107 Results for "

MG degrader-3

" in MedChemExpress (MCE) Product Catalog:
Products (107)

107 Results for "MG degrader-3" in MCE Product Catalog:

Cat. No.: HY-177728
CAS No.: 2413733-73-8
Research Areas:  

Cancer

MG degrader 3 is a molecular glue degrader that induces the degradation of multiple proteins including GSPT1, ZFP91 and CK1α via the ubiquitin-proteasome system, regulates protein stability and cellular signaling networks, and exhibits anti-proliferative activity against multiple myeloma cells. MG degrader 3 can be applied in the research of multiple myeloma .
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6 Publications Verification
Cat. No.: HY-100932
CAS No.: 105637-50-1
Purity:  99.86%
Target:  

Myosin

Research Areas:  

Cancer

ML-9 is a selective and potent inhibitor of Akt kinase, inhibits myosin light-chain kinase (MLCK) and stromal interaction molecule 1 (STIM1) activity . ML-9 inhibits inhibits MLCK, PKA and PKC activity with Ki values of 4, 32 and 54 μM, respectively . ML-9 induces autophagy by stimulating autophagosome formation and inhibiting their degradation .
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1 Cited Publications
Cat. No.: HY-139185
CAS No.: 2306388-65-6
Purity:  98.74%
Research Areas:  

Cancer

PROTAC ERRα Degrader-3 is a potent and selective ERRα degrader based on von Hippel-Lindau ligand. PROTAC ERRα Degrader-3 is capable of specifically degrading ERRα protein by >80% at a concentration of 30 nM. PROTAC ERRα Degrader-3 is inactive against ERRβ and ERRγ proteins .
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1 Cited Publications
Cat. No.: HY-135345
CAS No.: 2079056-43-0
Purity:  99.48%
Target:  

PROTACs FKBP

Research Areas:  

Cancer

PROTAC FKBP Degrader-3 is a selective FKBP PROTAC degrader with an IC50 of 1.8 nM. PROTAC FKBP Degrader-3 targets and degrades the FKBP protein by recruiting the VHL E3 ligase, and this degradation process is primarily mediated by K11 and K48 ubiquitin chain linkages. PROTAC FKBP Degrader-3 can be applied in cancer research .
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1 Cited Publications
Cat. No.: HY-114229
CAS No.: 3031993-61-7
Research Areas:  

Cancer

PROTAC BET Degrader-3 (Example C-55) is a BET PROTAC degrader and can be used in cancer research .
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1 Cited Publications
Cat. No.: HY-128842
CAS No.: 2249750-23-8
Purity:  96.06%
Target:  

PROTACs MDM-2/p53

Research Areas:  

Cancer

PROTAC MDM2 Degrader-3 is a MDM2 self-degrading (dimeric) PROTAC. PROTAC MDM2 Degrader-3 can be used in cancer research .
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Cat. No.: HY-177456
CAS No.: 3077464-19-5
Target:  

STAT

Research Areas:  

Inflammation/Immunology

STAT6 degrader-3 is a potent, bifunctional STAT6 degrader that recruits STAT6 to an E3 ubiquitin ligase, promoting STAT6 ubiquitination and subsequently inducing its degradation. STAT6 degrader-3 can be used in research concerning STAT6-related inflammation and immune signaling .
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Cat. No.: HY-164827
CAS No.: 2862772-71-0
Target:  

Molecular Glues CDK

Research Areas:  

Cancer

CDK2 degrader 3 is a selective CDK2 molecular glue-like degrader. CDK2 degrader 3 induces G1 cell cycle arrest in CCNE1-amplified cancer cells. CDK2 degrader 3 is applicable to breast cancer-related research .
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Cat. No.: HY-136857
CAS No.: 2413382-30-4
Purity:  98.41%
Research Areas:  

Cancer

BRD4 degrader-3 is a molecular glue degrader targeting BRD4, with binding activity towards the BD1 and BD2 domains of BRD4. BRD4 degrader-3 regulates the activity of BRD4. BRD4 degrader-3 inhibits MYC expression in cancer cells. BRD4 degrader-3 suppresses cell proliferation. BRD4 degrader-3 can be used in research related to acute myeloid leukemia and prostate cancer .
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Cat. No.: HY-69260
CAS No.: 137076-22-3
Target:  

PROTAC Linkers

Research Areas:  

Others

tert-Butyl 4-formylpiperidine-1-carboxylate is a PROTAC linker and can be used in the synthesis of PROTAC BRM/BRG1 degrader-3 (HY-168251) .
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Cat. No.: HY-135382A
CAS No.: 2374122-43-5
Purity:  97.22%
Target:  

PROTACs IRAK

Research Areas:  

