12 Results for "

meiosis

" in MedChemExpress (MCE) Product Catalog:
Products (12)

12 Results for "meiosis" in MCE Product Catalog:

5
5 Cited Publications
Cat. No.: HY-111556
CAS No.: 2361493-16-3
Purity:  ≥98.0%
Target:  

PROTACs CDK Apoptosis

Research Areas:  

Cancer

BSJ-03-123 is a selective PROTAC degrader of CDK6. BSJ-03-123 degrades CDK6, thereby inhibiting Rb S780 phosphorylation and inducing G1 phase arrest, while remodeling cell cycle and transcriptional signaling, with no effect on CDK4-dependent cancer cells. BSJ-03-123 reduces CDK6 protein levels in mouse ovarian tissues, increases the proportion of primordial follicles, and induces granulosa cell apoptosis, without impairing the ability of oocytes to resume meiosis and mature to the MII stage. BSJ-03-123 alleviates uveitis by blocking the HDACs-CDK6/ID2 axis. BSJ-03-123 can be used in studies related to acute myeloid leukemia, mantle cell lymphoma and autoimmune uveitis .
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3
3 Cited Publications
Cat. No.: HY-108330
CAS No.: 118409-62-4
Purity:  ≥98.0%
Synonyms: Tyrphostin AG126
Target:  

ERK Mitosis

Research Areas:  

Inflammation/Immunology

AG126 is a tyrosine kinase inhibitor, can inhibit the phosphorylation of ERK1 and ERK2 at 25-50 μM. AG126 can be used in meiosis, mitosis, and postmitotic research .
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Cat. No.: HY-138084
CAS No.: 2410846-16-9
Purity:  99.83%
Target:  

Separase Mitosis

Research Areas:  

Cancer

SIC5-6 is a potent Separase inhibitor. Separase, a large cysteine protease, involves in chromosome segregation during mitosis and meiosis, DNA damage repair, centrosome disengagement and duplication, spindle stabilization and elongation. Separase is highly overexpressed in many solid cancers, serves as an attractive chemotherapeutic target .
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Cat. No.: HY-N11274
CAS No.: 7448-02-4
Synonyms: 4,4-Dimethylzymosterol; 14-Norlanosterol
T-MAS (4,4-Dimethylzymosterol) serves as an intermediate in cholesterol biosynthesis, stimulating oocytes for meiosis and modulating cumulus expansion .
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Cat. No.: HY-121337
CAS No.: 61213-25-0
Purity:  99.61%
Synonyms: R-40244
Flurochloridone (R-40244) is an orally active herbicide and an inducer of ER stress, apoptosis, and cytotoxicity. Flurochloridone upregulates GRP78 and activates the PERK-eIF2α-ATF4 UPR axis, ATF6, CHOP, Bax, and Bim. Flurochloridone decreases Akt, p-Akt, GSK3β, and p-GSK3β levels, and induces ROS, oxidative stress, γ-glutamyl cycle activation, and GSH accumulation. Flurochloridone inhibits mitochondrial respiration and ATP production while enhancing glycolysis and cell viability inhibition. Flurochloridone inhibits spermatogonial proliferation, spermatocyte meiosis, and sperm mitochondrial membrane potential, and induces Sertoli cell apoptosis and mitochondrial damage. Flurochloridone non-competitively binds phytoene desaturase, blocking phytoene desaturation and carotenoid synthesis, leading to leaf bleaching and phytotoxicity. Flurochloridone can be used for research on male reproductive toxicity, hepatotoxicity, and as a herbicide .
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Cat. No.: HY-P3894
CAS No.: 309247-52-7
Research Areas:  

Others

P34cdc2 Kinase Fragment is associated with the completion of DNA replication in yeast mitosis. P34cdc2 Kinase can phosphorylate mitogen-activated protein 2 (MAP2) to regulate microtubules polymerization in Xenopus oocytes meiosis .
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Cat. No.: HY-108330R
CAS No.: 118409-62-4
Synonyms: Tyrphostin AG126 (Standard)
Research Areas:  

Inflammation/Immunology

AG126 (Standard) is the analytical standard of AG126. This product is intended for research and analytical applications. AG126 is a tyrosine kinase inhibitor, can inhibit the phosphorylation of ERK1 and ERK2 at 25-50 μM. AG126 can be used in meiosis, mitosis, and postmitotic research .
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Cat. No.: HY-121337R
CAS No.: 61213-25-0
Synonyms: R-40244 (Standard)
Flurochloridone (Standard) (R-40244 (Standard)) is the analytical standard of Flurochloridone (HY-121337). This product is intended for research and analytical applications. Flurochloridone (R-40244) is an orally active herbicide and an inducer of ER stress, apoptosis, and cytotoxicity. Flurochloridone upregulates GRP78 and activates the PERK-eIF2α-ATF4 UPR axis, ATF6, CHOP, Bax, and Bim. Flurochloridone decreases Akt, p-Akt, GSK3β, and p-GSK3β levels, and induces ROS, oxidative stress, γ-glutamyl cycle activation, and GSH accumulation. Flurochloridone inhibits mitochondrial respiration and ATP production while enhancing glycolysis and cell viability inhibition. Flurochloridone inhibits spermatogonial proliferation, spermatocyte meiosis, and sperm mitochondrial membrane potential, and induces Sertoli cell apoptosis and mitochondrial damage. Flurochloridone non-competitively binds phytoene desaturase, blocking phytoene desaturation and carotenoid synthesis, leading to leaf bleaching and phytotoxicity. Flurochloridone can be used for research on male reproductive toxicity, hepatotoxicity, and as a herbicide .
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Cat. No.: HY-DY2049
Target:  

Fluorescent Dye

Research Areas:  

Others

Thionin Staining Solution (1%) is mainly used for chromosome staining, such as somatic chromosome and meiosis staining, in which metachromatic substances appear purplish red, while other substances appear blue .
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Cat. No.: HY-W782762
CAS No.: 19456-83-8
Target:  

Endogenous Metabolite

Research Areas:  

Metabolic Disease

Dihydro FF-MAS is a steroid triterpenoid compound. Dihydro FF-MAS is an intermediate in the cholesterol synthesis pathway. Dihydro FF-MAS triggers the resumption of meiosis in cultured mouse oocytes in vitro, but not in vivo. Dihydro FF-MAS can be used in studies of reproduction and lipid metabolism .
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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-111556R
CAS No.: 2361493-16-3
Research Areas:  

Cancer

BSJ-03-123 (Standard) is the analytical standard of BSJ-03-123 (HY-111556). This product is intended for research and analytical applications. BSJ-03-123 is a selective PROTAC degrader of CDK6. BSJ-03-123 degrades CDK6, thereby inhibiting Rb S780 phosphorylation and inducing G1 phase arrest, while remodeling cell cycle and transcriptional signaling, with no effect on CDK4-dependent cancer cells. BSJ-03-123 reduces CDK6 protein levels in mouse ovarian tissues, increases the proportion of primordial follicles, and induces granulosa cell apoptosis, without impairing the ability of oocytes to resume meiosis and mature to the MII stage. BSJ-03-123 alleviates uveitis by blocking the HDACs-CDK6/ID2 axis. BSJ-03-123 can be used in studies related to acute myeloid leukemia, mantle cell lymphoma and autoimmune uveitis .
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