S3136
[pGlu6]-Substance P Fragment 6-11
≥95% (HPLC)
Synonym(s):
pGlu-Phe-Phe-Gly-Leu-Met-NH2
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About This Item
Empirical Formula (Hill Notation):
C36H49N7O7S
CAS Number:
Molecular Weight:
723.88
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
Assay
≥95% (HPLC)
UniProt accession no.
storage temp.
−20°C
SMILES string
CSCCC(NC(=O)C(CC(C)C)NC(=O)CNC(=O)C(Cc1ccccc1)NC(=O)C(Cc2ccccc2)NC(=O)C3CCC(=O)N3)C(N)=O
Gene Information
human ... TAC1(6863)
Biochem/physiol Actions
Substance P agonist; increased blood pressure when injected into cerebral ventricles of rat.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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M E Hall et al.
Peptides, 5(1), 85-89 (1984-01-01)
Substance P (SP) significantly reduced fighting in mice made aggressive by prolonged isolation. The N-terminal heptapeptide fragment SP (1-7) also reduced fighting. The C-terminal fragment SP(4-11) was without activity, while the shorter C-terminal fragment analog less than E-SP(7-11) significantly increased
W A Turski et al.
The International journal of biochemistry, 19(12), 1233-1236 (1987-01-01)
1. Peptidase(s) activity of nuclear and synaptosomal fraction from cortex and hippocampus of rat brain against pyroGlu6[125I-Tyr8]SP6-11 was evaluated in different concentration of Ca2+, Mg2+, K+ and Na+ in about "isotonic" conditions. 2. The effects of studied ions on the
U Wormser et al.
Biochimica et biophysica acta, 798(1), 28-36 (1984-03-22)
Inactivation of substance P and its C-terminal hexapeptide analog [p-Glu6]substance P6-11 was studied in rat parotid and hypothalamic slices. It was found that in the parotid slice system the decay of substance P induced K+ release occurs concurrently with a
U Wormser et al.
Neuropeptides, 16(1), 41-49 (1990-05-01)
Five synthetic N-methylated analogs (II-V) of the C-terminal hexapeptide analog of substance P (SP), [pGlu6]SP6-11 (I) were evaluated for their metabolic stability and in vitro spasmogenic activity. The metabolic resistance of the analogs was tested by two SP degrading systems
The pressor response to substance P and hexapeptide [pGlu6]SP 6--11 injections into the cerebral ventricles in rats.
W Z Traczyk et al.
Neuropharmacology, 19(7), 607-611 (1980-07-01)
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