Summary

IMPPAT Phytochemical identifier: IMPPAT3_PHYID011163

Phytochemical name: Dihydrozeatin riboside

Synonymous chemical names:
dihydrozeatin riboside

External chemical identifiers:
CID:CID_10522005, ChEBI:CHEBI:80498

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Chemical structure information

SMILES:
OCC(CCNc1ncnc2c1ncn2[C@@H]1O[C@@H]([C@H]([C@H]1O)O)CO)C

InChI:
InChI=1S/C15H23N5O5/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/h6-9,11-12,15,21-24H,2-5H2,1H3,(H,16,17,18)/t8?,9-,11-,12-,15-/m1/s1

InChIKey:
DBVVQDGIJAUEAZ-YXYADJKSSA-N

DeepSMILES:
OCCCCNcncncc6ncn5[C@@H]O[C@@H][C@H][C@H]5O))O))CO)))))))))))))))))C

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

Link to spectral information:
MSBNK-RIKEN-PR020103, MSBNK-RIKEN-PR020104, MSBNK-RIKEN-PR020102

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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: Carbohydrates

NP Classifier Superclass: Nucleosides

NP Classifier Class: Purine nucleos(t)ides

NP-Likeness score: 1.033

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Chemical structure download