U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

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

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:47:43 GMT 2023
Edited
by admin
on Fri Dec 15 15:47:43 GMT 2023
Record UNII
8EU82FAZ5J
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
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
N6-(2-ISOPENTENYL)-ADENOSINE
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 Fri Dec 15 15:47:43 GMT 2023 , Edited by admin on Fri Dec 15 15:47:43 GMT 2023
PRIMARY RxNorm
EPA CompTox
DTXSID1057828
Created by admin on Fri Dec 15 15:47:43 GMT 2023 , Edited by admin on Fri Dec 15 15:47:43 GMT 2023
PRIMARY
INN
2514
Created by admin on Fri Dec 15 15:47:43 GMT 2023 , Edited by admin on Fri Dec 15 15:47:43 GMT 2023
PRIMARY
CHEBI
62881
Created by admin on Fri Dec 15 15:47:43 GMT 2023 , Edited by admin on Fri Dec 15 15:47:43 GMT 2023
PRIMARY
SMS_ID
100000080576
Created by admin on Fri Dec 15 15:47:43 GMT 2023 , Edited by admin on Fri Dec 15 15:47:43 GMT 2023
PRIMARY
CAS
7724-76-7
Created by admin on Fri Dec 15 15:47:43 GMT 2023 , Edited by admin on Fri Dec 15 15:47:43 GMT 2023
PRIMARY
DAILYMED
8EU82FAZ5J
Created by admin on Fri Dec 15 15:47:43 GMT 2023 , Edited by admin on Fri Dec 15 15:47:43 GMT 2023
PRIMARY
DRUG BANK
DB11933
Created by admin on Fri Dec 15 15:47:43 GMT 2023 , Edited by admin on Fri Dec 15 15:47:43 GMT 2023
PRIMARY
FDA UNII
8EU82FAZ5J
Created by admin on Fri Dec 15 15:47:43 GMT 2023 , Edited by admin on Fri Dec 15 15:47:43 GMT 2023
PRIMARY
ECHA (EC/EINECS)
231-771-3
Created by admin on Fri Dec 15 15:47:43 GMT 2023 , Edited by admin on Fri Dec 15 15:47:43 GMT 2023
PRIMARY
NCI_THESAURUS
C175199
Created by admin on Fri Dec 15 15:47:43 GMT 2023 , Edited by admin on Fri Dec 15 15:47:43 GMT 2023
PRIMARY
PUBCHEM
24405
Created by admin on Fri Dec 15 15:47:43 GMT 2023 , Edited by admin on Fri Dec 15 15:47:43 GMT 2023
PRIMARY
EVMPD
SUB10299MIG
Created by admin on Fri Dec 15 15:47:43 GMT 2023 , Edited by admin on Fri Dec 15 15:47:43 GMT 2023
PRIMARY
ChEMBL
CHEMBL452867
Created by admin on Fri Dec 15 15:47:43 GMT 2023 , Edited by admin on Fri Dec 15 15:47:43 GMT 2023
PRIMARY
NSC
105546
Created by admin on Fri Dec 15 15:47:43 GMT 2023 , Edited by admin on Fri Dec 15 15:47:43 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY