1913319-59-1
Chemical Structure
Caesappanin C
- CAS No.: 1913319-59-1
- Formula:C32H32O12
- Molecular Weight:608.59
IUPAC Name: (11R,23S)-11,23-bis(hydroxymethyl)-11,12,23,24-tetrahydro-10H,22H-tetrabenzo[b,d,j,l][1,9]dioxacyclohexadecin-2,3,7,11,14,15,19,23-octaol
InChIKey: QRIDWFOMLAURDW-MEKGRNQZSA-N
SMILES: OC1=C(O)C=C2C(C3=CC=C(O)C=C3OC[C@](O)(CC4=CC(O)=C(O)C=C4C5=CC=C(O)C=C5OC[C@@](CO)(O)C2)CO)=C1
Biological Activity: Caesappanin C, a biphenyl dimer from the ethanolic extract of the heartwood of Indonesian Caesalpinia sappan L., shows strong proliferation stimulating activity against the primary osteoblastic cells in vitro. Caesappanin C has the potential to stimulate bone formation and regeneration[1]. Caesappanin C can effectively deactivate HSV particles and bind HSV surface glycoprotein B (gB) to inhibit membrane fusion[2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Caesappanin C | 98.09% | Caesappanin C, a biphenyl dimer from the ethanolic extract of the heartwood of Indonesian Caesalpinia sappan L., shows strong proliferation stimulating activity against the primary osteoblastic cells in vitro. Caesappanin C has the potential to stimulate bone formation and regeneration. Caesappanin C can effectively deactivate HSV particles and bind HSV surface glycoprotein B (gB) to inhibit membrane fusion. | ||||||||||||||||||||
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References
- [1]. Subehan, et al. Phytochemical investigation of the active constituents from Caesalpinia sappan on stimulation of osteoblastic cells. Plant Biotechnology, 2014,31(5), 505–509.
- [2]. Yang J, Wang J, Yan H, Xu Z, Hao C, Wang W. Inhibition of herpes simplex virus infection by Caesappanin C targeting virus gB protein and host HSP90β. Phytomedicine. 2026;151:157802. [Content Brief]
