Interesting facts
Interesting Facts About 4-amino-N-(1-benzyl-4-piperidyl)-5-chloro-2-methoxy-benzamide
This intriguing compound, known for its complex structure and pharmacological properties, belongs to a class of molecules that are actively researched for their potential therapeutic applications. Here are some key facts about this compound:
- Pharmacological Relevance: The presence of an amino group and a benzamide moiety suggests potential activity in areas such as antipsychotics or antidepressants, making it a subject of interest in medicinal chemistry.
- Structural Features: This compound features a piperidine ring, which is known for its role in enhancing the solubility and bioavailability of drugs. The addition of a benzyl group further enhances its lipid affinity, potentially increasing its efficacy.
- Chlorine Substitution: The incorporation of a chlorine atom can significantly affect the compound's reactivity and interactions with biological targets, often improving selectivity and potency.
- Research Applications: Compounds of this nature, often undergoing extensive biological testing, may lead to discovering new modalities of treatment for various ailments, including neurological disorders and cancer therapies.
- Synthetic Pathways: The synthesis of such complex compounds involves multi-step reactions, showcasing the ingenuity of organic chemistry. Researchers often employ techniques like coupling reactions and functional group transformations to achieve these intricate structures.
As a compound rich in chemical diversity, 4-amino-N-(1-benzyl-4-piperidyl)-5-chloro-2-methoxy-benzamide serves as a perfect example of how small structural variations can lead to significant shifts in biological activity, making it an exciting area for future research and development!
Synonyms
Clebopride
55905-53-8
Cleboril
Cleboprida
Clebopridum
4-amino-N-(1-benzylpiperidin-4-yl)-5-chloro-2-methoxybenzamide
LAS 9273
EINECS 259-885-9
Clebopridum [INN-Latin]
Cleboprida [INN-Spanish]
Cleboril (TN)
Clebopride [USAN:INN:BAN]
Clebopride (USAN)
BRN 0493934
N-(1'-Benzyl-4'-piperidyl)-2-methoxy-4-amino-5-chlorobenzamide
UNII-I0A84520Y9
4-Amino-N-(1-benzyl-4-piperidyl)-5-chloro-o-anisamide
CLEBOPRIDE [MI]
LAS-9273
CLEBOPRIDE [INN]
CLEBOPRIDE [USAN]
I0A84520Y9
CLEBOPRIDE [MART.]
CLEBOPRIDE [WHO-DD]
CHEMBL325109
DTXSID7022831
4-Amino-5-chloro-2-methoxy-N-(1-benzyl-4-piperidyl)benzamide
5-22-08-00086 (Beilstein Handbook Reference)
Clanzol
Cleprid
Motilex
Amicos
Clast
BENZAMIDE, 4-AMINO-5-CHLORO-2-METHOXY-N-(1-(PHENYLMETHYL)-4-PIPERIDINYL)-
clebopride malate
Clebopridum (INN-Latin)
Cleboprida (INN-Spanish)
CLEBOPRIDE (MART.)
Clebopride hydrogen malate
4-Amino-5-chloro-2-methoxy-N-[1-(phenylmethyl)-4-piperidinyl]benzamide
4-AMINO-5-CHLORO-2-METHOXY-N-(1-(PHENYLMETHYL)-4-PIPERIDINYL)BENZAMIDE
NCGC00016951-01
CAS-84370-95-6
Clanzoflat
Clebopride,(S)
Spectrum_001692
N-1-benzyl-4 piperidil-3-methoxy-4-amino-5-chlorobenzamide
SpecPlus_000752
Prestwick0_000380
Prestwick1_000380
Prestwick2_000380
Prestwick3_000380
Spectrum2_000767
Spectrum3_001997
Spectrum4_000083
Spectrum5_001571
SCHEMBL25710
BSPBio_000539
BSPBio_003597
KBioGR_000346
KBioSS_002172
DivK1c_006848
SPBio_000814
SPBio_002460
BPBio1_000593
DTXCID102831
SCHEMBL25259199
CHEBI:92309
KBio1_001792
KBio2_002172
KBio2_004740
KBio2_007308
KBio3_003039
A03FA06
BVPWJMCABCPUQY-UHFFFAOYSA-N
BDBM50132693
AKOS027420458
DB13511
NCGC00016951-02
NCGC00016951-03
NCGC00177974-01
NCGC00177974-02
AB00053707
NS00033420
D03534
4-amino-N-(1-benzylpiperidin-4-yl)-5-chloro-
L000785
Q5131021
BRD-K17294426-050-05-7
BRD-K17294426-050-12-3
4-amino-N-(1-benzyl-4-piperidinyl)-5-chloro-2-methoxybenzamide
4-Amino-N-(1-benzyl-piperidin-4-yl)-5-chloro-2-methoxy-benzamide
4-amino-5-chloro-2-(methyloxy)-N-[1-(phenylmethyl)piperidin-4-yl]benzamide
4-Amino-N-(1-benzyl-piperidin-4-yl)-5-chloro-2-methoxy-benzamide(Clebopride)
259-885-9
Solubility of 4-amino-N-(1-benzyl-4-piperidyl)-5-chloro-2-methoxy-benzamide
The compound 4-amino-N-(1-benzyl-4-piperidyl)-5-chloro-2-methoxy-benzamide (C20H24ClN3O2) exhibits unique solubility characteristics that are important to consider. Here are some key points regarding its solubility:
In conclusion, careful consideration of the solubility properties of this compound is crucial for its applications, as solubility can significantly influence bioavailability and interaction with biological systems. The factors above can help in determining the most effective solvent systems for various experimental procedures.