Interesting facts
Interesting Facts about 3-(1H-indol-3-yl)propanoic Acid
3-(1H-indol-3-yl)propanoic acid is a fascinating compound with intriguing properties and applications. Here are some key points that highlight its significance:
- Biological Activity: This compound is known for its potential biological activities, making it a subject of research in pharmacology. It exhibits properties that may influence various biochemical pathways, which could lead to therapeutic applications.
- Structure and Aesthetics: The unique structure of this compound, featuring an indole moiety, is not only essential for its biological functions but also contributes to its visual identification in molecular modeling.
- Indole Derivatives: Belonging to the family of indole derivatives, 3-(1H-indol-3-yl)propanoic acid can serve as a starting material in synthesizing various dye and drug compounds. Indoles, in general, are a significant class of heterocyclic compounds found widely in nature.
- Research Potential: Studies have suggested that compounds like 3-(1H-indol-3-yl)propanoic acid may possess antidepressant effects, potentially aiding in the development of new treatments for mood disorders.
- Impact on Neurotransmission: Due to the structural similarity to neurotransmitters, this compound may interact with neural receptors, enhancing our understanding of the chemistry behind neural signaling.
Overall, 3-(1H-indol-3-yl)propanoic acid holds promise not just in academic research but also in medicinal chemistry. Its potential applications and biological significance open doors for future investigations, enriching the scientific community's knowledge base.
Synonyms
3-Indolepropionic acid
830-96-6
Indole-3-propionic acid
3-(1H-Indol-3-yl)propanoic acid
1H-Indole-3-propanoic acid
Indolepropionic acid
3-(3-Indolyl)propionic acid
3-(3-Indolyl)propanoic acid
Indolylpropionic Acid
IPA (auxin)
3-(Indol-3-yl)propionic acid
1H-INDOLE-3-PROPIONIC ACID
3-(3-Indole)propionic acid
Oxigon
beta-Indolylpropionate
3-(2-Carboxyethyl)-1H-indole
3-Indolepropionicacid
indole propionate
indole-3-propanoic acid
MFCD00005660
beta-(3-Indolyl)propionic acid
NSC 3252
1H-Indole-3-proponoic acid
NSC 47831
CCRIS 4424
3-(Indol-3-yl)propanoic acid
3-(1H-Indol-3-yl)propionic acid
EINECS 212-600-1
JF49U1Q7KN
BRN 0147733
VP-20629
CHEBI:43580
AI3-17433
NSC-3252
3-(1H-indol-3-yl)-propionic acid
NSC-47831
.beta.-Indolepropionic acid
VP 20629
.beta.-Indole-3-propionic acid
DTXSID7061192
.beta.-(3-Indolyl)propionic acid
5-22-03-00114 (Beilstein Handbook Reference)
.beta.-Indolylpropionate
3-(1H-Indol-3-yl)propionate
UNII-JF49U1Q7KN
b-Indolepropionate
4ejl
3-Indolepropionate
Indole-3-propionic
beta-Indolepropionate
3-indolpropionic acid
b-Indolepropionic acid
b-Indole-3-propionate
Acid, 7
3-Indole propionic acid
Indole 3-propionic acid
1H-Indole-3-propionate
beta-Indolepropionic acid
indole-3-proprionic acid
b-(3-Indolyl)propionate
beta-Indole-3-propionate
Maybridge1_002431
3-(3-Indolyl)propanoate
3-(3-Indolyl)propionate
b-Indole-3-propionic acid
beta-(3-Indolyl)propionate
Oprea1_071255
b-(3-Indolyl)propionic acid
beta-Indole-3-propionic acid
BIDD:GT0788
DivK1c_001183
SCHEMBL195405
3-Indolepropionic acid (IPA)
3-(3-indolyl)-propionic acid
CHEMBL207225
GTPL4709
SCHEMBL1767754
SHP622
DTXCID5048342
BDBM31879
HMS548G11
NSC3252
SHP-622
1F1-N
3-Indolepropionic acid (Standard)
GLXC-03350
HMS3604I20
HMS3886E03
ALBB-034983
BCP26573
HY-W015229R
NSC47831
BBL001406
s4809
STK247053
3-(1H-Indol-3-yl)propanoic acid #
AKOS000120911
CCG-115418
CS-W015945
DB02758
FI30477
FS-3158
HY-W015229
SDCCGMLS-0065895.P001
VP20629
CDS1_000143
NCGC00340705-01
AC-10570
BP-21044
SY015400
DB-011207
Indole-3-propionic acid, >=97.0% (T)
Indole-3-propionic acid, >=99.0% (T)
I0032
NS00038237
EN300-20789
3-Indolepropionic acid, ReagentPlus(R), 99%
C22236
AB01333057-02
BRD-K21071223-001-02-8
Q21098993
3-Indolepropionic acid, Vetec(TM) reagent grade, 99%
F0849-0388
Z104482518
10265-77-7
212-600-1
Solubility of 3-(1H-indol-3-yl)propanoic acid
3-(1H-indol-3-yl)propanoic acid, with the chemical formula C11H11NO2, exhibits interesting solubility characteristics. Understanding the solubility of this compound can be essential for its applications in various fields, including pharmaceuticals and research. Here are some key points regarding its solubility:
In summary, the solubility of 3-(1H-indol-3-yl)propanoic acid is significantly influenced by its chemical structure, specifically the balance between its polar and non-polar regions. For optimal use, it is crucial to consider these solubility properties when selecting solvents for experiments or formulations.