Interesting facts
Interesting Facts about 2-(2-hydroxy-1H-indol-3-yl)indol-3-one
The compound 2-(2-hydroxy-1H-indol-3-yl)indol-3-one belongs to a unique family of chemical species that demonstrate intriguing properties and potential applications in various fields. Here are some key points of interest:
- Indole-based Structure: This compound features the indole moiety, a versatile structure that is prevalent in many biologically active molecules. Indoles are known for their ability to modulate biological activities and have been the subject of numerous research endeavors.
- Biological Significance: Compounds containing indole structures are often found in nature and play significant roles in pharmacology. They can exhibit a variety of biological activities, such as antimicrobial, antitumor, and anti-inflammatory effects, making them valuable in medicinal chemistry.
- Potential Therapeutic Uses: The presence of the hydroxyl group in the compound hints at its potential interaction with biological systems. Research is ongoing to explore its efficacy and safety for therapeutic applications, particularly in cancer research and the treatment of neurological disorders.
- Research Applications: Due to its complex structure, this compound serves as a promising candidate for synthetic investigations in organic chemistry. Scientists are constantly seeking to synthesize derivatives that may enhance its pharmacological properties or increase its effectiveness.
- Implications in Dye Chemistry: The vibrantly colored indole derivatives are also utilized in dye chemistry, opening avenues for further exploration in materials science and organic light-emitting diodes (OLEDs).
Overall, 2-(2-hydroxy-1H-indol-3-yl)indol-3-one stands as a remarkable example of how chemical compounds can bridge the gap between nature and synthetic innovation. As research progresses, we might uncover even more fascinating aspects of this and similar compounds, highlighting the ever-evolving landscape of chemistry.
Synonyms
2H-Indol-2-one, 3-(1,3-dihydro-3-oxo-2H-indol-2-ylidene)-1,3-dihydro-
2H-Indol-2-one, 3-(1,3-dihydro-3-oxo-2H-indol-2-ylidene)-1,3-dihydro-(9CI)
610-392-0
Indirubin
479-41-4
Indigo Red
906748-38-7
Couroupitine B
Indigopurpurin
(Z)-[2,3'-biindolinylidene]-2',3-dione
(E)-[2,3'-biindolinylidene]-2',3-dione
397242-72-7
Isoindirubin
Isoindirubine
Isoindogotin
Indirubin [MI]
NSC-105327
INDARUBICIN
2-(2-hydroxy-1H-indol-3-yl)indol-3-one
2H-Indol-2-one,3-(1,3-dihydro-3-oxo-2H-indol-2-ylidene)-1,3-dihydro-
C.I. 73200
MFCD00956441
Indirubin 3E-form [MI]
NSC 105327
1LXW6D3W2Z
(Z)-[2,3 inverted exclamation mark -Biindolinylidene]-2 inverted exclamation mark ,3-dione
V86L8P74GI
C.I. 75790
3-(1,3-dihydro-3-oxo-2h-indol-2-ylidene)-1,3-dihydro-2h-indol-2-one
[2,3'-Biindolinylidene]-2',3-dione
3-(1,3-dihydro-3-oxo-2h-indol-2-ylidene)-1,3-dihydro-2h-indol-2-on
(3Z)-3-(1,3-Dihydro-3-oxo-2H-indol-2-ylidene)-1,3-dihydro-2H-indol-2-one
(3~{Z})-3-(3-oxidanylidene-1~{H}-indol-2-ylidene)-1~{H}-indol-2-one
(3E)-3-(1,3-Dihydro-3-oxo-2H-indol-2-ylidene)-1,3-dihydro-2H-indol-2-one
2H-Indol-2-one, 3-(1,3-dihydro-3-oxo-2H-indol-2-ylidene)-1,3-dihydro-, (3E)-
SMR000466311
BRN 0088279
UNII-V86L8P74GI
Indirubin?
