IMPPAT Phytochemical information: 
trans-4-Methoxy-1-methyl-L-proline; trans-N-Methyl-4-methoxyproline

trans-4-Methoxy-1-methyl-L-proline; trans-N-Methyl-4-methoxyproline
Summary

IMPPAT Phytochemical identifier: IMPHY014672

Phytochemical name: trans-4-Methoxy-1-methyl-L-proline; trans-N-Methyl-4-methoxyproline

Synonymous chemical names:
trans-n-methyl-4-methoxyproline

External chemical identifiers:
CID:134714825
Chemical structure information

SMILES:
CO[C@H]1CN([C@@H](C1)C(=O)O)C.CO[C@H]1CN([C@@H](C1)C(=O)O)C

InChI:
InChI=1S/2C7H13NO3/c2*1-8-4-5(11-2)3-6(8)7(9)10/h2*5-6H,3-4H2,1-2H3,(H,9,10)/t2*5-,6+/m11/s1

InChIKey:
RTVARJGAIHUKCO-NTPRZCPUSA-N

DeepSMILES:
CO[C@H]CN[C@@H]C5)C=O)O)))C.CO[C@H]CN[C@@H]C5)C=O)O)))C

Functional groups:
CC(=O)O, CN(C)C, COC
Chemical classification

ClassyFire Kingdom: Organic compounds

ClassyFire Superclass:
Organic acids and derivatives

ClassyFire Class: Carboxylic acids and derivatives

ClassyFire Subclass: Amino acids, peptides, and analogues

NP Classifier Biosynthetic pathway: Alkaloids

NP Classifier Superclass: Ornithine alkaloids

NP Classifier Class: Pyrrolidine alkaloids

NP-Likeness score: 0.277


Chemical structure download