Malvaceae Extract

Hibiscus mutabilis polysaccharide is a polysaccharide derived from Hibiscus mutabilis.

Hibiscus sabdariffa polysaccharide is a polysaccharide derived from Hibiscus sabdariffa.

Abutilon indicum polysaccharide is a polysaccharide derived from Abutilon indicum.

Hibiscus syriacus polysaccharide is a polysaccharide derived from Hibiscus syriacus.

Abutilon theophrasti polysaccharide is a polysaccharide derived from Abutilon theophrasti.

Althaea rosea polysaccharide is a polysaccharide derived from Althaea rosea.

(S)-Mansonone E is the S-configurational form of Mansonone E (HY-118401). Mansonone E acts as an insecticide.

β-Sitosterol 3-O-galactopyranoside is a steroidal glycoside that can be found in the leaves of Hibiscus sabdariffa.

Feruloylaspartic acid (Compound 19) is an N-cinnamoyl-L-amino acid, and it is a key astringent compound responsible for the puckering sensation in roasted cocoa beans. Feruloylaspartic acid elicits a puckering, astringent oral sensation without exhibiting a bitter taste.

Cryptolepine is an orally active multi-potent alkaloid with anti-cancer, anti-bacterial, anti-viral, anti-malarial, anti-inflammatory, anti-hyperglycemic, relieve pain and other properties. Cryptolepine acts as an inhibitor of c-Myc, mTOR, NF-κB, HIF-1, MAPK and an activator of AMPKα1/2. It intercalates into DNA, inhibits topoisomerase II (Top II), disrupts mitochondrial dynamics and induces apoptosis. Cryptolepine also exhibits anti-plasmodial and cholinesterase inhibitory activities. Cryptolepine can be used in research related to tumors (melanoma, hepatocellular carcinoma, mammary adenocarcinoma, etc.), malaria, inflammatory diseases and diabetes, particularly in studies focused on inhibiting tumor growth and anti-plasmodial infection.

(±)-Dihydrodehydrodiconiferyl alcohol is a natural lignan.

Floramanoside F is a type of flavonol glycoside compound. Floramanoside F has a moderate free radical scavenging effect, with a SC₅₀ value of 25.1 μM. Floramanoside F has a relatively weak inhibitory activity on aldose reductase, with a IC₅₀ value greater than 100 μM. Floramanoside F has strong binding affinity with key target enzymes of type 1 diabetic nephropathy (T1DN) (Fasn, Cyp2e1, Cyp4a32), and can inhibit lipid accumulation and oxidative stress, thereby alleviating renal inflammation and fibrosis. Floramanoside F can be used to study type 1 diabetic nephropathy and diabetic complications.

trans-Ditiliroside is a natural flavonoid.

(2Z,6E)-Farnesyl acetate is a natural sesquiterpene.

Durianol A is a natural coumarin.

Naringenin 7-O-β-D-glucuronide methyl ester is a natural flavonoid.

Vavain is a natural flavonoid.

Cavaol E is a natural phenolic compound.

Flindulatin is a flavone that can be isolated from C. spinosa.