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iCRT-14
iCRT-14
United States Biological

A potent inhibitor of b-catenin-responsive transcription (CRT) (IC50 = 40.3 nM in assays of Wnt pathway activity). Studies suggest that it may directly...

Diisopropyl Fluorophosphate
Diisopropyl Fluorophosphate
United States Biological

A potent inhibitor of serine proteases such as trypsin and chymotrypsin, and of acetylcholinesterase. Form: Colourless Liquid Boiling Point: 46 degrees C/5mm...

Chaetomellic Acid B Anhydride
Chaetomellic Acid B Anhydride
United States Biological

A potent inhibitor of Ras protein farnesyltransferase.

Chaetomellic Acid A Anhydride
Chaetomellic Acid A Anhydride
United States Biological

A potent inhibitor of Ras protein farnesyltransferase.

Paullone
Paullone
United States Biological

A potent inhibitor of cyclin-dependent kinases (CDKs). The CDKs are a family of protein kinases that are involved in the regulation of the cell cycle.

Ascomycin
Ascomycin
United States Biological

A potent immunosuppressive agent and could be used as a potential therapeutic agent for autoimmune diseases. Form: White Solid Melting Point: 153-157 degrees...

Raltegravir-d3 Potassium Salt
Raltegravir-d3 Potassium Salt
United States Biological

A potent human immunodeficiency virus (HIV) integrase inhibitor. A novel anti-AIDS drug. Form: Off-White to Pale Yellow Solid Melting Point: 160-164 degrees...

Raltegravir Potassium Salt
Raltegravir Potassium Salt
United States Biological

A potent human immunodeficiency virus (HIV) integrase inhibitor. A novel anti-AIDS drug. Form: Off-White Solid Melting Point: 155-157 degrees C (dec.)...

(R)-(-)-Bromo Dragonfly Hydrochloride
(R)-(-)-Bromo Dragonfly Hydrochloride
United States Biological

A potent hallucinogenic drug. The 5-HT2A receptor is known to act as the biologic target for a series of hallucinogenic substances including substituted...

Inotilone
Inotilone
United States Biological

A potent COX-2 inhibitor. Inotilone is used for treating degenerative conditions from overexpression of iNOS.

N-(2-Aminoethyl)-5-isoquinolinesulfonamide Hydrochloride
N-(2-Aminoethyl)-5-isoquinolinesulfonamide Hydrochloride
United States Biological

A potent competitive inhibitor of protein kinase C, cGMP-, and cAMP-dependent protein kinase with respect to ATP. Form: Off-White Solid Melting Point: >244...

CP-775146
CP-775146
United States Biological

A potent and selective PPARa agonist. It exhibits hypolipidemic activity in vivo. Form: Off-White Solid Melting Point: 70-76 degrees C Solubility: DMSO,...

SC-57461A
SC-57461A
United States Biological

A potent and selective orally active leukotriene A4 hydrolase inhibitor. Form: White Solid Melting Point: 163-165 degrees C Solubility: DMSO, Methanol Pfizer...

MLN 4924
MLN 4924
United States Biological

A potent and selective inhibitor of NAE. Form: White Solid Melting Point: 148-150 degrees C Solubility: Methanol

SAG
SAG
United States Biological

A potent agonist of Hedgehog (Hh) signalling by activating the Smoothened (Smo) protein function. Studies identify novel properties of molecules displaying...

Diethyldithiocarbamic Acid Sodium Salt Trihydrate
Diethyldithiocarbamic Acid Sodium Salt Trihydrate
United States Biological

A possible nuclear factor kappa B inhibitor. Form: White to Off-White Solid Melting Point: 88-92 degrees C Solubility: Methanol, Water

Trazodone 1,4-Di-N-Oxide
Trazodone 1,4-Di-N-Oxide
United States Biological

A possible metabolite of Trazodone-HCl. Form: White Solid Melting Point: 157-159 degrees C Solubility: Methanol, Water

Hydroxy Brimonidine Trifluoroacetate Salt
Hydroxy Brimonidine Trifluoroacetate Salt
United States Biological

A possible metabolite of Brimonidine. Form: Off-White to Pale Yellow Solid Melting Point: 228-232 degrees C Solubility: Methanol

11-Hydroxy Myristic Acid
11-Hydroxy Myristic Acid
United States Biological

A possible fatty acyl pheromone precursors in Spodoptera littoralis

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