Cancer

5-Br-4-Cl-Pyrrolo-pyroxypyridine is a synthetic intermediate for molecular glues. 5-Br-4-Cl-Pyrrolo-pyroxypyridine can be used for synthesis GSPT1 degrader-9 (HY-159609) .
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Cat. No.: HY-159620
CAS No.: 3034310-00-1
Research Areas:  

Cancer

Thalidomide 5-azetidine-2C-oxotetrahydropyrimidin-bromophenyl is an E3 Ligase Ligand-Linker Conjugate. Thalidomide 5-azetidine-2C-oxotetrahydropyrimidin-bromophenyl can be used to synthesize PROTAC GSPT1 degrader-1 (HY-159609) .
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Cat. No.: HY-132862
CAS No.: 2711006-74-3
Target:  

PROTACs

Research Areas:  

Cancer

ZXH-4-137 is a CRBN PROTAC degrader. ZXH-4-137 brings CRBN and VHL E3 ligase into proximity, induces CRBN ubiquitination and proteasomal degradation, and exhibits high selectivity for CRBN. ZXH-4-137 blocks the degradation of CRBN-dependent target proteins such as GSPT1 and CDK9. ZXH-4-137 serves as a chemical knockdown tool compound for investigating CRBN-dependent biological processes .
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Cat. No.: HY-177751
Research Areas:  

Cancer

GSPT1 degrader-12 is a selective molecular glue GSPT1 degrader. GSPT1 degrader-12 exhibits antiproliferative activity against cancer cells in a CRBN- and GSPT1-dependent manner. GSPT1 degrader-12 can be used for leukemia research .
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Cat. No.: HY-188006
CAS No.: 3052938-18-5
Research Areas:  

Cancer

GSPT1 degrader-18 is a GSPT1 degrader that inhibits the proliferation of cancer cells. GSPT1 degrader-18 has weak ability to induce the formation of the GSPT1-CRBN/DDB1 ternary complex and belongs to a weak molecular glue. GSPT1 degrader-18 can be used in cancer-related research .
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Cat. No.: HY-181084
CAS No.: 3039500-55-2
PROTAC BCL6/GSPT1 Degrader-1 is a dual-target PROTAC degrader that targets BCL6 and GSPT1. PROTAC BCL6/GSPT1 Degrader-1 inhibits cell proliferation, promotes DNA damage, and induces cell cycle arrest and apoptosis in diffuse large B-cell lymphoma. PROTAC BCL6/GSPT1 Degrader-1 can be used for research on tumors such as lymphoma .
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Cat. No.: HY-170407
CAS No.: 2250062-05-4
mTOR/GSPT1 ligand-1 is a mTOR/GSPT1 ligand, which can be used for the synthesis of PROTACs, such as YB-3-17 (HY-170405) .
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Cat. No.: HY-RS16544
Research Areas:  

Others

Gspt1 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Gspt1 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS22976
Research Areas:  

Others

Gspt1 Rat Pre-designed siRNA Set A contains three designed siRNAs for Gspt1 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-130800R
CAS No.: 1860875-51-9
Synonyms: CC-90009 (Standard)
Eragidomide (Standard) is the analytical standard of Eragidomide (HY-130800). This product is intended for research and analytical applications. Eragidomide (CC-90009) is a first-in-class GSPT1-selective cereblon (CRBN) E3 ligase modulator, acts as a molecular glue. Eragidomide coopts the CRL4 CRBN to selectively target GSPT1 for ubiquitination and proteasomal degradation .
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Cat. No.: HY-180836
DIX-01 is a CRBN-recruiting molecular glue and cytotoxic agent targeting GSPT1, with an EC50 of 173 nM against human GSPT1. DIX-01 drives proteasomal degradation of GSPT1, IKZF1 and IKZF3, and induces cytotoxicity in cancer cells. DIX-01 inhibits tumor growth in a zebrafish xenograft model and can be used for research on acute myeloid leukemia and prostate cancer .
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Cat. No.: HY-P88836
Synonyms: ERF3B; GST2

Host:  

Mouse

Application:  

ICC/IF, FC

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-157830
CAS No.: 870120-63-1
Research Areas:  

Cancer

MDM2 ligand 6 is an MDM2 ligand that can be used in PROTAC synthesis-related research. MDM2 ligand 6 can serve as the target protein ligand moiety of the MDM2/GSPT1 PROTAC degrader WB156 (HY-174266) .
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