2365 Results for "

nucleophilic arylboronic acid coupling partner

" in MedChemExpress (MCE) Product Catalog:
Products (2365)

2365 Results for "nucleophilic arylboronic acid coupling partner" in MCE Product Catalog:

53
53 Publications Verification
Cat. No.: HY-B0445A
CAS No.: 20111-18-6
Synonyms: β-DPN sodium; β-NAD sodium; β-Nicotinamide Adenine Dinucleotide sodium
NAD sodium is an orally effective cofactor and homeostatic regulator. NAD sodium can be reduced to β-nicotinamide adenine dinucleotide (NADH) during coupling with reactions that oxidize organic substrates. NAD sodium can be converted to β-nicotinamide adenine dinucleotide (NADH) and passes to the inside of mitochondria, which indirectly generates ATP. NAD sodium can be used for the research of non-alcoholic fatty liver disease, obesity, and glucose intolerance .
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43
43 Cited Publications
Cat. No.: HY-P0014
CAS No.: 204656-20-2
Liraglutide is a glucagon-like peptide-1 (GLP-1) receptor agonist used clinically to treat type 2 diabetes mellitus.
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43
43 Cited Publications
Cat. No.: HY-P0014B
Target:  

GLP Receptor

Research Areas:  

Metabolic Disease

Liraglutide (TFA) is an agonist of glucagon-like peptide 1 receptor (GLP-1). Liraglutide (TFA) can activate GLP-1, leading to the release of insulin in the presence of increased glucose concentration. Liraglutide (TFA) also reduces glucagon secretion in a glucose-dependent manner. Liraglutide (TFA) can be studied in research on type 2 diabetes .
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18
18 Cited Publications
Cat. No.: HY-113466
CAS No.: 75899-68-2
Purity:  99.35%
Synonyms: 4-HNE
4-Hydroxynonenal (4-HNE) is an α,β unsaturated hydroxyalkenal and an oxidative/nitrosative stress biomarker. 4-Hydroxynonenal is a substrate and an inhibitor of acetaldehyde dehydrogenase 2 (ALDH2). 4-Hydroxynonenal can modulate a number of signaling processes mainly through forming covalent adducts with nucleophilic functional groups in proteins, nucleic acids, and membrane lipids. 4-Hydroxynonenal plays an important role in cancer through mitochondria .
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13
13 Cited Publications
Cat. No.: HY-W016319
CAS No.: 138-15-8
Research Areas:  

Others

(S)-2-aminopentanedioic acid hydrochloride is a glutamic acid derivative .
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12
12 Cited Publications
Cat. No.: HY-101444A
CAS No.: 100929-99-5
Purity:  99.89%
Synonyms: MC-207,110 dihydrochloride; Phe-Arg-β-naphthylamide dihydrochloride
Target:  

Bacterial

Research Areas:  

Infection

PAβN dihydrochloride (MC-207110 dihydrochloride) is an efflux pump inhibitor.
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10
10 Cited Publications
Cat. No.: HY-N0473A
CAS No.: 69847-45-6
Research Areas:  

Others Cancer

L-Tyrosine (disodium) is a tyrosine derivative .
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8
8 Cited Publications
Cat. No.: HY-15578
CAS No.: 863971-19-1
Purity:  99.96%
Synonyms: Maleimidocaproyl monomethylauristatin F
McMMAF (Maleimidocaproyl monomethylauristatin F) is a drug-linker conjugate for ADCs, formed by coupling the potent microtubule inhibitor Monomethyl auristatin F (MMAF) (HY-15579) with a maleimidocaproyl (mc) linker. McMMAF can be conjugated with anti-BCMA antibodies to form J6M0-mcMMAF, promoting apoptosis and inhibiting tumor growth .
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7
7 Cited Publications
Cat. No.: HY-112096
CAS No.: 1914078-41-3
Purity:  99.17%
Synonyms: NXP900
Target:  

Src

Research Areas:  

Cancer

eCF506 (NXP900) is a highly potent and orally active YES1/SRC kinase inhibitor with an IC50 of 0.47 nM. eCF506 locks its target into its native “closed” conformation, thereby inhibiting both kinase activity and complex formation with protein partners. eCF506 can be used for the study of esophageal squamous cancer and breast cancer .
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7
7 Cited Publications
Cat. No.: HY-100788
CAS No.: 173039-10-6
Purity:  ≥98.0%
Synonyms: 2-(Phosphonomethyl)pentanedioic acid
Target:  

Carboxypeptidase

Research Areas:  

