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Details

Stereochemistry ACHIRAL
Molecular Formula C8H7NO
Molecular Weight 133.1476
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of OXINDOLE

SMILES

O=C1CC2=CC=CC=C2N1

InChI

InChIKey=JYGFTBXVXVMTGB-UHFFFAOYSA-N
InChI=1S/C8H7NO/c10-8-5-6-3-1-2-4-7(6)9-8/h1-4H,5H2,(H,9,10)

HIDE SMILES / InChI

Molecular Formula C8H7NO
Molecular Weight 133.1476
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Design, synthesis and biological evaluations of novel oxindoles as HIV-1 non-nucleoside reverse transcriptase inhibitors. Part I.
2006-04-15
Design, synthesis, and biological evaluations of novel oxindoles as HIV-1 non-nucleoside reverse transcriptase inhibitors. Part 2.
2006-04-15
Highly diastereoselective one-pot synthesis of spirocyclic oxindoles through intramolecular Ullmann coupling and Claisen rearrangement.
2006-03-27
Targeting receptor kinases by a novel indolinone derivative in multiple myeloma: abrogation of stroma-derived interleukin-6 secretion and induction of apoptosis in cytogenetically defined subgroups.
2006-03-01
Fate of 3,3'-diindolylmethane in cultured MCF-7 human breast cancer cells.
2006-03
Synthesis and pharmacological profile of an orally-active growth hormone secretagogue, SM-130686.
2006-03
A water soluble extract from Uncaria tomentosa (Cat's Claw) is a potent enhancer of DNA repair in primary organ cultures of human skin.
2006-03
Oxindole alkaloids from Uncaria tomentosa induce apoptosis in proliferating, G0/G1-arrested and bcl-2-expressing acute lymphoblastic leukaemia cells.
2006-03
Distribution, metabolism, and excretion of the anti-angiogenic compound SU5416.
2006-03
Synthesis of the putative structure of fistulosin using the ruthenium-catalyzed cycloisomerization of diene.
2006-02-03
A new chemical tool for exploring the physiological function of the PDE2 isozyme.
2006-01-15
Oxindole synthesis through intramolecular nucleophilic addition of vinylpalladiums to aryl isocyanates.
2005-12-02
In silico fragment-based discovery of indolin-2-one analogues as potent DNA gyrase inhibitors.
2005-12-01
Preparation of 3-spirocyclic indolin-2-ones as ligands for the ORL-1 receptor.
2005-11-15
Facile synthesis of active antitubercular, cytotoxic and antibacterial agents: a Michael addition approach.
2005-11
Early relief of osteoarthritis symptoms with a natural mineral supplement and a herbomineral combination: a randomized controlled trial [ISRCTN38432711].
2005-10-21
Inflammation 2005 - Seventh World Congress. Highlights I.
2005-10
Rapid access to the Welwitindolinone alkaloid skeleton by cyclization of indolecarboxaldehyde substituted cyclohexanones.
2005-09-15
Biological basis for the use of botanicals in osteoarthritis and rheumatoid arthritis: a review.
2005-09
Indolin-2-ones with high in vivo efficacy in a model for multiple sclerosis.
2005-08-25
Stereoselective synthesis of 3-alkylideneoxindoles via palladium-catalyzed domino reactions.
2005-08-19
SAR studies of 6-aryl-1,3-dihydrobenzimidazol-2-ones as progesterone receptor antagonists.
2005-08-01
Catalytic enantioselective fluorination of oxindoles.
2005-07-27
Identification of degradation products of diclofenac by electrospray ion trap mass spectrometry.
2005-07-15
Suppressive effects of isorhynchophylline on 5-HT2A receptor function in the brain: behavioural and electrophysiological studies.
2005-07-11
Investigating the neuroprotective mechanism of action of a CDK5 inhibitor by phosphoproteome analysis.
2005-07-01
Nitrated and oxidized products of a single tryptophan residue in human Cu,Zn-superoxide dismutase treated with either peroxynitrite-carbon dioxide or myeloperoxidase-hydrogen peroxide-nitrite.
2005-07
Involvement of 5-HT2 receptors in the antinociceptive effect of Uncaria tomentosa.
2005-07
Scavenging of reactive oxygen species by novel indolin-2-one and indoline-2-thione derivatives.
2005-07
TiCl4 catalyzed tandem construction of C-C and C-O bonds: a simple and one-pot atom-economical stereoselective synthesis of spiro-oxindoles.
2005-05-28
Identification of natural dyes used in works of art by pyrolysis-gas chromatography/mass spectrometry combined with in situ trimethylsilylation.
2005-05
Structure-activity relationships of the oxindole growth hormone secretagogues.
2005-04-01
A-432411, a novel indolinone compound that disrupts spindle pole formation and inhibits human cancer cell growth.
2005-04
AG-041R, a novel indoline-2-one derivative, stimulates chondrogenesis in a bipotent chondroprogenitor cell line CL-1.
2005-04
