tiotidine
SMILES | N#CNC(=NC)NCCSCc1csc(n1)N=C(N)N |
InChIKey | YDDXVAXDYKBWDX-UHFFFAOYSA-N |
Chemical properties
Hydrogen bond acceptors | 6 |
Hydrogen bond donors | 4 |
Rotatable bonds | 6 |
Molecular weight (Da) | 312.1 |
Drug properties
Molecular type | Small molecule |
Endogenous/Surrogate | Surrogate |
Approved drug | No |
Database connections
Ligand site mutations | H2 |
Bioactivities
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
mGlu5 | GRM5 | Rat | Metabotropic glutamate | C | pEC50 | 6.57 | 6.57 | 6.57 | ChEMBL |
mGlu5 | GRM5 | Human | Metabotropic glutamate | C | pEC50 | 8.0 | 8.0 | 8.0 | ChEMBL |
mGlu5 | GRM5 | Rat | Metabotropic glutamate | C | pEC50 | 6.675 | 6.67 | 6.67 | Guide to Pharmacology |