CAS 64657-21-2: Isoforskolin
Formula:C22H34O7
InChI:InChI=1S/C22H34O7/c1-8-19(5)11-14(25)22(27)20(6)13(24)9-10-18(3,4)16(20)15(28-12(2)23)17(26)21(22,7)29-19/h8,13,15-17,24,26-27H,1,9-11H2,2-7H3/t13-,15-,16-,17-,19-,20-,21+,22-/m0/s1
InChI key:InChIKey=CLOQVZCSBYBUPB-KGGHGJDLSA-N
SMILES:C[C@@]12[C@]3(O)[C@@](C)([C@@H](O)[C@@H](OC(C)=O)[C@]1(C(C)(C)CC[C@@H]2O)[H])O[C@](C=C)(C)CC3=O
Synonyms:- (1α,5α,6β,7β)-6-(Acetyloxy)-8,13-epoxy-1,7,9-trihydroxylabd-14-en-11-one
- (3R,4aR,5S,6S,6aS,10S,10aR,10bS)-6-(Acetyloxy)-3-ethenyldodecahydro-5,10,10b-trihydroxy-3,4a,7,7,10a-pentamethyl-1H-naphtho[2,1-b]pyran-1-one
- 1H-Naphtho[2,1-b]pyran-1-one, 6-(acetyloxy)-3-ethenyldodecahydro-5,10,10b-trihydroxy-3,4a,7,7,10a-pentamethyl-, (3R,4aR,5S,6S,6aS,10S,10aR,10bS)-
- 1H-Naphtho[2,1-b]pyran-1-one, 6-(acetyloxy)-3-ethenyldodecahydro-5,10,10b-trihydroxy-3,4a,7,7,10a-pentamethyl-, [3R-(3α,4aβ,5β,6β,6aα,10α,10aβ,10bα)]-
- 6β-ACETOXY-8,13-EPOXY-1α,7β,9α-TRIHYDROXY-LABD-14-EN-11-ONE
- 6β-Acetoxy-8,13-epoxy-1α,7β,9α-trihydroxylabd-14-en-11-one
- Coleonol B
- Excolabdone C
- Isoforskolin
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Found 8 products.
(3R,4aR,5S,6S,6aS,10S,10aR,10bS)-6-(Acetyloxy)-3-ethenyldodecahydro-5,10,10b-trihydroxy-3,4a,7,7,10a-pentamethyl-1H-naphtho[2,1-b]pyran-1-one
CAS:Formula:C22H34O7Purity:98%Color and Shape:SolidMolecular weight:410.5011599999999Isoforskolin
CAS:Isoforskolin, from Coleus forskohlii, lowers TNF-α, IL-1β, IL-6, IL-8; studied for Lyme arthritis treatment.Formula:C22H34O7Purity:98.51%Color and Shape:SolidMolecular weight:410.5Isoforskolin
CAS:Oxygen-heterocyclic compoundFormula:C22H34O7Purity:≥ 90.0 % (HPLC)Color and Shape:PowderMolecular weight:410.51Isoforskolin
CAS:Isoforskolin is a forskolin derivative diterpenoid, which is extracted from the roots of *Coleus forskohlii*. This bioactive compound acts primarily by stimulating adenylate cyclase activity, leading to increased levels of cyclic adenosine monophosphate (cAMP) within cells. The elevated cAMP serves as a secondary messenger that can modulate various physiological responses, including lipolysis and vasodilation. Isoforskolin's ability to elevate cAMP levels makes it a compound of interest in several research domains, such as metabolic studies, cardiovascular research, and signal transduction analysis. Scientists have utilized isoforskolin to explore its effects on metabolic functions, investigating its potential role in energy expenditure and fat metabolism. Furthermore, its vasodilatory properties attract attention in cardiovascular research, where it may help elucidate mechanisms related to blood pressure regulation. While further studies are needed to fully understand its pharmacodynamics and therapeutic potential, isoforskolin remains an intriguing subject for researchers interested in natural compounds with significant biochemical activity.Formula:C22H34O7Purity:Min. 95%Color and Shape:White Off-White PowderMolecular weight:410.5 g/mol
