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BPTU 2 mg | 99.89%
TargetMol
Allosteric antagonist of P2Y1 (EC50 = 0.06-0.3 μM). Non-nucleotide ligand. Binds receptor outside of the helical bundle. Blocks inhibition of spontaneous contraction of rat and mouse colon induced by electrical field stimulation, nicotine and P2Y agonists. Antithrombotic; reduces platelet aggregation.
More Information Supplier PageOctreotide Acetate 200 mg | 99.57%
TargetMol
Octreotide Acetate (Sandostatin) is a potent, long-acting synthetic somatostatin octapeptide analog that inhibits secretion of growth hormone.
More Information Supplier PageOctreotide Acetate 100 mg | 99.57%
TargetMol
Octreotide Acetate (Sandostatin) is a potent, long-acting synthetic somatostatin octapeptide analog that inhibits secretion of growth hormone.
More Information Supplier PageMK-8617 2 mg | Purity Not Available
TargetMol
MK-8617 is an orally available HIF PHD1 3 pan-inhibitor, inhibiting PHD1/2/3 (IC50: 1.0/1.0/14 nM).
More Information Supplier PageGSK2981278 25 mg | 99.78%
TargetMol
GSK2981278 is a highly potent and selective inverse agonist of retinoic acid receptor-related orphan receptor gamma (ROR gamma).
More Information Supplier PageL-Argininamide dihydrochloride 200 mg | 100.00%
TargetMol
L-Argininamide (L-Arm) is used as a model compound in studies of the physicochemical characteristic of ligand binding DNA aptamers and their potential development as fluorescent aptasensors.
More Information Supplier PageVUF10460 2 mg | 99.53%
TargetMol
BPTU 5 mg | 99.89%
TargetMol
Allosteric antagonist of P2Y1 (EC50 = 0.06-0.3 μM). Non-nucleotide ligand. Binds receptor outside of the helical bundle. Blocks inhibition of spontaneous contraction of rat and mouse colon induced by electrical field stimulation, nicotine and P2Y agonists. Antithrombotic; reduces platelet aggregation.
More Information Supplier PagePCC0208009 1 mg | 99.89%
TargetMol
PCC0208009 (IDO-IN-2) is an IDO inhibitor extracted from patent WO/2015031295 A1, compound example 1.
More Information Supplier Page
