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| Product | Description | |
|---|---|---|
| Coleus Forskohlii 10% & 40% | Coleus Forskohlii 10% & 40%. |  CA, FL & NJ |
| Coleus forskohlii Extract | Coleus forskohlii Extract. Applications: It use for anti hypertensive, camp stimulator. Group: Others. Synonyms: Coleus forskohlii Extract; Coleus forskohlii. Purity: 10:1 by TLC. Appearance: Brown yellow to white fine powder. Storage: 2 years under well storage situation and stored away from direct sun light. Source: Whole herb. Species: Coleus forskohlii. Coleus forskohlii Extract; Coleus forskohlii; plant extract. Pack: 25KG/Drum with double plastic bag of foodstuff inside. Cat No: EXTW-177. |  |
| Coleus Forskohlii Root 4:1 | Coleus Forskohlii Root 4:1. | CA, FL & NJ |
| 1,9-Dideoxyforskolin from coleus forskohlii | 1,9-Dideoxyforskolin from coleus forskohlii. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 1,9-DIDEOXYFORSKOLIN; 1,9-Dideoxyforskolin. Appearance: white solid. CAS No. 64657-18-7. Molecular formula: C22H34O5. Mole weight: 378.5. Purity: 97%+. IUPACName: 1,9-dideoxyforskolin. Density: 1.12 g/cm³. Product ID: ACM64657187. Alfa Chemistry ISO 9001:2015 Certified. |  |
| 1,9-Dideoxyforskolin from Coleus forskohlii | ?97%, solid. Group: Fluorescence/luminescence spectroscopy. |  |
| Forskolin (Coleus forskohlii) | The major cell-permeable diterpene isolated from the Indian plant Coleus forskohlii. At low doses, it acts as a positive inotropic agent. At higher doses, it serves as a hypotensive and vasodilatory agent due to its actions as a smooth muscle relaxant. No major side effects are observed at effective doses. Forskolins pharmacological activities are due to its activation of adenylate cyclase (EC50 = 4uM), resulting in increased cAMP levels. The exact mechanism of forskolins positive inotropic effect is unknown but may be related to a cAMP-dependent increase in Na+ permeability that results in indirect augmentation of Ca2+ release. Inhibits MAP kinase in rat renal mesangial cells (IC50 = 25uM). Also acts as a Hh pathway antagonist. Shown to inhibit apoptosis in cerebellar granule cells and to induce apoptosis in resting human B lymphocytes. Group: Biochemicals. Grades: Highly Purified. CAS No. 66575-29-9. Pack Sizes: 5mg. US Biological Life Sciences. |  Worldwide |
| Forskolin, Coleus forskohlii (7b-Acetoxy-8,13-epoxy-1α,6 β,9α-trihydroxy-labd-14-en-11-one, Colforsin) | The major cell-permeable diterpene isolated from the Indian plant Coleus forskohlii. At low doses, it acts as a positive inotropic agent. At higher doses, it serves as a hypotensive and vasodilatory agent due to its actions as a smooth muscle relaxant. No major side effects are observed at effective doses. Forskolins pharmacological activities are due to its activation of adenylate cyclase (EC50=4uM), resulting in increased cAMP levels. The exact mechanism of forskolins positive inotropic effect