(10α,24R)-9β-Methyl-19-norlanosta-5-ene-3β,11α,24,25-tetrol
(10α,24R)-9β-Methyl-19-norlanosta-5-ene-3β,11α,24,25-tetrol Basic information
- Product Name:
- (10α,24R)-9β-Methyl-19-norlanosta-5-ene-3β,11α,24,25-tetrol
- Synonyms:
-
- (10α,24R)-3β,11α,24,25-Tetrahydroxy-9β-methyl-19-norlanosta-5-ene
- (10α,24R)-9β-Methyl-19-norlanosta-5-ene-3β,11α,24,25-tetrol
- (24R)-Cucurbit-5-ene-3β,11α,24,25-tetrol
- Mogrol
- Mogrol, >98%
- ERK,inhibit,Extracellular signal regulated kinases,STAT,Mogrol,Inhibitor
- Monascus alcohol
- Mogrol-RM
- CAS:
- 88930-15-8
- MF:
- C30H52O4
- MW:
- 476.73
- Mol File:
- 88930-15-8.mol
(10α,24R)-9β-Methyl-19-norlanosta-5-ene-3β,11α,24,25-tetrol Chemical Properties
- Boiling point:
- 595.6±50.0 °C(Predicted)
- Density
- 1.10±0.1 g/cm3(Predicted)
- storage temp.
- Store at -20°C
- solubility
- Soluble in DMSO
- form
- Solid
- pka
- 14.67±0.29(Predicted)
- color
- White to off-white
- InChIKey
- JLYBBRAAICDTIS-AYEHCKLZSA-N
- CAS DataBase Reference
- 88930-15-8
(10α,24R)-9β-Methyl-19-norlanosta-5-ene-3β,11α,24,25-tetrol Usage And Synthesis
Appearance
Constit. of Cucurbita foeridissimia (buffalo gourd).Amorph. powder.
Chemical Properties
Off-white powder, soluble in organic solvents such as methanol, ethanol, and DMSO, derived from Momordica grosvenori.
Uses
Mogrol is a biometabolite of mogrosides, and acts via inhibition of the ERK1/2 and STAT3 pathways, or reducing CREB activation and activating AMPK signaling.
Definition
ChEBI: Mogrol is a tetracyclic triterpenoid that is cucurbitadienol in which the side-chain double bond (position 24-25) has undergone formal oxidation to introduce hydroxy groups at positions 24 and 25 (the 24R stereoisomer). It is a biometabolite of mogrosides found in Siraitia grosvenorii. It has a role as an antineoplastic agent. It is a tetracyclic triterpenoid and a hydroxy seco-steroid. It is functionally related to a cucurbitadienol.
Biochem/physiol Actions
Mogrol is an aglycone of mogrosides from Siraitia grosvenorii that exhibits neuroprotective and anticancer activities. It induces apoptosis in K562 leukemia cells through suppression of ERK1/2 and STAT3 pathways. Mogrol appears to ameliorate the memory impairment caused by Aβ1-42 in mice. Mogrol increases AMPK activity in hepatocytes and suppresses adipocyte differentiation in 3T3-L1 cells.
IC 50
ERK1; ERK2; STAT3
References
[1] Liu C, et al. Mogrol represents a novel leukemia therapeutic, via ERK and STAT3 inhibition. Am J Cancer Res. 2015 Mar 15;5(4):1308-18.
[2] Naoki Harada, et al. Mogrol Derived from Siraitia grosvenorii Mogrosides Suppresses 3T3-L1 Adipocyte Differentiation by Reducing cAMP-Response Element-Binding Protein Phosphorylation and Increasing AMP-Activated Protein Kinase Phosphorylation. PLoS One. 2
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