Summary
IMPPAT Phytochemical identifier: IMPHY003595
Phytochemical name: cis-Zeatin riboside
Synonymous chemical names:cis-ribosylzeatin, cis-zeatin riboside, zeatin riboside,cis-
External chemical identifiers:CID:13935024, ChEBI:20833, ZINC:ZINC000013524330
Chemical structure information
SMILES:
OC/C(=CCNc1ncnc2c1ncn2[C@@H]1O[C@@H]([C@H]([C@H]1O)O)CO)/CInChI:
InChI=1S/C15H21N5O5/c1-8(4-21)2-3-16-13-10-14(18-6-17-13)20(7-19-10)15-12(24)11(23)9(5-22)25-15/h2,6-7,9,11-12,15,21-24H,3-5H2,1H3,(H,16,17,18)/b8-2-/t9-,11-,12-,15-/m1/s1InChIKey:
GOSWTRUMMSCNCW-BAJUWZQUSA-NDeepSMILES:
OC/C=CCNcncncc6ncn5[C@@H]O[C@@H][C@H][C@H]5O))O))CO)))))))))))))))))/CFunctional groups:
C/C=C(C)C, CO, COC, cNC, cn(c)C, cnc
Molecular scaffolds
Scaffold Graph/Node/Bond level:
c1ncc2ncn(C3CCCO3)c2n1Scaffold Graph/Node level:
C1COC(N2CNC3CNCNC32)C1Scaffold Graph level:
C1CCC2C(C1)CCC2C1CCCC1
Chemical classification
ClassyFire Kingdom: Organic compoundsClassyFire Superclass: Nucleosides, nucleotides, and analoguesClassyFire Class: Purine nucleosides
NP Classifier Biosynthetic pathway: Alkaloids
NP Classifier Superclass: Pseudoalkaloids
NP Classifier Class: Purine alkaloids
NP-Likeness score: 1.339
Chemical structure download