
P7C3-OMe
CAS No. 313268-18-7
P7C3-OMe( —— )
Catalog No. M22944 CAS No. 313268-18-7
P7C3-OMe, a pro-neurogenic agent, has therapeutic benefits in neurodegenerative diseases. The R-enantiomer of P7C3-OMe is far more active than the S-enantiomer.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
2MG | 88 | In Stock |
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5MG | 140 | In Stock |
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10MG | 205 | In Stock |
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25MG | 417 | In Stock |
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50MG | 614 | In Stock |
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100MG | 872 | In Stock |
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200MG | Get Quote | In Stock |
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500MG | Get Quote | In Stock |
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1G | Get Quote | In Stock |
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Biological Information
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Product NameP7C3-OMe
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NoteResearch use only, not for human use.
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Brief DescriptionP7C3-OMe, a pro-neurogenic agent, has therapeutic benefits in neurodegenerative diseases. The R-enantiomer of P7C3-OMe is far more active than the S-enantiomer.
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DescriptionP7C3-OMe, a pro-neurogenic agent, has therapeutic benefits in neurodegenerative diseases. The R-enantiomer of P7C3-OMe is far more active than the S-enantiomer.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptorOthers
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Research Area——
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Indication——
Chemical Information
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CAS Number313268-18-7
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Formula Weight504.21
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Molecular FormulaC22H20Br2N2O2
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Purity>98% (HPLC)
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SolubilityDMSO:100 mg/mL (198.33 mM)
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SMILESOC(CNC1=CC=CC(OC)=C1)CN2C3=C(C4=C2C=CC(Br)=C4)C=C(Br)C=C3
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference



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Hippuric acid
Hippuric acid is an acyl glycine formed by the conjugation of benzoic acid with glycine. Hippuric acid is a normal component of urine and is typically increased with increased consumption of phenolic compounds (tea wine fruit juices).
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Fructoheptasaccharid...
Fructoheptasaccharide belongs to fructooligosaccharides (FOS) with degree of polymerization (DP=7).
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2-Methylsuccinic aci...
Methylsuccinic acid is a normal metabolite found in human fluids. Increased urinary levels of Methylsuccinic acid (together with ethylmalonic acid) are the main biochemical measurable features in ethylmalonic encephalopathy a rare metabolic disorder with an autosomal recessive mode of inheritance that is clinically characterized by neuromotor delay hyperlactic acidemia recurrent petechiae orthostatic acrocyanosis and chronic diarrhea.