spinorphin (Human) [7420]



spinorphin (Human)


SMILES CC(C)C[C@H](N)C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](C(=O)O)[C@@H](C)O)C(C)C)C(C)C
InChIKey BXIFNVGZIMFBQB-DYDSHOKNSA-N
Sequence LVVYPWT
HELM PEPTIDE1{L.V.V.Y.P.W.T}$$$$

Chemical Properties

Hydrogen bond acceptors 10
Hydrogen bond donors 10
Rotatable bonds 21
Log P 1.224
Molecular weight (Da) 876.5
Stereochemistry info partial

Database connections

Model (AF2) FPR1


Bioactivities

Receptor Activity Source
Protein Gene Species Family Class Type Min Avg Max Database
Receptor Activity Source
Protein Gene Species Family Class Type Min Avg Max Database

spinorphin (Human)


Drug properties

Molecular type Peptide
Physiological/Surrogate Endogenous
Approved drug No

Distribution across phases (no. indications)

Phase I 0
Phase II 0
Phase III 0
Phase IV 0

Database connections

Model (AF2) FPR1


Compound is not listed as a drug.