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About This Item
Empirical Formula (Hill Notation):
C68H99N19O14S2
CAS Number:
Molecular Weight:
1470.76
UNSPSC Code:
12352200
MDL number:
SMILES string
NC(=N)NCCC[C@H](NC(=O)[C@H](Cc1cccs1)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@H](CO)NC(=O)[C@H](Cc3cccs3)NC(=O)CNC(=O)[C@@H]4C[C@@H](O)CN4C(=O)[C@@H]5CCCN5C(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](CCCNC(N)=N)NC(=O)CC67CC8CC(CC(C8)C6)C7)C(O)=O
assay
≥97% (HPLC)
storage temp.
−20°C
Gene Information
human ... BDKRB2(624)
mouse ... BDKRB2(12062)
rat ... BDKRB2(25245)
Biochem/physiol Actions
A highly potent antagonist at bradykinin B2 receptors with no agonist activity.
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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B Lammek et al.
Peptides, 11(5), 1041-1043 (1990-09-01)
We report that the acylation of the N-terminus of [D-Arg0,Hyp3,Thi5,8,D-Phe7]bradykinin, one of the most potent bradykinin antagonists described to date, with 1-adamantane-acetic acid, results in an analogue with more than ten times enhanced potency. The new analogue does not increase
J A García-Sáinz et al.
Biochemistry and molecular biology international, 47(6), 927-933 (1999-07-20)
In C9 rat liver cells bradykinin and kallidin increased (approximately 2-fold) the intracellular concentration of calcium, but the B1 agonist, des-Arg9-bradykinin did not. The effect of bradykinin was inhibited by the B2 antagonists, Hoe 140 and N-alpha-adamantaneacetyl-D-Arg-[Hyp3, Thi5,8, D-Phe7]-bradykinin, but
Man Zhang et al.
American journal of physiology. Cell physiology, 296(6), C1364-C1372 (2009-04-03)
Bradykinin (BK) is an endogenous peptide with diverse biological actions and is considered to be an important mediator of the inflammatory response in both the peripheral and the central nervous systems. BK has attracted recent interest as a potential mediator
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