Rhaphidophora pinnata (Lf) Schott leaves include alkaloids, saponins, flavonoids, tannins, steroids/triterpenoids, and glycosides, all of which are secondary metabolites with antioxidant, cholesterol-lowering, and anti-diabetic properties. Using n-hexane, ethyl acetate, and ethanol as solvents, layered percolation was used to extract. Anti-cholesterol activity using the Lieberman-Burchard Test and the antioxidant DPPH method (1,1-diphenyl-2-picryil hidrazin). The absorbance of antioxidant, antidiabetic, and anti-cholesterol activity was measured at a maximum wavelength of 516, 400, and 626 nm. The results of measurements of antioxidant activity, extracts of n-hexane, ethyl acetate, and ethanol of Rhaphidophora pinnata leaves obtained values of 516, 400, and 626 nm. The results of measurements of antioxidant activity, extracts of n-hexane, ethyl acetate, and ethanol of Rhaphidophora pinnata leaves obtained IC50 values of 74.2413; 27.8658; and 396,9975 µg/ml. The anti-cholesterol activity of the n-hexane extract with a concentration of 300 µg/ml was able to reduce cholesterol by 29.3395 % and ethyl acetate extract with a concentration of 35 µg/ml was 65.2030 %. Meanwhile, the ethanol extract of 100 µg/ml was 25.1489 %. Comparisons of fenofibrate and simvastatin with a concentration of 22.5 µg/ml of 65.8890 % and 76.3781 %. The results of the measurement of the antidiabetic activity of the extracts of n-hexane, ethyl acetate, and ethanol from the leaves of Rhaphidophora pinnata, aromas, and quercetin with IC50 values of 546.1511; 26.6306; 50.1951; 9.6862 and 2.4850 µg/ml. Ethyl acetate extract of Rhaphidophora pinnata leaves has an anti-cholesterol activity that is almost the same as fenofibrate at a concentration of 35 µg/ml.