Interesting facts
Interesting Facts about 7H-purine-2,6-diamine
7H-purine-2,6-diamine, often simply referred to as a purine derivative, has a notable presence in various biological processes. Here are some fascinating insights about this compound:
- Fundamental Role in Biology: Purines, including 7H-purine-2,6-diamine, are critical building blocks of nucleic acids—DNA and RNA. They play a vital role in the storage and transmission of genetic information.
- Cellular Energy Currency: This compound is also a part of adenosine triphosphate (ATP), the primary energy carrier in cells. ATP is essential for many biochemical reactions that sustain life.
- Involvement in Metabolism: As a purine derivative, it is involved in various metabolic pathways, including the purine nucleoside salvage pathway that recycles purines.
- Pharmaceutical Applications: Researchers are interested in purine derivatives for their potential therapeutic effects. Compounds related to 7H-purine-2,6-diamine are being studied for their roles in cancer treatment and antiviral therapies.
In the realm of scientific research, 7H-purine-2,6-diamine exemplifies the intricate connection between molecular structure and biological function. Its significance in both fundamental biology and medical applications underscores the importance of understanding chemical compounds at a deeper level.
Quote: "Exploring the intricacies of biochemical compounds like 7H-purine-2,6-diamine opens the door to understanding life's fundamental processes."
Synonyms
2,6-Diaminopurine
1904-98-9
7H-purine-2,6-diamine
2-Aminoadenine
9H-Purine-2,6-diamine
1H-Purine-2,6-diamine
49P95BAU4Z
CHEBI:40235
NSC-743
NSC743
DTXSID0062052
RefChem:445298
DTXCID6035998
CHEBI:38001
217-605-2
26-diaminopurine
Purine, 2,6-diamino-
2,6-diamino-9h-purine
NSC 743
SQ 21065
X 79
2,6-Diamino-purin-9-yl
purine-2,6-diamine
MFCD00047146
2,6-Diaminopurine, 98%
CHEMBL388596
133762-79-5
6AP
Purine-2,6-diyldiamine
CCRIS 923
EINECS 217-605-2
UNII-49P95BAU4Z
AI3-25010
CCRIS 3903
Group4_Adenines
2-6-Diaminopurine
Purine,6-diamino-
MFCD00071537
Purine, 2, 6-diamino-
Oprea1_670021
SCHEMBL24052
SCHEMBL24053
SCHEMBL95407
9H-Purine-2,6-diamine #
MLS001066366
SCHEMBL134492
DIAMINOPURINE, 2,6-
SCHEMBL2316818
SCHEMBL2867588
SCHEMBL2953673
SCHEMBL6322394
SCHEMBL8009783
SCHEMBL16513167
SCHEMBL29444619
2,6-DIAMINOPURINE [MI]
(2-amino-7H-purin-6-yl)-amine
HMS2267N10
ALBB-023319
BCP30955
BDBM50208879
BDBM50228488
SBB000103
AKOS003368184
AKOS015896933
AKOS028109333
9H-Purine-2,6-diamine0.5M H2SO4
AC-8693
CS-W014347
FD04050
GS-3048
HY-W013631
9H-Purine-2,6-diamine;2-Aminoadenine
BP-13206
SMR000112503
ST012425
SY036886
TS-00060
DB-015922
D1625
NS00026227
C22439
EN300-101012
904D989
AC-907/34116038
F037181
Q4596802
Z1255486094
Solubility of 7H-purine-2,6-diamine
7H-purine-2,6-diamine, a derivative of purine, exhibits unique solubility characteristics that are particularly relevant in biochemical contexts.
SOLUBILITY IN WATER:
This compound is known to be soluble in water due to its polar amino groups, which can form hydrogen bonds with water molecules. However, the extent of solubility can vary based on:
SOLUBILITY IN ORGANIC SOLVENTS:
When it comes to organic solvents, 7H-purine-2,6-diamine is generally:
In summary, while 7H-purine-2,6-diamine is readily soluble in aqueous solutions due to its polar characteristics, its solubility in organic solvents is contingent on the solvent's polarity. This solubility profile plays a crucial role in its applications within biochemistry and pharmacology, making it an interesting compound to study in relation to solubility behavior.