Interesting facts
Interesting Facts about 4-[2-(dipropylamino)ethyl]indolin-2-one
The compound 4-[2-(dipropylamino)ethyl]indolin-2-one belongs to the class of indolinones, which are important in various fields of research and applications. Here are some fascinating insights into this compound:
- Structural Significance: The indolinone structure is renowned for its versatile chemical properties and biological activities. The functional groups attached to the indole ring can significantly influence its reactivity.
- Biological Activity: Compounds with indolinone structures have been investigated for their potential in medicinal chemistry, particularly as antidepressants, antipsychotics, and even as anti-cancer agents.
- Role of Alkyl Amines: The dipropylamino group in this compound might enhance its lipophilicity and possibly lead to increased efficacy in biological systems by improving membrane penetration.
- Research Applications: Scientists often explore compounds like this for drug design. The ability to modify the amino chain could lead to derivatives that target specific receptors in the body.
- Synthetic Interest: The synthesis of compounds with indolinone frameworks often involves several interesting reactions, including cyclization and aromatic substitutions, showcasing the creativity of chemists.
A quote from renowned organic chemist Janet I. Van Horne emphasizes the significance of such compounds: "The diversity of indole derivatives in nature is a treasure trove for medicinal chemistry." This underlines the importance of 4-[2-(dipropylamino)ethyl]indolin-2-one as a potential lead compound in drug discovery.
In summary, the exploration of 4-[2-(dipropylamino)ethyl]indolin-2-one represents a blend of synthetic creativity and biological potential, making it an intriguing subject of study in modern chemistry.
Synonyms
ropinirole
91374-21-9
ropinirol
Ropinirolum
Ropinirolum [INN-Latin]
Ropinirol [INN-Spanish]
4-(2-(dipropylamino)ethyl)indolin-2-one
Ropitor
SKF 101468
SK&F 101468
4-[2-(dipropylamino)ethyl]-1,3-dihydroindol-2-one
Narapin
4-[2-(dipropylamino)ethyl]-1,3-dihydro-2H-indol-2-one
NSC-758917
CHEBI:8888
DTXSID8045195
UNII-030PYR8953
CHEMBL589
030PYR8953
DTXCID6025195
HSDB 8252
NSC 758917
SK&F-101468
NCGC00015893-02
Ropinirol (INN-Spanish)
Ropinirolum (INN-Latin)
4-(2-(Dipropylamino)ethyl)-1,3-dihydro-2H-indol-2-one
4-[2-(dipropylamino)ethyl]-2,3-dihydro-1h-indol-2-one
Ropitor (TN)
CAS-91374-21-9
Ropinirole [USAN:INN:BAN]
Ropinirolum (Latin)
ROPINIROLE [MI]
ROPINIROLE [INN]
Ropinirole (USAN/INN)
Lopac-R-4152
ROPINIROLE [USAN]
ROPINIROLE [VANDF]
ROPINIROLE [WHO-DD]
4-(2-(di-n-propylamino)ethyl)-2(3H)-indolone
Lopac0_001101
SCHEMBL35212
BIDD:GT0826
SPECTRUM1505178
GTPL7295
N04BC04
2H-Indol-2-one, 4-(2-(dipropylamino)ethyl)-1,3-dihydro-
HMS2093K04
Pharmakon1600-01505178
BCP09383
HY-B0623
Tox21_110256
BDBM50020680
NSC758917
STL454344
AKOS015843123
Tox21_110256_1
CCG-205177
DB00268
FR32034
SB65618
SDCCGSBI-0051070.P002
SKF-101468
4-[2-(Dipropylamino)ethyl]2-indolinone
NCGC00015893-01
NCGC00015893-03
NCGC00015893-04
NCGC00015893-06
NCGC00094373-12
NCGC00096064-01
NCGC00096064-02
4-[2-(dipropylamino)ethyl]-3H-indol-2-ol
CS-0009561
NS00008049
C07564
D08489
EN300-708794
G78293
AB01563044_01
AB01563044_02
4-(2-dipropylaminoethyl)-1,3-dihydroindol-2-one
L000520
Q420590
SR-01000076215-3
BRD-K15933101-003-01-2
BRD-K15933101-003-06-1
BRD-K15933101-003-07-9
4-[2-(dipropylamino)ethyl]-1.3-dihydro-2H-indol-2-one
Solubility of 4-[2-(dipropylamino)ethyl]indolin-2-one
The solubility of the compound 4-[2-(dipropylamino)ethyl]indolin-2-one (C17H26N2O) is an intriguing factor that influences its applications in various fields. This compound, possessing both hydrophobic and hydrophilic characteristics, showcases a range of solubility behavior:
In conclusion, the solubility profile of 4-[2-(dipropylamino)ethyl]indolin-2-one is essential for its effectiveness in chemical syntheses and biological contexts. When considering its use, one should meticulously evaluate the solvent system to optimize solvation characteristics.