83 Results for "

Embryonic development

" in MedChemExpress (MCE) Product Catalog:
Products (83)

83 Results for "Embryonic development" in MCE Product Catalog:

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17
17 Publications Verification
Art. -Nr.: HY-101117
CAS. Nr.: 2083627-02-3
Reinheit:  99.56%
Forschungsgebiete:  

Cancer

EED226 is a polycomb repressive complex 2 (PRC2) inhibitor, which binds to the K27me3-pocket on embryonic ectoderm development (EED) and shows strong antitumor activity in xenograft mice model . EED226 is a potent, selective, and orally bioavailable EED inhibitor . EED226 inhibits PRC2 with an IC50 of 23.4 nM when the H3K27me0 peptide is used as a substrate in the in vitro enzymatic assays .
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10
10 Cited Publications
Art. -Nr.: HY-B0631
CAS. Nr.: 66376-36-1
Forschungsgebiete:  

Metabolic Disease

Alendronate acid is an orally active bisphosphonate which binds to bone surfaces and inhibits bone resorption by osteoclasts. Alendronate acid induces skeletal alterations in the chicken embryonic development model. Alendronate acid can be used for osteoporosis research .
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10
10 Cited Publications
Art. -Nr.: HY-108685
CAS. Nr.: 129318-43-0
Reinheit:  ≥98.0%
Synonyms: Alendronic acid monosodium salt
Forschungsgebiete:  

Metabolic Disease

Alendronate sodium is an orally active bisphosphonate which binds to bone surfaces and inhibits bone resorption by osteoclasts. Alendronate sodium induces skeletal alterations in the chicken embryonic development model. Alendronate sodium can be used for osteoporosis research .
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6
6 Cited Publications
Art. -Nr.: HY-103663
CAS. Nr.: 1951408-58-4
Reinheit:  99.18%
Forschungsgebiete:  

Cancer

MAK683 is an embryonic ectoderm development (EED) inhibitor extracted from patent US20160176882 A1, compound example 2. MAK683 exhibits IC50s of 59, 89, 26 nM in EED Alphascreen binding, LC-MS and ELISA assay .
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2
2 Cited Publications
Art. -Nr.: HY-P0254
CAS. Nr.: 374675-21-5
Target:  

Kisspeptin Receptor

Forschungsgebiete:  

Cardiovascular Disease Cancer

Kisspeptin-10, human is a potent vasoconstrictor and inhibitor of angiogenesis. Kisspeptin-10, human acts as a tumor metastasis suppressor via its receptor GPR54. Kisspeptin-10-GPR54 system plays an important role in embryonic kidney development. Kisspeptin-10/GPR54 signaling induces osteoblast differentiation via NFATc4-mediated BMP2 expression .
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2
2 Cited Publications
Art. -Nr.: HY-156095
CAS. Nr.: 897109-93-2
Reinheit:  99.42%
Target:  

Wnt

Forschungsgebiete:  

Cancer

F7H is a Frizzled receptor FZD7 antagonist (IC50: 1.25 μM). Frizzled receptors (FZDs) influence Wnt signaling, mediating embryonic development and tissue homeostasis. F7H is a potent ligand for the FZD7 transmembrane domain (TMD) .
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2
2 Cited Publications
Art. -Nr.: HY-P0254A
Target:  

Kisspeptin Receptor

Forschungsgebiete:  

Cardiovascular Disease Cancer

Kisspeptin-10, human TFA is a potent vasoconstrictor and inhibitor of angiogenesis. Kisspeptin-10, human TFA acts as a tumor metastasis suppressor via its receptor GPR54. Kisspeptin-10-GPR54 system plays an important role in embryonic kidney development. Kisspeptin-10/GPR54 signaling induces osteoblast differentiation via NFATc4-mediated BMP2 expression .
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1
1 Cited Publications
Art. -Nr.: HY-N6612
CAS. Nr.: 6556-12-3
D-Glucuronic acid is a major component of many anti-inflammatory proteoglycans, which can promote embryonic development and inhibit cell aggregation. After being metabolized into ethyl glucuronide (HY-113093), D-Glucuronic acid activates Toll-like receptor 4 (TLR4), causing pain. D-Glucuronic acid and its derivative glucurono-lactone can serve as liver detoxifiers, and its derivatives also possess anti-tumor activity .
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1
1 Cited Publications
Art. -Nr.: HY-139400
CAS. Nr.: 2490676-18-9
Reinheit:  99.97%
Synonyms: FTX-6058
Forschungsgebiete:  

Cardiovascular Disease

Pociredir (FTX-6058) is a potent and orally active inhibitor of Embryonic Ectoderm Development (EED). Pociredir can induce HbF protein expression in cell and murine models. Pociredir can be used for the research of select hemoglobinopathies, including sickle cell disease and β-thalassemia .
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1
1 Cited Publications
Art. -Nr.: HY-136977
CAS. Nr.: 2488952-40-3
Reinheit:  99.87%
Forschungsgebiete:  

