Selank Co

T-09

Selank literature provenance explorer

The compound-unique data component for this site. Maps every selank paper we indexed by publication language, institutional country, species studied and evidence grade, so a reader can see for themselves that the evidence base is concentrated in one language and one research system. This is the interactive form of the argument the whole site makes.

The compound-unique data component for this site. Maps every selank paper we indexed by publication language, institutional country, species studied and evidence grade, so a reader can see for themselves that the evidence base is concentrated in one language and one research system. This is the interactive form of the argument the whole site makes.

Published records (13 of 13)

SpeciesDose as statedRouteContext
humanNot stated in abstractNot statedAll four Russian patient studies
humanNot stated in abstractInjection (unspecified)fMRI study, 52 healthy volunteers
rat0.3 mg/kg/dayintraperitonealEthanol memory impairment, 7 days
rat0.3 mg/kgintraperitonealMorphine withdrawal, single dose
mouse0.3 mg/kgintraperitonealEthanol hyperlocomotion, DBA/2 mice
rat300 mcg/kgnot statedFrontal cortex gene expression, single dose
mouse300 mcg/kg/dayintranasal and intraperitonealRoute comparison, 5 days
mouse100 mcg/kgintraperitonealSpleen inflammation genes, single dose
mouse100 mcg/kgnot statedOpen-field behaviour and plasma enkephalinase
rat80, 250 and 750 mcg/kgintraperitonealRestraint stress, colon morphology and microbiota
in vitro (human serum)IC50 20 micromolarin vitroEnkephalin-degrading enzyme inhibition
in vitro (human plasma)IC50 15 micromolarin vitroPlasma enkephalin hydrolysis
in vitro (rat slices)1 to 8 micromolarbath applicationCA1 inhibitory postsynaptic currents; no dose-dependence

Every row restates a published record; sources resolve on the sourced monograph. Species is part of the data: this table never scales an animal dose into a human figure.

Tools: educational calculators and references only.

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