T1266 |
Terfenadine
|
50679-08-8
|
99.36%
|
|
Terfenadine ((±)-Terfenadine) is a prodrug that is metabolized by intestinal CYP3A4 to the active form fexofenadine, a selective histamine H1-receptor antagonist...
|
T1146 |
Nifedipine
|
21829-25-4
|
99.30%
|
|
Nifedipine (Procardia) is a dihydropyridine calcium channel blocking agent. Nifedipine inhibits the transmembrane influx of extracellular calcium ions into myoca...
|
T8700 |
TKIM
|
326921-25-9
|
99.3%
|
|
TKIM is a TWIK-related potassium channel 1 (TREK-1) inhibitor, binding to the pocket of the intermediate (IM) state of TREK-1.
|
T1498 |
Indapamide
|
26807-65-8
|
99.28%
|
|
Indapamide (Noranat) is a non-thiazide sulphonamide diuretic compound, generally used in the treatment of hypertension, as well as decompensated cardiac failure....
|
T67917 |
ML353
|
|
99.28%
|
|
ML353 (VU0478006) is a selective activator of TREK-1 and TREK-2 and a selective ligand (Ki =18.2 nM) for the mGlu5 Silencing Allosteric Modulator (SAM). ML353 ha...
|
T0974 |
Novobiocin Sodium
|
1476-53-5
|
99.28%
|
|
Novobiocin Sodium (Albamycinsodium) binds to DNA gyrase and blocks adenosine triphosphatase (ATPase) activity. Novobiocin sodium is an antibiotic compound derive...
|
T11515 |
Gut restricted-7
|
2553218-46-3
|
99.27%
|
|
Gut restricted-7 (GR-7) (GR-7) is a covalent and orally active pan-bile salt hydrolase (BSH) inhibitor. It decreases gut bacterial BSHs and decreases deconjugate...
|
T15286 |
Flindokalner
|
187523-35-9
|
99.25%
|
|
Flindokalner (BMS-204352) is a potassium channel modulator and a positive modulator of all neuronal Kv7 channel subtypes expressed in HEK293 cells. Flindokalner ...
|
TP1852L |
Myomodulin acetate(110570-93-9 free base)
|
TP1852L
|
99.24%
|
|
Myomodulin acetate is present in two identified aplysia neurons that contain myomodulin A the ARC motor neuron B16 and the abdominal neuron L10.
|
T11529 |
H3B-120
|
2194903-42-7
|
99.2%
|
|
H3B-120 is a highly selective, competitive, and allosteric carbamoyl phosphate synthetase 1 (CPS1) inhibitor (IC50: 1.5 μM; Ki: 1.4 μM) with anti-cancer activity...
|
T0816 |
Acetohexamide
|
968-81-0
|
99.19%
|
|
Acetohexamide (Acetohexamid) is an intermediate-acting, first-generation sulfonylurea with hypoglycemic activity. It inhibits sulfonylurea receptor 1 (SUR1) link...
|
T1049 |
Oxybutynin chloride
|
1508-65-2
|
99.17%
|
|
Oxybutynin chloride (Oxybutynin HCl) is an anticholinergic medication used to relieve urinary and bladder difficulties. It competitively antagonizes the M1, M2, ...
|
T3465L |
Vesnarinone HCl
|
T3465L
|
99.17%
|
|
Vesnarinone HCl (OPC-8212 HCl) is an orally active phosphodiesterase 3 (PDE3) inhibitor.Vesnarinone HCl modulates calcium and potassium ions, increasing calcium ...
|
T1453 |
Phenformin hydrochloride
|
834-28-6
|
99.15%
|
|
Phenformin hydrochloride (Phenformin HCl) is an agent belonging to the biguanide class of antidiabetics with antihyperglycemic activity.
|
T7775 |
A2764 dihydrochloride
|
861038-72-4
|
99.08%
|
|
A2764 dihydrochloride is a highly selective inhibitor of TRESK.
|
T4369 |
SCH-23390 hydrochloride
|
125941-87-9
|
99.07%
|
|
SCH-23390 hydrochloride (R-(+)-SCH23390 hydrochloride) is an effective dopamine receptor antagonist, and for the D1(Ki=0.2 nM) and D5(Ki=0.3 nM).
|
T6476 |
Dofetilide
|
115256-11-6
|
99.06%
|
|
Dofetilide (UK 68789) is a sulfonamide class III antiarrhythmic agent and potassium channel blocker. Dofetilide selectively blocks cardiac ion channels of the ra...
|
T17227 |
Vernakalant Hydrochloride
|
748810-28-8
|
99.04%
|
|
Vernakalant Hydrochloride (RSD1235 hydrochloride) is a mixed voltage- and frequency-dependent Na+ and atria-preferred K+ channel blocker.
|
T78870 |
TWIK-1/TREK-1-IN-3
|
1440532-33-1
|
99.04%
|
|
TWIK-1/TREK-1-IN-3 is a selective and potent inhibitor of potassium channel TREK-1, inhibiting TREK-1 homodimers and TWIK-1/TREK-1 heterodimers containing two-po...
|
T6631 |
Quinine hydrochloride dihydrate
|
6119-47-7
|
99.04%
|
|
Quinine hydrochloride dihydrate (Quinine HCl Dihydrate) is a white crystalline K+ channel blocker, used to treat malaria.
|