| Catalog | name | Description | price |
|---|---|---|---|
| R-R-0756 | [D-Phe7]-Somatostatin-14 | [D-Phe7]-Somatostatin-14/CAS.64813-74-7 refers to a modified version of the natural peptide somatostatin-14, in which the seventh amino acid, phenylalanine, has been replaced with its D-enantiomer form. Somatostatin-14 is a biologically active peptide involved in the regulation of various physiological processes, including the inhibition of growth hormone secretion, inhibition of insulin and glucagon release, and modulation of gastrointestinal functions. | price> |
| R-R-0824 | [D-Leu2]-Melanocyte-Stimulating Hormone-Release Inhibiting Factor | [D-Leu2]-Melanocyte-Stimulating Hormone-Release Inhibiting Factor/CAS.39705-60-7 is a modified form of the naturally occurring Melanocyte-Stimulating Hormone-Release Inhibiting Factor (MIF). The modification involves substituting the amino acid Leucine with its D-stereoisomer (D-Leu) at position 2 within the peptide sequence. | price> |
| R-R-0831 | HIV-gp41-Fragment | HIV-gp41-Fragment/CAS:129426-47-7 from ruixi. The hexapeptide AVGIGA is identical in sequence to the first 6 N-terminal amino acids of the gp41 subunit of the HIV envelope glycoprotein. It was found to completely inhibit the HIV-induced syncytium formation (ID50 = 0.75 mM). | price> |
| R-R-0832 | C34, gp41 HIV Fragment | This C34 peptide, also known as HR2, belongs to the helical region of gp41 of HIV, C-terminal heptad repeat 2 (HR2) defined as C helix or C peptide. It is known that HIV-1 enters cells by membrane fusion, C34 gp41 peptide is a potent inhibitors of HIV-1 fusion. | price> |
| R-R-0833 | HIV -gp120- Fragment (421-438) | Understanding the biology of the HIV-gp120 protein, including specific fragments like (421-438), can aid in the development of strategies to prevent viral entry, neutralize viral infectivity, or elicit an effective immune response against HIV. | price> |
| R-R-0840 | a-Methyl-DL-aspartic acid | α-Methyl-DL-aspartic acid/Cas.2792-66-7 is a specific inhibitor of argininosuccinate synthase (ASS), and also is the rate-limiting enzyme for the recycling of 1-citrulline to 1-arginine. | price> |
| R-R-0844 | a-Methyltyrosine methyl ester hydrochloride | α-Methyltyrosine methyl ester hydrochloride/Cas .7361-31-1 is a competitive tyrosine hydroxylase inhibitor that inhibits the conversion of tyrosine to dopamine. α-Methyltyrosine methyl ester hydrochloride can be used as a tool for sympathetic nervous system research. | price> |
| R-R-0851 | 187-1, N-WASP inhibitor | 187-1, N-WASP inhibitor/Cas.380488-27-7 from ruixi. Inhibitor of neural Wiskott-Aldrich syndrome protein (N-WASP). | price> |
| R-R-0853 | BIO-1211 (trifluoroacetate salt) | BIO-1211 is a peptide inhibitor of α4β1 integrin (IC50 = 0.004 µM).1 It is selective for α4β1 integrin over α4β7 (IC50 = 2 µM), as well as α1β1, α5β1, α6β1, αLβ2, and αIIbβ3 (IC50s = >100 µM for all). BIO-1211 binds to α4β1 (IC50 = 1 nM) and inhibits Jurkat cell adhesion (IC50 = 4 nM). Inhaled administration of BIO-1211 (3 mg/animal) prevents carbachol-induced airway hyperresponsiveness in an ovine model of allergy-induced asthma. | price> |
| R-R-0860 | Retatrutide | Retatrutide (LY3437943)/CAS.2381089-83-2 is a triple agonist peptide of the glucagon receptor (GCGR), glucosedependent insulinotropic polypeptide receptor (GIPR), and glucagon-like peptide-1 receptor (GLP-1R). Retatrutide inhibits human GCGR, GIPR, and GLP-1R with EC50 values of 5.79, 0.0643 and 0.775 nM, respectively. Retatrutide can be used for the research of obesity. | price> |

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