indolem/indolem
IndoLEM is a comprehensive Indonesian NLU benchmark, comprising three pillars NLP task: morpho-syntax, semantic, and discourse. Presented in COLING 2020. (⭐ 107)
Indole - Wikipedia
In the 1930s, interest in indole intensified when it became known that the indole substituent is present in many important alkaloids, known as indole alkaloids (e.g., tryptophan and auxins), and it remains an …
Controlled Drugs and Substances Act - Wikipedia
1-pentyl-3-(1-naphthoyl)indole (JWH-018) 1-butyl-3-(1-naphthoyl)indole (JWH-073) 1-pentyl-3-(4-methyl-1-naphthoyl)indole (JWH-122) 1-hexyl-3-(1-naphthoyl)indole (JWH-019)
Indole-3-carbaldehyde - Wikipedia
Indole-3-carbaldehyde (I3A), also known as indole-3-aldehyde and 3-formylindole, is a metabolite of dietary L-tryptophan which is synthesized by human
Indole alkaloid - Wikipedia
Indole alkaloids are a class of alkaloids containing a structural moiety of indole; many indole alkaloids also include isoprene groups and are thus called
indole/indole
No description (⭐ 18)
Indole - Wikipedia
Indole is an organic compound with the formula C6H4CCNH3. Indole is classified as an aromatic heterocycle. It has a bicyclic structure, consisting of a
Indole: The Microbial Metabolite Connecting Gut Health, Brain, and ...
Indole serves as a key scaffold in many biologically active molecules including tryptophan, serotonin, melatonin, and several indole alkaloid drugs. It is a central motif not only in microbial metabolites but …
chengyumeng/Indole
Miss Indole’s homework (⭐ 2)
Indole-3-carbinol - Wikipedia
Indole-3-carbinol (I3C, C9H9NO) is produced by the breakdown of the glucosinolate glucobrassicin, which can be found at relatively high levels in cruciferous
Tryptophan synthase - Wikipedia
indole and glyceraldehyde-3-phosphate (G3P) from indole-3-glycerol phosphate (IGP). The β subunits catalyze the irreversible condensation of indole and
Indole-3-acetic acid - Wikipedia
Indole-3-acetic acid (IAA, 3-IAA) is the most common naturally occurring plant hormone of the auxin class. It is the best known of the auxins, and has
Indole moiety induced biological potency in pseudo- peptides derived from 2-amin…
We report the synthesis and theoretical investigations of three novel pseudo-peptide molecules derived from 2-amino-2-(1H-indole-2-yl) acetamides. The compounds were subjected to spectroscopic characterization ($^1$H, $^{13}$C-NMR and MS) and their c...
dinhanhx/the-indolent-game
"The indolent game" is an idle game coded in java. (⭐ 0)
Indole test - Wikipedia
The indole test is a biochemical test performed on bacterial species to determine the ability of the organism to convert tryptophan into indole. This
Fischer indole synthesis - Wikipedia
The Fischer indole synthesis is a chemical reaction that produces the aromatic heterocycle indole from a (substituted) phenylhydrazine and an aldehyde
Photophysics of indole upon x-ray absorption
A photofragmentation study of gas-phase indole (C$_8$H$_7$N) upon single-photon ionization at a photon energy of 420 eV is presented. Indole was primarily inner-shell ionized at its nitrogen and carbon $1s$ orbitals. Electrons and ions were measured...
What is Indole?_Chemicalbook
Apr 22, 2022 · Indole, also called benzopyrrole, an aromatic heterocyclic organic compound occurring in some flower oils, such as jasmine and orange blossom, in coal tar, and in fecal matter, is a colorless …
Indole: Chemical Properties, Synthesis, Applications, and Analysis
Learn about indole, its chemical properties, synthesis methods, biological role, applications in industry, and key analysis techniques used in research and industry.
Indole | Aromatic, Biosynthesis, Metabolism | Britannica
Indole, first isolated in 1866, has the molecular formula C 8 H 7 N, and it is commonly synthesized from phenylhydrazine and pyruvic acid, although several other procedures have been discovered.