All terms in DRUGBANK

Label Id Description
2,5-Xylidine DB02163
4,6-Dideoxy-4-{[4,5,6-Trihydroxy-3-(Hydroxymethyl)Cyclohex-2-En-1-Yl]Amino}-Alpha-D-Lyxo-Hexopyranosyl-(1->4)-Alpha-D-Threo-Hexopyranosyl-(1->6)-Alpha-L-Threo-Hexopyranose DB03495
N-sulfo-flavin mononucleotide DB02164
Hydroxy-Phenyl-Acetic Acid 8-Methyl-8-Aza-Bicyclo[3.2.1]Oct-3-Yl Ester DB02161
lambda-bis(2,2'-bipyridine)imidazole osmium (II) DB03492
5'-O-(N-Ethyl-Sulfamoyl)Adenosine DB02162
7-Methylguanosine DB03493
3-Pyridin-4-Yl-2,4-Dihydro-Indeno[1,2-.C.]Pyrazole DB03490
S-Butyryl-Cystein DB02160
2'-Deoxyguanosine-5'-Diphosphate DB03491
Glyceryl stearate SE DB14149
Human albumin microspheres DB14148
Zirconium chloride hydroxide DB15479
Nepidermin DB14145
Haemagglutinin-strain A(H1N1) DB15476
Haemagglutinin-strain A(H3N2) DB15475
p-Aminophenol DB14144
Frangula purshiana bark DB15478
Alloin DB15477
Loxicodegol DB14146 [Loxicodegol was developed by Nektar Therapeutics as an opioid analgesic with low abuse potential for the treatment of chronic pain [L3263]. The lack of abuse potential is believed to be due to the drug's slow rate of entry into brain, a unique characteristic compared to others in the opioid class [A33997, A34016]. This is also thought to be the reason behind the reduced frequency of CNS-mediated adverse effects, like sedation, seen with Loxicodegol. Nektar Therapeutics has filed an application for FDA approval of Loxicodegol for use in the treatment of chronic lower back pain [L3263]]