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

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.

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].

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].

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

-

, (2008/06/13)

A β-carbolin-3-carboxylic acid derivativ...

7730-20-3 Process route

formaldehyd
50-00-0,30525-89-4,61233-19-0

formaldehyd

6-fluoro-1,2,3,4-tetrahydro-β-carbolin-3-carboxylic acid ethyl ester

6-fluoro-1,2,3,4-tetrahydro-β-carbolin-3-carboxylic acid ethyl ester

DL-5-fluorotryptophan
154-08-5,343-91-9,97749-24-1

DL-5-fluorotryptophan

7-fluoro-1,2,3,4-tetrahydro-β-carbolin-3-carboxylic acid ethyl ester

7-fluoro-1,2,3,4-tetrahydro-β-carbolin-3-carboxylic acid ethyl ester

DL-6-fluorotryptophan
7730-20-3,108391-82-8,343-92-0

DL-6-fluorotryptophan

Conditions
Conditions Yield
In sodium hydroxide; ethanol; water; benzene;
51%
DL-6-fluorotryptophan
7730-20-3,108391-82-8,343-92-0

DL-6-fluorotryptophan

Conditions
Conditions Yield

7730-20-3 Upstream products

  • 50-00-0
    50-00-0

    formaldehyd

  • 154-08-5
    154-08-5

    DL-5-fluorotryptophan

7730-20-3 Downstream products

  • 461424-18-0
    461424-18-0

    7-fluoro-1-(2-fluoro-phenyl)-9H -β-carboline

  • 67308-25-2
    67308-25-2

    2-((tert-butoxycarbonyl)amino)-3-(6-fluoro-1H-indol-3-yl)propanoic acid

  • 108391-82-8
    108391-82-8

    D-6-fluorotryptophan

Online Inquiry
*Product Name
CAS
Purity
Quantity
Company name
*Email
*Other Description
*Code
Fields with* are required