humanin (Human) [3993]



humanin (Human)


SMILES CC[C@H](C)[C@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CS)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H]1CCCN1C(=O)[C@H](C)NC(=O)[C@@H](N)CCSC)[C@@H](C)O)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N1CCC[C@H]1C(=O)N[C@H](C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)O)C(C)C
InChIKey DPEUWKZJZIPZKE-OFANTOPUSA-N
Sequence MAPRGFSCLLLLTSEIDLPVKRRA
HELM PEPTIDE1{M.A.P.R.G.F.S.C.L.L.L.L.T.S.E.I.D.L.P.V.K.R.R.A}$$$$

Chemical Properties

Hydrogen bond acceptors 36
Hydrogen bond donors 39
Rotatable bonds 88
Log P -8.286
Molecular weight (Da) 2685.5
Stereochemistry info partial

Database connections

Model (AF2) FPR3 FPR2/ALX

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

humanin (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) FPR3 FPR2/ALX

Compound is not listed as a drug.