1815 Results for "

amino-acid

" in MedChemExpress (MCE) Product Catalog:

Products (1815)

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Liraglutide

43 Cited Publications

Cat. No.: HY-P0014

CAS No.: 204656-20-2

Target:

GCGR GLP Receptor

Research Areas:

Neurological Disease Metabolic Disease Inflammation/Immunology

Liraglutide is a glucagon-like peptide-1 (GLP-1) receptor agonist used clinically to treat type 2 diabetes mellitus.

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Liraglutide TFA

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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(S)-2-aminopentanedioic acid hydrochloride

13 Cited Publications

Cat. No.: HY-W016319

CAS No.: 138-15-8

Target:

Amino Acid Derivatives

Research Areas:

Others

(S)-2-aminopentanedioic acid hydrochloride is a glutamic acid derivative .

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PAβN dihydrochloride

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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L-Tyrosine disodium salt

10 Cited Publications

Cat. No.: HY-N0473A

CAS No.: 69847-45-6

Target:

Amino Acid Derivatives

Research Areas:

Others Cancer

L-Tyrosine (disodium) is a tyrosine derivative .

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L-γ-Glutamyl-p-nitroanilide

7 Cited Publications

Cat. No.: HY-W011391A

CAS No.: 7300-59-6

Target:

Amino Acid Derivatives

Research Areas:

Others

L-γ-Glutamyl-p-nitroanilide Monohydrate is a glutamic acid derivative .

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L-γ-Glutamyl-p-nitroanilide hydrate

7 Cited Publications

Cat. No.: HY-W345421

CAS No.: 122864-94-2

Target:

Amino Acid Derivatives

Research Areas:

Others

L-γ-Glutamyl-p-nitroanilide (hydrate) is aglutamic acid derivatives.

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L-Cystine dihydrochloride

5 Cited Publications

Cat. No.: HY-W009203

CAS No.: 30925-07-6

Category:

Ketones, Aldehydes, Acids Other Diseases Endogenous metabolite Disease Research Fields

Target:

Endogenous Metabolite Apoptosis Keap1-Nrf2 Reactive Oxygen Species (ROS) Ferroptosis

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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α-Methyl-DL-aspartic acid

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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CCZ01048 TFA

4 Cited Publications

Cat. No.: HY-P2336A

Target:

Melanocortin Receptor

Research Areas:

Cancer

CCZ01048 TFA, a α-MSH analogue, exhibits high binding affinity to melanocortin 1 receptor (MC1R) with a K_i of 0.31 nM. CCZ01048 TFA shows rapid internalization into B16F10 melanoma cells and high in vivo stability. CCZ01048 TFA is a promising candidate for PET imaging of malignant melanoma .

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Murepavadin TFA

4 Cited Publications

Cat. No.: HY-P1674A

CAS No.: 3053070-05-3

Synonyms: POL7080 TFA

Target:

Bacterial Antibiotic

Research Areas:

Infection

Murepavadin (POL7080) (TFA), a 14-amino-acid cyclic peptide, is a highly potent, specific antibiotic. Murepavadin exhibits a potent antimicrobial activity for P. aeruginosa with MIC₅₀ and MIC₉₀ values both of 0.12 mg/L. Murepavadin also can target the lipopolysaccharide transport portin D. Murepavadin can be used for the research of bacterial resistance .

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DL-Arginine hydrochloride

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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L-Histidine dihydrochloride

4 Cited Publications

Cat. No.: HY-W142162

CAS No.: 6027-02-7

Target:

Amino Acid Derivatives

Research Areas:

Others

L-Histidine dihydrochloride is a histidine derivative .

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Cagrilintide

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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Cagrilintide acetate

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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2-(Methylamino)acetic acid hydrochloride

3 Cited Publications

Cat. No.: HY-W012791

CAS No.: 637-96-7

Target:

Amino Acid Derivatives

Research Areas:

Others

2-(Methylamino)acetic acid hydrochloride is a Glycine (HY-Y0966) derivative .

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N-[3-(2-Furyl)acryloyl]-Phe-Gly-Gly

3 Cited Publications

Cat. No.: HY-W010991

CAS No.: 64967-39-1

Synonyms: FAPGG

Target:

Angiotensin-converting Enzyme (ACE)

Research Areas:

Others

N-[3-(2-Furyl)acryloyl]-Phe-Gly-Gly (FAPGG) is a specific substrate of angiotensin converting enzyme (ACE) with a Ki of 2.546×10 ^-4 M. It is used as a chromogenic probe for quantitative detection of ACE activity. N-[3-(2-Furyl)acryloyl]-Phe-Gly-Gly can be hydrolyzed by ACE to generate N-[3-(2-furyl)acryloyl]-Phe (FAP) and Gly-Gly, and the ACE inhibitory effect is monitored by photometry. FAPGG competitively binds to the active center of ACE and is a key tool for screening ACE inhibitors such as Captopril (HY-B0368) and Dioscorin. Its reversible mechanism of action supports hypertension research and drug development targeting the renin-angiotensin system .

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Glycyl-L-histidyl-L-lysine

3 Cited Publications

Cat. No.: HY-P0046

CAS No.: 49557-75-7

Synonyms: GHK; Tripeptide-1

Target:

Inhibitory Antibodies

Research Areas:

Neurological Disease Inflammation/Immunology

Glycyl-L-histidyl-L-lysine is a tripeptide consisting of glycine, L-histidine and L-lysine residues joined in sequence. Glycyl-L-histidyl-L-lysine is a hepatotropic immunosuppressor and shows anxiolytic effect. Glycyl-L-histidyl-L-lysine and its copper complexes show good skin tolerance .

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Chlorotoxin

2 Cited Publications

Cat. No.: HY-P0173A

CAS No.: 163515-35-3

Category:

Natural Products Animals Disease Research Fields Cancer

Target:

Chloride Channel

Chlorotoxin is a 36 amino-acid peptide from the venom of the Israeli scorpion Leiurus quinquestriatus with anticancer activity. Chlorotoxin is a chloride channel blocker.

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Angstrom6

2 Cited Publications

Cat. No.: HY-P2230

CAS No.: 220334-14-5

Synonyms: A6 Peptide

Target:

PAI-1

Research Areas:

Cancer

Angstrom6 (A6 Peptide) is an 8 amino-acid peptide derived from single-chain urokinase plasminogen activator (scuPA) and interferes with the uPA/uPAR cascade and abrogates downstream effects. Angstrom6 binds to CD44 resulting in the inhibition of migration, invasion, and metastasis of tumor cells, and the modulation of CD44-mediated cell signaling .

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