serw-MX  [xml]  
 
    
 DeCS Categories

D02 Organic Chemicals .
D02.806 Quinones .
D02.806.400 Indolequinones .
D03 Heterocyclic Compounds .
D03.066 Acids, Heterocyclic .
D03.066.288 Indoleacetic Acids .
D03.383 Heterocyclic Compounds, 1-Ring .
D03.383.129 Azoles .
D03.383.129.539 Pyrazoles .
D03.383.129.539.487 Indazoles .
D03.633 Heterocyclic Compounds, Fused-Ring .
D03.633.100 Heterocyclic Compounds, 2-Ring .
D03.633.100.449 Indazoles .
D03.633.100.473 Indoles .
D03.633.100.473.404 Indoleacetic Acids .
D03.633.100.473.412 Indolequinones .
D03.633.100.473.420 Indomethacin .
D03.633.100.496 Indolizines .
D03.633.100.496.500 Indolizidines .
HP4 Materia Medica .
HP4.018 Homeopathic Remedy .
HP4.018.375 Homeopathic Remedy I .
HP4.018.375.466 Indolum .
 
 Terms
 Synonyms & Historicals		Documents
LILACS e MDL		 
Indoles .
Benzopyrroles with the nitrogen at the number one carbon adjacent to the benzyl portion, in contrast to ISOINDOLES which have the nitrogen away from the six-membered ring. .
1.00
6447661
 
Indolum .
Homeopathic remedy. Abbrev.: "indol.". Chemical origin. Substance used: indol. .
0.74
00
 
Indolizines .
0.62
01136
 
Indolequinones .
Indole-Quinones .
Indoloquinones .
Indole Quinones .
INDOLES which have two keto groups forming QUINONES like structures of the indole aromatic ring. .
0.62
0695
 
Indomethacin .
Amuno .
Indocid .
Indocin .
Indomet 140 .
Indometacin .
Indomethacin Hydrochloride .
Metindol .
Osmosin .
Hydrochloride, Indomethacin .
A non-steroidal anti-inflammatory agent (NSAID) that inhibits the enzyme cyclooxygenase necessary for the formation of prostaglandins and other autacoids. It also inhibits the motility of polymorphonuclear leukocytes. .
0.60
28427416
 
Indazoles .
0.59
123485
 
Indoleacetic Acids .
Auxin .
Auxins .
Indolylacetic Acids .
Acids, Indoleacetic .
Acids, Indolylacetic .
Auxins .
Acetic acid derivatives of the heterocyclic compound indole. (Merck Index, 11th ed) .
0.57
327274
 
Indolizidines .
Saturated indolizines that are fused six and five-membered rings with a nitrogen atom at the ring fusion. They are biosynthesized in PLANTS by cyclization of a LYSINE coupled to ACETYL COENZYME A. Many of them are naturally occurring ALKALOIDS. .
0.57
0107