Isoprenoids - Natural Products

Cat.No. Product Name Information

BCC8200 Linalyl Acetate Linalyl acetate is the principal components of many plant essential oils with potentially anti-inflammatory activity. (CAS NO.: 115-95-7) Linalyl Acetate chemical structure

BCC8302 Beta-Pinene Botanical source: (CAS NO.: 127-91-3) Beta-Pinene chemical structure

BCC8259 Teucrin A Botanical source: (CAS NO.: 12798-51-5) Teucrin A chemical structure

BCC8156 Cucurbitacin E-2-O-Glucoside Botanical source: 1 Citrullus sp. 2 Cucumis sp. 3 Cucurbita sp. 4 Gratiola sp. 5 Iberis sp. (CAS NO.: 1398-78-3) Cucurbitacin E-2-O-Glucoside chemical structure

Cucurbitacin E-2-O-Glucoside chemical structure

BCC8328 18alpha-Glycyrrhetinic acid Botanical source: (CAS NO.: 1449-05-4) 18alpha-Glycyrrhetinic acid chemical structure

BCN8540 D-Isomenthol Botanical source: (CAS NO.: 23283-97-8) D-Isomenthol chemical structure

BCC8240 Protoaescigenin Botanical source: (CAS NO.: 20853-07-0) Protoaescigenin chemical structure

BCC8237 Primulic Acid 2 Botanical source: (CAS NO.: 208599-88-6) Primulic Acid 2 chemical structure

BCC2439 Cucurbitacin I Cucurbitacin I is a natural selective inhibitor of JAK2/STAT3, with potent anti-cancer activity. (CAS NO.: 2222-07-3) Cucurbitacin I chemical structure

BCN8546 Cnicin Botanical source: 1 Centaurea sp. (CAS NO.: 24394-09-0) Cnicin chemical structure

BCN8381 Gummiferin Carboxyatractyloside dipotassium is a toxic natural product, acts as an inhibitor of ADP/ATP carrier, inhibits mitochondrial ADP/ATP transport. (CAS NO.: 33286-30-5) Gummiferin chemical structure

BCC7546 Valerenic acid Botanical source: (CAS NO.: 3569-10-6) Valerenic acid chemical structure

BCC7712 Z-Guggulsterone Z-guggulsterone, a constituent of Indian Ayurvedic medicinal plant Commiphora mukul, inhibits the growth of human prostate cancer cells by causing apoptosis. Z-guggulsterone inhibits angiogenesis by suppressing the VEGF–VEGF-R2–Akt signaling axis. (CAS NO.: 39025-23-5) Z-Guggulsterone chemical structure

BCC8181 Guggulsterone E Botanical source: (CAS NO.: 39025-24-6) Guggulsterone E chemical structure

BCC8195 Larixyl acetate Botanical source: (CAS NO.: 4608-49-5) Larixyl acetate chemical structure

BCC8897 (-)-Borneol (-)-Borneol has a highly efficacious positive modulating action at GABA receptor with an EC50 of 237 μM. (CAS NO.: 464-45-9) (-)-Borneol chemical structure

BCC8208 Marrubiin Marrubiin, isolated from Marrubium vulgare, exhibits vasorelaxant and antioedematogenic activity. Marrubiin alleviates diabetic symptoms in animals. (CAS NO.: 465-92-9) Marrubiin chemical structure

BCC8239 Proscillaridin A Proscillaridin A is a potent poison of topoisomerase I/II activity with IC50 values of 30 nM and 100 nM, respectively. (CAS NO.: 466-06-8) Proscillaridin A chemical structure

BCC8155 Convallatoxin Convallatoxin is a cardiac glycoside isolated from Adonis amurensis Regel et Radde. Convallatoxin ameliorates colitic inflammation via activation of PPARγ and suppression of NF-κB. Convallatoxin is a P-glycoprotein (P-gp) substrate and recognized Val982 as an important amino acid involved in its transport. Convallatoxin is an enhancer of ligand-induced MOR endocytosis with high potency and efficacy. Anti-inflammatory and anti-proliferative properties. (CAS NO.: 508-75-8) Convallatoxin chemical structure

BCN8277 Yamogenin Yamogenin (Neodiosgenin) is a diastereomer of diosgenin. Yamogenin (Neodiosgenin) antagonizes the activation of the liver X receptor (LXR) in luciferase ligand assay. Yamogenin (Neodiosgenin) inhibits triacylglyceride (TG) accumulation through the suppression of gene expression of fatty acid synthesis in HepG2 hepatocytes. (CAS NO.: 512-06-1) Yamogenin chemical structure

BCC8118 Anisatin Botanical source: 1 Juniperus sp. 2 Persicaria sp. 3 Saxifraga sp. (CAS NO.: 5230-87-5) Anisatin chemical structure

BCC8145 Chamazulene Botanical source: 1 Chamaemelum sp. 2 Chamomilla sp. 3 Dendranthema sp. 4 Ferula sp. 5 Tanacetum sp. (CAS NO.: 529-05-5) Chamazulene chemical structure

BCC8271 α-Thujone α-Thujone is a monoterpene isolated from Thuja occidentalis essential oil with potent anti-tumor activities. α-Thujone is a reversible modulator of the GABA type A receptor and the IC50 for α-Thujone is 21 μM in suppressing the GABA-induced currents. α-Thujone induces ROS accumulation-dependent cytotoxicity, also induces cell apoptosis and autophagy. α-Thujone has antinociceptive, insecticidal, and anthelmintic activity, and easily penetrates the blood-brain barrier. (CAS NO.: 546-80-5) α-Thujone chemical structure

BCC8296 Androstenedione Botanical source: (CAS NO.: 63-05-8) Androstenedione chemical structure

BCC5069 Ouabain Ouabain is a selective Na+/K+, -ATPase inhibitor, binds to α2 /α3 subunit with Ki of 41 nM/15 nM. (CAS NO.: 630-60-4) Ouabain chemical structure