|Description||Fuberidazole is a benzimidazole based fungicide used in cereal seed dressing and fungicidal non-mercurial seed dressing with special action against fusarium.|
|Appearance||Off-White to Pale Beige Solid|
|Synonyms||2-(furan-2-yl)-1H-benzimidazole; BAY 33172;|
|Solubility||Soluble in DMSO|
|Storage||Store at -20 °C|
|Application||A fungicidal seed treatment of barley.|
|Quality Standard||Enterprise standard|
|Shelf Life||As supplied, 2 years from the QC date provided on the Certificate of Analysis, when stored properly.|
|Melting Point||>280ºC (dec.)|
Cinoctramide is an intermediate of pharmaceutical synthesis.
Astragaloside A (Astragaloside IV) is the primary pure saponin isolated from Astragalus membranaceus, which has been widely used for the treatment of cardiovasc...
CID 2745687 has been found to be a GPR35 antagonist and could probably be used in immune or gastrointestinal system regulation.
(+/-)-J 113397 has been found to be a NOP receptor antagonist and could restrain nociceptin/orphanin FQ-induced hyperalgesia in the mouse tail-flick test.
R 428 dihydrochloride is a potent and selective inhibitor of Axl receptor tyrosine kinases (IC50 = 14 nM). R428 inhibits Axl kinase and Axl-dependent events, in...
FR-217840 is a matrix metalloproteinase inhibitor. It can suppress joint destruction. FR217840 may have potential as a novel anti-rheumatic drug.
A potent and selective inhibitor of E-selectin (IC50= 7 nM) and ICAM-1 (IC50= 5 nM)
(+)-Catechin is a flavonoid found primarily in higher woody plants as (+)-Catechin along with (-)-Epicatechin (cis form). Antidiarrheal.
A 804598 is a potent and competitive P2X7 receptor antagonist (IC50 = 8.9, 9.9 and 10.9 nM for mouse, rat and human P2X7 receptors, respectively).
CGP-42454A is a epimer of Benazepril ,an approved drug using for the treatment of Hypertension.
CB-403, a cinnamaldehyde derivative, which has antitumor effect through the arrest of cell cycle progression in the G2/M phase.
OSU 6162 hydrochloride
OSU 6162 hydrochloride is a dopamine stabilizer. It is highly active on dopamine synthesis and turnover. It can antagonize the expression of L-DOPA induced beha...
D-erythro-Sphingosine is a natural isomer of sphingosine and acts as an inhibitor of protein kinase C and calmodulin-dependent enzymes with no effects on protei...
NSC 636819 is a KDM4A/KDM4B inhibitor. It induces apoptosis in cultured prostate cancer cells.
Probenecid inhibits the renal excretion of organic anions and reduces tubular reabsorption of urate. It is able to prevent the efflux of calcium-sensitive fluor...
FR-181157, an oxazol derivative, has been found to be a prostaglandin mimetic and could have potential biological activities as a IP receptor agonist.
Ani 9 is a highly selective and potent anoctamin1 (ANO1)/transmembrane protein 16A (TMEM16A) inhibitor with IC50 value of 77 nM. It completely inhibits ANO1 chl...
Aconine is extracted form the roots of Aconitum kusnezoffii Reichb, a derivative of Aconitine.
GKT137831 attenuates hypoxia-induced H(2)O(2) release, cell proliferation, and TGF-β1 expression and blunted reductions in PPARγ in HPAECs and HPASMCs.
CEP dipeptide 1
CEP dipeptide 1 is a CEP dipeptide which has potent angiogenic activity. It is used as mediators of age-related macular degeneration (AMD).