Summary
IMPPAT Phytochemical identifier: IMPHY000080
Phytochemical name: Tetrahydropteroylglutamate
Synonymous chemical names:tetrahydropteroylglutamate
External chemical identifiers:CID:1129
Chemical structure information
SMILES:
OC(=O)CCC(C(=O)O)NC(=O)c1ccc(cc1)NCC1CNc2c(N1)c(=O)nc([nH]2)NInChI:
InChI=1S/C19H23N7O6/c20-19-25-15-14(17(30)26-19)23-11(8-22-15)7-21-10-3-1-9(2-4-10)16(29)24-12(18(31)32)5-6-13(27)28/h1-4,11-12,21,23H,5-8H2,(H,24,29)(H,27,28)(H,31,32)(H4,20,22,25,26,30)InChIKey:
MSTNYGQPCMXVAQ-UHFFFAOYSA-NDeepSMILES:
OC=O)CCCC=O)O))NC=O)cccccc6))NCCCNccN6)c=O)nc[nH]6)NFunctional groups:
CC(=O)O, c=O, cC(=O)NC, cN, cNC, c[nH]c, cnc
Molecular scaffolds
Scaffold Graph/Node/Bond level:
O=c1nc[nH]c2c1NC(CNc1ccccc1)CN2Scaffold Graph/Node level:
OC1NCNC2NCC(CNC3CCCCC3)NC12Scaffold Graph level:
CC1CCCC2CCC(CCC3CCCCC3)CC12
Chemical classification
ClassyFire Kingdom: Organic compoundsClassyFire Superclass: Organoheterocyclic compoundsClassyFire Class: Pteridines and derivatives
ClassyFire Subclass: Pterins and derivatives
NP Classifier Biosynthetic pathway: Alkaloids
NP Classifier Superclass: Pseudoalkaloids
NP Classifier Class: pteridine alkaloids
NP-Likeness score: 0.374
Chemical structure download