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Results for "

bay 55 9837 acetate

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    9
    TargetMol | Activity
  • Peptide Products
    8
    TargetMol | inventory
Bay 55-9837 acetate
TP2071L
Bay 55-9837 acetate is a potent and highly selective VPAC2 agonist(Kd = 0.65 nM) and can be used in type 2 diabetes studies.
  • $539
In Stock
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Urotensin II, mouse acetate (9047-55-6 free base)
TP2165
Urotensin II, mouse acetate (9047-55-6 free base) is an endogenous ligand for the orphan GPR14 or SENR. It is a potent vasoconstrictor.
  • $101
In Stock
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QTY
TargetMol | Inhibitor Sale
gamma-DGG acetate(6729-55-1 free base)
T15369L2935387-13-4
gamma-DGG acetate(6729-55-1 free base) (γ-D-Glutamylglycine) is a competitive blocker of AMPA receptor.
  • $29
In Stock
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QTY
TargetMol | Inhibitor Sale
MOG peptide (35-55) , mouse, rat acetate
T7657L
Myelin Oligodendrocyte Glycoprotein (MOG) peptide (35-55) , mouse, rat acetate is a MOG peptide (35-55) derivative. MOG peptide (35-55) is a part of myelin oligodendrocyte glycoprotein (MOG) immunogenic peptide and can be used to study immune-related diseases.
  • $135
In Stock
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Cys-TAT(47-57) acetate(583836-55-9 Free base)
TP1185L
Cys-TAT(47-57) acetate is derived from the HIV-1 transactivating protein. Cys-TAT(47-57) acetate is an arginine rich peptide that can penetrate cells.
  • $117
In Stock
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QTY
TargetMol | Inhibitor Sale
p2Ca acetate(142606-55-1 free base)
TP1777L
p2Ca acetate is a naturally processed peptide that derives from a ubiquitous enzyme, alpha-ketoglutarate dehydrogenase, and is recognized in association with the class I MHC protein, Ld, by a CTL clone (2C).
  • $123
In Stock
Size
QTY
TargetMol | Inhibitor Sale
Bay 55-9837
TP2071463930-25-8
Selective VPAC2 receptor agonist (EC50 values are 0.4, 100 and >1000 nM for VPAC2, VPAC1 and PAC1, respectively in a cAMP accumulation assay; IC50 values are 60, 8700 and >10000 nM for VPAC2, VPAC1 and PAC1, respectively in a competition binding assay). S
  • $1,200
35 days
Size
QTY
Bay 55-9837 TFA
T75825
Bay 55-9837 TFA, a potent and highly selective VPAC2 agonist with a dissociation constant (Kd) of 0.65 nM, represents a potential research therapy for type 2 diabetes [1].
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