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(2S,4S)-1-((S)-2-amino-3,3-dimethylbutanoyl)-4-hydroxy-N-((S)-1-(4-(4-methylthiazol-5-yl)phenyl)ethyl)pyrrolidine-2-carboxamide hydrochloride is a synthetic peptidomimetic intermediate used in pharmaceutical research and synthesis. It is supplied as a white to yellow solid with molecular weight 481.05 g/mol and CAS 2380273-26-5; batch COA reports LCMS purity 98.59%. Recommended storage is -20°C, sealed, protected from moisture and light.
Hydrochloride salt suitable for synthetic intermediates
High purity (98.6%) by LCMS
White to yellow solid appearance
Molecular weight 481.05 g/mol; CAS 2380273-26-5
Intended for use as a drug intermediate and research chemical
Store at -20°C, sealed, protect from moisture and light
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Pyridin-4-ol is a biochemical reagent primarily used in life science research. It functions as a biological material or organic compound, supporting various scientific investigations.
Used as a biochemical reagent
Suitable for life science related research
Functions as a biological material or organic compound
Appears as a white to yellow solid
Soluble in DMSO
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N-Boc-dolaproine-amide-Me-Phe is a Boc-protected amino acid fragment derived from the pentapeptide Dolastatin 10, provided as a high-purity research reagent for studies of tubulin polymerization and antimitotic activity.
High purity suitable for research applications.
Available as a solid and as a 10 mM solution in DMSO.
Stable when stored sealed at 4°C; in solution, store at -80°C for long-term storage.
Light yellow solid appearance.
Commonly used for peptide synthesis and structure-activity studies.
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Human GIP(3-30), amide TFA is the TFA salt form of human GIP(3-30), amide (HY-P10138). It is a high affinity antagonist of the human GIP receptor in vitro. Human GIP(3-30), amide TFA has potential anti-obesity and anti-diabetic effects.
High affinity antagonist of the human GIP receptor in vitro.
Potential anti-obesity effects.
Potential anti-diabetic effects.
Competitively binds to GIP receptor (GIPR), blocking GIP-mediated cAMP accumulation (Ki=16.8 nM), β-arrestin recruitment (Ki for β-arrestin-1/2 recruitment is 10.6 nM and 10.2 nM) and receptor internalization.
Inhibits GIP mediated insulin secretion and signal transduction in adipocytes.
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