332 Results for "

Zebrafish

" in MedChemExpress (MCE) Product Catalog:
Products (332)

332 Results for "Zebrafish" in MCE Product Catalog:

48
48 Publications Verification
Art. -Nr.: HY-119738
CAS. Nr.: 1681056-61-0
Reinheit:  99.90%
Target:  

OGT Acyltransferase

Forschungsgebiete:  

Metabolic Disease

OSMI-1 is a cell-permeable O-GlcNAc transferase (OGT) inhibitor with an IC50 value of 2.7 μM. OSMI-1 inhibits protein O-linked N-acetylglucosamine (O-GlcNAcylation) in several mammalian cell lines without qualitatively altering cell surface N- or O-linked glycans .
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17
17 Cited Publications
Art. -Nr.: HY-15858
CAS. Nr.: 1177827-73-4
Reinheit:  99.87%
Synonyms: ENOblock
Target:  

Enolase Apoptosis

Forschungsgebiete:  

Metabolic Disease Cancer

AP-III-a4 (ENOblock) is a nonsubstrate analogue enolase inhibitor with an IC50 of 0.576 uM. AP-III-a4 can be used for the research of cancer and diabetic .
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17
17 Cited Publications
Art. -Nr.: HY-15858A
CAS. Nr.: 2070014-95-6
Reinheit:  99.24%
Synonyms: ENOblock hydrochloride
Target:  

Enolase Apoptosis

Forschungsgebiete:  

Metabolic Disease Cancer

AP-III-a4 (ENOblock) hydrochloride is a nonsubstrate analogue enolase inhibitor with an IC50 of 0.576 uM. AP-III-a4 hydrochloride can be used for the research of cancer and diabetic .
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7
7 Cited Publications
Art. -Nr.: HY-144828
CAS. Nr.: 2682850-41-3
Reinheit:  ≥97.0%
Forschungsgebiete:  

Cancer

RIP1/RIP3/MLKL activator 1 (Compound 6i) is a potent anti-glioma agent. RIP1/RIP3/MLKL activator 1 induces necroptosis through RIP1/RIP3/MLKL pathway. RIP1/RIP3/MLKL activator 1 exerts acceptable BBB permeability .
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6
6 Cited Publications
Art. -Nr.: HY-B0717
CAS. Nr.: 9002-96-4
Synonyms: TPGS; D-α-Tocopherol polyethylene glycol 1000 succinate; Vitamin E-TPGS
Target:  

Drug Derivative

Forschungsgebiete:  

Neurological Disease Metabolic Disease

Tocofersolan is synthetic polyethylene glycol derivative of α-tocopherol. Tocofersolan is an orally active and water-soluble analog of vitamin E. Tocofersolan can reduce neurobehavioral deficits in zebrafish embryos exposed to moderate and high concentrations of BaP during early development. Tocofersolan shows antioxidant activity. Tocofersolan can be used to provide an orally bioavailable source of vitamin E .
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5
5 Cited Publications
Art. -Nr.: HY-B0642
CAS. Nr.: 16051-77-7
Synonyms: Isosorbide-5-mononitrate
Isosorbide mononitrate (Isosorbide-5-mononitrate) is an orally active nitric acid compound used for angina pectoris by dilating blood vessels and lowering blood pressure. Isosorbide mononitrate increases the viability and proliferation of HUVECs by decreasing Apoptosis and elevated the expressions of vedf, kdrl, pdgfr in zebrafish embryos. Isosorbide mononitrate is promising for research of heart failure and coronary heart disease .
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4
4 Cited Publications
Art. -Nr.: HY-W583749
CAS. Nr.: 73606-19-6
Forschungsgebiete:  

Endocrinology

6:2 Cl-PFAES is an orally effective alternative to Perfluorooctane sulfonate. 6:2 Cl-PFAES significantly inhibits the growth of zebrafish and induces reproductive toxicity. 6:2 Cl-PFAES reduces the relative weights of epididymis and testis in male BALB/c mice. 6:2 Cl-PFAES can be used in the chrome plating industry .
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4
4 Cited Publications
Art. -Nr.: HY-15825
CAS. Nr.: 1427782-89-5
Reinheit:  99.50%
Synonyms: Porcn Inhibitor III
Target:  

Porcupine

Forschungsgebiete:  