Phosphoproteome and transcriptome analysis of the neuronal response to a CDK5 inhibitor.
2005-04
Antiangiogenic drugs synergize with a membrane macrophage colony-stimulating factor-based tumor vaccine to therapeutically treat rats with an established malignant intracranial glioma.
2005-03-01
Indol-2-one intermediates: mechanistic evidence and synthetic utility. Total syntheses of (+/-)-flustramines A and C.
2005-02-17
HPLC quantification of uncarine D and the anti-plasmodial activity of alkaloids from leaves of Mitragyna inermis (Willd.) O. Kuntze.
2005-02-04
An active ingredient of Cat's Claw water extracts identification and efficacy of quinic acid.
2005-01-15
Genotoxic and cytotoxic studies of beta-sitosterol and pteropodine in mouse.
2005
Toxicological aspects of the South American herbs cat's claw (Uncaria tomentosa) and Maca (Lepidium meyenii) : a critical synopsis.
2005
Palladium-catalyzed asymmetric allylation of prochiral nucleophiles: synthesis of 3-allyl-3-aryl oxindoles.
2004-12-27
MAZ51, an indolinone that inhibits endothelial cell and tumor cell growth in vitro, suppresses tumor growth in vivo.
2004-12-20
Identification of indigoid dyes in natural organic pigments used in historical art objects by high-performance liquid chromatography coupled to electrospray ionization mass spectrometry.
2004-12
A Lewis acid-promoted cyclization of ethenetricarboxylate derivative aromatic compounds. Novel syntheses of oxindoles and benzofuranones via Friedel-Crafts intramolecular Michael addition.
2004-11-07
3-amino thioacridone inhibits DNA synthesis and induce DNA damage in T-cell acute lymphoblastic leukemia (T-ALL) in a p16-dependent manner.
2004-10
Methanol extracts of Hamelia patens containing oxindole alkaloids relax KCl-induced contraction in rat myometrium.
2004-10
One-pot homolytic aromatic substitutions/HWE olefinations under microwave conditions for the formation of a small oxindole library.
2004-09-30
Tissue distribution of molidone in a multidrug overdose.
2004-09
Cellular effects and antitumor activity of RET inhibitor RPI-1 on MEN2A-associated medullary thyroid carcinoma.
2004-07-07
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:01:34 GMT 2025
Edited
by admin
on Mon Mar 31 19:01:34 GMT 2025
Record UNII
0S9338U62H
Record Status FAILED
Record Version
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Name Type Language
OXINDOLE
Systematic Name English
NSC-274863
Preferred Name English
2-OXINDOLE
Common Name English
INDOL-2-OL
Systematic Name English
DICLOFENAC POTASSIUM IMPURITY I [EP IMPURITY]
Common Name English
2-HYDROXYINDOLE
Systematic Name English
INDOLINE-2-ONE
Systematic Name English
DICLOFENAC SODIUM IMPURITY E [EP IMPURITY]
Common Name English
1,3-DIHYDROINDOL-2-ONE
Systematic Name English
2-INDOLINONE
Systematic Name English
1H-INDOL-2-OL
Systematic Name English
2H-INDOL-2-ONE, 1,3-DIHYDRO-
Systematic Name English
1,3-DIHYDRO-2H-INDOL-2-ONE
Systematic Name English
DICLOFENAC IMPURITY E
Common Name English
DICLOFENAC POTASSIUM IMPURITY E [EP IMPURITY]
Common Name English
INDOL-2(3H)-ONE
Systematic Name English
Code System Code Type Description
CHEBI
31697
Created by admin on Mon Mar 31 19:01:34 GMT 2025 , Edited by admin on Mon Mar 31 19:01:34 GMT 2025
PRIMARY
PUBCHEM
321710
Created by admin on Mon Mar 31 19:01:34 GMT 2025 , Edited by admin on Mon Mar 31 19:01:34 GMT 2025
PRIMARY
NSC
274863
Created by admin on Mon Mar 31 19:01:34 GMT 2025 , Edited by admin on Mon Mar 31 19:01:34 GMT 2025
PRIMARY
CAS
59-48-3
Created by admin on Mon Mar 31 19:01:34 GMT 2025 , Edited by admin on Mon Mar 31 19:01:34 GMT 2025
PRIMARY
ECHA (EC/EINECS)
241-069-9
Created by admin on Mon Mar 31 19:01:34 GMT 2025 , Edited by admin on Mon Mar 31 19:01:34 GMT 2025
ALTERNATIVE
CAS
16990-73-1
Created by admin on Mon Mar 31 19:01:34 GMT 2025 , Edited by admin on Mon Mar 31 19:01:34 GMT 2025
ALTERNATIVE
WIKIPEDIA
OXINDOLE
Created by admin on Mon Mar 31 19:01:34 GMT 2025 , Edited by admin on Mon Mar 31 19:01:34 GMT 2025
PRIMARY
ECHA (EC/EINECS)
200-429-5
Created by admin on Mon Mar 31 19:01:34 GMT 2025 , Edited by admin on Mon Mar 31 19:01:34 GMT 2025
PRIMARY
EPA CompTox
DTXSID80870389
Created by admin on Mon Mar 31 19:01:34 GMT 2025 , Edited by admin on Mon Mar 31 19:01:34 GMT 2025
PRIMARY
FDA UNII
0S9338U62H
Created by admin on Mon Mar 31 19:01:34 GMT 2025 , Edited by admin on Mon Mar 31 19:01:34 GMT 2025
PRIMARY
MESH
C022960
Created by admin on Mon Mar 31 19:01:34 GMT 2025 , Edited by admin on Mon Mar 31 19:01:34 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> IMPURITY
PARENT -> IMPURITY