1279 Results for "

CRBN ligand

" in MedChemExpress (MCE) Product Catalog:
Products (1279)

1279 Results for "CRBN ligand" in MCE Product Catalog:

5
5 Cited Publications
Cat. No.: HY-122562
CAS No.: 2231744-29-7
Purity:  98.35%
Target:  

PROTACs Btk

Research Areas:  

Cancer

MT-802 is a BTK PROTAC degrader. MT-802 degrades wild-type BTK (DC50 = 14.6 nM) and BTK mutants including E41K, C481S (DC50 = 14.9 nM), C481R, C481Y, C481T, C481F, L528W, and inhibits their Y223 phosphorylation. BI-4732 can be used for the study of Ibrutinib (HY-10997)-resistant chronic lymphocytic leukemia (CLL). (Pink: BTK ligand (HY-150885), Blue: CRBN Ligand (HY-14658), Black: Linker (HY-141371), E3 ligase ligand-linker conjugate (HY-176340)) .
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4
4 Cited Publications
Cat. No.: HY-153321
CAS No.: 2649400-34-8
Purity:  98.67%
Synonyms: NX-5948; BTK-IN-24
Target:  

PROTACs Btk

Research Areas:  

Inflammation/Immunology

Bexobrutideg (NX-5948) is an orally active chimeric targeting molecule (CTM) that induces specific BTK protein degradation by the cereblon E3 ligase (CRBN) complex without degradation of other cereblon neo-substrates. Bexobrutideg mediates potent anti-inflammatory activity via BTK degradation with resultant inhibition of B cell activation. Bexobrutideg exhibits potent tumor growth inhibition in TMD8 xenograft models that contain either wild-type BTK or BTKi-resistant mutations. Bexobrutideg is efficacious in a mouse collageninduced arthritis (CIA) model. Bexobrutideg can cross the blood brain barrier (BBB). Bexobrutideg is a PROTAC composed of the ligand for target protein, a linker, and a cereblon E3 ligase (CRBN) complex (Red: BTK ligand (HY-170324); Blue: CRBN ligand (HY-171893); Black: linker) .
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3
3 Cited Publications
Cat. No.: HY-126534
CAS No.: 2704316-81-2
Purity:  98.01%
Synonyms: LSN3106729
Research Areas:  

Cancer

Abemaciclib metabolite M18 (LSN3106729), the metabolite of Abemaciclib (HY-16297A), is a CDK inhibitor with antitumor activity. Abemaciclib metabolite M18 and a CRBN ligand have been used to design PROTAC CDK4/6 degrader .
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3
3 Cited Publications
Cat. No.: HY-126534A
CAS No.: 2704316-82-3
Purity:  98.18%
Synonyms: LSN3106729 hydrochloride
Research Areas:  

Cancer

Abemaciclib metabolite M18 (LSN3106729) hydrochloride, the metabolite of Abemaciclib (HY-16297A), is a CDK inhibitor with antitumor activity. Abemaciclib metabolite M18 hydrochloride and a CRBN ligand have been used to design PROTAC CDK4/6 degrader .
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3
3 Cited Publications
Cat. No.: HY-148333
CAS No.: 2225938-86-1
Purity:  98.00%
Research Areas:  

Cancer

MS177 is an effective and fast-acting EZH2 degrader. MS177 is a PROTAC that consists of a CRBN ligand, linker, and a potent enzymatic EZH2 inhibitor C24 (C24 IC50): 12 nM). MS177 effectively depletes both canonical EZH2-PRC2 and noncanonical EZH2-cMyc complexes. MS177 induces leukaemia cell growth inhibition, apoptosis and cell cycle progression arrest .
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2
2 Cited Publications
Cat. No.: HY-103597
CAS No.: 1061605-21-7
Purity:  99.85%
Synonyms: Cereblon ligand 3; E3 ligase ligand 3
Target:  

Ligands for E3 Ligase

Research Areas:  

Cancer

Thalidomide-O-COOH (Cereblon ligand 3) is the Thalidomide-based Cereblon ligand used in the recruitment of CRBN protein. Thalidomide-O-COOH (Cereblon ligand 3) can be connected to the ligand for protein by a linker to form PROTACs .
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2
2 Cited Publications
Cat. No.: HY-131295
CAS No.: 2581116-22-3
Purity:  98.62%
Research Areas:  

Cancer

PD0325901-O-C2-dioxolane has main portion of MEK inhibitor PD0325901. PD0325901-O-C2-dioxolane and a ligand of VHL or CRBN E3 ligase can be used in the synthesis of MEK1/2 degrader .
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2
2 Cited Publications
Cat. No.: HY-129603
CAS No.: 2429877-30-3
Purity:  98.96%
Research Areas:  

Cancer

SI-109 is a potent STAT3 SH2 domain inhibitor (Ki=9 nM) with antitumor activity. SI-109 effectively inhibits the transcriptional activity of STAT3 (IC50=3 μM). SI-109 and an analog of CRBN ligand lenalidomide have been used to design PROTAC STAT3 degrader SD-36 .
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2
2 Cited Publications
Cat. No.: HY-155008
CAS No.: 3033812-84-6
Purity:  98.98%
Target:  

PROTACs Hexokinase

Research Areas:  

