Shopping Cart
Remove All
  • TargetMol
    Your shopping cart is currently empty
Filter
Applied FilterClear all
TargetMol | Tags By Target
  • Sodium Channel
    (2)
  • Antifungal
    (1)
  • Autophagy
    (1)
  • GluR
    (1)
  • Opioid Receptor
    (1)
  • PI3K
    (1)
  • Others
    (1)
TargetMol | Tags By ResearchField
  • Cardiovascular System
    (2)
  • Nervous System
    (2)
  • Cancer
    (1)
  • Infection
    (1)
Filter
Search Result
Results for "

T2199

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    6
    TargetMol | All_Pathways
Myclobutanil
Systhane
T219988671-89-0
Myclobutanil (Systhane) is a triazole chemical used as a fungicide. It is a steroid demethylation inhibitor, specifically inhibiting ergosterol biosynthesis. Ergosterol is a critical component of fungal cell membranes.
  • $30
In Stock
Size
QTY
Zoniporide hydrochloride
CP-597396 hydrochloride
T21996241800-97-5In house
Zoniporide hydrochloride is a selective inhibitor of NHE-1 with IC50 of 14 nM which is >150-fold selectivity versus other NHE isoforms. Zoniporide hydrochloride shows an IC50 of 59 nM for NHE-1-dependent swelling of human platelets.
  • $57
In Stock
Size
QTY
Vacuolin-1
T21992351986-85-1
Vacuolin-1 is a cell-permeable inhibitor of Ca2+ dependent fusion of lysosomes to the cell membrane. It acts by inhibiting release of lysosomal content.vacuolin‐1 is a potent and selective PIKfyve inhibitor and inhibits late‐stage autophagy by impairing lysosomal maturation
  • $31
In Stock
Size
QTY
TargetMol | Citations Cited
XAP044
T21995196928-50-4
XAP044 is a mGlu7-selective antagonist which inhibits lateral amygdala long term potentiation (LTP) in brain slices from wild type mice with a half-maximal blockade at 88 nm[1].
  • $56
In Stock
Size
QTY
Zoniporide
CP-597396, CP597396, CP 597396
T21996L241800-98-6
Zoniporide (CP-597396) is an NHE-1 inhibitor that inhibits the uptake of 22Na+ by fibroblasts expressing human NHE-1 in a concentration-dependent manner, inhibits platelet swelling, and can be used in the study of cardiovascular diseases.
  • $45
In Stock
Size
QTY
(±)-J 113397
T21999217461-40-0
(±)-J-113397 is a potent and selective non-peptidyl ORL1 receptor antagonist (K(i): cloned human ORL1=1.8 nM). J-113397 inhibited nociceptin/orphanin FQ-stimulated GTPγS binding to CHO cells expressing ORL1 with an IC50 value of 5.3 nM. J-113397 can be used for researching the physiological roles of nociceptin/orphanin FQ [1].
  • $931
10-14 weeks
Size
QTY