CHEBI:141949 - pseudoyohimbine

ChEBI IDCHEBI:141949
ChEBI Namepseudoyohimbine
Stars
Last Modified7 December 2018
Submittermwilliams
DownloadsMolfile
FormulaC21H26N2O3
Net Charge0
Average Mass354.450
Monoisotopic Mass354.19434
SMILES[H][C@@]12CC[C@H](O)[C@H](C(=O)OC)[C@@]1([H])C[C@]1([H])c3nc4ccccc4c3CCN1C2
InChIInChI=1S/C21H26N2O3/c1-26-21(25)19-15-10-17-20-14(13-4-2-3-5-16(13)22-20)8-9-23(17)11-12(15)6-7-18(19)24/h2-5,12,15,17-19,22,24H,6-11H2,1H3/t12-,15-,17+,18-,19+/m0/s1
InChIKeyBLGXFZZNTVWLAY-AECJZGCLSA-N
Species of MetaboliteComponentSourceComments
Catharanthus trichophyllus (ncbitaxon:319559) root (BTO:0001188) PubMed (1263083)
Uncaria callophylla (IPNI:768220-1) stem (BTO:0001300) Article (Goh, S.H. and Junan, S.A.A. (1985) Alkaloids of Uncaria callophylla. Phytochemistry, 24(4), 880-881.)
Uncaria attenuata (ncbitaxon:1840405) leaf (BTO:0000713) Article (Phillipson, J.D. and Hemingway, S.R. (1975) Alkaloids of Uncaria attenuata, U. orientalis and U. canescens. Phytochemistry, 14, 1855-1863.)
Rauvolfia canescens (IPNI:81522-1) root (BTO:0001188) Article (Stoll, A. and Hofmann, A. (1955) Canescine and pseudoyohimbine from the roots of Rauwolfia canescens L. J. Am. Chem. Soc., 77(3), 820-821.)
Uncaria borneensis (IPNI:768216-1) leaf (BTO:0000713) Article (Kam, T.S., Lee, K.H. and Goh, S.H. (1992) Alkaloid distribution in Malaysian Uncaria. Phytochemistry, 31(6), 2031-2034.)
Roles Classification
Biological Role:
metabolite  Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
ChEBI Ontology
Outgoing Relation(s)
pseudoyohimbine (CHEBI:141949) is a methyl 17-hydroxy-20ξ-yohimban-16-carboxylate (CHEBI:48565)
IUPAC Name 
methyl (3β,16α,17α)-17-hydroxyyohimban-16-carboxylate
Synonyms  Source
(3R)-17α-hydroxyyohimban-16α-carboxylic acid methyl esterChEBI
(3β)-17α-hydroxyyohimban-16α-carboxylic acid methyl esterChEBI
pseudoyohimbineChemIDplus
Registry NumbersSources
CAS:84-37-7ChemIDplus
Citations