5 Results for "

forskolin derivative

" in MedChemExpress (MCE) Product Catalog:
Products (5)

5 Results for "forskolin derivative" in MCE Product Catalog:

Cat. No.: HY-103193
CAS No.: 138605-00-2
Purity:  99.86%
Synonyms: Colforsin dapropate hydrochloride
Target:  

Adenylate Cyclase

Research Areas:  

Cardiovascular Disease

NKH477 (Colforsin dapropate hydrochloride) directly activates the catalytic unit of adenylate cyclase and increases intracellular cAMP. NKH477 is a forskolin derivative that improves cardiac failure mainly through its beneficial effects on diastolic cardiac function. NKH477 exerts an antiproliferative effect in vivo with an altered cytokine profile to inhibit the acute rejection of rat orthotopic lung allografts .
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Cat. No.: HY-173215
3-Dimethylaminopropyl deacetylforskolin is a dehydro derivative of adenylate cyclase activator Forskolin (HY-15371) and may cause cross-immunoreactivity with anti-Forskolin antibodies .
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Cat. No.: HY-137934
CAS No.: 64657-20-1
Synonyms: 7-Deacetylforskolin
Deacetylforskolin is a deacetylated derivative of forskolin (HY-15371) that can be extracted from C. forskohlii. Deacetylforskolin activates rat adipocyte adenylyl cyclase (IC50 = 20 µM), inhibits glucose transport in rat adipocyte plasma membranes and exhibits antihypertensive activity .
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Cat. No.: HY-136974
CAS No.: 84048-28-2
9-Deoxyforskolin (compound 2) is a labdane-type diterpenoid, and also a forskolin derivative identified in hairy root cultures of Coleus forskohlii .
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Cat. No.: HY-103193R
CAS No.: 138605-00-2
Synonyms: Colforsin dapropate hydrochloride (Standard)
NKH477 (Standard) is the analytical standard of NKH477 (HY-103193). This product is intended for research and analytical applications. NKH477 (Colforsin dapropate hydrochloride) directly activates the catalytic unit of adenylate cyclase and increases intracellular cAMP. NKH477 is a forskolin derivative that improves cardiac failure mainly through its beneficial effects on diastolic cardiac function. NKH477 exerts an antiproliferative effect in vivo with an altered cytokine profile to inhibit the acute rejection of rat orthotopic lung allografts .
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