Cancer

PROTAC HK2 Degrader-1 is a PROTAC consisting of Lonidamine (HY-B0486) as a target protein Hexokinase 2 (HK2) inhibitor and Thalidomide (HY-14658) as a CRBN ligand-linked PROTAC. PROTAC HK2 Degrader-1 selectively inhibits the proliferation of breast cancer cells by forming a ternary complex through the ubiquitin-proteasome system to degrade Hexokinase 2 (HK2) protein leading to mitochondrial damage and cell death. PROTAC HK2 Degrader-1 effectively inhibits breast tumor growth and reduces the colonic side effects of cisplatin for breast cancer research .
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1
1 Cited Publications
Cat. No.: HY-130714
CAS No.: 2305936-56-3
Purity:  99.41%
Target:  

PROTACs

Research Areas:  

Cancer

TD-165 is a PROTAC-based cereblon (CRBN) degrader. TD-165 comprises a cereblon (CRBN) ligand binding group, a linker and an von Hippel-Landau (VHL) binding group .
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1
1 Cited Publications
Cat. No.: HY-136262
CAS No.: 2362575-45-7
Purity:  98.97%
Target:  

PROTACs E1/E2/E3 Enzyme

Research Areas:  

Cancer

CRBN-6-5-5-VHL is a potent and selective VHL E3 ligand-based Cereblon (CRBN) PROTAC degrader with a DC50 value of 1.5 nM. CRBN-6-5-5-VHL forms a heterotrimeric complex with CRBN and VHL E3 ligase, thereby promoting CRBN ubiquitination and proteasomal degradation without inducing VHL degradation. CRBN-6-5-5-VHL protects myeloma from the toxic effects of IMiDs. CRBN-6-5-5-VHL can be used in the research of multiple myeloma .
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1
1 Cited Publications
Cat. No.: HY-114420
CAS No.: 2230613-03-1
Purity:  99.85%
Synonyms: PROTAC FKBP12-binding moiety 2
Research Areas:  

Cancer

AP1867-2-(carboxymethoxy), the AP1867 (a synthetic FKBP12 F36V-directed ligand) based moiety, binds to CRBN ligand via a linker to form dTAG molecules .
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1
1 Cited Publications
Cat. No.: HY-131717
CAS No.: 927670-97-1
Purity:  98.07%
Research Areas:  

Cancer

Thalidomide-NH-CH2-COOH is the Thalidomide-based cereblon ligand used in the recruitment of CRBN protein. Thalidomide-NH-CH2-COOH can be connected to the ligand for protein by a linker to form PROTACs, such as THAL-SNS-032 (HY-123937) .
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1
1 Cited Publications
Cat. No.: HY-125876
CAS No.: 2378801-85-3
Purity:  99.80%
Target:  

PROTACs Bcl-2 Family

Research Areas:  

Cancer

PROTAC Bcl2 degrader-1 (Compound C5) is a PROTAC based on Cereblon ligand, which potently and selectively induces the degradation of Bcl-2 (IC50, 4.94 μM; DC50, 3.0 μM) and Mcl-1 (IC50, 11.81 μM) by introducing the E3 ligase cereblon (CRBN)-binding ligand pomalidomide to Mcl-1/Bcl-2 dual inhibitor Nap-1 .
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1
1 Cited Publications
Cat. No.: HY-130683
CAS No.: 2489242-23-9
Purity:  98.04%
Research Areas:  

Cancer

Lenalidomide-propargyl-C2-NH2 hydrochloride incorporates a cereblon (CRBN) ligand for the E3 ubiquitin ligase, and a linker. Lenalidomide-propargyl-C2-NH2 hydrochloride can be used to design the PROTAC MD-224 (HY-114312) . Lenalidomide-propargyl-C2-NH2 (hydrochloride) is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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Cat. No.: HY-24538
CAS No.: 1267337-47-2
Target:  

Ligands for E3 Ligase

Research Areas:  

Cancer

CRBN ligand-880 is an E3 ubiquitin ligase cereblon (CRBN) ligand used to recruit the cereblon protein. CRBN ligand-880 can be linked to a target protein ligand via a linker to form a PROTAC.
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Cat. No.: HY-43983
CAS No.: 1448189-90-9
Target:  

Ligands for E3 Ligase

Research Areas:  

Cancer

CRBN ligand-798 is an E3 ubiquitin ligase cereblon (CRBN) ligand used to recruit the cereblon protein. CRBN ligand-798 can be linked to a target protein ligand via a linker to form a PROTAC.
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Cat. No.: HY-W442918
CAS No.: 92137-90-1
Target:  

Ligands for E3 Ligase

Research Areas:  

Cancer

CRBN ligand-881 is an E3 ubiquitin ligase cereblon (CRBN) ligand used to recruit the cereblon protein. CRBN ligand-881 can be linked to a target protein ligand via a linker to form a PROTAC.
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Cat. No.: HY-48024
CAS No.: 2758531-21-2
Target:  

Ligands for E3 Ligase

Research Areas:  

Cancer

CRBN ligand-885 is an E3 ubiquitin ligase cereblon (CRBN) ligand used to recruit the cereblon protein. CRBN ligand-885 can be linked to a target protein ligand via a linker to form a PROTAC.
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Cat. No.: HY-W733888
CAS No.: 2883704-28-5
Target:  

Ligands for E3 Ligase

Research Areas:  

Cancer

CRBN ligand-187 is a CRBN-type E3 ubiquitin ligase ligand that can be used for synthesis of TQ-3959 (HY-175541) .
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