Quinones - Natural Products

Cat.No. Product Name Information

BCN4806 4-Hydroxysapriparaquinone Botanical source: The herbs of Salvia prionitis Hance (CAS NO.: 120278-25-3) 4-Hydroxysapriparaquinone chemical structure

4-Hydroxysapriparaquinone chemical structure

BCN7871 Rubioncolin C Botanical source: The roots and rhizomes of Rubia podantha. (CAS NO.: 132242-52-5) Rubioncolin C chemical structure

BCN6781 Triptoquinone A Botanical source: The roots of Tripterygium wilfordii Hook.f. (CAS NO.: 142950-86-5) Triptoquinone A chemical structure

BCN2729 Primin Primin is a natural product stored in trichomes on leaves and stems of Primula obconica, with antimicrobial and antitumour properties. (CAS NO.: 15121-94-5) Primin chemical structure

BCN1683 Dehydro-alpha-lapachone Botanical source: The roots of Radermachera sinica (CAS NO.: 15297-92-4) Dehydro-alpha-lapachone chemical structure

Dehydro-alpha-lapachone chemical structure

BCN6895 Prerubialatin Botanical source: The herbs of Rubia cordifolia (CAS NO.: 1667718-89-9) Prerubialatin chemical structure

BCN4883 Isodiospyrin Botanical source: The herbs of Diospyros morrisiana (CAS NO.: 20175-84-2) Isodiospyrin chemical structure

BCN6660 Taxoquinone Botanical source: The herbs of Salvia deserta Schang. (CAS NO.: 21764-41-0) Taxoquinone chemical structure

BCN5052 2,6-Dimethoxy-1-acetonylquinol Botanical source: The barks of Ailanthus altissima (CAS NO.: 2215-96-5)

2,6-Dimethoxy-1-acetonylquinol chemical structure

BCN8249 Lucidin 3-O-glucoside Botanical source: The root of Rubia cordifolia (CAS NO.: 22255-29-4) Lucidin 3-O-glucoside chemical structure

BCN5060 9-Hydroxy-alpha-lapachone Botanical source: The herbs of Catalpa ovata (CAS NO.: 22333-58-0) 9-Hydroxy-alpha-lapachone chemical structure

BCN2665 Acetylshikonin Acetylshikonin, derived from the root of Lithospermum erythrorhizon, has anti-cancer and antiinflammation activity. Acetylshikonin is a non-selective cytochrome P450 inhibitor against all P450s (IC50 values range from 1.4-4.0 μM). Acetylshikonin is an AChE inhibitor and exhibits potent antiapoptosis activity. (CAS NO.: 24502-78-1) Acetylshikonin chemical structure

BCN2310 Dimethylacrylshikonin Botanical source: The roots of Lithosperraum erythrorhizon Sieb. et Zucc. (CAS NO.: 23444-70-4) Dimethylacrylshikonin chemical structure

Dimethylacrylshikonin chemical structure

BCN4821 Salvisyrianone Botanical source: The herbs of Salvia syriaca (CAS NO.: 250691-57-7) Salvisyrianone chemical structure

BCN5390 Luteosporin Botanical source: The body of Cordyceps sienesis (Berkeley) Saccardo (CAS NO.: 2530-39-4) Luteosporin chemical structure

BCN4773 Phyllostine Botanical source: The Pencillium urticae (CAS NO.: 27270-89-9) Phyllostine chemical structure

BCN5954 Coenzyme Q10 Coenzyme Q10 is an essential cofactor of the electron transport chain and a potent antioxidant agent. (CAS NO.: 303-98-0) Coenzyme Q10 chemical structure

BCN7912 3,3'-Bilawsone Botanical source: The herbs of Lomatia ferruginea (CAS NO.: 33440-64-1) 3,3'-Bilawsone chemical structure

BCN2767 Beta,beta-Dimethylacrylalkannin β,β-Dimethylacrylalkannin is a napthoquinone isolated from Arnebia nobilis Reichb.f, increases collagen and involucrin content in skin cells. (CAS NO.: 34539-65-6)

Beta,beta-Dimethylacrylalkannin chemical structure

BCN5289 9-Methoxy-alpha-lapachone Botanical source: The stems of Catalpa ovata (CAS NO.: 35241-80-6) 9-Methoxy-alpha-lapachone chemical structure

BCN5299 Deoxylapachol Botanical source: The leaves of Catalpa ovata G. Don. (CAS NO.: 3568-90-9) Deoxylapachol chemical structure

BCN7986 Isoshinanolone Botanical source: The herbs of Plumbago zeylanica (CAS NO.: 39626-91-0) Isoshinanolone chemical structure

BCN3006 Deoxyshikonin Deoxyshikonin is isolated from Lithospermum erythrorhizon Sieb with antitumor activity. Deoxyshikonin increases the expression of VEGF-C and VEGF-A mRNA in HMVEC-dLy, promotes HIF-1α and HIF-1β subunit interaction and binds to specific DNA sequences targeted by HIF, indicates a prolymphangiogenesis as well as a proangiogenesis effect in vitro. Deoxyshikonin shows significant synergic antimicrobial activity against S. pneumonia (MIC=17 μg/mL), also shows significantly inhibitory activities against MRSA. (CAS NO.: 43043-74-9) Deoxyshikonin chemical structure

BCN5520 alpha-Lapachone Botanical source: The barks of Catalpa ovata (CAS NO.: 4707-33-9) alpha-Lapachone chemical structure

BCN7985 Droserone Botanical source: The herbs of Plumbago zeylanica (CAS NO.: 478-40-0) Droserone chemical structure