is unknown but may be related to a cAMP-dependent increase in Na+ permeability that results in indirect augmentation of Ca2+ release. Inhibits MAP kinase in rat renal mesangial cells (IC50= 25uM). Also acts as a Hh pathway antagonist. Shown to inhibit apoptosis in cerebellar granule cells and to induce apoptosis in resting human B lymphocytes. Group: Biochemicals. Grades: Highly Purified. CAS No. 66575-29-9. Pack Sizes: 10mg, 25mg. Molecular Formula: C??H??O?. US Biological Life Sciences. | Worldwide |
| 1,9-Dideoxyforskolin | 1,9-Dideoxyforkskolin does not activate adenylyl cyclase and is an inactive analog of Forskolin, a diterpene isolated from Coleus forskohlii, possessing vasodilating and cardiostimulatory properties. Forskolin resensitizes cell receptors by activating the enzyme adenylyl cyclase and increasing the intracellular levels of cAMP. Group: Biochemicals. Grades: Highly Purified. CAS No. 64657-18-7. Pack Sizes: 1mg, 5mg. Molecular Formula: C22H34O5, Molecular Weight: 378.5. US Biological Life Sciences. | Worldwide |
| 1-Deoxyforskolin | 1-Deoxyforskolin. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 1-Deoxyforskolin from Coleus forskohlii, SureCN4922859, D1290_SIGMA, 7|A-Acetoxy-6|A,9|A-dihydroxy-8,13-epoxy-labd-14-en-11-one, 7beta-Acetoxy-6beta,9alpha-dihydroxy-8,13-epoxy-labd-14-en-11-one, 72963-77-0. Product Category: Heterocyclic Organic Compound. CAS No. 72963-77-0. Molecular formula: C22H34O6. Mole weight: 394.5. Purity: 0.96. IUPACName: [(3R,4aR,5S,6S,6aS,10aS,10bS)-3-ethenyl-6,10b-dihydroxy-3,4a,7,7,10a-pentamethyl-1-oxo-5,6,6a,8,9,10-hexahydro-2H-benzo[f]chromen-5-yl] acetate. Canonical SMILES: CC(=O)OC1C(C2C(CCCC2(C3(C1(OC(CC3=O)(C)C=C)C)O)C)(C)C)O. Density: 1.183 g/cm³. Product ID: ACM72963770. Alfa Chemistry ISO 9001:2015 Certified. | |
| 6-Epidemethylesquirolin D | 6-Epidemethylesquirolin D is isolated from the herbs of Coleus forskohlii. Synonyms: 6-epi-O-Demethylesquirolin D. Grade: 97%. CAS No. 165074-00-0. Molecular formula: C20H28O5. Mole weight: 348.4. |  |
| 7Beta-acetoxy-1alpha,6beta-dihydroxy-8,13-epoxy-labd-14-en-11-one | 7Beta-acetoxy-1alpha,6beta-dihydroxy-8,13-epoxy-labd-14-en-11-one. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 7beta-acetoxy-8,13-epoxy-1alpha,6beta-dihydroxylabd-14-en-11-one; 7beta-Acetoxy-1alpha,6beta-dihydroxy-8,13-epoxy-labd-14-en-11-one; 9-deoxyforskolin; 7|A-Acetoxy-1|A,6|A-dihydroxy-8,13-epoxy-labd-14-en-11-one; 9-Deoxyforskolin from Coleus forskohlii. Product Category: Heterocyclic Organic Compound. CAS No. 84048-28-2. Molecular formula: C22H34O6. Mole weight: 394.5. Purity: 0.96. IUPACName: [(3R,4aS,5S,6S,6aS,10S,10aS,10bR)-3-ethenyl-6,10-dihydroxy-3,4a,7,7,10a-pentamethyl-1-oxo-2,5,6,6a,8,9,10,10b-octahydrobenzo[f]chromen-5-yl] acetate. Canonical SMILES: CC(=O)OC1C(C2C(CCC(C2(C3C1(OC(CC3=O)(C)C=C)C)C)O)(C)C)O. Density: 1.18g/cm³. Product ID: ACM84048282. Alfa Chemistry ISO 9001:2015 Certified. | |
