labradimil [4619]



labradimil


SMILES COc1ccc(C[C@@H](CN[C@@H](CCCN=C(N)N)C(=O)O)NC(=O)[C@@H]2CCCN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2C[C@@H](O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](N)CCCN=C(N)N)cc1
InChIKey IDXCXSCCZNCXCL-XMADEQCMSA-N
Sequence RPXGXSPYR

Chemical Properties

Hydrogen bond acceptors 16
Hydrogen bond donors 13
Rotatable bonds 29
Log P -4.474
Molecular weight (Da) 1097.5
Stereochemistry info partial

Database connections

Model (AF2) B2


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

labradimil


Drug properties

Molecular type Peptide
Physiological/Surrogate Surrogate
Approved drug Yes

Distribution across phases (no. indications)

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

Database connections

Model (AF2) B2


Compound is not listed as a drug.