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alpha-Methyl-DL-tryptophan (CAS 153-91-3)

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Alternate Names:
DL-α-Methyltryptophan
CAS Number:
153-91-3
Purity:
99%
Molecular Weight:
218.22
Molecular Formula:
C12H14N2O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Latent Transforming Growth Factor Beta Binding Proteins (LTBPs) are essential components in the cellular matrix and have significant roles in the signaling pathways that regulate cell growth, differentiation, and function. They are best known for their function in regulating the bioavailability and activation of Transforming Growth Factor-Beta (TGF-β). LTBPs form a complex with TGF-β, holding it in a latent (inactive) form until activated by various stimuli such as mechanical force or specific proteolytic enzymes. This sequestering and subsequent release mechanism is an important aspect of modulating TGF-β signaling pathways. Aside from their interaction with TGF-β, LTBPs are involved in the organization of extracellular matrix (ECM) through their interactions with other matrix components like fibronectin and fibrillins. Latent Transforming Growth Factor Beta Binding Protein (LTBP) Inhibitors focus on the disruption or modulation of LTBP functions and interactions. These molecules can operate through various mechanisms, such as disrupting the LTBP-TGF-β complex, inhibiting LTBP-fibronectin or LTBP-fibrillin interactions, or interfering with the processes that lead to the activation of the latent TGF-β. Some inhibitors target pathways that are upstream or downstream of LTBP, thus having an indirect effect on its activity. Additionally, some LTBP inhibitors act by affecting substrate availability for LTBP or through complex signaling cascades that ultimately influence LTBP function. This category of chemicals is particularly nuanced given the multifaceted roles that LTBPs play in cellular signaling and ECM organization.


alpha-Methyl-DL-tryptophan (CAS 153-91-3) References

  1. Contribution of serum albumin to the transport of orally administered L-tryptophan into liver of rats with L-tryptophan depletion.  |  Sasaki, E., et al. 1999. Amino Acids. 16: 29-39. PMID: 10078332
  2. The influence of endogenous dopamine levels on the density of [3H]SCH23390-binding sites in the brain of the honey bee, Apis mellifera L.  |  Purnell, MT., et al. 2000. Brain Res. 855: 206-16. PMID: 10677592
  3. Evaluation and application of liquid chromatographic columns coated with 'intelligent' ligands: (I) acylcarnitine column.  |  Kamimori, H. and Konishi, M. 2001. J Chromatogr A. 929: 1-12. PMID: 11594390
  4. Effects of alpha-methyl-DL-tryptophan on the oxidation of tryptophan.  |  SOURKES, TL. and TOWNSEND, E. 1955. Can J Biochem Physiol. 33: 735-40. PMID: 13260953
  5. The weight-depressing action of alpha-methyl-DL-tryptophan in the rat.  |  SANKOFF, I. and SOURKES, TL. 1962. Can J Biochem Physiol. 40: 739-47. PMID: 14496957
  6. SLC6A14 (ATB0,+) protein, a highly concentrative and broad specific amino acid transporter, is a novel and effective drug target for treatment of estrogen receptor-positive breast cancer.  |  Karunakaran, S., et al. 2011. J Biol Chem. 286: 31830-8. PMID: 21771784
  7. Transporter targeted gatifloxacin prodrugs: synthesis, permeability, and topical ocular delivery.  |  Vooturi, SK., et al. 2012. Mol Pharm. 9: 3136-46. PMID: 23003105
  8. Multianalytical approach for surface- and tip-enhanced infrared spectroscopy study of a molecule-metal conjugate: deducing its adsorption geometry.  |  Pięta, E., et al. 2018. Phys Chem Chem Phys. 20: 27992-28000. PMID: 30382272
  9. Nanoengineered sonosensitive platelets for synergistically augmented sonodynamic tumor therapy by glutamine deprivation and cascading thrombosis.  |  Zhou, L., et al. 2023. Bioact Mater. 24: 26-36. PMID: 36582345
  10. Infrared spectra of carbon monoxide complexes of indoleamine 2,3-dioxygenase and L-tryptophan 2,3-dioxygenases. Effects of substrates on the CO-stretching frequencies.  |  Uchida, K., et al. 1985. J Biol Chem. 260: 1400-6. PMID: 3871436
  11. Action of alpha-methyl-DL-tryptophan in vivo on catabolism of amino acids and their conversion to liver glycogen.  |  Oravec, M. and Sourkes, TL. 1969. Can J Biochem. 47: 179-84. PMID: 5774807
  12. Effect of alpha-methyl-DL-tryptophan on tryptophan metabolism of Musca domestica L.  |  Lancaster, GA. and Sourkes, TL. 1969. Comp Biochem Physiol. 28: 1435-41. PMID: 5786836
  13. Induction by L-tryptophan and an analogue, alpha-methyl-DL-tryptophan, of the enzymes catabolizing L-tryptophan in Pseudomonas.  |  Tremblay, GC., et al. 1967. J Bacteriol. 93: 168-76. PMID: 6020404
  14. Relationship between changes in the translational apparatus and actinomycin production in Streptomyces antibioticus.  |  Jones, GH. 1977. J Bacteriol. 129: 81-6. PMID: 63458
  15. Actinomycin biosynthesis by protoplasts derived from Streptomyces parvulus.  |  Hitchcock, MJ. and Katz, E. 1978. Antimicrob Agents Chemother. 13: 104-14. PMID: 75712

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

alpha-Methyl-DL-tryptophan, 1 g

sc-300182
1 g
$140.00

alpha-Methyl-DL-tryptophan, 5 g

sc-300182A
5 g
$612.00