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Results for "

[des-arg-9]-bradykinin

" in TargetMol Product Catalog
  • Inhibitor Products
    18
    TargetMol | Activity
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    18
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    TargetMol | composition
[Des-Arg9]-Bradykinin TFA
T8809199433-70-0
[Des-Arg9]-Bradykinin is an agonist of Bradykinin (B1) receptor that displays selectivity for B1 over B2 receptors.
  • $50
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Lys-[Des-Arg9]Bradykinin acetate
TP1918L1
Lys-[Des-Arg9]Bradykinin acetate is an endogenous potent and highly selective bradykinin B1 receptor agonist (Ki values are 0.12 and > 30000 nM at human B1 and B2 receptors respectively). Hypotensive agent that reduces peripheral vascular resistance in vivo. 16-fold more potent than [Des-Arg9]-Bradykinin.
  • $81
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Lys-[Des-Arg9]Bradykinin,TFA
TP1918L
Lys-[Des-Arg9]Bradykinin,TFA is Endogenous potent and highly selective bradykinin B1 receptor agonist (Ki values are 0.12 and > 30000 nM at human B1 and B2 receptors respectively). Hypotensive agent that reduces peripheral vascular resistance in vivo. 16-fold more potent than [Des-Arg9]-Bradykinin.
  • $79
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Lys-Bradykinin acetate(342-10-9 free base)
TP2268L84640-50-6
Lys-Bradykinin acetate is an endogenous bradykinin receptor agonist.
  • $98
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Sar-[D-Phe8]-des-Arg9-Bradykinin acetate
TP1917L1
Sar-[D-Phe8]-des-Arg9-Bradykinin acetate is a potent and selective bradykinin B1 receptor agonist (EC50 = 9.02 nM in rabbit aorta) that is resistant to aminopeptidase, kininase I and II (ACE) and neutral endopeptidase cleavage. Exhibits hypotensive and angiogenic activity in vivo.
  • $308
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(Arg)9 TFA (143413-47-2 free base)
TP10792283335-13-5
(Arg)9 TFA (Peptide R9 TFA) is a cell-penetrating peptide. (Arg)9 TFA (Nona-L-arginine TFA) exhibits neuroprotective activity with an IC50 of 0.78 μM in the glutamic acid model.
  • $139
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[Des-Arg9]-Bradykinin
T764515958-92-6
[Des-Arg9]-Bradykinin ([Des-Arg9]-Bradykinin(2TFA))(2TFA) is an agonist of Bradykinin (B1) receptor.
  • $265
35 days
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Lys-[Des-Arg9]Bradykinin
TP191871800-36-7
Endogenous potent and highly selective bradykinin B1 receptor agonist (Ki values are 0.12 and > 30000 nM at human B1 and B2 receptors respectively). Hypotensive agent that reduces peripheral vascular resistance in vivo. 16-fold more potent than [Des-Arg9]
  • $81
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Arg-Gly-Asp-Ser (TFA)(91037-65-9,free)
TP1043
Arg-Gly-Asp-Ser (TFA) is an integrin binding sequence that inhibits integrin receptor function.
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Bradykinin (2-9)
TP118116875-11-9
Bradykinin (2-9) (Des-Arg1-bradykinin) is an amino-truncated peptide compound that is a metabolite of Bradykinin. It is formed by the cleavage action of Aminopeptidase P.
  • $44
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Sar-[D-Phe8]-des-Arg9-Bradykinin
TP1917126959-88-4
Potent and selective bradykinin B1 receptor agonist (EC50 = 9.02 nM in rabbit aorta) that is resistant to aminopeptidase, kininase I and II (ACE) and neutral endopeptidase cleavage. Exhibits hypotensive and angiogenic activity in vivo.
  • $229
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Argipressin, des-glynh2(9)-
TP245037552-33-3
Argipressin, des-glynh2(9)-, can effect on aggregation of blood platelets.
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[Des-Arg9]-Bradykinin acetate
TP144523827-91-0
[Des-Arg9]-Bradykinin acetate is a selective agonist of Bradykinin B1 receptor.
  • $47
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Lys-(Des-Arg9,Leu8)-Bradykinin
T8011771800-37-8
Lys-(Des-Arg9,Leu8)-Bradykinin is a selective antagonist of the bradykinin B1 receptor [1].
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(Arg)9 acetate
T77998
Nona-L-arginine (Arg)9 acetate, a cell-penetrating peptide (CPP) consisting of 9 arginine residues, displays neuroprotective properties, with an IC50 of 0.78 μM in the glutamic acid model [1] [2].
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Des-Arg9-[Leu8]-Bradykinin acetate
T80072115035-45-5
Des-Arg9-[Leu8]-Bradykinin acetate is a potent antagonist of the bradykinin receptor 1 (B1R), utilized in renal fibrosis research [1].
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(Arg)9
T13976143413-47-2
(Arg)9 (Nona-L-arginine;Peptide R9) is a cell-penetrating peptide,and exhibits neuroprotective activity(IC50 of 0.78 μM, in the glutamic acid model).
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7-10 days
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Lys-[Des-Arg9]Bradykinin TFA
T736462763588-90-3
Lys-[Des-Arg9]Bradykinin TFA is a naturally occurring kinin that serves as a potent and highly selective agonist for the bradykinin B1 receptor, demonstrating binding affinities (K i values) of 0.12 nM, 1.7 nM, and 0.23 nM for the human, mouse, and rabbit B1 receptors, respectively. This compound exhibits low inhibitory activity on B2 receptors [1] [2].
  • $61
5 days
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