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Natriuretic Peptide, C-Type_Molecular_structure_CAS_127869-51-6)
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Natriuretic Peptide, C-Type

Catalog No. N8768 Name Sigma Aldrich
CAS Number 127869-51-6 Website http://www.sigmaaldrich.com
M. F. C93H157N27O28S3 Telephone 1-800-521-8956
M. W. 2197.60078 Fax
Purity ≥95% (HPLC) Email
Storage Chembase ID: 133940

SYNONYMS

IUPAC name
(4R,10S,16S,19S,22S,28S,31S,34S,37S,40S,43S,49S,52R)-52-{2-[(2S)-6-amino-2-[(2S)-2-[(2S)-2-(2-aminoacetamido)-4-methylpentanamido]-3-hydroxypropanamido]hexanamido]acetamido}-40-(4-aminobutyl)-49-benzyl-28-[(2S)-butan-2-yl]-31-(3-carbamimidamidopropyl)-34-(carboxymethyl)-16,22-bis(hydroxymethyl)-10,37,43-tris(2-methylpropyl)-19-[2-(methylsulfanyl)ethyl]-6,9,12,15,18,21,24,27,30,33,36,39,42,45,48,51-hexadecaoxo-1,2-dithia-5,8,11,14,17,20,23,26,29,32,35,38,41,44,47,50-hexadecaazacyclotripentacontane-4-carboxylic acid
IUPAC Traditional name
(4R,10S,16S,19S,22S,28S,31S,34S,37S,40S,43S,49S,52R)-52-{2-[(2S)-6-amino-2-[(2S)-2-[(2S)-2-(2-aminoacetamido)-4-methylpentanamido]-3-hydroxypropanamido]hexanamido]acetamido}-40-(4-aminobutyl)-49-benzyl-28-[(2S)-butan-2-yl]-31-(3-carbamimidamidopropyl)-34-(carboxymethyl)-16,22-bis(hydroxymethyl)-10,37,43-tris(2-methylpropyl)-19-[2-(methylsulfanyl)ethyl]-6,9,12,15,18,21,24,27,30,33,36,39,42,45,48,51-hexadecaoxo-1,2-dithia-5,8,11,14,17,20,23,26,29,32,35,38,41,44,47,50-hexadecaazacyclotripentacontane-4-carboxylic acid
Synonyms
CNP

DATABASE IDS

MDL Number MFCD00080348
CAS Number 127869-51-6

PROPERTIES

Compostion Peptide content, ≥65%
Purity ≥95% (HPLC)
Gene Information human ... NPPC(4880)
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Storage Temperature -20°C
German water hazard class 3

DETAILS

Description (English)
Amino Acid Sequence
Gly-Leu-Ser-Lys-Gly-Cys-Phe-Gly-Leu-Lys-Leu-Asp-Arg-Ile-Gly-Ser-Met-Ser-Gly-Leu-Gly-Cys [Disulfide Bridge: 6-22]
Biochem/physiol Actions
C-type natriuretic peptide is produced in the hypothalamus, anterior pituitary, and most major endocrine glands. It has potent venodilatory and coronary vasodilatory effects, but minimal effects on renal function.

REFERENCES