Interesting facts
Interesting Facts about (2R,4R,5R,6S)-4-(hydroxymethyl)-10-imino-3,7-dioxa-1,9-diazatricyclo[6.4.0.02,6]dodeca-8,11-dien-5-ol; hydrochloride
The compound (2R,4R,5R,6S)-4-(hydroxymethyl)-10-imino-3,7-dioxa-1,9-diazatricyclo[6.4.0.02,6]dodeca-8,11-dien-5-ol; hydrochloride is a fascinating example of a multi-functional compound, showcasing a complex architecture that contributes to its chemical properties and potential applications. Here are some captivating aspects of this compound:
- Structural Complexity: The compound's bicyclic structure, featuring diazatricycles and hydroxymethyl groups, exemplifies how intricate molecular arrangements can influence reactivity and interaction with biological systems.
- Biological Relevance: Compounds similar to this one are often investigated for their biological activity, particularly in relation to drug design and medicinal chemistry. The presence of functional groups may provide valuable pathways for biochemical interactions.
- Chirality: With specified stereochemistry at multiple centers (2R, 4R, 5R, 6S), this compound emphasizes the importance of chirality in chemistry. Chirality can significantly impact how a molecule interacts with enzymes and receptors in the body, adding another layer to its potential applications.
- Legacy and Research: Compounds like this have sparked interest in ongoing research, particularly in fields such as pharmaceutical chemistry and organic synthesis. The quest for new active compounds continues to drive scientists to explore the unique characteristics of such molecular designs.
Ultimately, the intricate dynamics of (2R,4R,5R,6S)-4-(hydroxymethyl)-10-imino-3,7-dioxa-1,9-diazatricyclo[6.4.0.02,6]dodeca-8,11-dien-5-ol; hydrochloride reflect the broader complexity of chemical compounds, stirring a curiosity that drives exploration and discovery in the scientific community.
Synonyms
Cyclocytidine hydrochloride
ANCITABINE HYDROCHLORIDE
(-)-Cyclocytidine hydrochloride
OCTD hydrochloride
2,2'-O-Cyclocytidine hydrochloride
Ancitabin hydrochlorid
ancitabine HCl
Cyclo-cmp hydrochloride
2,2'-Anhydro-1-beta-D-arabinofuranosylcytosine hydrochloride
Ancitabine (hydrochloride)
2,2'-Anhydrocytidine hydrochloride
Cyclocytidine HCl
2,2'-Anhydrocytarabine hydrochloride
2,2'-Anhydroaracytidine hydrochloride
Ancitabine hydrochloride [JAN]
2,2'-Anhydroarabinosylcytosine hydrochloride
2,2'-Cyclocytidine hydrochloride
MFCD00012636
CHEBI:74843
Cyclo-C
3T6920M469
(2R,3R,3aS,9aR)-2-(hydroxymethyl)-6-imino-3,3a,6,9a-tetrahydro-2H-furo[2',3':4,5]oxazolo[3,2-a]pyrimidin-3-ol hydrochloride
Ancitabine hydrochloride (JAN)
MLS001173324
Ancitabin HCl
Ancitabin hydrochloride
SMR000538927
EINECS 233-515-6
2,2'-Cyclocytidine, monohydrochloride
O-2,2'-Cyclocytidine monohydrochloride
UNII-3T6920M469
2,2'-Anhydro-1-ss-D-arabinofuranosylcytosine HCl; 2,2'-O-Cyclocytidine HCl; Ancitabine HCl; Cyclo-CMP HCl
2,2'-Anhydro-1beta-D-arabinofuranosylcytosine hydrochloride
1beta-D-Arabinofuranosylcytosine, 2,2'-anhydro-, hydrochloride
1-beta-D-Arabinofuranosylcytosine, 2,2'-anhydro-, hydrochloride
Cytosine, 1-beta-D-arabinofuranosyl-2,2'-anhydro-, hydrochloride
Cytosine, 1beta-D-arabinofuranosyl-2,2'-anhydro-, hydrochloride
2,2'-Anhydrocytidine HCl
SCHEMBL98180
2,2'-Anhydro-(1-beta-D-arabinofuranosyl)cytosine hydrochloride
MLS000766878
MLS001032024
MLS006011603
NSC 145668 HCl
CHEMBL1255937
HY-N0093
2,2'-cyclocytidine monohydrochloride
ANCITABINE HYDROCHLORIDE [MI]
s1973
AKOS015896930
AC-8697
CCG-267066
CS-5313
NA01967
ANCITABINE HYDROCHLORIDE [MART.]
