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tolbutamide
1st gen sulfonylurea

chlorpropamide
1st gen sulfonylurea

tolazamide
1st gen sulfonylurea

acetohexamide
1st gen sulfonylurea

glipizide
2nd gen sulfonylurea

glyburide
2nd gen sulfonylurea

glimepiride
2nd gen sulfonylurea

repaglinide
meglitinide

nateglinide
meglitinide

troglitazone
PPARg/a agonist (withdrawn due to serious liver injury)

rosiglitazone
PPARg agonist

pioglitazone
PPARg agonist/weak PPARa agonist

metformin (glucophage)
biguanide

canagliflozin (invokana)
SGLT2i

empagliflozin (jardiance)
SGLT2i

dapagliflozin (farxiga)
SGLT2i

ertugliflozin (steglatro)
SGLT2i

sitagliptin
DPP4 inhibitor

saxagliptin
DPP4 inhibitor

linagliptin
DPP4 inhibitor

alogliptin
DPP4 inhibitor

acarbose
alpha-amylase and alpha-glucosidase inhibitor for T2DM

miglitol
alpha-glucosidase inhibitor

morphine
potent, selective mu-opioid agonist

heroin

codeine sulfate
less potent than morphine

hydromorphone
more potent than morphine b/c of C ring ketone

oxymorphone
more potent than morphine b/c of C ring ketone AND -OH

hydrocodone
similar potency to morphine

oxycodone (oxycontin)
more potent than morphine

buprenorphine
mu partial agonist & ORL-1 agonist/kappa antagonist

nalbuphine
mu partial agonist/kappa agonist

butorphanol
mu partial agonist/kappa agonist

pentazocine
mu partial agonist/kappa agonist

fentanyl
flexible mu agonist

meperidine (demerol)
mu agonist

methadone (dolophine)
R - mu agonist / S - NMDA antagonist

tramadol
mu agonist and monoamine reuptake inhibition

tapentadol
mu agonist and NE reuptake inhibitor

oliceridine
biased mu agonist (G protein NOT beta-arrestin)

loperamide (imodium)
mu agonist - pgp substrate (doesnt cross BBB)

diphenoxylate
PRODRUG for difenoxin, weak mu agonist

difenoxin

naloxone
mu antagonist

naltrexone
mu antagonist
nasal spray - Narcan
SQ/IM - Evzio

methylnaltrexone bromide
mu antagonist

naloxegol
mu antagonist

aspirin
non selective irreversible COX inhibitor

acetaminophen
weak non selective COX enzyme (peroxidase fxn), activation of serotonergic descending inhibitory pathways, activation of endocannabinoids and TRPV1 ion channels

indomethacin
non selective pseudo irreversible COX inhibitor

diclofenac
potent reversible COX inhibitor (COX2>COX1)

ibuprofen (advil, motrin)
non selective reversible COX inhibitor equipotent to aspirin

naproxen (aleve, naprosyn)
non selective reversible COX inhibitor equipotent to aspirin and ibuprofen

meloxicam
reversible COX2 preferring inhibitor

celecoxib (celebrex)
moderately selective reversible COX2 inhibitor

methotrexate
DHFR inhibitor, increases adenosine, ATIC inhibitor

leflunomide
PRODRUG for teriflunomide, DHODH inhibitor

teriflunomide

sulfasalazine
metabolized to SP and 5-ASA to increase adenosine, suppress NF-kappaB activation, reduce TNF, inhibit PG synthesis

hydroxychloroquine
increase pH in lysosomes and inhibit toll like receptors

tofacitinib
JAK1/3 inhibitor

upadacitinib
JAK1 inhhibitor

baricitinib
JAK1/2 inhibitor

colchicine (colcrys)
reduce inflammation, DOES NOT ALTER SERUM URIC ACID

allopurinol
suicide inhibitor of xanthine oxidase

febuxostat
reversible non competitive xanthine oxidase inhibitor

probenecid
URAT1 inhibitor less selective

lesinurad
URAT1 inhibitor more selective
