Compound
angiotensin I
No description recorded for this entry yet. Everything this graph holds about angiotensin I is below.
Structure
No depiction stored for this entry. The InChIKey and SMILES beside this define the structure exactly.
- Class
- Organic compound
- Formula
- C62H89N17O14
- Mass
- 1296.499 g/mol
- Charge
- 0
- InChIKey
- ORWYRWWVDCYOMK-HBZPZAIKSA-N
- SMILES
- CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(N)=[NH2+])NC(=O)[C@@H]([NH3+])CC(=O)[O-])C(C)C)C(=O)N[C@@H](Cc1cncn1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cncn1)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 angiotensin I 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.
2 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
2 entities
2 entities reached, most connected first. Hub metabolites are excluded, so this is not a claim that the compound touches everything.
0 reported hops2 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 angiotensin I: 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
2 statements
2 statements in 1 reference database name angiotensin I — Rhea. Press a relation to see only its rows; every count is the rows behind it.
- angiotensin I is a substrate of ACEProteinRhea RHEA:63560Inferred only
- angiotensin I is a substrate of ACE2ProteinRhea RHEA:63532Inferred only
Other names
4 names
Every name this graph resolves to angiotensin I. Searching any of them lands here.
- Also called
- Asp-Arg-Val-Tyr-Ile-His-Pro-Phe-His-LeuL-aspartyl-L-arginyl-L-valyl-L-tyrosyl-L-isoleucyl-L-histidyl-L-prolyl-L-phenylalanyl-L-histidyl-L-leucine
- Systematic name
- N(5)-[amino(iminio)methyl]-N(2)-[(2S)-2-azaniumyl-3-carboxylatopropanoyl]-L-ornithyl-L-valyl-L-tyrosyl-L-isoleucyl-L-histidyl-L-prolyl-L-phenylalanyl-N-[(1S)-1-carboxylato-3-methylbutyl]-L-histidinamideN5-[amino(iminio)methyl]-N2-[(2S)-2-azaniumyl-3-carboxylatopropanoyl]-L-ornithyl-L-valyl-L-tyrosyl-L-isoleucyl-L-histidyl-L-prolyl-L-phenylalanyl-N-[(1S)-1-carboxylato-3-methylbutyl]-L-histidinamide