63 Results for "

wee1

" in MedChemExpress (MCE) Product Catalog:
Products (63)

63 Results for "wee1" in MCE Product Catalog:

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Cat. No.: HY-P701726
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: wee1; wee1 G2 Checkpoint Kinase; wee1-Like Protein Kinase; wee1A; wee1A Kinase; wee1hu; Non-Specific Protein-Tyrosine Kinase; wee1+ (S. Pombe) Homolog; wee1 Homolog (S. Pombe); Protein Kinase; wee1+ Homolog; wee1 Homolog
Species:  
Human
Source:  
Sf9 insect cells
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Cat. No.: HY-P701727
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: wee1; wee1 G2 Checkpoint Kinase; wee1-Like Protein Kinase; wee1A; wee1A Kinase; wee1hu; Non-Specific Protein-Tyrosine Kinase; wee1+ (S. Pombe) Homolog; wee1 Homolog (S. Pombe); Protein Kinase; wee1+ Homolog; wee1 Homolog
Species:  
Human
Source:  
Sf9 insect cells
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Cat. No.: HY-P705896
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: wee1; wee1 G2 Checkpoint Kinase; wee1-Like Protein Kinase; wee1A; wee1A Kinase; wee1hu; Non-Specific Protein-Tyrosine Kinase; wee1+ (S. Pombe) Homolog; wee1 Homolog (S. Pombe); Protein Kinase; wee1+ Homolog; wee1 Homolog
Species:  
Human
Source:  
sf9 insect cells
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Cat. No.: HY-189307
Target:  

Wee1 CDK DNA/RNA Synthesis

Research Areas:  

Cancer

WEE1-IN-15 is an ATP-competitive, selective WEE1 kinase inhibitor (IC50: 42 nM). WEE1-IN-15 abolishes CDK1 phosphorylation. WEE1-IN-15 induces DNA damage and replication stress, and increases the S-phase cell population. WEE1-IN-15 shows selective anticancer effects on colorectal cancer organoids. WEE1-IN-15 can be used for research on colorectal cancer [1].
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Cat. No.: HY-P706113
Purity:  ≥ 85%, as determined by reducing SDS-PAGE.
Synonyms: wee1; wee1 G2 Checkpoint Kinase; wee1-Like Protein Kinase; wee1A; wee1A Kinase; wee1hu; Non-Specific Protein-Tyrosine Kinase; wee1+ (S. Pombe) Homolog; wee1 Homolog (S. Pombe); Protein Kinase; wee1+ Homolog; wee1 Homolog
Species:  
Human
Source:  
Sf9 insect cells
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Cat. No.: HY-108343R
CAS No.: 622855-37-2
Research Areas:  

Cancer

WEE1-IN-4 (Standard) is the analytical standard of WEE1-IN-4 (HY-108343). This product is intended for research and analytical applications. WEE1-IN-4 (Compound 15) is a potent checkpoint Wee1 Kinase inhibitor with an IC50 of 0.011 μM. Wee1 inhibitors can abrogate the G2/M checkpoint [1].
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Cat. No.: HY-183547
CAS No.: 3055032-68-0
Target:  

Wee1 CDK

Research Areas:  

Cancer

WEE1/PKMYT1-IN-4 is a selective WEE1/PKMYT1 inhibitor, with IC50 values of 0.185 μM and 2.2 nM for human WEE1 and PKMYT1, respectively. WEE1/PKMYT1-IN-4 inhibits phosphorylation of CDK1 at T14 and Y15, disrupting the G2/M cell cycle checkpoint. WEE1/PKMYT1-IN-4 can be used for the research of colorectal cancer and amplified breast cancer [1].
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Cat. No.: HY-112409
CAS No.: 622855-50-9
Target:  

Drug Derivative

Research Areas:  

Others

WEE1-IN-2 is an active compound.
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Cat. No.: HY-143343
CAS No.: 2858812-88-9
Target:  

DUBTACs Wee1

Research Areas:  

Cancer

LEB-03-153 is a WEE1 DUBTAC (deubiquitinase-targeting chimera) linking AZD1775 (Adavosertib) to the OTUB1 recruiter EN523 through no linker [1].
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Cat. No.: HY-143340
CAS No.: 2858812-90-3
Target:  

DUBTACs Wee1

Research Areas:  

Cancer

LEB-03-145 is a WEE1 DUBTAC (deubiquitinase-targeting chimera) linking AZD1775 (Adavosertib) to the OTUB1 recruiter EN523 through a C5 alkyl linker [1].
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Cat. No.: HY-13925A
CAS No.: 212391-63-4
Target:  

Wee1 Apoptosis

Research Areas:  

