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PRUNINDIHYDROCHALCONE

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Category Human immunodeficiency Virus (HIV)
CAS 4192-90-9
Description Trilobatin, coming from the herbs of Lithocarpus pachyphyllus, potentially inhibits the LPS-induced inflammatory response by suppressing the NF-κB signaling pathway. It increased superoxide dismutase (SOD) activity. Besides, Trilobatin is a potential effective α-glucosidase inhibitor for management of postprandial hyperglycemia with less side effect.
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Product Information

Synonyms Prunindihydrochalcone; 1-[4-(β-D-Glucopyranosyloxy)-2,6-dihydroxyphenyl]-3-(4-hydroxyphenyl)-1-propanone; Phloretin 4'-glucoside; p-Phloridzin; Trilobatin
IUPAC Name 1-[2,6-dihydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3-(4-hydroxyphenyl)propan-1-one
Molecular Weight 436.4
Molecular Formula C21H24O10
Canonical SMILES C1=CC(=CC=C1CCC(=O)C2=C(C=C(C=C2O)OC3C(C(C(C(O3)CO)O)O)O)O)O
InChI InChI=1S/C21H24O10/c22-9-16-18(27)19(28)20(29)21(31-16)30-12-7-14(25)17(15(26)8-12)13(24)6-3-10-1-4-11(23)5-2-10/h1-2,4-5,7-8,16,18-23,25-29H,3,6,9H2/t16-,18-,19+,20-,21-/m1/s1
InChIKey GSTCPEBQYSOEHV-QNDFHXLGSA-N
Boiling Point 787.9±60.0 °C at 760 mmHg
Melting Point 163 °C
Flash Point 277.1±26.4 °C
Purity >98%
Density 1.6±0.1 g/cm3
Solubility In vitro:
10 mM in DMSO
Appearance Powder
Application Anti-inflammatory
Storage 4°C, protect from light
* In solvent :
-80°C, 6 months
-20°C, 1 month (protect from light)
Complexity 569
Exact Mass 436.13694696
Index Of Refraction 1.686
In Vitro Trilobatin protects against oxidative injury in neuronal PC12 cells through regulating mitochondrial reactive oxygen species (mtROS) homeostasis in the first time, which is, at least partly, mediated through the AMPK/Nrf2/Sirt3 signaling pathway.
PSA 177.14000
Target HIV; SGLT
Vapor Pressure 0.0±2.9 mmHg at 25°C
XLogP3-AA 1.2

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