Cheminformatic Tools and Databases for Pharmacology

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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
DEGARELIX

DEGARELIX


ATC L02BX02

ANTINEOPLASTIC
PROSTATE CANCER
GONADOTROPIN-RELEASING HORMONE (GNRH) ANTAGONIST
IT BINDS REVERSIBLY TO THE PITUITARY GNRH RECEPTORS THEREBY REDUCING THE RELEASE OF GONADOTROPINS AND CONSEQUENTLY TESTOSTERONE

SUBCUTANEOUS

Cmax 16 NANOMOLAR (240 MILLIGRAM)

VD 1000 LITER

PPB 90 PERCENT

Cl 9 LITER / HOUR

HT 1272 HOUR

GONADOTROPIN-RELEASING HORMONE

GONADOTROPIN-RELEASING HORMONE RECEPTOR ANTAGONIST CHEMBL1855 GONADOTROPIN-RELEASING HORMONE RECEPTOR P30968 GONADOTROPIN-RELEASING HORMONE RECEPTOR HOMO SAPIENS MEMBRANE RECEPTOR 7TM1 PEPTIDE SHORT PEPTIDE GNRH RECEPTORANSM (in French)

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