Summary

IMPPAT Phytochemical identifier: IMPHY003593

Phytochemical name: Zeatin riboside

Synonymous chemical names:
ribosyl-trans-zeatin, ribosylzeatin, trans-ribosylzeatin, zeatin riboside

External chemical identifiers:
CID:6440982, ChEBI:71693, ZINC:ZINC000004521935, FDASRS:7LG4D082A9, SureChEMBL:SCHEMBL4058989, MolPort-003-939-929

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Chemical structure information

SMILES:
OC/C(=C/CNc1ncnc2c1ncn2[C@@H]1O[C@@H]([C@H]([C@H]1O)O)CO)/C

InChI:
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/s1

InChIKey:
GOSWTRUMMSCNCW-HNNGNKQASA-N

DeepSMILES:
OC/C=C/CNcncncc6ncn5[C@@H]O[C@@H][C@H][C@H]5O))O))CO)))))))))))))))))/C

Functional groups:
C/C=C(/C)C, CO, COC, cNC, cn(c)C, cnc

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Molecular scaffolds

Scaffold Graph/Node/Bond level:
c1ncc2ncn(C3CCCO3)c2n1

Scaffold Graph/Node level:
C1COC(N2CNC3CNCNC32)C1

Scaffold Graph level:
C1CCC2C(C1)CCC2C1CCCC1

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Chemical classification

ClassyFire Kingdom: Organic compounds

ClassyFire Superclass: Nucleosides, nucleotides, and analogues

ClassyFire Class: Purine nucleosides

NP Classifier Biosynthetic pathway: Alkaloids

NP Classifier Superclass: Pseudoalkaloids

NP Classifier Class: Purine alkaloids

NP-Likeness score: 1.339

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Chemical structure download