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Results for "

p-11

" in TargetMol Product Catalog
  • Inhibitors & Agonists
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hsdvhk-nh2
P11
TP1879848644-86-0
Potent antagonist of the integrin αvβ3-vitronectin interaction (IC50 = 25.72 nM). Blocks proliferation and induces apoptosis in HUVECs; antiangiogenic.
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P-113 acetate
T25913L
P-113 acetate is an antimicrobial peptide (AMP) derived from the human salivary protein histatin 5, shows good safety and efficacy profiles in gingivitis and human immunodeficiency virus (HIV) patients with oral candidiasis.
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Substance P (7-11)
Substance P 7-11(TFA)
T755451165-05-0
Substance P (7-11) (Substance P 7-11(TFA)) is a C-terminal fragment of Substance P .
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[Glp6] Substance P (6-11)
T7640261123-13-5
[Glp6] Substance P (6-11) is an analogue of the native peptide Substance P (6-11), acting on 'septide-sensitive' tachykinin receptors and stimulating the formation of [3H]-inositol monophosphate ([3H]-IP1) in rat urinary bladder, as evidenced by references [1] [2].
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[Glp5] Substance P (5-11)
T7640356104-22-4
[Glp5] Substance P (5-11), an octapeptide, is a key fragment of substance P in the rat central nervous system (CNS) and plays a localized role in modulating dopamine release in the rat striatum [1].
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[Glp5,(Me)Phe8,Sar9] Substance P (5-11)
T7640477128-69-9
[Glp5,(Me)Phe8,Sar9] Substance P (5-11) (DiMe-C7) is an analogue of Substance P that acts on the neurokinin 1 receptor (NK1R) in rat brain, similarly to Substance P but with a significantly extended duration of action. This compound selectively enhances dopamine metabolism within the mesencephalon and midbrain cortex, increases motor activity, and facilitates the resumption of addictive agent-seeking behavior in rats [1] [2] [3].
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[D-Pro4,D-Trp7,9,Nle11] Substance P (4-11)
T7640689430-34-2
[D-Pro4,D-Trp7,9,Nle11] Substance P (4-11) is a potent neurokinin NK1 antagonist that effectively inhibits the actions of gold-protein-substance P (GPSP) and substance P (SP), demonstrating its efficacy in neutralizing their effects [1].
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[DAla4] Substance P (4-11)
T7644781381-50-2
[DAla4] Substance P (4-11), an analog of Substance P (Substance P), effectively inhibits the binding of 125I-Bolton Hunter-conjugated Eledoisin (Eledoisin) and 125I-Bolton Hunter-conjugated Substance P to rat brain cortex membranes, with IC50 values of 0.5 μM and 0.15 μM, respectively [1].
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Substance P (6-11)
T7645351165-07-2
Substance P (6-11), the C-terminal hexapeptideamide of Substance P, exhibits affinity for the NK-1 tachykinin receptor, leading to motoneuron depolarization and a hypotensive effect [1] [2].
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Substance P (5-11)
T7645451165-09-4
Substance P (5-11), the C-terminal heptapeptide derived from Substance P, functions as a neuropeptide that specifically interacts with the NK-1 tachykinin receptor [1].
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Substance P (4-11)
T7645553749-60-3
Substance P (4-11), a C-terminal fragment of Substance P, acts as a highly selective agonist for NK1 receptors, demonstrating specificity in its interaction.
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[Glp5,Sar9] Substance P (5-11)
T7646277128-78-0
[Glp5,Sar9] Substance P (5-11) is an analogue of Substance P [1].
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[Sar4] Substance P (4-11)
T76483
[Sar4] Substance P (4-11) is a Substance P agonist and an analog of the C-terminus fragment of Substance P known as Substance P (4-11) [1].
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[Sar9,Met(O2)11]-Substance P
Bhsar-sp, NA
T7828110880-55-2
[Sar9,Met(O2)11]-Substance P (NA) is an NK1 receptor agonist.
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Substance P (3-11)
T8107851165-11-8
Substance P (3-11), an SP fragment peptide capable of crossing the blood-brain barrier (BBB), induces contraction in guinea pig ileum and facilitates chemotaxis in human monocytes [1] [2] [5].
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Substance P (2-11)
T8107953749-61-4
Substance P (2-11), a fragment peptide of Substance P (SP), exhibits contractile effects on the guinea pig ileum and inhibits the permeation of tritiated SP (3 H SP) across brain microvessel endothelial cell (BBMEC) monolayers [1] [2].
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[D-Pro4,D-Trp7,9] Substance P (4-11)
T8349581039-85-2
[D-Pro4,D-Trp7,9] Substance P (4-11) acts as a potent Substance P antagonist, significantly reducing plasma aldosterone (ALDO) concentrations[1].
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[D-Pro4,D-Trp7,9,10] Substance P (4-11)
T8349686917-57-9
[D-Pro4,D-Trp7,9,10] Substance P (4-11) is a potent antagonist of the tachykinin family of neuropeptides [1].
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[Sar9,Met(O2)11]-Substance P TFA(110880-55-2,free)
[Sar9,Met(O2)11]-Substance P TFA
TP1369
[Sar9,Met(O2)11]-Substance P TFA is a selective tachykinin NK1 receptor agonist.[Sar9,Met(O2)11]-Substance P and septide (10-100 pmol per rat, i.c.v.) are equipotent in increasing mean arterial blood pressure (MAP) and heart rate (HR), yet they have dissi
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[Sar9,Met(O2)11]-Substance P acetate
[Sar9,Met(O2)11]-Substance P acetate(110880-55-2 free base)
TP1369L
[Sar9,Met(O2)11]-Substance P acetate is a tachykinin NK1 receptor selective agonist. [Sar9,Met(O2)11]-Substance P acetate is a selective tachykinin NK1 receptor agonist.[Sar9,Met(O2)11]-Substance P acetate and septide (10-100 pmol per rat, i.c.v.) are equipotent in increasing mean arterial blood pressure (MAP) and heart rate (HR), yet they have dissimilar time-course. Both agonists increase dose-dependently face washing and sniffing while [Sar9,Met(O2)11]-Substance P acetate is the sole to produce grooming.
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P-113
P 113,Ala-lys-arg-his-his-gly-tyr-lys-arg-lys-phe-his-NH2
T25913190673-58-6
P-113 is a peptide with antimicrobial activity.
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Oligopeptide P11-4 acetate
Oligopeptide P11-4 acetate(593266-60-5 free base)
TP2326L
Oligopeptide P11-4 acetate is a peptide
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ω-Conotoxin MVIIC TFA
Omega-conotoxin MVIIC TFA
T75726
ω-Conotoxin MVIIC TFA is a peptide and neurotoxin with 26 residues that preferentially blocks P-type and Q-type Ca ++ currents by binding with high affinity to voltage-sensitive neuronal Ca ++ channels (VGCCs) and can be radiolabeled and used in immunoprecipitation assays.
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Substance P
Neurokinin P
TP108733507-63-0
Substance P (Neurokinin P) (SP) is an undecapeptide (a peptide composed of a chain of 11 amino acid residues) member of the tachykinin neuropeptide family.
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