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Details

Stereochemistry ACHIRAL
Molecular Formula C7H9N5
Molecular Weight 163.1799
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 6,6-DIMETHYLADENINE

SMILES

CN(C)C1=C2NC=NC2=NC=N1

InChI

InChIKey=BVIAOQMSVZHOJM-UHFFFAOYSA-N
InChI=1S/C7H9N5/c1-12(2)7-5-6(9-3-8-5)10-4-11-7/h3-4H,1-2H3,(H,8,9,10,11)

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Effect of inhibitors on the montmorillonite clay-catalyzed formation of RNA: studies on the reaction pathway.
2001 Aug-Oct
Development of cloned embryos from adult rabbit fibroblasts: effect of activation treatment and donor cell preparation.
2001 Jan
c-Mos proteolysis is independent of the CA(2+) rise induced by 6-DMAP in Xenopus oocytes.
2001 May 15
Effect of 6-dimethylaminopurine on electrically activated in vitro matured porcine oocytes.
2002 Jul
Conditions for in vitro maturation and artificial activation of ferret oocytes.
2002 May
[Effects of different activation methods on in vitro development of bovine somatic cloned embryos].
2002 Sep
Developmental kinetics of bovine nuclear transfer and parthenogenetic embryos.
2003
Effect of activation methods for bovine oocytes after intracytoplasmic injection.
2003 Feb
The fenestrin antigen in submembrane skeleton of the ciliate Tetrahymena thermophila is proposed as a marker of cell polarity during cell division and in oral replacement.
2003 Jul
Production of nuclear transfer-derived piglets using porcine fetal fibroblasts transfected with the enhanced green fluorescent protein.
2003 Sep
Xenopus cell-free extracts to study the DNA damage response.
2004
Chemical activation of buffalo (Bubalus bubalis) oocytes by different methods: effects of aging on post-parthenogenetic development.
2004 Dec
Activation of equine nuclear transfer oocytes: methods and timing of treatment in relation to nuclear remodeling.
2004 Jan
Development of reconstituted embryos derived from somatic cell nuclei in the rabbit.
2004 Mar
Effects of post-treatment with 6-dimethylaminopurine (6-DMAP) on ethanol activation of mouse oocytes at different ages.
2004 Oct 1
Parthenogenetic and nuclear transfer rabbit embryo development and apoptosis after activation treatments.
2005 Sep
[Effects of different donor cells and passages on the development of nuclear transfer porcine embryos].
2006 Apr
CD40 mediated human cholangiocyte apoptosis requires JAK2 dependent activation of STAT3 in addition to activation of JNK1/2 and ERK1/2.
2006 Apr
Contribution of spermatozoal centrosomes to the microtubule-organizing centre in Antarctic minke whale ( Balaenoptera bonaerensis ).
2006 Feb
The effect of 6-dimethylaminopurine (6-DMAP) and cycloheximide (CHX) on the development and chromosomal complement of sheep parthenogenetic and nuclear transfer embryos.
2006 Jan
Cell cycle analysis of in vitro cultured goral (Naemorhedus caudatus) adult skin fibroblasts.
2006 Sep
Effect of different parthenogenetic activation methods on the developmental competence of in vitro matured porcine oocytes.
2007
Morphology of dromedary camel oocytes and their ability to spontaneous and chemical parthenogenetic activation.
2007 Feb
A comparative study of parthenogenic activation and in vitro fertilization of bubaline oocytes.
2008 Jan 30
The effect of activation treatments on the development of reconstructed bovine oocytes.
2008 Jun
Name Type Language
6,6-DIMETHYLADENINE
Common Name English
6-(DIMETHYLAMINO)PURINE
Systematic Name English
N(6),N(6)-DIMETHYLADENINE
Systematic Name English
PURINE, 6-(DIMETHYLAMINO)-
Systematic Name English
9H-PURIN-6-AMINE, N,N-DIMETHYL-
Systematic Name English
N,N-DIMETHYLADENINE
Systematic Name English
ADENINE, N6,N6-DIMETHYL-
Systematic Name English
N,N-DIMETHYL-6-AMINOPURINE
Common Name English
NSC-401568
Code English
1H-PURIN-6-AMINE, N,N-DIMETHYL-
Systematic Name English
6-DIMETHYLADENINE
Common Name English
N6,N6-DIMETHYLADENINE
Systematic Name English
DIMETHYLADENINE
Systematic Name English
6-DIMETHYLAMINOPURINE
Systematic Name English
ADENINE, N,N-DIMETHYL-
Systematic Name English
Code System Code Type Description
ECHA (EC/EINECS)
213-344-3
Created by admin on Fri Dec 15 18:17:29 GMT 2023 , Edited by admin on Fri Dec 15 18:17:29 GMT 2023
PRIMARY
CAS
938-55-6
Created by admin on Fri Dec 15 18:17:29 GMT 2023 , Edited by admin on Fri Dec 15 18:17:29 GMT 2023
PRIMARY
FDA UNII
649SA4S2CV
Created by admin on Fri Dec 15 18:17:29 GMT 2023 , Edited by admin on Fri Dec 15 18:17:29 GMT 2023
PRIMARY
CHEBI
60281
Created by admin on Fri Dec 15 18:17:29 GMT 2023 , Edited by admin on Fri Dec 15 18:17:29 GMT 2023
PRIMARY
NSC
401568
Created by admin on Fri Dec 15 18:17:29 GMT 2023 , Edited by admin on Fri Dec 15 18:17:29 GMT 2023
PRIMARY
PUBCHEM
3134
Created by admin on Fri Dec 15 18:17:29 GMT 2023 , Edited by admin on Fri Dec 15 18:17:29 GMT 2023
PRIMARY
EPA CompTox
DTXSID20239658
Created by admin on Fri Dec 15 18:17:29 GMT 2023 , Edited by admin on Fri Dec 15 18:17:29 GMT 2023
PRIMARY