SPRi3 , CAS No.S613680, Inhibitor of sepiapterin reductase

Item Number
S613680
Grouped product items
SKUSizeAvailabilityPrice Qty
S613680-5mg
5mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$1,334.90
S613680-25mg
25mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$2,001.90
View related series
sepiapterin reductase Inhibitor

Basic Description

Synonymsexample 23 [WO2011047156];SPR inhibitor 3
Specifications & PurityMoligand™
GradeMoligand™
Action TypeINHIBITOR
Mechanism of actionInhibitor of sepiapterin reductase

Associated Targets(Human)

SPR Tchem Sepiapterin reductase (4 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Names and Identifiers

IUPAC Name N-[2-(5-hydroxy-2-methyl-1H-indol-3-yl)ethyl]-2-methoxyacetamide
INCHI InChI=1S/C14H18N2O3/c1-9-11(5-6-15-14(18)8-19-2)12-7-10(17)3-4-13(12)16-9/h3-4,7,16-17H,5-6,8H2,1-2H3,(H,15,18)
InChi Key YBXBWBBVLXZQBJ-UHFFFAOYSA-N
Canonical SMILES COCC(=O)NCCc1c(C)[nH]c2c1cc(O)cc2
Isomeric SMILES CC1=C(C2=C(N1)C=CC(=C2)O)CCNC(=O)COC
PubChem CID 52911386

Certificates

Certificate of Analysis(COA)

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Related Documents

References

1. Latremoliere A, Latini A, Andrews N, Cronin SJ, Fujita M, Gorska K, Hovius R, Romero C, Chuaiphichai S, Painter M et al..  (2015)  Reduction of Neuropathic and Inflammatory Pain through Inhibition of the Tetrahydrobiopterin Pathway..  Neuron,  86  (6): (1393-406).  [PMID:26087165] [10.1021/op500134e]
2. Haruki H, Hovius R, Pedersen MG, Johnsson K.  (2016)  Tetrahydrobiopterin Biosynthesis as a Potential Target of the Kynurenine Pathway Metabolite Xanthurenic Acid..  J Biol Chem,  291  (2): (652-7).  [PMID:26565027] [10.1021/op500134e]

Solution Calculators