|
T27205 |
DPI 201-106
|
DPI-201-106 |
Sodium Channel
|
|
DPI-201-106 is a cardioselective inhibitor of the TTX-resistant h1 Na channel inactivation. DPI-201-106 inhibits the L-type calcium current, and inward and delayed rectifier potassium currents. |
|
T7191 |
Diphenyleneiodonium chloride
|
DPI |
NOS
,
Reactive Oxygen Species
,
NADPH
,
TRP/TRPV Channel
|
|
Diphenyleneiodonium chloride (DPI)(DPI) is an irreversible inhibitor of iNOS and eNOS (IC50 values of 50 nM and 0.3 μM, respectively),and displays broad-spectrum bactericidal activity. |
|
T15165 |
DPI-3290
|
Org 41793 |
Opioid Receptor
|
|
DPI-3290 is a specific agonist of opioid receptors (Ki: 0.18 nM, 0.46 nM, and 0.62 nM for δ-, μ-, and κ-opioid receptors, respectively) with potent antinociceptive activity. DPI-3290 is one of a series of novel centrally... |
|
T10700 |
(+)-CBI-CDPI1
|
|
Others
|
|
(+)-CBI-CDPI1 is an enhanced functional analog of CC-1065. It is a DNA alkylating agent and an antibody-drug conjugates (ADCs) toxin. |
|
T10701 |
(+)-CBI-CDPI2
|
|
Others
|
|
(+)-CBI-CDPI2 is an enhanced functional analog of CC-1065. |
|
TQ0095 |
Brincidofovir
|
CMX001,HDP-CDV |
Others
,
Antiviral
,
HSV
|
|
Brincidofovir (HDP-CDV) is an orally active, lipophilic form of cidofovir. It has enhanced activity compared to CDV against certain adenoviruses, herpesviruses, and orthopoxviruses. |
