Metabolic Modeling Tutorial
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Metabolic Modeling Tutorial
early discounted registration
ends Feb 21th, 2015
Metabolic Modeling Tutorial
early discounted registration
ends Feb 21th, 2015
Metabolic Modeling Tutorial
early discounted registration
ends Feb 21th, 2015
Metabolic Modeling Tutorial
early discounted registration
ends Feb 21th, 2015
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MetaCyc Pathways Class: Alkaloids Biosynthesis

Summary:
This class contains biosynthetic pathways of alkaloids. Most alkaloids contain cyclic nitrogen. They function as defense compounds. Many alkaloids, including morphine and cocaine, have a high affinity for receptors of neurotransmitters and have pharmacological activities.

Parent Classes:
Nitrogen-Containing Secondary Compounds Biosynthesis

Child Classes:
Betalaine Alkaloids Biosynthesis (8) ,
Indole Alkaloids Biosynthesis (10) ,
Isoquinoline and Benzylisoquinoline Alkaloids Biosynthesis (12) ,
Peptide Alkaloids Biosynthesis (0) ,
Polyketide Alkaloids Biosynthesis (0) ,
Purine Alkaloids Biosynthesis (4) ,
Pyrrolidine, Piperidine and Pyridine Alkaloids Biosynthesis (4) ,
Pyrrolizidine Alkaloids Biosynthesis (1) ,
Quinoline Alkaloids Biosynthesis (2) ,
Quinolizidine Alkaloids Biosynthesis (1) ,
Terpenoid Alkaloids Biosynthesis (3) ,
Tropane Alkaloids Biosynthesis (5)

Instances:
α-cyclopiazonate biosynthesis ,
α-cyclopiazonate detoxification ,
γ-coniciene and coniine biosynthesis ,
5-N-acetylardeemin biosynthesis ,
acridone alkaloid biosynthesis ,
asperlicin E biosynthesis ,
capsaicin biosynthesis ,
capsiconiate biosynthesis ,
emetine biosynthesis ,
ephedrine biosynthesis ,
fumiquinazoline D biosynthesis ,
fumitremorgin A biosynthesis ,
fumitremorgin C biosynthesis ,
lampranthin biosynthesis ,
N-methyl-Δ1-pyrrolinium cation biosynthesis ,
noscapine biosynthesis ,
ricinine degradation ,
steroidal glycoalkaloid biosynthesis ,
superpathway of ergotamine biosynthesis ,
tryptophan degradation VI (via tryptamine)


Report Errors or Provide Feedback
Please cite the following article in publications resulting from the use of MetaCyc: Caspi et al, Nucleic Acids Research 42:D459-D471 2014
Page generated by SRI International Pathway Tools version 18.5 on Fri Feb 27, 2015, BIOCYC13B.