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Merck
모든 사진(1)

주요 문서

S3136

Sigma-Aldrich

[pGlu6]-Substance P Fragment 6-11

≥95% (HPLC)

동의어(들):

pGlu-Phe-Phe-Gly-Leu-Met-NH2

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About This Item

실험식(Hill 표기법):
C36H49N7O7S
CAS Number:
Molecular Weight:
723.88
MDL number:
UNSPSC 코드:
12352200
PubChem Substance ID:

분석

≥95% (HPLC)

UniProt 수납 번호

저장 온도

−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

유전자 정보

human ... TAC1(6863)

생화학적/생리학적 작용

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

개인 보호 장비

Eyeshields, Gloves, type N95 (US)


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문서 라이브러리 방문

M E Hall et al.
Peptides, 4(5), 763-768 (1983-09-01)
Most of the biological actions of substance P (SP) have been thought to be mediated by the carboxy-terminal portion of the peptide. Some of the behavioral effects produced by exogenous SP exhibit a strikingly different structure-activity relationship. The N-terminal heptapeptide
R Laufer et al.
Journal of medicinal chemistry, 29(7), 1284-1288 (1986-07-01)
Substitution of a single amino acid residue, proline for glycine-9 in [pGlu6]SP6-11, a hexapeptide analogue of substance P, confers on the peptide selective agonist activity toward the SP-P receptor subtype. [pGlu6,Pro9]SP6-11 had 20% and 75% of the activity of [pGlu6]SP6-11
O Gaffori et al.
Experientia, 40(1), 89-91 (1984-01-15)
N-terminal and C-terminal fragments of substance P (SP) have been shown to exert opposite effects on antinociception, grooming and fighting in mice. The present experiments explored whether these findings could be generalized to passive avoidance behavior. Substance P (SP-(1-11] and
Conformational studies on substance P. C-terminal pentapeptide pGlu-Phe-Phe-Gly-Leu-Met NH2.
M Cotrait et al.
Biochemical and biophysical research communications, 109(4), 1123-1128 (1982-12-31)
Z Y Friedman et al.
European journal of pharmacology, 117(3), 323-328 (1985-11-19)
Challenge of rat parotid slices with substance P or its analogs, at concentrations which cause less than maximal response resulted in the transient release of K+ into the medium. Reuptake of the released K+ into the cell was accompanied by

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