Product Name

  • Name

    Tectoridin

  • EINECS
  • CAS No. 611-40-5
  • Density 1.609 g/cm3
  • Solubility
  • Melting Point 261.8-263.2oC
  • Formula C22H22O11
  • Boiling Point 798.1 °C at 760 mmHg
  • Molecular Weight 462.41
  • Flash Point 279.7 °C
  • Transport Information
  • Appearance
  • Safety
  • Risk Codes
  • Molecular Structure Molecular Structure of 611-40-5 (Tectoridin)
  • Hazard Symbols
  • Synonyms Tectoridin(7CI,8CI);Shekanin;Tectorigenin 7-O-b-D-glucopyranoside;Tectoridin;4',5-Dihydro-6-methoxy-7-(o-glucoside)isoflavone;
  • PSA 179.28000
  • LogP 0.05850

Tectoridin Specification

The IUPAC name of Tectoridin is 5-hydroxy-3-(4-hydroxyphenyl)-6-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one. With the CAS registry number 611-40-5, it is also named as 4',5-Dihydro-6-methoxy-7-(o-glucoside)isoflavone. The product's classification codes are Drug / Therapeutic Agent; Natural Product. Besides, it is the 7-glucoside of tectorigenin, which can be isolated from flowers of Pueraria thunbergiana. In addition, its molecular formula is C22H22O11 and molecular weight is 462.40.

The other characteristics of Tectoridin can be summarized as: (1)ACD/LogP: 0.29; (2)# of Rule of 5 Violations: 2; (3)ACD/LogD (pH 5.5): 0.2; (4)ACD/LogD (pH 7.4): -1.02; (5)ACD/BCF (pH 5.5): 1; (6)ACD/BCF (pH 7.4): 1; (7)ACD/KOC (pH 5.5): 27.55; (8)ACD/KOC (pH 7.4): 1.69; (9)#H bond acceptors: 11; (10)#H bond donors: 6; (11)#Freely Rotating Bonds: 11; (12)Polar Surface Area: 109.37 Å2; (13)Index of Refraction: 1.694; (14)Molar Refractivity: 110.35 cm3; (15)Molar Volume: 287.2 cm3; (16)Polarizability: 43.74×10-24cm3; (17)Surface Tension: 85.1 dyne/cm; (18)Density: 1.609 g/cm3; (19)Flash Point: 279.7 °C; (20)Enthalpy of Vaporization: 121.71 kJ/mol; (21)Boiling Point: 798.1 °C at 760 mmHg; (22)Vapour Pressure: 7.19E-27 mmHg at 25 °C.

People can use the following data to convert to the molecule structure.
(1)SMILES: O=C4C(/c1ccc(O)cc1)=C\Oc3cc(O[C@@H]2O[C@@H]([C@@H](O)[C@H](O)[C@H]2O)CO)c(OC)c(O)c34
(2)InChI: InChI=1/C22H22O11/c1-30-21-13(32-22-20(29)19(28)17(26)14(7-23)33-22)6-12-15(18(21)27)16(25)11(8-31-12)9-2-4-10(24)5-3-9/h2-6,8,14,17,19-20,22-24,26-29H,7H2,1H3/t14-,17-,19+,20-,22-/m1/s1
(3)InChIKey: CNOURESJATUGPN-UDEBZQQRBO
(4)Std. InChI: InChI=1S/C22H22O11/c1-30-21-13(32-22-20(29)19(28)17(26)14(7-23)33-22)6-12-15(18(21)27)16(25)11(8-31-12)9-2-4-10(24)5-3-9/h2-6,8,14,17,19-20,22-24,26-29H,7H2,1H3/t14-,17-,19+,20-,22-/m1/s1
(5)Std. InChIKey: CNOURESJATUGPN-UDEBZQQRSA-N

The toxicity data is as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD50 intraperitoneal 4200mg/kg (4200mg/kg) BEHAVIORAL: ALTERED SLEEP TIME (INCLUDING CHANGE IN RIGHTING REFLEX)

BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)

LUNGS, THORAX, OR RESPIRATION: DYSPNEA
Nippon Yakurigaku Zasshi. Japanese Journal of Pharmacology. Vol. 64, Pg. 186, 1968.

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