Compound Identification
SMILES
CC1=NC=C(COP(O)(O)=O)C(C=O)=C1O.CC[C@@]12CCCN3CCC4=C([C@H]13)N(C1=CC=CC=C41)[C@](O)(C2)C(=O)OC
InChIKey
InChIKey=ZSUDTJHEHYTFQB-YAFGAGFVSA-N
Formula
C29H36N3O9P
Mass
601.593
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Alkaloids and derivatives
- Class Eburnan-type alkaloids
-
Superclass
Alkaloids and derivatives
Kingdom
Organic compounds
Superclass
Alkaloids and derivatives
Class
Eburnan-type alkaloids
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Eburnan-type alkaloids
Alternative Parents
Indolonaphthyridine alkaloids Beta carbolines Pyridoxals and derivatives 3-alkylindoles Alpha amino acids and derivatives Naphthyridines Aralkylamines Monoalkyl phosphates Methylpyridines Aryl-aldehydes Hydroxypyridines Piperidines Benzenoids Pyrroles Methyl esters Vinylogous acids Heteroaromatic compounds Trialkylamines Azacyclic compounds Alkanolamines Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives
Molecular Framework
Not available
Substituents
Eburna alkaloid - Indolo[3,2-1de][1,5]naphthyridine - Beta-carboline - Pyridoindole - Pyridoxal - Alpha-amino acid or derivatives - Naphthyridine - 3-alkylindole - Indole - Indole or derivatives - 4-pyridine carboxaldehyde - Methylpyridine - Hydroxypyridine - Aralkylamine - Aryl-aldehyde - Monoalkyl phosphate - Benzenoid - Pyridine - Alkyl phosphate - Piperidine - Phosphoric acid ester - Organic phosphoric acid derivative - Methyl ester - Pyrrole - Vinylogous acid - Heteroaromatic compound - Tertiary aliphatic amine - Tertiary amine - Amino acid or derivatives - Carboxylic acid ester - Organoheterocyclic compound - Alkanolamine - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Azacycle - Organooxygen compound - Organic oxygen compound - Carbonyl group - Aldehyde - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen compound - Amine - Organic oxide - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as eburnan-type alkaloids. These are alkaloids with a structure based on the eburnan skeleton, that arises from rearrangement of the aspidospermidine ring system, involving migration of C-21 from C-7 to C-2, fission of the 2,16-bond, and attachment of C-16 to N-1.
External Descriptors
Not available