Cancer

PD0166285 dihydrochloride, a substrate of P-gp, is a WEE1 inhibitor and a weak Myt1 inhibitor with IC50 values of 24 and 72 nM, respectively. PD0166285 dihydrochloride exhibits an IC50 of 3.433 μM for Chk1 [1].
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Cat. No.: HY-P706186
Purity:  ≥ 85%, as determined by reducing SDS-PAGE.
Synonyms: wee1-like protein kinase; wee1A kinase
Species:  
Human
Source:  
Sf9 insect cells
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Cat. No.: HY-P87147
Synonyms: DKFZp686I18166 antibody; EC 2.7.10.2 antibody; FLJ16446 antibody; MGC105683 antibody; OTTHUMP00000231338 antibody; OTTHUMP00000231339 antibody; wee 1 antibody; wee 1 homolog 1 (S. pombe) antibody; wee1 antibody; wee1 homolog (S. pombe) antibody; DKFZp686I18166 antibody; EC 2.7.10.2 antibody; FLJ16446 antibody; MGC105683 antibody; OTTHUMP00000231338 antibody; OTTHUMP00000231339 antibody; wee 1 antibody; wee 1 homolog 1 (S. pombe) antibody; wee1 antibody; wee1 homolog (S. pombe) antibody; wee1 homolog antibody; wee1 homolog S. pombe antibody; wee1 like protein kinase antibody; wee1 tyrosine kinase antibody; wee1+ homolog antibody; wee1+ S. pombe homolog antibody; wee1, S. pombe, homolog of antibody; wee1, somatic antibody; wee1-like protein kinase antibody; wee1_HUMAN antibody; wee1A antibody; wee1A kinase antibody; wee1hu antibody;

Host:  

Rabbit

Application:  

WB, IHC-P

Reactivity:  

Human, Monkey

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Cat. No.: HY-N0819R
CAS No.: 89412-79-3
Raddeanin A (Standard) is the analytical standard of Raddeanin A (HY-N0819). This product is intended for research and analytical applications. Raddeanin A is an oleanane-type triterpenoid saponin with oral activity. Raddeanin A inhibits SRC, mTOR, JNK, VEGFR2, NLRP3 inflammasome, Wnt/β-catenin, Wee1, PI3K/AKT signaling pathway, MAPK/ERK signaling pathway, AR-FL, AR-Vs, and downregulates the expression of p-PI3K and p-AKT. Raddeanin A inhibits osteoclast formation, bone resorption, osteolysis, cancer cell invasion, migration, proliferation, angiogenesis and epithelial-mesenchymal transition, while induces apoptosis, cell cycle arrest, ROS production, immunogenic cell death and dendritic cell maturation. Raddeanin A improves blood-retinal barrier function, alleviates inflammation, regulates the tumor microenvironment, and enhances the activity of anti-PD-1 antibody. Raddeanin A is applicable to the research of breast cancer-associated osteolysis, human osteosarcoma, colorectal cancer, glioblastoma, Alzheimer's disease, cholangiocarcinoma, melanoma, non-small cell lung cancer, castration-resistant prostate cancer and multiple myeloma.
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Cat. No.: HY-P701729
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: wee2; wee2 Oocyte Meiosis Inhibiting Kinase; wee1B; wee1-Like Protein Kinase 1B; wee1-Like Protein Kinase 2; wee1B Kinase; wee1 Homolog 2; FLJ16107; wee1 Homolog 2 (S. Pombe); OZEMA5; OOMD5
Species:  
Human
Source:  
Sf9 insect cells
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Cat. No.: HY-187907
CAS No.: 3038330-83-2
Synonyms: SGR-3515
Target:  

Wee1

Research Areas:  

Cancer

Surbinsertib (SGR-3515) is an orally active dual inhibitor of the Wee1 and Myt1 kinases. Surbinsertib is used in cancer research [1] .
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Cat. No.: HY-208742
CAS No.: 2414418-56-5
ZNL-02-096 is a selective Wee1 PROTAC degrader. ZNL-02-096 binds to CRBN and Wee1 to form a ternary complex, inducing CRBN- and proteasome-dependent ubiquitination and proteasomal degradation of Wee1. ZNL-02-096 inhibits recombinant PLK1 with an IC50 of 102 nM, but does not induce its degradation in cells. ZNL-02-096 induces G2/M phase arrest, Apoptosis, transient integrated stress response, upregulation of ATF4, and phosphorylation of GCN2. ZNL-02-096 reduces Tyr15 phosphorylation of CDK1. ZNL-02-096 can be used in research related to ovarian cancer, acute lymphoblastic leukemia, triple-negative breast cancer, multiple myeloma, and pancreatic ductal adenocarcinoma [1] .
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Cat. No.: HY-182433
CAS No.: 1847445-87-7
Target:  

Wee1

Research Areas:  

Neurological Disease Cancer

CJM061 is a WEE1 kinase inhibitor with a target IC50 of 2.8 nM. CJM061 acts as a sensitizer and exhibits synergistic effects with Cisplatin (HY-17394) in medulloblastoma cells. CJM061 can be used for the research of medulloblastoma [1].
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Cat. No.: HY-183278
Target:  

Wee1 Apoptosis

Research Areas:  

Cancer

APO-50815 is a WEE1 kinase inhibitor with a human IC50 of 9 nM. APO-50815 induces DNA damage, replication stress, S-phase cell accumulation, and apoptosis. APO-50815 can be used for the research of metastatic colorectal cancer [1].
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Cat. No.: HY-W1135319
Research Areas:  

Cancer

SB-405483 is a CRBN orthosteric ligand bindign enhancer. SB-405483 potentiates degradation of CRBN substrates including CK1α, Wee1, IKZF1/3. SB-405483 stabilizes CRBN and reduces CRBN autoubiquitination. SB-405483 can be used for the research of cancer, such as multiple myeloma and acute myeloid leukemia [1].
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