Lobetyolin
Lobetyolin Basic information
- Product Name:
- Lobetyolin
- Synonyms:
-
- β-D-Glucopyranoside, (1R,2R,7E)-2-hydroxy-1-[(1E)-5-hydroxy-1-pentenyl]-7-nonene-3,5-diynyl (9CI)
- CAS:
- 129277-38-9
- MF:
- C20H28O8
- MW:
- 396.44
- Mol File:
- 129277-38-9.mol
Lobetyolin Chemical Properties
- Boiling point:
- 698.5±55.0 °C(Predicted)
- Density
- 1.35±0.1 g/cm3(Predicted)
- pka
- 11.39±0.20(Predicted)
- form
- Solid
- color
- White to yellow
- InChIKey
- MMMUDYVKKPDZHS-FHMAEMBXNA-N
- SMILES
- O([C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)[C@]([H])(/C=C/CCCO)[C@H](O)C#CC#C/C=C/C |&1:1,2,3,5,7,12,20,r|
Lobetyolin Usage And Synthesis
Uses
Lobetyolin, a bioactive compound, is derived from Codonopsis pilosula. Lobetyolin has anti-inflammatory, anti-oxidative and xanthine oxidase inhibiting activities. Lobetyolin also induces the apoptosis via the inhibition of ASCT2-mediated glutamine metabolism[1][2]. Lobetyolin is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
References
[1] Yoon YP, et al. Effects of Lobetyolin, Lobetyol and Methyl linoleate on Secretion, Production and Gene Expression of MUC5AC Mucin from Airway Epithelial Cells. Tuberc Respir Dis (Seoul). 2014 Nov;77(5):203-8. DOI:10.4046/trd.2014.77.5.203
[2] He W, et, al. Lobetyolin induces apoptosis of colon cancer cells by inhibiting glutamine metabolism. J Cell Mol Med. 2020 Mar;24(6):3359-3369. DOI:10.1111/jcmm.15009
LobetyolinSupplier
- Tel
- 028-81700200 13308200041
- 2851167782@qq.com
- Tel
- 0510-85629785 18013409632
- sales@reading-chemicals.com
- Tel
- 010-60605840 18892239720
- psaitong@jm-bio.com
- Tel
- 028-028-85370565-229-229 18080489829
- 18080489829@163.com
- Tel
- 0512-56316828
- info@amateksci.com