6-FLUORO-DL-TRYPTOPHAN
Base Information
- Chemical Name: 6-FLUORO-DL-TRYPTOPHAN
- CAS No.: 7730-20-3
Reputable supplier selling 6-FLUORO-DL-TRYPTOPHAN 7730-20-3 with stock
- Molecular Formula: C11H11FN2O2
- Molecular Weight: 222.219
- Appearance/Colour: almost white to beige powder
- Vapor Pressure: 6.54E-09mmHg at 25°C
- Melting Point: 280-285 °C (dec.)(lit.)
- Refractive Index: 1.673
- Boiling Point: 450.7 °C at 760 mmHg
- PKA: 2.22±0.10(Predicted)
- Flash Point: 226.4 °C
- PSA: 79.11000
- Density: 1.442 g/cm3
- LogP: 1.96170
6-FLUORO-DL-TRYPTOPHAN(Cas 7730-20-3) Usage
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Biological Activity |
6-fluoro-dl-tryptophan is a serotonin (5-ht) synthesis inhibitor.serotonin or 5-hydroxytryptamine (5-ht), a monoamine neurotransmitter, is biochemically derived from tryptophan. serotonin is primarily present in the gastrointestinal tract, blood platelets, and the central nervous system of animals. serotonin is considered to be a contributor to feelings of well-being and happiness. |
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in vitro |
the potential competition was investigated between l-tryptophan (trp) and 6-fluoro-dl-tryptophan (6-f-trp). in equilibrium dialysis experiments, albumin bound about 80% of trp and 50% of 6-f-trp. competitive inhibition was assessed as the decrease in the apparent ka of trp in the presence of 6-f-trp, with no modification of the n value [1]. |
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in vivo |
rats werer administered 6-fluoro-dl-tryptophan (6f-trp) and its neurochemical effects on central catechole and indole were evaluated. results showed that neither norepinephrine nor dopamine and its major metabolites were affected by 6f-trp. with regard to serotonin (5-ht), 6f-trp could induce a transient depletion in all the studied brain areas, with a maximum of about 60-65% obtained between 1 and 3 hr. after 6 hr, 5-ht levels returned to control values. in addition, the 5-hydroxyindolacetic acid (5-hiaa) level was also reduced 3 hr after 6f-trp administration. a large dose-dependent increase in tryptophan was seen in the four brain areas, mainly due to an inhibition of tryptophan incorporation into protein, as demonstrated by experiments with mouse neuroblastoma cells [2]. |
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references |
[1] chanut, e. ,zini, r.,trouvin, j.h., et al. albumin binding and brain uptake of 6-fluoro-dl-tryptophan: competition with l-tryptophan. biochemical pharmacology 44(10), 2082-2085 (1992).[2] chanut, e. ,trouvin, j.h.,bondoux, d., et al. metabolism of 6-fluoro-dl-tryptophan and its specific effects on the rat brain serotoninergic pathway. biochemical pharmacology 45(5), 1049-1057 (1992). |
InChI:InChI=1/C11H11FN2O2/c12-7-1-2-8-6(3-9(13)11(15)16)5-14-10(8)4-7/h1-2,4-5,9,14H,3,13H2,(H,15,16)/t9-/m1/s1
7730-20-3 Relevant articles
β-Carbolin-3-carboxylic acid derivatives
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, (2008/06/13)
A β-carbolin-3-carboxylic acid derivativ...
7730-20-3 Process route
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50-00-0,30525-89-4,61233-19-0
formaldehyd
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6-fluoro-1,2,3,4-tetrahydro-β-carbolin-3-carboxylic acid ethyl ester
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154-08-5,343-91-9,97749-24-1
DL-5-fluorotryptophan
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7-fluoro-1,2,3,4-tetrahydro-β-carbolin-3-carboxylic acid ethyl ester
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7730-20-3,108391-82-8,343-92-0
DL-6-fluorotryptophan
| Conditions | Yield |
|---|---|
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In
sodium hydroxide; ethanol; water; benzene;
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51%
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7730-20-3,108391-82-8,343-92-0
DL-6-fluorotryptophan
| Conditions | Yield |
|---|---|
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7730-20-3 Upstream products
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50-00-0
formaldehyd
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154-08-5
DL-5-fluorotryptophan
7730-20-3 Downstream products
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461424-18-0
7-fluoro-1-(2-fluoro-phenyl)-9H -β-carboline
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67308-25-2
2-((tert-butoxycarbonyl)amino)-3-(6-fluoro-1H-indol-3-yl)propanoic acid
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108391-82-8
D-6-fluorotryptophan