|
gptkb:Rydberg_blockade
|
strong dipole-dipole interaction between Rydberg atoms
|
|
gptkb:Cefcapene_pivoxil_hydrochloride_hydrate
|
inhibits bacterial cell wall synthesis
|
|
gptkb:penciclovir
|
inhibits viral DNA polymerase
|
|
gptkb:Ponatinib
|
inhibits VEGFR
|
|
gptkb:teprotide
|
angiotensin-converting enzyme inhibitor
|
|
gptkb:doxylamine_succinate
|
histamine H1 receptor antagonist
|
|
gptkb:Sovaldi
|
gptkb:NS5B_polymerase_inhibitor
|
|
gptkb:sulpiride
|
dopamine D2 receptor antagonist
|
|
gptkb:somavaratan
|
VEGF inhibitor
|
|
gptkb:E-605_(parathion)
|
gptkb:acetylcholinesterase_inhibitor
|
|
gptkb:felzartamab
|
CD38 inhibition
|
|
gptkb:V.A.C._Therapy
|
applies negative pressure to wound
|
|
gptkb:Pioglitazone
|
PPARγ agonist
|
|
gptkb:Molidustat
|
HIF prolyl-hydroxylase inhibitor
|
|
gptkb:NDM-2
|
hydrolyzes beta-lactam ring
|
|
gptkb:Tranexamic_acid
|
inhibits activation of plasminogen to plasmin
|
|
gptkb:Erythromycin_D
|
inhibits bacterial protein synthesis
|
|
gptkb:buprenorphine
|
partial agonist at mu-opioid receptor
|
|
gptkb:sucralfate
|
forms a protective barrier on ulcers
|
|
gptkb:satraplatin
|
DNA crosslinking
|