Interesting facts
Interesting Facts about 3-(1-Piperidylmethyl)-1H-indole
3-(1-Piperidylmethyl)-1H-indole is a fascinating compound with connections to both medicinal chemistry and pharmacology. Here are some intriguing aspects of this compound:
- Chemical Structure: The compound features an indole ring, which is notable for its participation in a variety of biochemical processes. Indoles are often found in many natural products and play a crucial role in the structure of numerous alkaloids.
- Biological Activity: Compounds containing both piperidine and indole moieties are of great interest in drug discovery. They exhibit diverse biological activities, including potential roles as analgesics, anti-inflammatory agents, and even anticancer properties.
- Influence on Neurochemistry: The piperidine group is known for its influence on neurotransmitter systems. This compound may act as a ligand for certain receptors in the brain, making it a subject of interest for studies related to mood disorders and cognitive function.
- Pharmacological Research: Researchers often investigate indole derivatives for their therapeutic potential. The combination of the piperidyl group with the indole structure suggests that 3-(1-Piperidylmethyl)-1H-indole could interact with various target proteins in the human body.
- Synthetic Pathways: The synthesis of this compound typically involves strategies that interconnect piperidine and indole derivatives. Understanding these synthetic routes not only sheds light on the compound itself but also on broader methodologies in organic chemistry.
In summary, 3-(1-Piperidylmethyl)-1H-indole represents a significant area of research due to its structural complexity and potential pharmacological benefits. As a professional in the field, one can appreciate the balance of chemistry and biology that this compound epitomizes.
Synonyms
5355-42-0
INDOLE, 3-(PIPERIDINOMETHYL)-
N-Skatylpiperidine
3-(1-Piperidinylmethyl)-1H-indole
3-(Piperidinomethyl) indole
NSC 24532
3ED9JU5XWE
3-(Piperidinomethyl)indole
NSC 47186
BRN 0176547
UNII-3ED9JU5XWE
NSC-24532
NSC-47186
3-N-Piperidinomethyl indole
DTXSID20201759
5-22-10-00029 (Beilstein Handbook Reference)
1H-Indole, 3-(1-piperidylmethyl)-
1H-Indole, 3-(1-piperidinylmethyl)-
3-(PIPERIDIN-1-YLMETHYL)INDOLE
DTXCID00124250
hpkxpfrrvvwapd-uhfffaoysa-n
3-((PIPERIDIN-1-YL)METHYL)-1H-INDOLE
3-(piperidin-1-ylmethyl)-1H-indole
CHEMBL57535
3-Piperidin-1-ylmethyl-1H-indole
3-[(piperidin-1-yl)methyl]-1H-indole
3-(Piperidinomethyl)-1H-indole
TimTec1_004365
Oprea1_229223
Oprea1_800570
MLS000780429
N-(3-Indolylmethyl)-piperidin
SCHEMBL8789790
HMS1546G09
HMS2788N12
NSC24532
NSC47186
BDBM50050466
MFCD00458412
STK001853
AKOS000291489
3-(1-Piperidinylmethyl)-1H-indole #
NCGC00246449-01
SMR000424731
DB-071700
CS-0313178
3-((Piperidin-1-yl)methyl)-1H-indole,98%
AG-670/31507045
SR-01000391787
SR-01000391787-1
Solubility of 3-(1-piperidylmethyl)-1H-indole
The solubility of 3-(1-piperidylmethyl)-1H-indole can be influenced by several factors that are intrinsic to its molecular structure. This compound, a derivative of indole, contains both aromatic and aliphatic moieties, which may enhance or hinder its solubility in various solvents.
Factors Affecting Solubility:
In general, indole derivatives can exhibit varying degrees of solubility depending on their substituents and the medium. As a result:
Ultimately, the solubility profile will determine the practical applications of 3-(1-piperidylmethyl)-1H-indole in various fields, including pharmaceuticals and chemical research.