UCSF

ZINC04492886

Physical Representations

Type pH range xlogP Des A‑Pol Apolar desolvation (kcal/mol) Des Pol Polar desolvation (kcal/mol) H Don H-bond donors H Acc H-bond acceptors Chg Net charge tPSA (Ų) MWT Molecular weight (g/mol) RB Rotatable bonds DL
Ref Reference (pH 7) 2.09 6.85 -12.29 0 3 0 39 248.322 0

Vendor Notes

Note Type Comments Provided By
MP 115-116 °C(lit.) Indofine
MP 115o C Indofine
Purity >98% Fluorochem
UniProt Database Links ANKR1_HUMAN ChEBI
Therapy antiinflammatory, immune suppressant SMDC MicroSource
PUBCHEM_PATENT_ID EP0098041A2; EP0553658B1; EP0565578A1; EP0614459A1; EP0805680A2; EP1053246A1; US4758433; US5384121; US5466451; US5795909; US5905089; US6068999; US6103218; US6117896; WO1992011857A1; WO1994006800A1; WO1996022774A2; WO1997039355A1; WO1998005333A1; WO1998027 IBM Patent Data
Therapy Inhibitors: IkappaB kinase inhibitor SMDC Iconix
Reactome Database Links REACT_15538; REACT_163726; REACT_22239; REACT_22289 ChEBI

Activity (Go SEA)

Direct Reactome Annotations (via ChEBI)

Description Species
Class C/3 (Metabotropic glutamate/pheromone receptors)
G alpha (i) signalling events

Analogs ( Draw Identity 99% 90% 80% 70% )