Inflammation/Immunology

PROTAC IRAK4 degrader-3 is a PROTAC-induced IRAK4 degrader based on von Hippel-Lindau .
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Cat. No.: HY-168054
CAS No.: 3043670-68-1
Target:  

PROTACs Ras

Research Areas:  

Cancer

PROTAC K-Ras Degrader-3 (compound 40) is a PROTAC degrader of K-Ras with a DC50 of ≤ 1 nM against SW620 KRAS G12D, and a GI50 of ≤ 10 nM against SW620 3D cell growth. PROTAC K-Ras Degrader-3 can be utilized in cancer research, such as non-small-cell lung cancer (NSCLC) .
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Cat. No.: HY-168543
Target:  

PROTACs Aurora Kinase Mps1

Research Areas:  

Cancer

PROTAC AURKA degrader 3 is a selective AURKA PROTAC degrader, with DC50 values of 2.05, 157.85 and 43.05 nM against AURKA, AURKB and TTK, respectively. PROTAC AURKA degrader 3 exhibits cytotoxicity against acute myeloid leukemia cells. PROTAC AURKA degrader 3 can be used for research related to acute myeloid leukemia .
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Cat. No.: HY-163502
CAS No.: 3033746-17-4
Target:  

PROTACs STAT

Research Areas:  

Cancer

PROTAC STAT3 degrader-3 is a STAT3 PROTAC degrader. PROTAC STAT3 degrader-3 recruits the E3 ubiquitin ligase CRBN and induces the degradation of STAT3 protein. PROTAC STAT3 degrader-3 inhibits the proliferation of malignant tumor cells. PROTAC STAT3 degrader-3 can be used for the research of non-small cell lung cancer and liver cancer .
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Cat. No.: HY-132997
CAS No.: 2471970-60-0
Target:  

PROTACs Bcl-2 Family

Research Areas:  

Cancer

PROTAC Bcl-xL degrader-3 is a potent PROTAC Bcl-xL degrader. PROTAC Bcl-xL degrader-3 forms ternary complexes with the VHL-complex and BCL-XL. PROTAC Bcl-xL degrader-3 can be used in research on acute lymphoblastic leukemia .
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Cat. No.: HY-173414
CAS No.: 3109967-69-0
Target:  

PROTACs STING NF-κB

Research Areas:  

Inflammation/Immunology

PROTAC STING degrader-3 is a STING PROTAC degrader (DC50: 0.62 μM). PROTAC STING degrader-3 induces STING degradation via the ubiquitin-proteasome pathway. PROTAC STING degrader-3 exerts anti-inflammatory effects by inhibiting STING/TBK1/NF-κB signaling. PROTAC STING degrader-3 has renal protective effects and can be used in the study of acute kidney injury (AKI) .
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Cat. No.: HY-176919
CAS No.: 3077385-98-6
Target:  

PROTACs STAT

Research Areas:  

Inflammation/Immunology Cancer

PROTAC STAT6 degrader-3 is a potent STAT6 PROTAC degrader with a DC50 of less than 1 nM. PROTAC STAT6 degrader-3 can be used for research on allergic/inflammatory diseases and cancer .
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Cat. No.: HY-136001
CAS No.: 2412273-77-7
Purity:  99.61%
Target:  

α-synuclein PROTACs

Research Areas:  

Neurological Disease

PROTAC α-synuclein degrader 3 is a selective α-Synuclein PROTAC degrader. PROTAC α-synuclein degrader 3 promotes ubiquitination and degradation of α-Synuclein. PROTAC α-synuclein degrader 3 can be used in research related to Parkinson's disease and Alzheimer's disease .
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Cat. No.: HY-171140
Research Areas:  

Cancer

PROTAC HDAC6 degrader 3 is a selective HDAC6 PROTAC degrader with an IC50 of 0.686 μM and shows high selectivity for HDAC6 over HDAC1-4. PROTAC HDAC6 degrader 3 recruits cereblon (CRBN) to trigger HDAC6 ubiquitination and subsequent proteasomal degradation. PROTAC HDAC6 degrader 3 selectively elevates acetylated α-tubulin levels in cancer cells, and does not induce histone H3 hyperacetylation or obvious loss of cell viability. PROTAC HDAC6 degrader 3 is applicable for research on multiple myeloma .
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Cat. No.: HY-174210
Research Areas:  

Cancer

PROTAC BRD4 Degrader-3 is a potent BRD4 PROTAC degrader with DC50 values ​​of 164 nM and 80 nM at 4 h and 24 h, respectively. PROTAC BRD4 Degrader-3 induces the ubiquitination and subsequent proteasomal degradation of BRD4 by recruiting the ubiquitin E3 ligase KLHDC2. PROTAC BRD4 Degrader-3 can be used in breast cancer research .
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