| Forskolin | Forskolin is a diterpene isolated from Coleus forskohlii, possessing vasodilating and cardiostimulatory properties. Forskolin resensitizes cell receptors by activating the enzyme adenylyl cyclase and increasing the intracellular levels of cAMP. Alternative Names: 7BETA-ACETOXY-1ALPHA,6BETA,9ALPHA-TRIHYDROXY-8,13-EPOXY-LABD-14-EN-11-ONE;7BETA-ACETOXY-8,13-EPOXY-1ALPHA,6BETA,9ALPHA-TRIHYDROXY-LABD-14-EN-11-ONE;7BETA-ACETOXY-8,13-EPOXY-1ALPHA,6BETA,9ALPHA-TRIHYDROXY-LABD-14-ENE-11-ONE;[3R-(3A,4AB,5B,6B,6AA,10A,10AB,10BA)]-5-(ACETYLOXY)-3-ETHENYLDODECAHYDRO-6,10,10B-TRIHYDROXY-3,4A,7,7,10A-PENTAMETHYL-1H-NAPHTHO[2,1-B]PYRAN-1-ONE;10a-beta,10b-alpha))-10-alph;1-b)pyran-1-one,dodecahydro-5-(acetyloxy)-3-ethenyl-3,4a,7,7,10a-1h-naphtho(;pentamethyl-6,10,10b-trihydroxy-,(3r-(3-alpha,4a-beta,5-beta,6-beta,6a-alpha,;FORSKOLIN FROM COLEUS FORSKOHLII. CAS No. 66575-29-9. Product ID: PIPE-0355. Molecular formula: C22H34O7. Mole weight: 410.5. EINECS: 266-410-9. SMILES: CC(=O)O[C@H]1[C@H]([C@@H]2[C@]([C@H](CCC2(C)C)O)([C@@]3([C@@]1(O[C@@](CC3=O)(C)C=C)C)O)C)O. Appearance: Powder. Category: Natural Extract. |  |
| Forskolin | Forskolin is a diterpene isolated from Coleus forskohlii, possessing vasodilating and cardiostimulatory properties. Forskolin resensitizes cell receptors by activating the enzyme adenylyl cyclase and increasing the intracellular levels of cAMP. Group: Biochemicals. Alternative Names: (3R, 4aR, 5S, 6S, 6aS, 10S, 10aR, 10bS)-5-(Acetyloxy)-3-ethenyldodecahydro-6, 10, 10b-trihydroxy-3, 4a, 7, 7, 10a-pentamethyl-1H-Naphtho[2, 1-b]pyran-1-one; (-)-Forskolin; Coleonol; Colforsin; ForsLean; HL 362; L 75-1362B; NSC 357088. Grades: Highly Purified. CAS No. 66575-29-9. Pack Sizes: 25mg. US Biological Life Sciences. | Worldwide |
| Forskolin (7b-Acetoxy-8,13-epoxy-1a,6b,9a-trihydroxy- labd-14-ene-11-one, Coleonol, Colforsin) | Forskolin is a naturally occurring diterpene from the Indian plant, Coleus forskohlii, that works as an activator of adenylate cyclase resulting in an increase in the intracellular concentration of cAMP. Group: Biochemicals. Grades: Highly Purified. CAS No. 66575-29-9. Pack Sizes: 50mg. US Biological Life Sciences. | Worldwide |
| Forskolin Hemisuccinate | Forskolin Hemisuccinate is a derivative fo Forskolin (F701800), a diterpene isolated from Coleus forskohlii, possessing vasodilating and cardiostimulatory properties. Forskolin Hemisuccinate was found to inhibit E-selectin gene transcription through a cAMP-dependent protein kinase pathway. Group: Biochemicals. Alternative Names: 1-[(3R, 4aR, 5S, 6S, 6aS, 10S, 10aR, 10bS)-3-Ethenyldodecahydro-6, 10, 10b-trihydroxy-3, 4a, 7, 7, 10a-pentamethyl-1-oxo-1H-naphtho[2, 1-b]pyran-5-yl] Ester Butanedioic Acid; 1H-Naphtho[2,1-b]pyran, Butanedioic Acid Deriv. Grades: Highly Purified. CAS No. 83797-56-2. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
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