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Hemopressin trifluoroacetate salt_Molecular_structure_CAS_568588-77-2(freebase))
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Hemopressin trifluoroacetate salt

Catalog No. H3042 Name Sigma Aldrich
CAS Number 568588-77-2(freebase) Website http://www.sigmaaldrich.com
M. F. C55H78F3N13O14 Telephone 1-800-521-8956
M. W. 1202.2817296 Fax
Purity ≥98% (HPLC) Email
Storage Chembase ID: 154857

SYNONYMS

IUPAC name
(2S)-2-[(2S)-2-[(2S)-2-[(2S)-2-[(2S)-6-amino-2-[(2S)-2-[(2S)-3-carbamoyl-2-[(2S)-3-methyl-2-[(2S)-pyrrolidin-2-ylformamido]butanamido]propanamido]-3-phenylpropanamido]hexanamido]-3-phenylpropanamido]-4-methylpentanamido]-3-hydroxypropanamido]-3-(1H-imidazol-4-yl)propanoic acid; trifluoroacetic acid
IUPAC Traditional name
(2S)-2-[(2S)-2-[(2S)-2-[(2S)-2-[(2S)-6-amino-2-[(2S)-2-[(2S)-3-carbamoyl-2-[(2S)-3-methyl-2-[(2S)-pyrrolidin-2-ylformamido]butanamido]propanamido]-3-phenylpropanamido]hexanamido]-3-phenylpropanamido]-4-methylpentanamido]-3-hydroxypropanamido]-3-(1H-imidazol-4-yl)propanoic acid; trifluoroacetic acid
Synonyms
Hemopressin from rat brain
L-Prolyl-L-valyl-L-asparaginyl-L-phenylalanyl-L-lysyl-L-phenylalanyl-L-leucyl-L-seryl-L-histidine trifluoroacetate salt
Pro-Val-Asn-Phe-Lys-Phe-Leu-Ser-His trifluoroacetate salt
Hemopressin from rat

DATABASE IDS

MDL Number MFCD19443861
CAS Number 568588-77-2(freebase)

PROPERTIES

Empirical Formula (Hill Notation) C53H77N13O12 · xC2HF3O2
Purity ≥98% (HPLC)
Shipped in wet ice
Apperance white to off-white powder
Solubility H2O: ≥2 mg/mL
MSDS Link Download
Storage Temperature -20°C
German water hazard class 3

DETAILS

Description (English)
Biochem/physiol Actions
Hemopressin is an endogenous hypotensive nonapeptide derived from hemoglobin. Hemopressin reduces appetite, acting as a cannabinoid CB1 inverse agonist. It blocks signaling by CB(1) receptors but not by other members of family A G protein-coupled receptors (including the closely related CB(2) receptors.
Description (简体中文)
Biochem/physiol Actions
Hemopressin is an endogenous hypotensive nonapeptide derived from hemoglobin. Hemopressin reduces appetite, acting as a cannabinoid CB1 inverse agonist. It blocks signaling by CB(1) receptors but not by other members of family A G protein-coupled receptors (including the closely related CB(2) receptors.

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