Tectorigenin

Bezeichnung:Tectorigenin

CAS-Nr548-77-6

Englisch Name:Tectorigenin

CBNumberCB11040716

SummenformelC16H12O6

Molgewicht300.26

MOL-Datei548-77-6.mol

Tectorigenin physikalisch-chemischer Eigenschaften

Schmelzpunkt	225-226°
Siedepunkt	361.5°C (rough estimate)
Dichte	1.512
Brechungsindex	1.4600 (estimate)
storage temp.	Sealed in dry,2-8°C
Löslichkeit	DMSO : 150 mg/mL (499.57 mM; Need ultrasonic and warming)
Aggregatzustand	powder to crystal
pka	6.49±0.20(Predicted)
Farbe	White to Orange to Green
BRN	305601
InChI	InChI=1S/C16H12O6/c1-21-16-11(18)6-12-13(15(16)20)14(19)10(7-22-12)8-2-4-9(17)5-3-8/h2-7,17-18,20H,1H3
InChIKey	OBBCRPUNCUPUOS-UHFFFAOYSA-N
SMILES	C1OC2=CC(O)=C(OC)C(O)=C2C(=O)C=1C1=CC=C(O)C=C1
CAS Datenbank	548-77-6

Sicherheit

WGK Germany	3
RTECS-Nr.	NR2400000
HS Code	2932.99.6100

Gefahreninformationscode (GHS)

Tectorigenin Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung
Tectorigenin is an isoflavone that exists in numerous plant resources, and it is especially abundant in Belamcandae Rhizoma and Puerariae flos, which both have the effects of clearing away heat, removing toxic substances, relieving sore throat, and reducing swelling. As one of the most important active ingredients, the pharmacological effects of tectorigenin have been demonstrated by an increasing number of investigators. Due to its extensive pharmacological activities, including anticancer, antioxidation, hepatoprotection, anti-inflammation, etc., tectorigenin has received a large amount of attention[1].
Occurrence
Tectorigenin, a methoxy isoflavone with three hydroxyl groups, is chemically noted as 5,7-dihydroxy-3-(4-hydroxyphenyl)-6-methoxy-4H-chromen-4-one. As a bioactive compound, tectorigenin is found in several plant species, most notably in the rhizomes of Belamcanda chinensis (L.) DC., a traditional Chinese medicine (TCM) named Belamcandae Rhizoma. The Iris family is the major source of tectorigenin, and many Iridaceous plants, such as Iris spuria L. (Calizona), Iris tectorum Maxim, Iris japonica Thunb., Iris dichotoma Pall., Iris germanica L., Iris unguicularis Poiret, Iris loczyi Kan., Iris kashmiriana Baker, Iris crocea Jacq. ex R. C. Foster, Iris ensata Thunb., Iris germanica L., Iris hungarica Waldst. et Kit., Iris confusa Sealy, and Iris pseudacorus L. contain abundant tectorigenin, so tectorigenin is also known as iris flavone. Tectorigenin also exists in some leguminous plants, such as the flowers of Pueraria lobata (Willd.) Ohwi, Pueraria thomsonii Benth., and Pueraria thunbergiana Benth. are also TCM called Puerariae Flos. Tectorigenin was isolated from the leaves of Dalbergia odorifera T. Chen, the heartwood of Dalbergia parviflora Roxb., and the roots of Euchresta formosana (Hayata) Ohwi as well. Moreover, some plants in other families also contain tectorigenin, including Codonopsis pilosula (Franch.) Nannf. (Campanulaceae), Morus alba L. (Moraceae), Viola hondoensis W. Becker et H. Boissieu. (Violaceae), and Eleocharis dulcis (Burm. f.) Trin. ex Hensch. (Cyperaceae)[1].
Verwenden
Tectorigenin is identified as an α-glucosidase inhibitors. Potent lactate dehydrogenase (LDH) inhibitor.
Definition
ChEBI: A methoxyisoflavone that is isoflavone substituted by a methoxy group at position 6 and hydroxy groups at positions 5, 7 and 4' respectively.
Synthesis Reference(s)
Synthetic Communications, 38, p. 525, 2008 DOI: 10.1080/00397910701796725
Einzelnachweise
[1] Juan Rong. “Tectorigenin: A Review of Its Sources, Pharmacology, Toxicity, and Pharmacokinetics.” Molecules 28 15 (2023).

Tectorigenin Upstream-Materialien And Downstream Produkte

Tectorigenin Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

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