Structure
No three-dimensional record for this entry.
- Class
- Organic compound, cation
- Formula
- C75H131N24O15
- Mass
- 1609.026 g/mol
- Charge
- +5
- InChIKey
- OVVIBUHLQIYUEU-IWIISZHXSA-S
- SMILES
- CC[C@H](C)[C@H](NC(=O)[C@H](CCCNC(N)=[NH2+])NC(=O)[C@H](CCCNC(N)=[NH2+])NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)CNC(=O)[C@@H]([NH3+])Cc1ccc(O)cc1)C(=O)N[C@@H](CCCNC(N)=[NH2+])C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCC[NH3+])C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCC[NH3+])C(=O)[O-]
- Look it up
- ChEBIBy InChIKey
Identity from ChEBI. Not evidence.
What it touches on the way
Mechanistic reach
1 entity
1 entities reached.
0 reported hops1 assembled from the scaffold
What the reference databases state
Statements
1 statement
1 statement · 1 reference database · Subject: dynorphin A-(1-13) · Sources: Rhea
- dynorphin A-(1-13) is a substrate of ACE2ProteinRhea RHEA:63556Inferred only
Reactions
1 reaction
dynorphin A-(1-13)+waterdynorphin A-(1-12)+L-lysine
Catalysed by ACE2
Reaction pageLeft to rightBalanced
Rhea RHEA:63556CC BY 4.0Reference data
Other names
2 names
Resolves to: dynorphin A-(1-13)
- Also called
- L-tyrosyl-glycyl-glycyl-L-phenylalanyl-L-leucyl-L-arginyl-L-arginyl-L-isoleucyl-L-arginyl-L-prolyl-L-lysyl-L-leucyl-L-lysineTyr-Gly-Gly-Phe-Leu-Arg-Arg-Ile-Arg-Pro-Lys-Leu-Lys