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Category of Chemicals

Natural quinones

Quinones are organic compounds known for their distinct chemical structure, which includes a conjugated ring system with carbonyl groups. They are commonly found in nature and are crucial in biological processes. Quinones have diverse applications, including serving as redox cofactors in enzymatic reactions, participating in electron transport chains, and acting as precursors for the synthesis of various compounds, including synthetic dyes. Additionally, some quinones exhibit antioxidant properties and have potential health benefits, making them a subject of interest in medicine and nutrition.

Products of Natural quinones
CAS No.Product NameMolecular Formula
103646-20-41,4-Dihydro-3-hydroxy-1,4-dioxo-2-naphthalenecarboxamideC11H7NO4
120278-25-34-HydroxysapriparaquinoneC20H26O4
132242-52-5Rubioncolin CC27H22O6
142763-37-93,4-DidehydrosapriparaquioneC20H24O3
142950-86-5Triptoquinonoic acid AC20H24O4
15297-92-4Dehydro-alpha-lapachoneC15H12O3
17397-93-2Tanshinone IIBC19H18O4
20175-84-2IsodiospyrinC22H14O6
20958-18-3DihydrotanshinoneC18H14O3
21764-41-0TaxoquinoneC20H28O4
21887-01-4HorminoneC20H28O4
2215-96-52,6-Dimethoxy-1-acetonylquinolC11H14O5
22333-58-09-Hydroxy-alpha-lapachoneC15H14O4
250691-57-7SalvisyrianoneC20H24O3
260397-58-8Dihydroisotanshinone IIC18H14O3
269742-39-416-Acetoxy-7-O-acetylhorminoneC24H32O7
27270-89-9PhyllostineC7H6O4
27468-20-8DeoxyneocryptotanshinoneC19H22O3
35241-80-69-Methoxy-alpha-lapachoneC16H16O4
4707-33-9alpha-LapachoneC15H14O3
56473-67-74,9-Dihydroxy-alpha-lapachoneC15H14O5
60263-06-1Ethyl (1-hydroxy-4-oxocyclohexa-2,5-dien-1-yl)acetate C10H12O4
630057-39-5Neoprzewaquinone AC36H28O6
65907-75-7Danshenxinkun AC18H16O4
6812-87-9RoyleanoneC20H28O3
76843-23-7Przewaquinone AC19H18O4
77029-83-5HypocrellinC30H26O10
85122-21-02-MethoxystypandroneC14H12O5
87205-99-0Dihydrotanshinone IC18H14O3



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