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is a mAChR agonist that exerts its effects via directly stimulating the mAChR (M1
γ-Butyrobetaine hydrochloride
hypertension
InChi: InChI=1S/C7H8N4O2/c1-10-5-4(8-3-9-5)6(12)11(2)7(10)13/h3H
Gypenoside LI inhibited the colony formation ability of melanoma through inhibition of the Wnt/β-catenin signaling pathway
PI-55 minobutanoic acid) is a mAChR agonist thatPI 55 is a specific cytokinin receptor inhibitor. PI 55 is structurally related to 6 benzylaminopurine (BAP) and was shown to inhibit competitively BAP binding on Arabidopsis specific receptors CRE1 AHK4 and AHK3. PI 55 inhibits cytokinins induced haustorium formation and increased parasite aggressiveness. Product information CAS Number: 1122579 42 3 Molecular Weight: 255. 28 Formula: C13H13N5O Chemical Name: 2 methyl 6 {[(7H purin 6
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