Sparstolonin B
Sparstolonin B Basic information
- Product Name:
- Sparstolonin B
- Synonyms:
-
- Sparstolonin B
- 3H-Pyrano[3,4,5-kl]xanthen-3-one, 4,10-dihydroxy-
- Sparstolonin B >=98% (HPLC)
- Sparstolonin B (SsnB)
- CAS:
- 1259330-61-4
- MF:
- C15H8O5
- MW:
- 268.22
- Mol File:
- 1259330-61-4.mol
Sparstolonin B Chemical Properties
- storage temp.
- 2-8°C
- solubility
- DMSO : 10 mg/mL (Need ultrasonic and warming)
- form
- powder
- color
- white to beige
Sparstolonin B Usage And Synthesis
Uses
Sparstolonin B acts as a selective TLR2 and TLR4 antagonist and selectively blocks TLR2- and TLR4-mediated inflammatory signaling. Sparstolonin B has anti-HIV and anticancer activities[1][2].
Biochem/physiol Actions
Sparstolonin B (SsnB) is a polyphenol. It has a structural features similar to xanthone and isocoumarin. SsnB exerts anti-inflammatory properties on mouse and human macrophages. SsnB can significantly reduce hypoxia–reoxygenation-induced inflammation of cardiomyocytes by blocking extracellular signal-regulated protein kinase (ERK1/2) and c-jun N-terminal kinases (JNK) signaling pathways. Thus, SsnB acts as a potent therapeutic for the treatment of myocardial ischemia–reperfusion (MIR) injury.
in vivo
Sparstolonin B (100 μg/mouse; i.p.) suppresses LPS-provoked inflammation in mice[1].
| Animal Model: | 5-6-week-old male C57Bl/6 mice (body weight 18-20 g)[1] |
| Dosage: | 100 μg/mouse |
| Administration: | I.p. |
| Result: | Significantly lower TNFα and IL-1β expression levels in LPS-induced sepsis mouse model. |
IC 50
TLR2; TLR4; HIV-1
References
[1] Liang Q, et al. Characterization of sparstolonin B, a Chinese herb-derived compound, as a selective Toll-like receptor antagonist with potent anti-inflammatory properties. J Biol Chem. 2011;286(30):26470-26479. DOI:10.1074/jbc.M111.227934
[2] Deng X, et al. The Chinese herb-derived Sparstolonin B suppresses HIV-1 transcription. Virol J. 2015;12:108. Published 2015 Jul 25. DOI:10.1186/s12985-015-0339-8
[3] Kumar A, et al. Sparstolonin B, a novel plant derived compound, arrests cell cycle and induces apoptosis in N-myc amplified and N-myc nonamplified neuroblastoma cells [published correction appears in PLoS One. 2016;11(7):e0159082]. PLoS One. 2014;9(5):e96343. Published 2014 May 1. DOI:10.1371/journal.pone.0096343
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