Chalepensin
Names
IUPAC name
6-(2-Methylbut-3-en-2-yl)furo[3,2-g]chromen-7-one
Other names
Xyloltenin; 3-(α,α-dimethylallyl)psoralen
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
KEGG
  • InChI=1S/C16H14O3/c1-4-16(2,3)12-8-11-7-10-5-6-18-13(10)9-14(11)19-15(12)17/h4-9H,1H2,2-3H3
    Key: FYCCCUNGXGKNJV-UHFFFAOYSA-N
  • CC(C)(C=C)C1=CC2=C(C=C3C(=C2)C=CO3)OC1=O
Properties
C16H14O3
Molar mass 254.285 g·mol−1
Melting point 82–83 °C (180–181 °F; 355–356 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Chalepensin is a chemical compound of the furanocoumarin class. Originally isolated in 1967 from fringed rue (Ruta chalepensis),[1] from which it derives its name, it has also been found in other plants of the genus Ruta including common rue (Ruta graveolens)[2] and mountain rue (Ruta montana).[3]

Chemical properties

Chalepensin forms colorless crystalline needles with a melting point of 82-83 °C.[4]

Research

Chalepensin has been shown to have antifertility effects in female rats.[2][5][6] This may be the result of toxic effects chalepensin has on the ovaries.[5] This antifertility effect may provide some scientific evidence in support of the traditional uses of fringed rue[6] and modern use of rue oil (oil from plants of the genus Ruta) in South America[7] as an abortifacient.

Chalepensis has also been shown to have antibacterial activity against Streptococcus mutans and methicillin-resistant Staphylococcus aureus (MRSA).[8]

Several chemical compounds that have the same core chemical structure as chalepensin are known, including chalepin, rutamarin, 5-methoxychalepensin, and 5,8-dimethoxychalepensin.

References

  1. ↑ Brooker, Robert M.; Eble, John N.; Starkovsky, Nicolas A. (1967). "Chalepensin, chalepin, and chalepin acetate, three novel furocoumarins from ruta chalepensis". Lloydia. 30 (1): 73–77.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  2. 1 2 Kong, Y.; Lau, C.; Wat, K.; Ng, K.; But, P.; Cheng, K.; Waterman, P. (1989). "Antifertility Principle of Ruta graveolens". Planta Medica. 55 (2): 176–178. doi:10.1055/s-2006-961917. PMID 2748734.
  3. ↑ Touati, Driss; Atta-Ur-Rahman; Ulubelen, Ayhan (2000). "Alkaloids from Ruta montana". Phytochemistry. 53 (2): 277–279. doi:10.1016/S0031-9422(99)00486-0. PMID 10680183.
  4. ↑ Wu, Tian-Shung; Shi, Li-Shian; Wang, Jhi-Joung; Iou, Song-Chou; Chang, Hsien-Chang; Chen, Yuh-Pan; Kuo, Yao-Haur; Chang, Ya-Ling; Tenge, Che-Ming (2003). "Cytotoxic and Antiplatelet Aggregation Principles of Ruta Graveolens". Journal of the Chinese Chemical Society. 50: 171–178. doi:10.1002/jccs.200300024.
  5. 1 2 Ulubelen, A.; Ertugrul, L.; Birman, H.; Yigit, R.; Erseven, G.; Olgac, V. (1994). "Antifertility effects of some coumarins isolated from Ruta chalepensis andR. Chalepensis var.latifolia in rodents". Phytotherapy Research. 8 (4): 233–236. doi:10.1002/ptr.2650080409. S2CID 85292230.
  6. 1 2 Nahar, Lutfun; Al-Majmaie, Shaymaa; Al-Groshi, Afaf; Rasul, Azhar; Sarker, Satyajit D. (2021). "Chalepin and Chalepensin: Occurrence, Biosynthesis and Therapeutic Potential". Molecules. 26 (6): 1609. doi:10.3390/molecules26061609. PMC 7999183. PMID 33799365.
  7. ↑ Ciganda, Carmen; Laborde, Amalia (2003). "Herbal Infusions Used for Induced Abortion". Journal of Toxicology: Clinical Toxicology. 41 (3): 235–239. doi:10.1081/CLT-120021104. PMID 12807304. S2CID 44851492.
  8. ↑ Al-Majmaie, Shaymaa; Nahar, Lutfun; Rahman, M. Mukhlesur; Nath, Sushmita; Saha, Priyanka; Talukdar, Anupam Das; Sharples, George P.; Sarker, Satyajit D. (2021). "Anti-MRSA Constituents from Ruta chalepensis (Rutaceae) Grown in Iraq, and in Silico Studies on Two of Most Active Compounds, Chalepensin and 6-Hydroxy-rutin 3′,7-Dimethyl ether". Molecules. 26 (4): 1114. doi:10.3390/molecules26041114. PMC 7923287. PMID 33669881.
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