Wet Ice

3-Amino-1,2,4-Triazole

3-Amino-1,2,4-Triazole

3-Amino-1,2,4-Triazole

3-Aminopropyl-Triethoxysilane

3-Aminopropyl-Triethoxysilane

Molecular Formula : C24 H29 B F2 N4 O5

Molecular Formula : C24 H29 B F2 N4 O5

Molecular Formula : C7 H8 Br N O4

Molecular Formula : C5H7NS

Molecular Formula : C5H7NS

Molecular Formula : C5H7NS

Molecular Formula : C4H6O

Molecular Formula : C4H6O

Molecular Formula : C4H6O

Molecular Formula : C4H6Cl2

Molecular Formula : C4H6Cl2

Molecular Formula : C4H6Cl2

Molecular Formula : No Data Available

Molecular Formula : C7H4Cl4

Molecular Formula : C7H4Cl4

Molecular Formula : C4H7OCl

Molecular Formula : C4H7OCl

Molecular Formula : C4H7OCl

Molecular Formula : C6 H10 O5

Molecular Formula : C6 H10 O5

Molecular Formula : C6 H10 O5

Molecular Formula : C7 H11 N3 O4

Molecular Formula : C7 H11 N3 O4

Molecular Formula : C7 H11 N3 O4

Molecular Formula : C36 H30 Cl N3 O9

Molecular Formula : C36 H30 Cl N3 O9

Molecular Formula : C8 H18

Molecular Formula : C8 H18

Molecular Formula : C8 H18

Molecular Formula : C10H22

Molecular Formula : C10H22

Molecular Formula : C10H22

Molecular Formula : C8 H18

Molecular Formula : C8 H18

Molecular Formula : C6H10O2

Molecular Formula : C6H10O2

Molecular Formula : C6H10O2

Molecular Formula : C8 H7 N O2

Molecular Formula : C3H5NaO3

Molecular Formula : C3H5NaO3

3-Indoxyl Phosphate Disodium Salt

3-Indoxyl Phosphate Disodium Salt

IBMX has been shown to be a potent, non-specific inhibitor of adenosine 3′,5′-cyclic monophosphate phosphodiesterase (cAMP PDE)4, significantly more effective than theophylline. Also inhibits cGMP phosphodiesterases. IBMX inhibits cyclic nucleotide PDE with subsequent inhibition of cyclic nucleotide hydrolysis, resulting in accumulation of cyclic AMP and guanosine 3′,5′-cyclic monophosphate.

IBMX has been shown to be a potent, non-specific inhibitor of adenosine 3′,5′-cyclic monophosphate phosphodiesterase (cAMP PDE)4, significantly more effective than theophylline. Also inhibits cGMP phosphodiesterases. IBMX inhibits cyclic nucleotide PDE with subsequent inhibition of cyclic nucleotide hydrolysis, resulting in accumulation of cyclic AMP and guanosine 3′,5′-cyclic monophosphate.

IBMX has been shown to be a potent, non-specific inhibitor of adenosine 3′,5′-cyclic monophosphate phosphodiesterase (cAMP PDE)4, significantly more effective than theophylline. Also inhibits cGMP phosphodiesterases. IBMX inhibits cyclic nucleotide PDE with subsequent inhibition of cyclic nucleotide hydrolysis, resulting in accumulation of cyclic AMP and guanosine 3′,5′-cyclic monophosphate.