46 Results for "

BF

" in MedChemExpress (MCE) Product Catalog:
Products (46)

46 Results for "BF" in MCE Product Catalog:

12
12 Publications Verification
Cat. No.: HY-12054
CAS No.: 422513-13-1
Purity:  98.89%
Research Areas:  

Cancer

Hesperadin is an ATP competitive indolinone inhibitor of Aurora A and B. Hesperadin inhibits Aurora B with an IC50 of 250 nM. Hesperadin inhibits the growth of Trypanosoma brucei by blocking nuclear division and cytokinesis. Hesperadin also is a broad-spectrum influenza antiviral .
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6
6 Cited Publications
Cat. No.: HY-U00426
CAS No.: 1436383-95-7
Research Areas:  

Infection

BF738735 is a phosphatidylinositol 4-kinase III beta (PI4KIIIβ) inhibitor with an IC50 of 5.7 nM.
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2
2 Cited Publications
Cat. No.: HY-12199B
CAS No.: 903576-44-3
Purity:  99.51%
Synonyms: Ciproxidine; BF 2649
Target:  

Histamine Receptor

Research Areas:  

Neurological Disease Endocrinology

Pitolisant hydrochloride is a potent and selective nonimidazole inverse agonist at the recombinant human histamine H3 receptor (Ki=0.16 nM).
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2
2 Cited Publications
Cat. No.: HY-141487
CAS No.: 312749-73-8
Purity:  99.92%
CLP-3094 is a potent BF3 (binding function 3)-directed inhibitor of the androgen receptor (AR). CLP-3094 inhibits AR transcriptional activity (IC50=4 μM) . CLP-3094 is a selective, potent GPR142 antagonist .
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1
1 Cited Publications
Cat. No.: HY-P72137
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: Cfb; BF; H2-BFComplement factor B; EC 3.4.21.47; C3/C5 convertase; Complement factor B Ba fragment; Complement factor B Bb fragment
Species:  
Source:  
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Cat. No.: HY-105252A
CAS No.: 845647-80-5
Purity:  98.88%
Target:  

Amyloid-β

Research Areas:  

Neurological Disease

BF 227 is a candidate for an amyloid imaging probe for PET, with a Ki of 4.3 nM for Aβ1-42 fibrils.
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Cat. No.: HY-161746
CAS No.: 2941386-44-1
Target:  

AUTOTACs Autophagy

Research Areas:  

Neurological Disease

Anle138b-F105 is an autophagy-targeting chimera (AUTOTAC) that targets p62/Sequestosome-1/SQSTM1. Anle138b-F105 binds to the ZZ domain of p62, induces conformational activation, self-oligomerization, interaction with LC3, and formation of autophagosomes. Anle138b-F105 induces autophagic flux of ubiquitin-conjugated aggregated proteins, leading to their lysosomal degradation. Anle138b-F105 is applicable for the research of neurodegenerative proteinopathies .
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Cat. No.: HY-W033277
CAS No.: 21797-13-7
Synonyms: NSC 307191; Palladium(II) tetrafluoroborate tetraacetonitrile complex
Research Areas:  

Others

Tetrakis(acetonitrile)palladium(II) tetrafluoroborate (NSC 307191) acts as a potent Lewis acid and facilitates the formation of the 2:1 complex [Pd(1,2-bis(2′-pyridylethynyl)benzene)2](BF4)2 through the Sonogashira cross-coupling reaction.
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Cat. No.: HY-120018
CAS No.: 218464-59-6
Purity:  99.87%
Target:  

Androgen Receptor

Research Areas:  

Cancer

VPC-13566, a BF3-specific small molecule, is an androgen receptor (AR) inhibitor. VPC-13566 is effective in inhibiting AR transcriptional activity in vitro as well as the growth of AR-dependent PCa cell lines. VPC-13566 can be used as a chemical probe to help identify unknown AR partners.VPC-13566 can be used for the research of cancer.
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Cat. No.: HY-W338446
CAS No.: 22191-97-5
Target:  

Tau Protein

Research Areas:  

Neurological Disease

BF-170 is a selective tau fibril binding agent with an EC50 of 221 nM. It exhibits good blood-brain barrier permeability, and after intravenous injection in mice, the concentration in brain tissue reaches 9.1% ID/g within 2 minutes (with a brain clearance rate of 0.25% ID/g after 30 minutes). BF-170 can be used as a probe for tau protein pathology imaging in Alzheimer's disease (AD). It plays an important role in early-stage AD research and holds potential for imaging studies of tau-related neurodegenerative diseases .
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Cat. No.: HY-138443A
CAS No.: 1333375-02-2
BF-175 is a selective SIRT1 agonist. BF175 increases SIRT1-mediated activation of PGC1-α, induces Apoptosis, induces Autophagy and inhibits SREBP activity. BF-175 protects against high glucose-mediated mitochondrial injury. BF-175 attenuates diabetic kidney disease progression. BF175 inhibits endometrial carcinoma .
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Cat. No.: HY-P3350
CAS No.: 2892148-58-0
Target:  

Bacterial

Research Areas:  

Infection

LS-BF1 is a stable and low toxic cationic antimicrobial peptide. LS-BF1 displays broad spectrum of antibacterial activity, including the challenging ESKAPE pathogens, by cell membrane disruptive mechanism. LS-BF1 shows good in vivo efficacy for elimination of bacteria in a mouse infection model[1].
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Cat. No.: HY-170799
CAS No.: 2127358-36-3
Research Areas:  

Infection

HNC-1664 is the orally active inhibitor for RNA-dependent RNA polymerase (RdRP). HNC-1664 exhibits broad-spectrum antiviral activity against coronavirus (SARS-CoV-2 wildtype and its mutants XBB.1.18, HK.3.1, BF.7.14, BA.1HCoV-229E, HCoV-OC43) and arenavirus. HNC-1664 exhibits anti-infectious activity in SARS-CoV-2 Delta infected mouse models .
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Cat. No.: HY-139046
CAS No.: 331948-99-3
Target:  

Adrenergic Receptor

Research Areas:  

Neurological Disease

MEPB is a modulator of AF-2 of the androgen receptor. MEPB increases co-repressor binding of AR. MEPB can bind to the BF3 pocket of AR specifically, thereby modulating the binding of co-regulators to the AF2 domain. MEPB alleviates degeneration in spinal bulbar muscular atrophy mouse model .
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Cat. No.: HY-120726
CAS No.: 1404506-35-9
Target:  

HSP

Research Areas:  

Others

BF844 mitigate hearing loss associated with USH3 (usher syndrome type III) mutation CLRN1 (clarin-1) N48K. BF844 induces CLRN1 N48K transportes to the plasma membrane. BF844 shows significantly preserves hearing in vivo .
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Cat. No.: HY-W007489
CAS No.: 3581-89-3
Research Areas:  

Others

5-Methylthiazole can be used to generate mobile ionic liquids through alkylation with n-butyl bromide and anion exchange of Br - for BF4 - .
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Cat. No.: HY-12054A
Research Areas:  

Cancer

Hesperadin hydrochloride is an ATP competitive indolinone inhibitor of Aurora A and B. Hesperadin hydrochloride inhibits Aurora B with an IC50 of 250 nM .
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Cat. No.: HY-119946
CAS No.: 518980-66-0
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

BF-1 is a 5-HT2B receptor antagonist with a pKi value of 10.05 and an IC50 value of 2.6 nM .
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Cat. No.: HY-112830
CAS No.: 634911-47-0
Purity:  99.68%
Target:  

Amyloid-β

Research Areas:  

Neurological Disease

BF-168, a candidate probe for PET, is found to specifically recognize both neuritic and diffuse plaques, with a Ki of 6.4 nM for Aβ1-42.
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Cat. No.: HY-106897
CAS No.: 127245-22-1
Synonyms: Biofor 389
Target:  

COX Lipoxygenase

Research Areas:  

Inflammation/Immunology

BF389 (Biofor 389) is an orally active anti-inflammatory and analesis agent. BF389 is also an inhibitor of cyclooxygenase and 5-lipoxygenase, with IC50s of 4 and 8 ug/mL for COX-1 and COX-2 respectively. BF389 can be used for arthritis research .
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