(Z)-Indirubin
3-(3-oxo-1H-indol-2-ylidene)-1H-indol-2-one
(2_Z)-Indirubin
MFCD00221745
Indirubin (Standard)
(delta2,3'-Biindoline)-2',3-dione
CPD000466311
Indirubin derivative, 1
BiomolKI_000069
EM-A05-INDIRUBIN
[.DELTA.2,3-dione
BiomolKI2_000073
UNII-1LXW6D3W2Z
INDIRUBIN [WHO-DD]
(3Z)-3-(3-oxoindolin-2-ylidene)indolin-2-one
(delta(sup 2,3')-BIINDOLINE)-2',3-DIONE
SCHEMBL27678
BMK1-G9
BSPBio_001110
KBioGR_000450
KBioSS_000450
5-24-08-00507 (Beilstein Handbook Reference)
MLS000759416
MLS001424211
MLS002473308
MLS006010732
CHEMBL35349
Indirubin - Bio-X trade mark
BDBM7392
SCHEMBL9899338
CHEMBL1276127
CHEMBL3185783
CHEBI:92322
cid_5318433
HY-N0117A
HY-N0117R
KBio2_000450
KBio2_003018
KBio2_005586
KBio3_000839
KBio3_000840
EX-A347
CRDNMYFJWFXOCH-UHFFFAOYSA-N
Bio2_000395
Bio2_000875
DTXSID201026053
DTXSID501026052
GLXC-05476
HMS1362H11
HMS1792H11
HMS1990H11
HMS2051H20
HMS2234G06
HMS3369O15
HMS3393H20
HMS3403H11
HMS3656O13
BCP28869
HY-N0117
AC1180
BDBM50023867
BDBM50349806
FD9058
MSK157073
MSK181279
NSC105327
NSC827101
s2386
AKOS015895136
AKOS028108775
AKOS032455876
AC-8003
BCP9000788
CCG-100673
CCG-101058
CCG-267073
CS-3682
DB12379
FI65043
IndirubinCouroupitine B; Indigopurpurin
NC00308
NSC-827101
SB64698
SDCCGSBI-0634263.P002
IDI1_002150
(2'Z)-Indirubin, >=98% (HPLC)
NCGC00163356-01
NCGC00163356-02
NCGC00163356-03
NCGC00163356-04
NCGC00179302-02
(Z)-[2,3-Biindolinylidene]-2,3-dione
AC-29931
BI164578
CS-12423
DA-54305
LS-14462
PD003207
SMR004701694
SY058396
3-(3-oxoindolin-2-ylidene)indolin-2-one
3-(3-indolinone-2-ylidene)-indolin-2-one
DB-179341
UNM-0000305766
I0868
NS00011738
NS00101121
SW197688-2
(E)-3-(3-oxoindolin-2-ylidene)indolin-2-one
AB00639939-06
2-(2-oxo-1H-indol-3-ylidene)-1H-indol-3-one
SR-01000759396
Q1661452
SR-01000759396-5
BRD-K17894950-001-03-6
BRD-K17894950-001-04-4
BRD-K17894950-001-14-3
Q27164070
2H-Indol-2-one,3-dihydro-3-oxo-2H-indol-2-ylidene)-1,3-dihydro-
(3z)-3-(3-oxo-1,3-dihydro-2h-indol-2-ylidene)-1,3-dihydro-2h-indol-2-one
(Z)-[2,3invertedexclamationmark-Biindolinylidene]-2invertedexclamationmark,3-dione
2-[(3Z)-2-oxo-2,3-dihydro-1H-indol-3-ylidene]-2,3-dihydro-1H-indol-3-one
Solubility of 2-(2-hydroxy-1H-indol-3-yl)indol-3-one
The compound 2-(2-hydroxy-1H-indol-3-yl)indol-3-one, often referred to for its complex indole structure, exhibits unique solubility properties that can impressively vary based on the conditions. Here are some key points to consider:
In general, it is observed that a compound's solubility can be a fundamental property influencing its functionality and application in various fields. As the saying goes, "like dissolves like." Therefore, careful selection of solvents is crucial when working with such compounds to achieve the desired outcomes in experiments or formulations.