Cancer

EEDi-5285 is an exceptionally potent and orally active embryonic ectoderm development (EED) inhibitor with an IC50 value of 0.2 nM for binds to the EED protein. EEDi-5285 has anti-cancer activity .
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1
1 Cited Publications
Art. -Nr.: HY-14608R
CAS. Nr.: 56-86-0
L-Glutamic acid (Standard) is the analytical standard of L-Glutamic acid. This product is intended for research and analytical applications. L-Glutamic acid is an excitatory amino acid neurotransmitter that acts as an agonist for all subtypes of glutamate receptors (metabolic rhodophylline, NMDA, and AMPA). L-Glutamic acid has an agonist effect on the release of DA from dopaminergic nerve endings. L-Glutamic acid can be used in the study of neurological diseases . IC50 & Target:DA . In Vitro: L-Glutamic acid (120, 500, 750, 1000 mg/dL) can reduce the harmful effect of lithium on the embryonic development of Xenopus Xenopus .
L-Glutamic acid (2, 5, 10, 20 mM, 24-48 h) can induce neuroexcitotoxicity in neuroblastoma .
In Vivo: L-Glutamic acid (3 g/kg, subcutaneous injection) can promote excitotoxic degeneration of retinal ganglion cells in mice .
L-Glutamic acid (750 mg/kg, intraperitoneal injection) can reduce and inhibit oxidative stress induced by chlorpyrifos (CPF) in rats .
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1
1 Cited Publications
Art. -Nr.: HY-103073
CAS. Nr.: 864716-85-8
Reinheit:  99.19%
Target:  

TRP Channel

Forschungsgebiete:  

Others

Mesendogen is a TRPM6 inhibitor. Mesendogen enhances the mesoderm and definitive endoderm (DE) differentiations of human embryonic stem cells (hESCs) and human induced pluripotent stem cells (hiPSCs). Mesendogen can be used for the research of magnesium homeostasis during early embryonic cell development .
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1
1 Cited Publications
Art. -Nr.: HY-124838
CAS. Nr.: 693241-54-2
Reinheit:  98.26%
Target:  

DNA/RNA Synthesis

Forschungsgebiete:  

Cancer

EG1, a specific Pax2 inhibitor, directly binds the paired domain of Pax2 (Kd=1.35-1.5 μM) and inhibits Pax2-DNA interactions. EG1 can inhibit embryonic kidney development, a process directly dependent on Pax2 activity .
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1
1 Cited Publications
Art. -Nr.: HY-139400A
CAS. Nr.: 2490676-19-0
Reinheit:  99.89%
Synonyms: FTX-6058 hydrochloride
Forschungsgebiete:  

Cardiovascular Disease

Pociredir (FTX-6058) hydrochloride is a potent and orally active inhibitor of Embryonic Ectoderm Development (EED). Pociredir hydrochloride can induce HbF protein expression in cell and murine models. Pociredir hydrochloride can be used for the research of select hemoglobinopathies, including sickle cell disease and β-thalassemia .
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1
1 Cited Publications
Art. -Nr.: HY-W011215
CAS. Nr.: 84-75-3
Dihexyl phthalate is an orally active phthalate ester (PAEs) widely used as a plasticizer, and it acts as an environmental endocrine disruptor. Dihexyl phthalate exhibits endocrine-disrupting and reproductive toxic properties, induces oxidative stress and inflammation, and ultimately causes apoptosis and damage to reproductive organs such as the testes. Dihexyl phthalate can be used in studies related to developmental toxicity, embryonic lethality, teratogenicity, and abnormal development of the male reproductive system .
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1
1 Cited Publications
Art. -Nr.: HY-N6612A
CAS. Nr.: 207300-70-7
D-Glucuronic acid sodium salt monohydrate is a major component of many anti-inflammatory proteoglycans, which can promote embryonic development and inhibit cell aggregation. After being metabolized into ethyl glucuronide (HY-113093), D-Glucuronic acid sodium salt monohydrate activates Toll-like receptor 4 (TLR4), causing pain. D-Glucuronic acid sodium salt monohydrate and its derivative glucurono-lactone can serve as liver detoxifiers, and its derivatives also possess anti-tumor activity .
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Art. -Nr.: HY-W013272
CAS. Nr.: 52806-53-8
Synonyms: HFT
Hydroxyflutamide (HFT) is the active metabolite of Flutamide (HY-B0022) and exhibits oral activity. Hydroxyflutamide is a potent androgen receptor antagonist with an IC50 of 700 nM. Hydroxyflutamide can affect embryonic development and reproductive tract development in mice. Additionally, Hydroxyflutamide can enhance the efficacy of Bacillus Calmette-Guérin (BCG) to better inhibit the progression of bladder cancer. Hydroxyflutamide can be used in research related to tumors and reproductive diseases .
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Art. -Nr.: HY-132922
CAS. Nr.: 2585648-55-9
Reinheit:  99.09%
Synonyms: APG-5918
Forschungsgebiete:  

Cancer

EEDi-5273 (APG-5918) is a potent and orally active embryonic ectoderm development (EED) inhibitor with an IC50 of 0.2 nM. EEDi-5273 can inhibit the polycomb repressive complex 2 (PRC2) activity and block trimethylation of histone H3 lysine 27. EEDi-5273 can be used for the research of cancer, such as ovarian cancer .
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Art. -Nr.: HY-N6612R
CAS. Nr.: 6556-12-3
D-Glucuronic acid (Standard) is the analytical standard of D-Glucuronic acid. This product is intended for research and analytical applications. D-Glucuronic acid is a major component of many anti-inflammatory proteoglycans, which can promote embryonic development and inhibit cell aggregation. After being metabolized into ethyl glucuronide (HY-113093), D-Glucuronic acid activates Toll-like receptor 4 (TLR4), causing pain. D-Glucuronic acid and its derivative glucurono-lactone can serve as liver detoxifiers for human health prevention, and its derivatives also possess anti-tumor activity .
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Art. -Nr.: HY-130815A
CAS. Nr.: 2938997-23-8
Reinheit:  98.03%
MAK683-CH2CH2COOH binds to EED (embryonic ectoderm development protein). MAK683-CH2CH2COOH and a VHL ligand for the E3 ubiquitin ligase have been used to design PROTAC EED degrader-1 (HY-130614) and PROTAC EED degrader-2 (HY-130615) .
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