ANCITABINE HYDROCHLORIDE [WHO-DD]
6H-Furo(2',3':4,5)oxazolo(3,2-a)-pyrimidine-2-methanol, 2,3,3a,9a-tetrahydro-3-hydroxy-6-imino-, monohydrochloride, stereoisomer
6H-Furo(2',3':4,5)oxazolo(3,2-a)pyrimidine-2-methanol, 2,3,3a,9a-tetrahydro-3-hydroxy-6-imino-, monohydrochloride, (2R-(2alpha,3beta,3abeta,9abeta))-
AS-12870
TL8000113
D01651
EN300-7400814
Ancitabine hydrochloride (Cyclocytidine hydrochloride)
Q27144957
Z2044737748
2,2'-anhydro-(1-beta-D-arabinofuranosylcytosine) hydrochloride
2,2'-anhydro-1-(beta-D-arabinofuranosyl)cytosine hydrochloride
(2R,3R,3AS,9AR)-2,3,3A,9A-TETRAHYDRO-3-HYDROXY-6-IMINO-6H-FURO(2',3';4,5)OXAZOLO(3,2-A)PYRIMIDINE-2-METHANOL, HYDROCHLORIDE
(2R,3R,3aS,9aR)-2-(hydroxymethyl)-6-imino-2,3,3a,9a-tetrahydro-6H-furo[2',3':4,5][1,3]oxazolo[3,2-a]pyrimidin-3-ol hydrochloride
(2R,3R,3aS,9aR)-2-(hydroxymethyl)-6-imino-2,3,3a,9a-tetrahydrofuro[1,2]oxazolo[3,4-a]pyrimidin-3-ol
(2R,3R,3aS,9aR)-2-(hydroxymethyl)-6-imino-3,3a,6,9a-tetrahydro-2H-furo[2',3':4,5]oxazolo[3,2-a]pyrimidin-3-olhydrochloride
(2R,4R,5R,6S)-4-(hydroxymethyl)-10-imino-3,7-dioxa-1,9-diazatricyclo[6.4.0.0,2,6]dodeca-8,11-dien-5-ol hydrochloride
(2R,4R,5R,6S)-4-(hydroxymethyl)-10-imino-3,7-dioxa-1,9-diazatricyclo[6.4.0.02,6]dodeca-8,11-dien-5-ol;hydrochloride
2,2'-Anhydro-b-D-arabinofuranosyl cytosine HCl;Cyclocytidine HCl;2,2'-Anhydro-D-cytidine HCl
Solubility of (2R,4R,5R,6S)-4-(hydroxymethyl)-10-imino-3,7-dioxa-1,9-diazatricyclo[6.4.0.02,6]dodeca-8,11-dien-5-ol; hydrochloride
The solubility of the compound (2R,4R,5R,6S)-4-(hydroxymethyl)-10-imino-3,7-dioxa-1,9-diazatricyclo[6.4.0.02,6]dodeca-8,11-dien-5-ol; hydrochloride (C8H12N5O3Cl) can be influenced by several factors:
In summary, the solubility of (2R,4R,5R,6S)-4-(hydroxymethyl)-10-imino-3,7-dioxa-1,9-diazatricyclo[6.4.0.02,6]dodeca-8,11-dien-5-ol; hydrochloride is expected to be quite favorable in aqueous solutions, exhibiting the typical characteristics of many amino-rich compounds, which often demonstrate excellent solvation properties.