32 Results for "

Fragile

" in MedChemExpress (MCE) Product Catalog:
Products (32)

32 Results for "Fragile" in MCE Product Catalog:

Cat. No.: HY-N16480
CAS No.: 651750-97-9
Synonyms: Lindetannin trimer
Lindetannin (Lindetannin trimer) is an A-type trimer of proanthocyanidin (HY-N0794) found in the bark of Cinnamomum trees. Proanthocyanidin are a class of polyphenolic that are widely distributed in higher plants, consisted of an electrophilic flavanyl unit. Proanthocyanidin can be used as antioxidant and anti-cancer agent. Proanthocyanidin also exhibit anti-inflammatory, cardioprotective, antibacterial and antifungal properties, which can be used in the treatment of chronic venous insufficiency, capillary fragility, sunburn and retinopathy .
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Cat. No.: HY-181828
CAS No.: 3118902-53-4
Target:  

iGluR Dopamine Receptor

Research Areas:  

Neurological Disease

SePP is a blood-brain barrier-permeable NMDAR antagonist and dopamine/norepinephrine reuptake inhibitor, with a Ki of 28.7 nM for rat NMDAR. SePP exerts anticonvulsant effects. SePP can be used in research related to fragile X syndrome .
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Cat. No.: HY-P75187
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: FHIT; AP3A Hydrolase; Fragile Histidine Triad Diadenosine Triphosphatase; FRA3B; Bis(5'-Adenosyl)-Triphosphatase; Fragile Histidine Triad Protein; AP3Aase; Fragile Histidine Triad; Diadenosine 5',5'''-P1,P3-Triphosphate Hydrolase; Truncated Diadenosine Tr
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-182587
CAS No.: 1359087-83-4
Target:  

mAChR

Research Areas:  

Neurological Disease

VU0415248 is a selective muscarinic acetylcholine receptor 1 (M1) inhibitor. VU0415248 inhibits acetylcholine-induced calcium mobilization in cells expressing human and rat M1 muscarinic acetylcholine receptors, with an IC50 of 0.4 and 0.18 μM, respectively. VU0415248 is applicable to the research of Parkinson's disease, movement disorders and fragile X syndrome .
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Cat. No.: HY-114515
CAS No.: 1034442-21-1
Synonyms: RG7090 sulfate; RO4917523 sulfate
Target:  

mGluR

Research Areas:  

Neurological Disease

Basimglurant (RG7090; RO4917523) sulfate is a selective, orally active, blood-brain barrier permeable negative allosteric modulator of metabotropic glutamate receptor 5 (mGluR5), with a Ki of 1.4 nM (against [ 3H]-ABP688 (HY-110141)) and 35.6 nM (against [ 3H]-MPEP (HY-14609A)). Basimglurant sulfate inhibits mGlu5-mediated signaling pathways and receptor constitutive activity, regulates dopamine levels in the nucleus accumbens, exerts anxiolytic, antidepressant-like, analgesic and arousal-promoting effects, and alters δ-wave power during non-rapid eye movement sleep. Basimglurant sulfate can be used in research on depression, fragile X syndrome, anxiety disorders, etc .
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Cat. No.: HY-DY1111
CAS No.: 1539318-40-5
Target:  

DNA Stain

Research Areas:  

Neurological Disease

DFHBI-2T solution is a membrane-permeable, RNA aptamer-activated fluorescent probe (Ex/Em=500 nm/523 nm), with a Kd value of 1300 nM for the RNA aptamer Spinach2. DFHBI-2T solution binds to Spinach2, converting the fluorophore to a fluorescent state, stabilizing its planar structure to facilitate the radiative fluorescence decay pathway, and forming a complex with red-shifted excitation and emission peaks. DFHBI-2T solution can be used for RNA imaging in live cells. It is also applicable to research related to fragile X-associated tremor/ataxia syndrome .
Solvent and concentration: DMSO: 5 mM
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Cat. No.: HY-P86610
Synonyms: Fragile X mental retardation syndrome-related protein 1; hFXR1p;

Host:  

Rabbit

Application:  

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

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-P705480
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: FXR1; MYOPMIL; FMR1 Autosomal Homolog 1; MYORIBF; RNA-Binding Protein FXR1; CMYO9A; CDNA FLJ58644, Highly Similar To Fragile X Mental Retardation Syndrome-Related Protein 1; CMYO9B; Fragile X Mental Retardation Autosomal Homolog Variant P1K; CMYP9A; Fragi
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-W747508
CAS No.: 58814-86-1
Target:  

Fungal Antibiotic

Research Areas:  

Infection

Aculeacin A is a β-1,3-glucan synthase inhibitor. Aculeacin A is an antifungal antibiotic. Aculeacin A inhibits cell wall glucan synthesis in growing yeast cells, induces cell lysis, osmotic fragility, cell aggregation and abnormal cell morphology, without affecting the synthesis of proteins, nucleic acids or mannan. Aculeacin A acts only on growing yeast cells and has a narrow antifungal spectrum, mainly targeting Candida and Torulopsis species. Aculeacin A shows reduced activity in human serum and exhibits a paradoxical dose-response pattern. Aculeacin A has an inoculum effect against some Candida albicans strains, and its activity is pH-stable. Aculeacin A can be used in studies of fungal infections, such as those caused by Candida, Torulopsis and other species .
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Cat. No.: HY-15446R
CAS No.: 802906-73-6
Synonyms: RG7090 (Standard); RO4917523 (Standard)
Research Areas:  

Neurological Disease

Basimglurant (RG7090; RO4917523) (Standard) is the analytical standard of Basimglurant. This product is intended for research and analytical applications. Basimglurant is a selective, orally active, blood-brain barrier permeable negative allosteric modulator of metabotropic glutamate receptor 5 (mGluR5), with a Ki of 1.4 nM (against [ 3H]-ABP688 (HY-110141)) and 35.6 nM (against [ 3H]-MPEP (HY-14609A)). Basimglurant inhibits mGlu5-mediated signaling pathways and receptor constitutive activity, regulates dopamine levels in the nucleus accumbens, exerts anxiolytic, antidepressant-like, analgesic and arousal-promoting effects, and alters δ-wave power during non-rapid eye movement sleep. Basimglurant can be used in research on depression, fragile X syndrome, anxiety disorders, etc.
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Cat. No.: HY-P702888
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: CBL; RING-Type E3 Ubiquitin Transferase CBL; Prev. CBL2; RING Finger Protein 55; RNF55; Proto-Oncogene C-Cbl; E3 Ubiquitin-Protein Ligase CBL; Oncogene CBL2; C-Cbl; Fragile Site, Folic Acid Type, Rare, Fra(11)(Q23.3); Cas-Br-M (Murine) Ecotropic Retrovira
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-125444
CAS No.: 1622059-04-4
Target:  

LIM Kinase (LIMK)

Research Areas:  

Neurological Disease Cancer

TH251 is a LIMK1 and LIMK2 inhibitor with IC50s of 52 nM and 47 nM against LIMK1 and LIMK2, respectively. TH251 binds to inactive αC-out and DFG-out LIMK1 conformations, inhibits unphosphorylated LIMK1 and LIMK2 enzymatic activity, and exhibits unchanged potency despite PAK-mediated phosphorylation of either kinase. TH251 can be used for the research of cancers, glaucoma, and CNS diseases .
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