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  • Product Name: Trilobatin
  • Price: ¥Inquiry/5mg
  • Purity: 98.0%
  • Stocking Period: 10 Day
  • Contact: Xueping-Zheng


4192-90-9

4192-90-9 structure
4192-90-9 structure
  • Name: Trilobatin
  • Chemical 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
  • CAS Number: 4192-90-9
  • Molecular Formula: C21H24O10
  • Molecular Weight: 436.409
  • Catalog: Natural product Chalcone
  • Create Date: 2018-08-30 09:00:22
  • Modify Date: 2024-01-02 16:05:23
  • Trilobatin, a natural sweetener derived from Lithocarpus polystachyus Rehd[1], Trilobatin is an HIV-1 entry inhibitor targeting the HIV-1 Gp41 envelope[2]. Neuroprotective effects[1]. Trilobatin is also a SGLT1/2 inhibitor that selectively induces the proliferation of human hepatoblastoma cells[3].

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
Synonyms UNII:23298I791N
1-Propanone, 1-[4-(β-D-glucopyranosyloxy)-2,6-dihydroxyphenyl]-3-(4-hydroxyphenyl)-
3,5-Dihydroxy-4-[3-(4-hydroxyphenyl)propanoyl]phenyl β-D-glucopyranoside
p-Phloridzin
phloretin-4-D-glucoside
T6OTJ BOR CQ EQ DV2R DQ&& CQ DQ EQ F1Q &&β-D-Gluco Form
p-Phlorizin
1-Propanone, 1-(4-(β-D-glucopyranosyloxy)-2,6-dihydroxyphenyl)-3-(4-hydroxyphenyl)-
Trilobatin
1-(4-(β-D-Glucopyranosyloxy)-2,6-dihydroxyphenyl)-3-(4-hydroxyphenyl)-1-propanone
Description Trilobatin, a natural sweetener derived from Lithocarpus polystachyus Rehd[1], Trilobatin is an HIV-1 entry inhibitor targeting the HIV-1 Gp41 envelope[2]. Neuroprotective effects[1]. Trilobatin is also a SGLT1/2 inhibitor that selectively induces the proliferation of human hepatoblastoma cells[3].
Related Catalog
Target

HIV-1

SGLT1/2

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[1].
References

[1]. Gao J, et al. Trilobatin Protects Against Oxidative Injury in Neuronal PC12 Cells Through Regulating Mitochondrial ROS Homeostasis Mediated by AMPK/Nrf2/Sirt3 Signaling Pathway. Front Mol Neurosci. 2018 Jul 30;11:267.

[2]. Yin S, et al. Trilobatin as an HIV-1 entry inhibitor targeting the HIV-1 Gp41 envelope. FEBS Lett. 2018 Jul;592(13):2361-2377.

Density 1.6±0.1 g/cm3
Boiling Point 787.9±60.0 °C at 760 mmHg
Melting Point 163 °C
Molecular Formula C21H24O10
Molecular Weight 436.409
Flash Point 277.1±26.4 °C
Exact Mass 436.136932
PSA 177.14000
LogP 1.43
Vapour Pressure 0.0±2.9 mmHg at 25°C
Index of Refraction 1.686

~49%

4192-90-9 structure

4192-90-9

Literature: Gupte, Amol; Buolamwini, John K. Bioorganic and Medicinal Chemistry Letters, 2009 , vol. 19, # 3 p. 917 - 921

~%

4192-90-9 structure

4192-90-9

Literature: Jorio Annali di Chimica (Rome, Italy), 1959 , vol. 49, p. 1929,1936

~%

4192-90-9 structure

4192-90-9

Literature: Jorio Annali di Chimica (Rome, Italy), 1959 , vol. 49, p. 1929,1936

~%

4192-90-9 structure

4192-90-9

Literature: Jorio Annali di Chimica (Rome, Italy), 1959 , vol. 49, p. 1929,1936