Interesting facts
Interesting Facts about 3-[(4-chlorophenyl)methyl]-2-[3-(1H-imidazol-5-yl)propyl]isothiourea
This compound, a member of the isothiourea family, boasts a complex structure that intertwines various functional groups, making it a subject of great interest in the realm of medicinal chemistry. Here are some noteworthy points:
- Pharmacological Potential: Compounds like this one often exhibit a range of biological activities, including anti-inflammatory and antitumor properties. Research may unveil its potential in targeting specific diseases.
- Molecular Diversity: The presence of the 1H-imidazol-5-yl moiety suggests intriguing interactions with biological targets, especially in enzyme inhibition or receptor modulation.
- Bridge to Therapeutics: Isothioureas have been studied for their ability to act as enzyme inhibitors, which may lead to the development of new therapeutic agents in treating conditions such as cancer and diabetes.
- Halogen Influence: The 4-chlorophenyl group exemplifies how halogen substitutions can significantly modify the pharmacokinetic properties of organic compounds, potentially increasing their bioavailability and interaction with target sites.
- Synthetic Utility: The synthetic pathways leading to such compounds are of great interest, opening avenues for innovative chemical synthesis techniques that can yield structurally diverse derivatives.
In summary, the compound 3-[(4-chlorophenyl)methyl]-2-[3-(1H-imidazol-5-yl)propyl]isothiourea encompasses a rich tapestry of chemical properties and potential applications in the biomedical field. Its multifaceted structure not only holds promise for future research but also poses exciting questions in the study of structure-activity relationships.
Synonyms
clobenpropit
145231-45-4
Vuf-9153
Vuf 9153
CHEBI:64177
Carbamimidothioic acid, N-[(4-chlorophenyl)methyl]-, 3-(1H-imidazol-5-yl)propyl ester
S-(3-(4(5)-Imidazolyl))propyl-N-(4-chlorobenzyl)isothiourea
UNII-RKU631JF4H
RKU631JF4H
3-(1H-Imidazol-5-yl)propyl 4-chlorobenzylcarbamimidothioate
DTXSID3043738
3-(1H-imidazol-4-yl)propyl ((4-chlorophenyl)methyl)carbamimidothioate
Carbamimidothioic acid, ((4-chlorophenyl)methyl)-, 3-(1H-imidazol-4-yl)propyl ester
3-(1H-imidazol-4-yl)propyl N-(4-chlorobenzyl)carbamimidothioate
3-(1H-imidazol-5-yl)propyl N'-[(4-chlorophenyl)methyl]carbamimidothioate
CARBAMIMIDOTHIOIC ACID, N-((4-CHLOROPHENYL)METHYL)-, 3-(1H-IMIDAZOL-5-YL)PROPYL ESTER
N'-[(4-chlorophenyl)methyl]-1-[3-(3H-imidazol-4-yl)propylsulfanyl]methanimidamide
VUF9153
N'-((4-chlorophenyl)methyl)-1-(3-(3H-imidazol-4-yl)propylsulfanyl)methanimidamide
Carbamimidothioic acid,N-[(4-chlorophenyl)methyl]-, 3-(1H-imidazol-5-yl)propyl ester
Clobenpropit free base
Tocris-0752
SCHEMBL49050
MLS001424295
CHEMBL14690
GTPL1223
SCHEMBL8312286
DTXCID1023738
SCHEMBL19733457
BDBM22541
UCAIEVHKDLMIFL-UHFFFAOYSA-N
HMS2052B07
HMS3394B07
AAA30301
BDBM50214615
PDSP1_000537
PDSP2_000535
AKOS025405026
CCG-101167
NC00417
NCGC00024770-01
NCGC00024770-02
AS-77937
SMR000469632
HY-115447
CS-0086986
A11462
C17934
L000192
L010032
Q5134762
BRD-K71430621-303-01-5
BRD-K71430621-303-02-3
3-(1H-imidazol-4-yl)propyl 4-chlorobenzylcarbamimidothioate
3-(1~{H}-imidazol-4-yl)propyl ~{N}'-[(4-chlorophenyl)methyl]carbamimidothioate
N''''-[(4-chlorophenyl)methyl]{[3-(1H-imidazol-5-yl)propyl]sulfanyl}methanimidamide
Solubility of 3-[(4-chlorophenyl)methyl]-2-[3-(1H-imidazol-5-yl)propyl]isothiourea
The solubility of 3-[(4-chlorophenyl)methyl]-2-[3-(1H-imidazol-5-yl)propyl]isothiourea (C22H17ClN2S) is influenced by its complex molecular structure and functional groups. Understanding the solubility behavior is crucial for applications in pharmacology and medicinal chemistry.
Factors Affecting Solubility:
As with many isothiourea derivatives, solubility is often limited in standard conditions, leading to the following observations:
In summary, while 3-[(4-chlorophenyl)methyl]-2-[3-(1H-imidazol-5-yl)propyl]isothiourea presents intriguing solubility characteristics, its practical applications underscore the need for careful solvent selection and formulation strategies to optimize its solubility profile for specific uses.