Interesting facts
Exploring (2R,3R,4R,5S)-2-(hydroxymethyl)piperidine-3,4,5-triol
(2R,3R,4R,5S)-2-(hydroxymethyl)piperidine-3,4,5-triol is an intriguing compound with significant relevance in both organic chemistry and biochemistry. This compound stands out due to its unique structure and functional groups. Here are some fascinating facts about it:
- Chirality: The compound possesses multiple chiral centers, making it an interesting subject for stereochemistry studies. Its specific arrangement of substituents results in distinct stereoisomers, each potentially exhibiting different biological properties.
- Biological Relevance: Compounds similar to this one are often found in natural products, which can lead to interesting pharmacological applications. It may play a role as a sugar mimic or in glycosylation reactions. This hint at biological activity opens up avenues for further research.
- Functional Groups: The presence of hydroxymethyl groups indicates the compound's potential for participating in hydrogen bonding and further chemical reactivity. Hydroxymethyl groups are known to increase solubility, and they can influence the interactions in biological systems.
- Potential Applications: Given its structural characteristics, (2R,3R,4R,5S)-2-(hydroxymethyl)piperidine-3,4,5-triol might find use in the synthesis of pharmaceuticals or as a building block in organic synthesis.
- Research Opportunities: Ongoing studies may yield insights into how variations in the structure affect activity, making it a prime candidate for both theoretical and applied research in medicinal chemistry.
In conclusion, the study of (2R,3R,4R,5S)-2-(hydroxymethyl)piperidine-3,4,5-triol offers valuable perspectives on chirality, functional group chemistry, and the fascinating intersections between synthetic and natural compounds. As this area of chemistry evolves, we may uncover even more about how such compounds can impact our understanding of biology and medicine.
Synonyms
19130-96-2
DUVOGLUSTAT
deoxynojirimycin
Moranolin
1 Deoxynojirimycin
D-1-deoxynojirimycin
1,5-Dideoxy-1,5-imino-D-glucitol
Nojirimycin, 1-deoxy-
BAY-h-5595
5-Amino-1,5-dideoxy-D-glucopyranose
1,5-dideoxy-1,5-imino-
FZ56898FLE
CHEBI:44369
DTXSID70172647
3,4,5-Piperidinetriol, 2-(hydroxymethyl)-, (2R-(2alpha,3beta,4alpha,5beta))-
duvoglustatum
GlyTouCan:G62915MH
DTXCID4095138
G62915MH
606-239-2
RefChem:388743
1-DEOXYNOJIRIMYCIN
(2R,3R,4R,5S)-2-(hydroxymethyl)piperidine-3,4,5-triol
Moranoline
1,5-Deoxy-1,5-imino-D-mannitol
MFCD00063474
(2R,3R,4R,5S)-2-Hydroxymethyl-piperidine-3,4,5-triol
(+)-1-DEOXYNOJIRIMYCIN
1-deoxynojirimycin (DNJ)
3,4,5-Piperidinetriol, 2-(hydroxymethyl)-, (2R,3R,4R,5S)-
CHEMBL307429
DNJ
1-Deoxy-Nojirimycin
S-GI
1oim
DNM
1-Deoxynojirimycin (hydrochloride)
Duvoglustat (hydrochloride)
Duvoglustat [USAN:INN]
UNII-FZ56898FLE
BAY-h 5595
NOJ
DUVOGLUSTAT [INN]
Duvoglustat (USAN/INN)
DUVOGLUSTAT [USAN]
EC 606-239-2
SCHEMBL2969
1-DNJ
BSPBio_000993
1-Deoxynojirimycin (Standard)
GTPL4642
orb1303921
1-DEOXYNOJIRIMYCIN [MI]
BDBM18351
2j77
Bio1_000415
Bio1_000904
Bio1_001393
HMS1792A15
HMS1990A15
HMS3267J09
HMS3403A15
MSK10764
HB4599
HY-14860R
s3839
1,5-didesoxy-1,5-imino-D-glucitol
1, 5-dideoxy-1,5-imino-D-glucitol
AKOS006275143
1-Deoxynojirimycin, analytical standard
AC-1386
CCG-266301
CS-5594
DB03206
MD05255
SMP2_000333
NCGC00025085-02
NCGC00025085-03
BS-15755
HY-14860
SY032317
D5612
NS00009621
D09605
EN300-7411893
GLUCOPYRANOSE, 5-AMINO-1,5-DIDEOXY-, D-
SR-01000597392
SR-01000597392-1
Q15274561
(2R,3R,4R,5S)-2-(Hydroxymethyl)piperidine-3,4,5-triol, 10
1,5-Dideoxy-1,5-imino-D-glucitol;Moranoline;1,5-Dideoxy-1,5-imino-D-sorbitol;DNJ;2R- (hydroxymethyl)- 3R, 4R, 5S- piperidinetriol
3,4,5-PIPERIDINETRIOL, 2-(HYDROXYMETHYL)-, (2R-(2.ALPHA.,3.BETA.,4.ALPHA.,5.BETA.))-
Solubility of (2R,3R,4R,5S)-2-(hydroxymethyl)piperidine-3,4,5-triol
The solubility of (2R,3R,4R,5S)-2-(hydroxymethyl)piperidine-3,4,5-triol can be understood through several key factors that influence its behavior in different solvents:
In summary, one could reasonably predict that (2R,3R,4R,5S)-2-(hydroxymethyl)piperidine-3,4,5-triol will exhibit excellent solubility in polar solvents due to its hydroxyl functional groups that facilitate strong intermolecular interactions. As the old adage goes, "like dissolves like", and this compound aligns well with that principle when considering its affinity for polar media.