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1 INNClassRoute (list)PK parameters= Cmax; Tmax; F: bioavailability; t1/2: half-life; VD: volume of distribution; Cl: clearance; PPB: plasma protein binding;(EQN means that value was calculated using VD=(Cl*t1/2)/0.693)Primary Target and PDB code of Protein-Drug complexTargets from DrugCentral Links
RISEDRONATE

RISEDRONATE


ATC M05BA07
ATC M05BB02
ATC M05BB07
ATC M05BB04

MUSCULO-SKELETAL
OSTEOPOROSIS
OSTEOCLASTIC RESORPTION INHIBITOR
BISPHOSPHONATES
HAS AN AFFINITY FOR HYDROXYAPATITE CRYSTALS IN BONE AND ACTS AS AN ANTIRESORPTIVE AGENT

ORAL

Tmax 1 HOUR

F 0.63 PERCENT

VD 897 LITER (65 KILOGRAM)

PPB 24 PERCENT

Cl 7.3 LITER / HOUR

HT 561 HOUR

SOLUBILITY SOLUBLE IN WATER

FARNESYL PYROPHOSPHATE SYNTHASE

PDB 4KPD (CRYSTAL STRUCTURE OF HUMAN FARNESYL PYROPHOSPHATE SYNTHASE (Y204F) MUTANT COMPLEXED WITH MG, RISEDRONATE AND ISOPENTENYL PYROPHOSPHATE)

LIGAND CODE = RIS (link to the list of PDB complexes)

Download experimental 3D coordinates of RIS with added hydrogens

ENZYME FPPS_HUMAN INHIBITOR P14324EMA

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