NKH477

Modify Date: 2024-01-15 22:12:38

NKH477 Structure
NKH477 structure
Common Name NKH477
CAS Number 138605-00-2 Molecular Weight 546.093
Density N/A Boiling Point 571.4ºC at 760mmHg
Molecular Formula C27H44ClNO8 Melting Point N/A
MSDS Chinese USA Flash Point 176ºC
Symbol GHS06
GHS06
Signal Word Danger

 Use of NKH477


NKH477 (Colforsin dapropate hydrochloride) is a novel water-soluble forskolin derivative that improves cardiac failure mainly through its beneficial effects on diastolic cardiac function. NKH477 directly activates the catalytic unit of adenylate cyclase and increases intracellular cAMP. NKH477 exerts an antiproliferative effect in vivo with an altered cytokine profile to inhibit the acute rejection of rat orthotopic lung allografts[1].

 Names

Name N,N-Dimethyl-(3R,4aR,5S,6aS,10S,10aR,10bS)-5-(acetyloxy)-3-ethenyldodecahydro-10,10b-dihydroxy-3,4a,7,7,10a-pentamethyl-1-oxo-1H-naphtho[2,1-b]pyran-6-ylesterβ-alaninehydrochloride
Synonym More Synonyms

 NKH477 Biological Activity

Description NKH477 (Colforsin dapropate hydrochloride) is a novel water-soluble forskolin derivative that improves cardiac failure mainly through its beneficial effects on diastolic cardiac function. NKH477 directly activates the catalytic unit of adenylate cyclase and increases intracellular cAMP. NKH477 exerts an antiproliferative effect in vivo with an altered cytokine profile to inhibit the acute rejection of rat orthotopic lung allografts[1].
Related Catalog
Target

Adenylate Cyclase[1]

In Vivo NKH477 (Colforsin dapropate hydrochloride) (orally; 1-3 mg/kg/day; days 3 and 5) prolonged lung allograft survival in a dose dependent manner[1]. Animal Model: Specific-pathogen-free inbred male Lewis rats (LEW) weighing 250 to 280 g[1] Dosage: 1, 2 or 3 mg/kg/day Administration: Orally; daily; Days 3 and 5 Result: Prolonged lung allograft survival in a dose dependent manner.
References

[1]. Nakashima S, et al. Antiproliferative effects of NKH477, a forskolin derivative, on cytokine profile in rat lung allografts. J Heart Lung Transplant. 2005 Apr;24(4):462-9.

 Chemical & Physical Properties

Boiling Point 571.4ºC at 760mmHg
Molecular Formula C27H44ClNO8
Molecular Weight 546.093
Flash Point 176ºC
Exact Mass 545.275574
PSA 122.60000
LogP 2.82450
Vapour Pressure 5.29E-16mmHg at 25°C
Storage condition 2-8°C

 Safety Information

Symbol GHS06
GHS06
Signal Word Danger
Hazard Statements H300
Precautionary Statements P264-P301 + P310
Hazard Codes T
Safety Phrases 28-36/37-45
RIDADR UN 2811 6.1 / PGII
RTECS AY5992600

 Articles35

More Articles
Analysis of compartmentalized cAMP: a method to compare signals from differently targeted FRET reporters.

Methods Mol. Biol. 1071 , 59-71, (2014)

Förster resonance energy transfer (FRET)-based reporters are important tools to study the spatiotemporal compartmentalization of cyclic adenosine monophosphate (cAMP) in living cells. To increase the ...

Chemically induced pluripotent stem cells (CiPSCs): a transgene-free approach.

J. Mol. Cell Biol. 5(5) , 354-5, (2013)

Induced pluripotent stem cells (iPSCs) could be generated by a single gene Oct4 and chemical compounds, in which exogenous expression of Oct4 was indispensable for reprogramming. Recent advances in ch...

Activation of cAMP signaling attenuates impaired hepatic glucose disposal in aged male p21-activated protein kinase-1 knockout mice.

Endocrinology 155(6) , 2122-32, (2014)

p21-activated protein kinase-1 (Pak1) plays a role in insulin secretion and glucagon-like peptide-1 (GLP-1) production. Pak1(-/-) mice were found to carry a defect in ip pyruvate tolerance test (IPPTT...

 Synonyms

(3R,4aR,5S,6S,6aS,10S,10aR,10bS)-5-Acetoxy-10,10b-dihydroxy-3,4a,7,7,10a-pentamethyl-1-oxo-3-vinyldodecahydro-1H-benzo[f]chromen-6-yl N,N-dimethyl-β-alaninate hydrochloride (1:1)
colforsindapropatehydrochloride
Adehl
β-Alanine, N,N-dimethyl-, (3R,4aR,5S,6S,6aS,10S,10aR,10bS)-5-(acetyloxy)-3-ethenyldodecahydro-10,10b-dihydroxy-3,4a,7,7,10a-pentamethyl-1-oxo-1H-naphtho[2,1-b]pyran-6-yl ester, hydrochloride (1:1)
NKH 477
colforsin daropate hydrochloride
6-[3-(dimethylamino)propionyl]-forskolin,Colforsin dapropate hydrochloride,N,N-dimethyl
MKH 477
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