Compound
L-tyrosyl-L-isoleucyl-L-leucine
No description recorded for this entry yet. Everything this graph holds about L-tyrosyl-L-isoleucyl-L-leucine is below.
Structure
- Class
- Organic compound
- Formula
- C21H33N3O5
- Mass
- 407.511 g/mol
- Charge
- 0
- InChIKey
- HVPPEXXUDXAPOM-MGHWNKPDSA-N
- SMILES
- CC[C@H](C)[C@H](NC(=O)[C@@H]([NH3+])Cc1ccc(O)cc1)C(=O)N[C@@H](CC(C)C)C(=O)[O-]
- Look it up
- ChEBIBy InChIKey
Identity from ChEBI. Not evidence — none of it carries a grade.
What it touches on the way
A finding says L-tyrosyl-L-isoleucyl-L-leucine moved an endpoint. This is the biology in between: the proteins and reactions it runs through to get there. It is where to look for the two things a list of findings cannot answer — why a result might happen, and what else acts on the same machinery.
1 of these are proteins with a page of their own, and that is the door: a protein page says what else it carries, which is how one compound leads to the next.
Mechanistic reach
1 entity
1 entities reached, most connected first. Hub metabolites are excluded, so this is not a claim that the compound touches everything.
0 reported hops1 assembled from the scaffold
What the reference databases state
The section above shows paths a projection assembled. This is the reference layer itself, one step from L-tyrosyl-L-isoleucyl-L-leucine: what the cleared databases state it reacts with, is carried by, is converted to and takes part in, whether or not a projection has walked it yet.
Statements
1 statement
1 statement in 1 reference database name L-tyrosyl-L-isoleucyl-L-leucine — Rhea. Press a relation to see only its rows; every count is the rows behind it.
- L-tyrosyl-L-isoleucyl-L-leucine is a substrate of MMEProteinRhea RHEA:71479Inferred only
Other names
7 names
Every name this graph resolves to L-tyrosyl-L-isoleucyl-L-leucine. Searching any of them lands here.
- Also called
- L-Tyr-L-Ile-L-Leu zwitterionL-tyrosyl-L-isoleucyl-L-leucine zwitterionneurotensin (11-13) zwitterionneurotensin 11-13 zwitterionneurotensin zwitterion fragment 11-13YIL zwitterion
- Systematic name
- (2S)-2-({N-[(2S)-2-azaniumyl-3-(4-hydroxyphenyl)propanoyl]-L-isoleucyl}amino)-4-methylpentanoate