19 Results for "

Benzylamine

" in MedChemExpress (MCE) Product Catalog:
Products (19)

19 Results for "Benzylamine" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-17396
CAS No.: 101827-46-7
Synonyms: KP363 Hydrochloride
Target:  

Fungal Antibiotic

Research Areas:  

Infection

Butenafine Hydrochloride (KP363 Hydrochloride) is a synthetic benzylamine antifungal, works by inhibiting the synthesis of sterols by inhibiting squalene epoxidase.
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Cat. No.: HY-76253
CAS No.: 3287-99-8
Synonyms: Phenylmethylamine
Benzylamine hydrochloride is a substrate for benzylamine oxidase and monoamine oxidase B.
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Cat. No.: HY-W157055
CAS No.: 852180-47-3
Target:  

PROTAC Linkers

Research Areas:  

Cancer

4-(4-Boc-Piperazino)benzylamine is a PROTAC linker that can be used in the synthesis of PROTACs.
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Cat. No.: HY-P3983
CAS No.: 123380-68-7
Target:  

Peptides

Research Areas:  

Others

[Cys(Bzl)84] CD (81-92) is an acidic peptide. [Cys(Bzl)84] CD (81-92) can be sequencing by negative ion postsource decay (PSD) spectra .
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Cat. No.: HY-114518
CAS No.: 101828-21-1
Synonyms: KP363
Target:  

Fungal

Research Areas:  

Infection

Butenafine (KP363) is a potent and broad spectrum benzylamine antifungal agent . Butenafine inhibits fungal ergosterol biosynthesis at the point of squalene epoxidation, leading to a deficiency of the fungal cell membranes. Butenafine is effective against dermatophytes infections, such as  tinea pedis,  tinea cruris, tinea versicolor .
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Cat. No.: HY-W748107
(Rac)-Fosfomycin-d5 (benzylamine) is deuterium labeled (Rac)-Fosfomycin (benzylamine) .
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Cat. No.: HY-B1075AS
CAS No.: 1216461-18-5
Synonyms: MK-0955 (Benzylamine)-13C3
(Rac)-Fosfomycin (benzylamine)- 13C3 is the 13C labeled Fosfomycin . Fosfomycin (MK-0955) is a broad-spectrum antibiotic. Fosfomycin can cross blood-brain barrier penetrating, and irreversibly inhibits an early stage in cell wall synthesis. Fosfomycin shows anti-bacteria activity for a range of bacteria, including multidrug-resistant (MDR), extensively drug-resistant (XDR), and pan-drug-resistant (PDR) bacteria .
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Cat. No.: HY-19594
CAS No.: 5560-78-1
Synonyms: WIN 13146
Target:  

Parasite

Research Areas:  

Infection

Teclozan (WIN 13146) is an antiprotozoal agent, class in benzylamine derivatives. Teclozan intervenes in the phospholipid metabolism preventes the formation of arachidonic acid. Teclozan acts in the intestinal lumen being effective in Anti-G. intestinalis. Teclozan can be used for the research of protozoan infections .
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Cat. No.: HY-136653
CAS No.: 63269-31-8
Synonyms: WY 15705
Target:  

UGT

Research Areas:  

Neurological Disease

Ciramadol (WY 15705) is a potent and orally active analgesic agent with both narcotic agonist and UDP-glucuronyltransferase modulator properties . Ciramadol (WY 15705) can be used for postoperative pain research research.
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Cat. No.: HY-19594R
CAS No.: 5560-78-1
Synonyms: WIN 13146 (Standard)
Research Areas:  

Infection

Teclozan (Standard) is the analytical standard of Teclozan. This product is intended for research and analytical applications. Teclozan (WIN 13146) is an antiprotozoal agent, class in benzylamine derivatives. Teclozan intervenes in the phospholipid metabolism preventes the formation of arachidonic acid. Teclozan acts in the intestinal lumen being effective in Anti-G. intestinalis. Teclozan can be used for the research of protozoan infections .
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Cat. No.: HY-115771
CAS No.: 2627-27-2
Target:  

Others

Research Areas:  

Cancer

3-Phenylpropyl isothiocyanate has a stronger inhibitory effect on N-nitrosomethyl-benzylamine (NMBA) tumorigenesis. 3-Phenylpropyl isothiocyanate has chemopreventive effects .
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Cat. No.: HY-17396S
Synonyms: KP363-13C,d3 hydrochloride
Butenafine- 13C,d3 (hydrochloride) is the 13C- and deuterium labeled. Butenafine Hydrochloride (KP363 Hydrochloride) is a synthetic benzylamine antifungal, works by inhibiting the synthesis of sterols by inhibiting squalene epoxidase.
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Cat. No.: HY-114518S2
CAS No.: 1653964-70-5
Synonyms: KP363-d4
Butenafine-d4 (KP363-d4) is the deuterium labeled Butenafine (HY-114518). Butenafine (KP363) is a potent and broad spectrum benzylamine antifungal agent . Butenafine inhibits fungal ergosterol biosynthesis at the point of squalene epoxidation, leading to a deficiency of the fungal cell membranes. Butenafine is effective against dermatophytes infections, such as ?tinea pedis, ?tinea cruris, tinea versicolor .
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Cat. No.: HY-144743
CAS No.: 2771312-16-2
Research Areas:  

Others

ATX inhibitor 12 (compound 20) is an orally active and potent ATX (autotaxin) inhibitor, with an IC50 of 1.72 nM. ATX inhibitor 12 effectively alleviates lung structural damage with fewer fibrotic lesions at an oral dose of 60 mg/kg in C57Bl/6J mice. ATX inhibitor 12 can be uesd for idiopathic pulmonary fibrosis (IPF) research .
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Cat. No.: HY-161497
Research Areas:  

Cancer

Thalidomide-benzylamine-Py-NH2 is a conjugate of E3 ligase ligand and linker, which is consisted of a Thalidomide (HY-14658) and the Linker Boc-NHCH2-Ph-Py-NH2 (HY-161496). Thalidomide-benzylamine-Py-NH2 is utilized for synthesis of PROTAC molecule XYD190 (HY-161494) .
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Cat. No.: HY-76253S
CAS No.: 352431-27-7
Phenylmethanamine-d7 Hydrochloride is the deuterated-labeled Benzylamine hydrochloride (HY-76253). Benzylamine hydrochloride is a substrate for benzylamine oxidase and monoamine oxidase B.
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Cat. No.: HY-W659059
CAS No.: 76605-79-3
Target:  

Drug Derivative

Research Areas:  

Neurological Disease

N-Methyl-1-phenylpropan-1-amine hydrochloride is structurally categorized as a benzylamine.
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Cat. No.: HY-W017118A
CAS No.: 34967-23-2
Target:  

Monoamine Oxidase

Research Areas:  

Others

2,6-Dimethoxybenzylamine hydrochloride (Compound 5) exhibits reversible inhibitory activity against copper amine oxidase (CAO), that inhibits benzylamine oxidase (BAO) and monoamine oxidase B (MAO B) with IC50 of 120 μM and 190 μM .
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Cat. No.: HY-169651
CAS No.: 61-38-1
Target:  

GABA Receptor

Research Areas:  

Neurological Disease

GABA-IN-4 (Compound 17) is a N-(indol-3-ylglyoxylyl)benzylamine derivative. GABA-IN-4 exhibits high affinity for the benzodiazepine receptor (BzR) (binding site in GABAA receptor complex) with Ki value of 67 nM. Benzodiazepines are widely used as antianxiety, sedative-hypnotic and anticonvulsant agents .
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