7 Results for "

Cullin1

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

7 Results for "Cullin1" in MCE Product Catalog:

2
2 Cited Publications
Cat. No.: HY-133558
CAS No.: 2305757-96-2
Purity:  99.63%
Research Areas:  

Cancer

VII-31 is a potent NEDDylation pathway activator to inhibit the tumor progression in vitro and in vivo. VII-31 induces apoptosis via intrinsic and extrinsic pathways [1].
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Cat. No.: HY-156240
CAS No.: 2247060-97-3
Research Areas:  

Metabolic Disease

DI-1548 is a potent, selective, and irreversible covalent inhibitor of DCN1 (IC50 = 4.6 nM). DI-1548 potently and selectively inhibits cullin 3 neddylation at nanomolar concentrations, and exhibits no obvious effect on the neddylation of other cullin members (including cullin 1, 2, 4A, 4B, and 5). DI-1548 exhibits no cytotoxicity. DI-1548 covalently binds to DCN1, disrupting the DCN1-UBC12 interaction, causing the collapse of the neddylation complex, inactivating CRL3, leading to NRF2 accumulation and upregulation of its target genes, and ultimately protecting mice from liver damage. DI-1548 can be used in liver injury research [1].
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Cat. No.: HY-163524
Target:  

Apoptosis

Research Areas:  

Cancer

NAE-IN-2 (compound III-26) is N2–(1-benzylpiperidin-4-yl)quinazoline-2,4-diamine derivative, and inhibits Cullin1 and Cullin3. NAE-IN-2 inhibits migration and induces cell apoptosis of gastric cancer cells [1].
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Cat. No.: HY-P82633
Synonyms: CUL1; Cullin1

Host:  

Rabbit

Application:  

WB, IHC-P, ICC/IF, IP, FC

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-P703242
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Cullin-1; CUL1; Homo sapiens; Human; CUL-1
Species:  
Source:  
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Cat. No.: HY-P703243
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Cullin-1; CUL1; Homo sapiens; Human; CUL-1
Species:  
Source:  
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Cat. No.: HY-172252
Target:  

PD-1/PD-L1 RAD51

Research Areas:  

Cancer

CSN5-IN-2 (Compound 31) is a CSN5 inhibitor with an IC50 of 0.36 μM. CSN5-IN-2 can increase the level of Cullin 1 neddylation, and downregulate the expression of RAD51 and PD-L1 in cancer cells. CSN5-IN-2 has anti-tumor activity, and its effect is better when combined with Talazoparib (HY-16106) [1].
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