α-methyl-D,L-tryptophan

group of stereoisomers
Thing group_of_isomeric_entities Q27074404
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α-methyl-D,L-tryptophan

Summary

α-methyl-D,L-tryptophan is a group of isomeric entities[1].

Key Facts

  • α-methyl-D,L-tryptophan's instance of is recorded as group of isomeric entities[2].
  • α-methyl-D,L-tryptophan's canonical SMILES is recorded as CC(CC1=CNC2=CC=CC=C21)(C(=O)O)N[3].
  • α-methyl-D,L-tryptophan's InChI is recorded as InChI=1S/C12H14N2O2/c1-12(13,11(15)16)6-8-7-14-10-5-3-2-4-9(8)10/h2-5,7,14H,6,13H2,1H3,(H,15,16)[4].
  • α-methyl-D,L-tryptophan's InChIKey is recorded as ZTTWHZHBPDYSQB-UHFFFAOYSA-N[5].
  • α-methyl-D,L-tryptophan's chemical formula is recorded as C₁₂H₁₄N₂O₂[6].
  • α-methyl-D,L-tryptophan's subclass of is recorded as tryptamine alkaloid[7].
  • α-methyl-D,L-tryptophan's ChEMBL ID is recorded as CHEMBL559578[8].
  • α-methyl-D,L-tryptophan's Guide to Pharmacology Ligand ID is recorded as 4693[9].
  • α-methyl-D,L-tryptophan's UNII is recorded as 260VJL1C6Q[10].
  • α-methyl-D,L-tryptophan's ChemSpider ID is recorded as 86134[11].
  • α-methyl-D,L-tryptophan's PubChem CID is recorded as 95438[12].
  • α-methyl-D,L-tryptophan's PubChem CID is recorded as 25244123[13].
  • α-methyl-D,L-tryptophan's ChEBI ID is recorded as 233090[14].
  • α-methyl-D,L-tryptophan's found in taxon is recorded as Aspergillus fumigatus[15].
  • α-methyl-D,L-tryptophan's Human Metabolome Database ID is recorded as HMDB0248231[16].
  • α-methyl-D,L-tryptophan's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+218.105528'}[17].
  • α-methyl-D,L-tryptophan's SureChEMBL ID is recorded as 343309[18].
  • α-methyl-D,L-tryptophan's DSSTox substance ID is recorded as DTXSID001351919[19].
  • α-methyl-D,L-tryptophan's Probes And Drugs ID is recorded as PD050356[20].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] . wikidata.org.
  2. [3] . PubChem. Retrieved . wikidata.org.
  3. [4] . PubChem. Retrieved . wikidata.org.
  4. [5] . PubChem. Retrieved . wikidata.org.
  5. [6] . PubChem. Retrieved . wikidata.org.
  6. [7] . wikidata.org.
  7. [8] . ChEMBL. Retrieved . wikidata.org.
  8. [9] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  9. [10] . wikidata.org.
  10. [11] . Q2311683. Retrieved . wikidata.org.
  11. [12] . PubChem. Retrieved . wikidata.org.
  12. [13] . wikidata.org.
  13. [14] . wikidata.org.
  14. [15] . Substrate promiscuity of the cyclic dipeptide prenyltransferases from Aspergillus fumigatus ( section sign).. wikidata.org.
  15. [16] . wikidata.org.
  16. [17] . PubChem. Retrieved . wikidata.org.
  17. [18] . wikidata.org.
  18. [19] . wikidata.org.
  19. [20] . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). α-methyl-D,L-tryptophan. Retrieved May 3, 2026, from https://4ort.xyz/entity/-methyl-d-l-tryptophan
MLA “α-methyl-D,L-tryptophan.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/-methyl-d-l-tryptophan.
BibTeX @misc{4ortxyz_-methyl-d-l-tryptophan_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{α-methyl-D,L-tryptophan}}, year = {2026}, url = {https://4ort.xyz/entity/-methyl-d-l-tryptophan}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): α-methyl-D,L-tryptophan — https://4ort.xyz/entity/-methyl-d-l-tryptophan (retrieved 2026-05-03)

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