Cancer

IWP L6 (Porcn Inhibitor III) is a Porcupine (Porcn) inhibitor with an EC50 of 0.5 nM. IWP L6 disrupts well-established Wnt-dependent developmental processes of embryonic and juvenile zebrafish .
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4
4 Cited Publications
Art. -Nr.: HY-B1752
CAS. Nr.: 80373-22-4
Synonyms: LY 171555; (-)-LY 141865
Quinpirole (LY 171555; (-)-LY 141865) is a D2/D3 dopamine receptor agonist and a CaV1.3 calcium channel modulator. Quinpirole normalizes dendritic spine density in dopamine-depleted striatum, upregulates the protein expression of BCL2 and GluR2, downregulates the protein expression of BAX, and delays the onset of seizures. Quinpirole enhances learning and memory, inhibits neuronal apoptosis (apoptosis), and induces anxiety-like, stereotyped, and compulsive behaviors. Quinpirole disrupts prepulse inhibition in rhesus monkeys, enhances the activity of paraventricular thalamic neurons to promote recovery from Isoflurane anesthesia, and alters the composition of the gut microbiota in rats. Quinpirole can be used in research related to dyskinesia, pain, epilepsy, and neurological disorders including anxiety disorder, obsessive-compulsive disorder, and schizophrenia .
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3
3 Cited Publications
Art. -Nr.: HY-Y0921
CAS. Nr.: 57-55-6
Synonyms: 1,2-(RS)-Propanediol; 1,2-Propylene glycol; Propylene glycol
(±)-1, 2-propanediol (1,2-(RS)-Propanediol) is an aliphatic alcohol that is often used as an excipient in many active molecular preparations to increase the solubility and stability of the active molecule. (±)-1, 2-propanediol can affect the neurobehavior of zebrafish .
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3
3 Cited Publications
Art. -Nr.: HY-B0842
CAS. Nr.: 23564-05-8
Thiophanate-Methyl is a pesticide residue and fungicide. Thiophanate-Methyl induces hepatotoxicity via caspase-3-mediated apoptosis and oxidative stress, thereby causing metabolic imbalance in the liver of zebrafish. Thiophanate-Methyl impairs the rhizobacteria-mediated defense response of cucumber against fusarium wilt .
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3
3 Cited Publications
Art. -Nr.: HY-N6893
CAS. Nr.: 54999-07-4
Ergolide is an orally active dual inhibitor targeting NF-κB/p65 and NLRP3. Ergolide blocks the NF-κB signaling pathway and the nuclear translocation of p65, and irreversibly binds to the NACHT domain of NLRP3 to inhibit inflammasome assembly. Ergolide significantly reduces the production of inflammatory mediators (e.g., NO, PGE2) and cytokines, induces cancer cell apoptosis, autophagy and ROS generation. Ergolide also enhances the anti-tumor effect of vincristine. Ergolide alleviates acute lung injury via an NLRP3-dependent mechanism, and effectively improves the survival rate and behavioral function of septic mice and inflammatory zebrafish models. Ergolide is used in the research of metastatic uveal melanoma, neurodegenerative diseases (such as Alzheimer's disease, Parkinson's disease), sepsis and acute lymphoblastic leukemia .
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3
3 Cited Publications
Art. -Nr.: HY-107399
CAS. Nr.: 196961-43-0
Reinheit:  98.18%
Target:  

RAR/RXR

Forschungsgebiete:  

Metabolic Disease Cancer

CD3254 a potent and selective retinoid-X-receptor (RXR) agonist .
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3
3 Cited Publications
Art. -Nr.: HY-B0850
CAS. Nr.: 119446-68-3
Forschungsgebiete:  

Infection

Difenoconazole is a sterol demethylation inhibitor, as a fungicide. Difenoconazole binds the heme portion of the fungal cytochrome P450 51, interferes the mycelial growth and inhibits the spore germination of pathogens, suppressing fungal growth .
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3
3 Cited Publications
Art. -Nr.: HY-110135
CAS. Nr.: 374620-70-9
Reinheit:  98.88%
Target:  

IGF-1R

NBI-31772 is a non-selective IGFBP inhibitor (Ki=47 nM). NBI-31772 has neuroprotective effects and reduces infarct volume during cerebral ischemia. NBI-31772 can also restore or enhance proteoglycan synthesis in osteoarticular chondrocytes. In addition, NBI-31772 also increases the effect of IGF3 on zebrafish oocyte maturation .
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2
2 Cited Publications
Art. -Nr.: HY-P72854
Reinheit:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: BDA2; BMP-2; BMP-2A; Bone morphogenetic protein 2a; SSFSC
Species:  
Source:  
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2
2 Cited Publications
Art. -Nr.: HY-120870
CAS. Nr.: 1621326-32-6
Reinheit:  ≥99.0%
Target:  

Myosin

Forschungsgebiete:  

Metabolic Disease

para-Nitroblebbistatin is a derivative of Blebbistatin (HY-13813) and an inhibitor of myosin II. para-Nitroblebbistatin is photostable, non-cytotoxic, and non-phototoxic. para-Nitroblebbistatin can serve as an ideal substitute for Blebbistatin (HY-13813) to study the role of myosin II in physiology, development, and cell biology .
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2
2 Cited Publications
Art. -Nr.: HY-19753
CAS. Nr.: 1253452-78-6
Target:  

BCRP

Forschungsgebiete:  

Cancer

KS176 is a selective BCRP inhibitor (IC50 values are 0.59 and 1.39 μM in Pheo A and Hoechst assays, respectively). KS176 can be used in the research of cancer .
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2
2 Cited Publications
Art. -Nr.: HY-N6626
CAS. Nr.: 175013-18-0
Pyraclostrobin is a highly effective and broad-spectrum strobilurin fungicide. Pyraclostrobin can induce oxidative DNA damage, mitochondrial dysfunction and autophagy through the activation of AMPK/mTOR signaling. Pyraclostrobin can be used to control crop diseases .
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2
2 Cited Publications
Art. -Nr.: HY-P3434A
Target:  

Pyroptosis

Forschungsgebiete:  

Inflammation/Immunology

Ac-FEID-CMK TFA is a potent zebrafish-specific GSDMEb-derived peptide inhibitor. Ac-FEID-CMK TFA can attenuate the mortality and kidney injury during septic shock. Ac-FEID-CMK TFA inhibits pyroptosis and attenuates septic AKI (acute kidney injury) in vivo. Ac-FEID-CMK TFA can suppress the caspy2-mediated noncanonical inflammasome pathway .
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