Page last updated: 2024-11-08
7-chlorotryptophan
Description
7-chlorotryptophan: RN given refers to (DL)-isomer [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]
7-chloro-L-tryptophan : An L-tryptophan derivative having a chloro substituent at the 7-position. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]
7-chlorotryptophan : A tryptophan derivative having a chloro substituent at the 7-position of the indole ring. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]
Cross-References
| ID Source | ID |
|---|
| PubMed CID | 3081936 |
| CHEBI ID | 47356 |
| SCHEMBL ID | 837413 |
| MeSH ID | M0113623 |
Synonyms (22)
| Synonym |
|---|
| dl-tryptophan, 7-chloro- |
| 7-chlorotryptophan |
| CTE , |
| 73945-46-7 |
| CHEBI:47356 |
| 7-chloro-l-tryptophan |
| (2s)-2-amino-3-(7-chloro-1h-indol-3-yl)propanoic acid |
| C19687 |
| SCHEMBL837413 |
| (s)-2-amino-3-(7-chloro-1h-indol-3-yl)propanoic acid |
| W-204244 |
| AKOS025287309 |
| l-tryptophan, 7-chloro- |
| mfcd09264322 |
| 7-chloro-l-tryptophan (h-l-trp(7-cl)-oh) |
| CS-D0040 |
| DS-9523 |
| DTXSID70934646 |
| Q27120774 |
| A865991 |
| (s)-2-amino-3-(7-chloro-1h-indol-3-yl)propanoicacid |
| h-trp(7-cl)-oh |
Drug Classes (4)
| Class | Description |
|---|
| L-tryptophan derivative | A proteinogenic amino acid derivative resulting from reaction of L-tryptophan at the amino group or the carboxy group, or from the replacement of any hydrogen of L-tryptophan by a heteroatom. |
| 7-chlorotryptophan | A tryptophan derivative having a chloro substituent at the 7-position of the indole ring. |
| non-proteinogenic L-alpha-amino acid | Any L-alpha-amino acid which is not a member of the group of 23 proteinogenic amino acids. |
| amino acid zwitterion | The zwitterionic form of an amino acid having a negatively charged carboxyl group and a positively charged amino group. |
| [compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res] |
Research
Studies (7)
| Timeframe | Studies, This Drug (%) | All Drugs % |
|---|
| pre-1990 | 1 (14.29) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (42.86) | 29.6817 |
| 2010's | 3 (42.86) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| [information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Study Types
| Publication Type | This drug (%) | All Drugs (%) |
|---|
| Trials | 0 (0.00%) | 5.53% |
| Reviews | 0 (0.00%) | 6.00% |
| Case Studies | 0 (0.00%) | 4.05% |
| Observational | 0 (0.00%) | 0.25% |
| Other | 7 (100.00%) | 84.16% |
| [information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |