Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C19H21NO4 |
Molecular Weight | 327.3743 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=C[C@]23CCN(C)[C@H](CC4=C2C(O)=C(OC)C=C4)C3=CC1=O
InChI
InChIKey=GVTRUVGBZQJVTF-YJYMSZOUSA-N
InChI=1S/C19H21NO4/c1-20-7-6-19-10-16(24-3)14(21)9-12(19)13(20)8-11-4-5-15(23-2)18(22)17(11)19/h4-5,9-10,13,22H,6-8H2,1-3H3/t13-,19+/m1/s1
Approval Year
PubMed
Title | Date | PubMed |
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Transformation of opium poppy (Papaver somniferum L.) with antisense berberine bridge enzyme gene (anti-bbe) via somatic embryogenesis results in an altered ratio of alkaloids in latex but not in roots. | 2004 Dec |
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Saludimerines A and B, novel-type dimeric alkaloids with stereogenic centers and configurationally semistable biaryl axes. | 2004 Dec 10 |
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Reticuline exposure to invertebrate ganglia increases endogenous morphine levels. | 2004 Oct |
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Comparative transcript and alkaloid profiling in Papaver species identifies a short chain dehydrogenase/reductase involved in morphine biosynthesis. | 2006 Oct |
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Production of benzylisoquinoline alkaloids in Saccharomyces cerevisiae. | 2008 Sep |
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CYP719B1 is salutaridine synthase, the C-C phenol-coupling enzyme of morphine biosynthesis in opium poppy. | 2009 Sep 4 |
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Mammalian cytochrome P450 enzymes catalyze the phenol-coupling step in endogenous morphine biosynthesis. | 2009 Sep 4 |
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Biochemistry and occurrence of o-demethylation in plant metabolism. | 2010 |
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Engineering cofactor preference of ketone reducing biocatalysts: A mutagenesis study on a γ-diketone reductase from the yeast Saccharomyces cerevisiae serving as an example. | 2010 Apr 14 |
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[Alkaloids in stems and leaves of Stephania cepharantha]. | 2010 May |
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Integration of deep transcriptome and proteome analyses reveals the components of alkaloid metabolism in opium poppy cell cultures. | 2010 Nov 18 |
Patents
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Code System | Code | Type | Description | ||
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7X10PRH74D
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m9749
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58061
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1936-18-1
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SALUTARIDINE
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17225
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DTXSID60941041
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5408233
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8325
Created by
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SUBSTANCE RECORD