Neurological Disease

2-PMPA (2-(Phosphonomethyl)pentanedioic acid) is a glutamate carboxypeptidase II (GCPII) inhibitor with an IC50 of 0.0003 μM. 2-PMPA shows low blood-brain barrier penetration. 2-PMPA sodium blocks the hydrolysis of NAAG, regulates glutamate levels in the brain and neurovascular coupling. 2-PMPA is applicable to the research of neurological diseases .
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7
7 Cited Publications
Cat. No.: HY-100788C
CAS No.: 373645-42-2
Synonyms: 2-(Phosphonomethyl)pentanedioic acid sodium
Target:  

Carboxypeptidase

Research Areas:  

Neurological Disease

2-PMPA (2-(Phosphonomethyl)pentanedioic acid) sodium is a glutamate carboxypeptidase II (GCPII) inhibitor with an IC50 of 0.0003 μM. 2-PMPA sodium shows low blood-brain barrier penetration. 2-PMPA sodium blocks the hydrolysis of NAAG, regulates glutamate levels in the brain and neurovascular coupling. 2-PMPA sodium is applicable to the research of neurological diseases .
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7
7 Cited Publications
Cat. No.: HY-112461A
CAS No.: 627034-85-9
Purity:  97.39%
Target:  

P2X Receptor

Research Areas:  

Cardiovascular Disease

NF449 octasodium is a highly potent P2X1 receptor antagonist, with IC50s of 0.28, 0.69, and 120 nM for rP2X1, rP2X1+5, P2X2+3, respectively. NF449 octasodium is a Gsα-selective G Protein antagonist. NF449 octasodium suppresses the rate of GTP[γS] binding to Gsα-s, inhibits the stimulation of adenylyl cyclase activity, and blocks the coupling of β-adrenergic receptors to Gs .
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7
7 Cited Publications
Cat. No.: HY-W011391A
CAS No.: 7300-59-6
Research Areas:  

Others

L-γ-Glutamyl-p-nitroanilide Monohydrate is a glutamic acid derivative .
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7
7 Cited Publications
Cat. No.: HY-W345421
CAS No.: 122864-94-2
Research Areas:  

Others

L-γ-Glutamyl-p-nitroanilide (hydrate) is aglutamic acid derivatives.
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5
5 Cited Publications
Cat. No.: HY-W009203
CAS No.: 30925-07-6
L-Cystine dihydrochloride is the dihydrochloride salt form of L-Cystine (HY-N0394). L-Cystine dihydrochloride elevates Nrf2 protein expression and activates Nrf2 transcription factor. L-cystine dihydrochloride reduces ROS generation and protects against oxidant- or Doxorubicin (HY-15142A)-induced apoptosis. L-Cystine dihydrochloride combined with L-theanine (HY-15121) enhances the production of antigen-specific IgG by increasing glutathione (GSH) levels and T helper 2 (Th2) mediated responses in mice. L-Cystine dihydrochloride is promising for research of cystinuria and kidney stones
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5
5 Cited Publications
Cat. No.: HY-W142119
CAS No.: 2792-66-7
Target:  

Ser/Thr Protease

Research Areas:  

Neurological Disease

α-Methyl-DL-aspartic acid is a specific inhibitor of argininosuccinate synthase (ASS), and also is the rate-limiting enzyme for the recycling of 1-citrulline to 1-arginine .
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4
4 Cited Publications
Cat. No.: HY-W014375
CAS No.: 32042-43-6
Synonyms: (±)-Arginine hydrochloride
Target:  

Endogenous Metabolite

Research Areas:  

Cardiovascular Disease

DL-Arginine ((±)-Arginine) hydrochloride is the racemic compound of L-Arginine (HY-N0455) and D-Arginine (HY-W016781). Arginine is an essential amino acid that requires additional supplementation in traumatic or diseased conditions. Arginine is involved in T cell activation, proliferation, and differentiation, and affects the function of immune cells .
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4
4 Cited Publications
Cat. No.: HY-W142162
CAS No.: 6027-02-7
Research Areas:  

Others

L-Histidine dihydrochloride is a histidine derivative .
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3
3 Cited Publications
Cat. No.: HY-P3462
CAS No.: 1415456-99-3
Target:  

CGRP Receptor

Research Areas:  

Metabolic Disease

Cagrilintide is an investigational novel long-acting acylated amylin analogue, acts as nonselective amylin receptors (AMYR) and calcitonin G protein-coupled receptor (CTR) agonist. Cagrilintide induces significant weight loss and reduces food intake. Cagrilintide has the potential for the research of obesity .
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3
3 Cited Publications
Cat. No.: HY-P3462A
Target:  

CGRP Receptor

Research Areas:  

Metabolic Disease

Cagrilintide acetate is a non-selective AMYR/CTR agonist and long-acting acylated amylase analogue. Cagrilintide acetate causes a reduction in food intake and significant weight loss in a dose-dependent manner. Cagrilintide acetate can be used in obesity studies .
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