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Ψ-Tectorigenin: Difference between revisions

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{{lowercase title}}
{{chembox {{chembox
| verifiedrevid = 401016194
| Name = Psi-tectorigenin
| Name = ψ-Tectorigenin
| ImageFile = Psi-tectorigenin.PNG
| ImageFile = Psi-tectorigenin.svg
| ImageSize = 200px | ImageSize = 220px
| IUPACName = 5,7-dihydroxy-3-(4-hydroxyphenyl)-8-methoxychromen-4-one
| ImageFile1 = Psi-tectorigenin-3D-balls.png
| OtherNames = Isotectorigenin<br>Pseudotectorigenin<br>5,7,4'-Trihydroxy-8-methoxyisoflavone
| ImageSize1 = 220
| Section1 = {{Chembox Identifiers
| ImageAlt1 = Psi-Tectorigenin molecule
| IUPACName = 4′,5,7-Trihydroxy-8-methoxyisoflavone
| SystematicName = 5,7-Dihydroxy-3-(4-hydroxyphenyl)-8-methoxy-4''H''-1-benzopyran-4-one
| OtherNames = Isotectorigenin<br>Pseudotectorigenin
|Section1={{Chembox Identifiers
| CASNo = 13111-57-4 | CASNo = 13111-57-4
| CASNo_Ref = {{cascite|correct|CAS}}
| UNII = 8HXB4THX7F
| UNII_Ref = {{fdacite|correct|FDA}}
| PubChem = 5353911 | PubChem = 5353911
| ChEMBL = 242741
| Beilstein = | Beilstein =
| SMILES = COC1=C(C=C(C2=C1OC=C(C2=O)C3=CC=C(C=C3)O)O)O | SMILES = COC1=C(C=C(C2=C1OC=C(C2=O)C3=CC=C(C=C3)O)O)O
| ChemSpiderID = 4510255
| StdInChI = 1S/C16H12O6/c1-21-15-12(19)6-11(18)13-14(20)10(7-22-16(13)15)8-2-4-9(17)5-3-8/h2-7,17-19H,1H3
| StdInChIKey = UYLQOGTYNFVQQX-UHFFFAOYSA-N

}} }}
| Section2 = {{Chembox Properties |Section2={{Chembox Properties
| C=16 | H=12 | O=6
| Formula = C<sub>16</sub>H<sub>12</sub>O<sub>6</sub>
| MolarMass = 300.26 g/mol
| ExactMass = 300.063388
| Appearance = | Appearance =
| Density = | Density =
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| BoilingPt = | BoilingPt =
| Solubility = }} | Solubility = }}
| Section3 = {{Chembox Hazards |Section3={{Chembox Hazards
| MainHazards = | MainHazards =
| FlashPt = | FlashPt =
| Autoignition = }} | AutoignitionPt = }}
}} }}
'''Psi-tectorigenin''' is an ], a type of flavonoid. It can be isolated from ''] sp''<ref></ref>, '']'', '']'' and '']'' sp. No. 644<ref></ref>.


'''ψ-Tectorigenin''' is an ], a type of flavonoid. It can be isolated from '']'', '']''. It can also be isolated from the bacterium ''] sp'',<ref>{{cite journal | pmid = 1917707 | year = 1991 | last1 = Imoto | first1 = M | last2 = Shimura | first2 = N | last3 = Umezawa | first3 = K | title = Inhibition of epidermal growth factor-induced activation of phospholipase C by psi-tectorigenin | volume = 44 | issue = 8 | pages = 915–7 | journal = The Journal of Antibiotics | doi=10.7164/antibiotics.44.915| doi-access = free }}</ref> and from the mold '']'' sp. No. 644.<ref></ref>
==References==

==See also==
* ], a related favonoid

== References ==
{{reflist}} {{reflist}}


{{isoflavone}} {{isoflavone}}


{{DEFAULTSORT:Tectorigenin, psi-}}
]
] ]
]
] ]



{{Polyphenol-stub}} {{Aromatic-stub}}

Latest revision as of 19:08, 16 September 2023

ψ-Tectorigenin
Psi-Tectorigenin molecule
Names
IUPAC name 4′,5,7-Trihydroxy-8-methoxyisoflavone
Systematic IUPAC name 5,7-Dihydroxy-3-(4-hydroxyphenyl)-8-methoxy-4H-1-benzopyran-4-one
Other names Isotectorigenin
Pseudotectorigenin
Identifiers
CAS Number
3D model (JSmol)
ChEMBL
ChemSpider
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C16H12O6/c1-21-15-12(19)6-11(18)13-14(20)10(7-22-16(13)15)8-2-4-9(17)5-3-8/h2-7,17-19H,1H3Key: UYLQOGTYNFVQQX-UHFFFAOYSA-N
SMILES
  • COC1=C(C=C(C2=C1OC=C(C2=O)C3=CC=C(C=C3)O)O)O
Properties
Chemical formula C16H12O6
Molar mass 300.266 g·mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkverify (what is  ?) Infobox references
Chemical compound

ψ-Tectorigenin is an O-methylated isoflavone, a type of flavonoid. It can be isolated from Belamcanda chinensis, Dalbergia sissoo. It can also be isolated from the bacterium Nocardiopsis sp, and from the mold Stemphilium sp. No. 644.

See also

References

  1. Imoto, M; Shimura, N; Umezawa, K (1991). "Inhibition of epidermal growth factor-induced activation of phospholipase C by psi-tectorigenin". The Journal of Antibiotics. 44 (8): 915–7. doi:10.7164/antibiotics.44.915. PMID 1917707.
  2. Psi-tectorigenin on knapsack
Isoflavones and their glycosides
Isoflavones
O-methylated isoflavones
Glycosides
Prenylated isoflavones
Pyranoisoflavones
Derivatives
Synthetic


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