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Details

Stereochemistry ABSOLUTE
Molecular Formula C15H21N5O4
Molecular Weight 335.3583
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RIBOPRINE

SMILES

CC(C)=CCNC1=NC=NC2=C1N=CN2[C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O

InChI

InChIKey=USVMJSALORZVDV-SDBHATRESA-N
InChI=1S/C15H21N5O4/c1-8(2)3-4-16-13-10-14(18-6-17-13)20(7-19-10)15-12(23)11(22)9(5-21)24-15/h3,6-7,9,11-12,15,21-23H,4-5H2,1-2H3,(H,16,17,18)/t9-,11-,12-,15-/m1/s1

HIDE SMILES / InChI

Molecular Formula C15H21N5O4
Molecular Weight 335.3583
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

N(6)-[delta(3)-isopentenyl]adenosine also known as riboprine is an isopentenyl derivative of adenosine and is a member of the cytokinin family of plant growth regulators. It’s naturally present in certain transfer RNAs adjacent to the adenosine of ANN anti-dopes. Riboprine produced endogenously by plants and demonstrates the ability to induce cell cycle arrest and apoptosis.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
Identification of plant cytokinin biosynthetic enzymes as dimethylallyl diphosphate:ATP/ADP isopentenyltransferases.
2001-07
Summary: the modified nucleosides of RNA.
1994-06-25
6-(gamma,gamma-Dimethylallylamino)Purine As A Precursor of Zeatin.
1969-03

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:08:53 GMT 2025
Edited
by admin
on Mon Mar 31 18:08:53 GMT 2025
Record UNII
8EU82FAZ5J
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
N6-(2-ISOPENTENYL)-ADENOSINE
Preferred Name English
RIBOPRINE
INN   USAN  
USAN   INN  
Official Name English
RIBOPRINE [USAN]
Common Name English
NSC-105546
Code English
N-(3-Methyl-2-butenyl)adenosine
Systematic Name English
IPA
Code English
riboprine [INN]
Common Name English
6-N-((3-METHYL-2-BUTENYL)AMINO)-9-.BETA.-D-RIBOFURANOSYL-9H-PURINE
Common Name English
ADENOSINE, N-(3-METHYL-2-BUTENYL)-
Systematic Name English
Code System Code Type Description
RXCUI
1376156
Created by admin on Mon Mar 31 18:08:53 GMT 2025 , Edited by admin on Mon Mar 31 18:08:53 GMT 2025
PRIMARY RxNorm
EPA CompTox
DTXSID1057828
Created by admin on Mon Mar 31 18:08:53 GMT 2025 , Edited by admin on Mon Mar 31 18:08:53 GMT 2025
PRIMARY
INN
2514
Created by admin on Mon Mar 31 18:08:53 GMT 2025 , Edited by admin on Mon Mar 31 18:08:53 GMT 2025
PRIMARY
CHEBI
62881
Created by admin on Mon Mar 31 18:08:53 GMT 2025 , Edited by admin on Mon Mar 31 18:08:53 GMT 2025
PRIMARY
SMS_ID
100000080576
Created by admin on Mon Mar 31 18:08:53 GMT 2025 , Edited by admin on Mon Mar 31 18:08:53 GMT 2025
PRIMARY
CAS
7724-76-7
Created by admin on Mon Mar 31 18:08:53 GMT 2025 , Edited by admin on Mon Mar 31 18:08:53 GMT 2025
PRIMARY
DAILYMED
8EU82FAZ5J
Created by admin on Mon Mar 31 18:08:53 GMT 2025 , Edited by admin on Mon Mar 31 18:08:53 GMT 2025
PRIMARY
DRUG BANK
DB11933
Created by admin on Mon Mar 31 18:08:53 GMT 2025 , Edited by admin on Mon Mar 31 18:08:53 GMT 2025
PRIMARY
FDA UNII
8EU82FAZ5J
Created by admin on Mon Mar 31 18:08:53 GMT 2025 , Edited by admin on Mon Mar 31 18:08:53 GMT 2025
PRIMARY
ECHA (EC/EINECS)
231-771-3
Created by admin on Mon Mar 31 18:08:53 GMT 2025 , Edited by admin on Mon Mar 31 18:08:53 GMT 2025
PRIMARY
NCI_THESAURUS
C175199
Created by admin on Mon Mar 31 18:08:53 GMT 2025 , Edited by admin on Mon Mar 31 18:08:53 GMT 2025
PRIMARY
PUBCHEM
24405
Created by admin on Mon Mar 31 18:08:53 GMT 2025 , Edited by admin on Mon Mar 31 18:08:53 GMT 2025
PRIMARY
EVMPD
SUB10299MIG
Created by admin on Mon Mar 31 18:08:53 GMT 2025 , Edited by admin on Mon Mar 31 18:08:53 GMT 2025
PRIMARY
ChEMBL
CHEMBL452867
Created by admin on Mon Mar 31 18:08:53 GMT 2025 , Edited by admin on Mon Mar 31 18:08:53 GMT 2025
PRIMARY
NSC
105546
Created by admin on Mon Mar 31 18:08:53 GMT 2025 , Edited by admin on Mon Mar 31 18:08:53 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY