Sargachromanol

Sargachromanols
	File:Sargachromanol A.svg; Sargachromanol A
	File:Sargachromanol B.svg; Sargachromanol B
	File:Sargachromanol G.svg; Sargachromanol G
Identifiers
CAS Number	A: 856414-50-1 check; B: 856414-51-2; G: 856414-56-7;
3D model (JSmol)	A: Interactive image; B: Interactive image; G: Interactive image;
ChemSpider	A: 9511768; B: 9591548; G: 9582569;
PubChem CID	A: 11336823; B: 11416661; G: 11407674;
UNII	A: 3OG14YJA8B check;
	SMILES A: CC1=C2C(=CC(=C1)O)CCC(O2)(C)CCC=C(C)CCC=C(C)C=O; B: CC1=C2C(=CC(=C1)O)CCC(O2)(C)CCC=C(C)CCC=C(C)CO; G: CC1=C2C(=CC(=C1)O)CCC(O2)(C)CCC=C(C)CCC=C(C)C(=O)C(C=C(C)C)O;
Properties
Chemical formula	A: C22H30O3; B: C22H32O3; G: C27H38O4
Molar mass	A: 342.48 g/mol; B: 344.49 g/mol; G: 426.60 g/mol
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Sargachromanols are a group of related chemical compounds isolated from the brown alga Sargassum siliquastrum.^[1] At least 20 members of the class have been identified, named sargachromanol A through T.^[2] Sargachromanol G has in vitro anti-inflammatory effects in isolated mouse macrophage cells.^[3]

References

↑ Jang KH, Lee BH, Choi BW, Lee HS, Shin J (May 2005). "Chromenes from the brown alga Sargassum siliquastrum". Journal of Natural Products. 68 (5): 716–23. doi:10.1021/np058003i. PMID 15921416.
↑ Kang HS, Kim JP (2017). "New Chromene Derivatives with Radical Scavenging Activities from the Brown Alga Sargassum Siliquastrum". Journal of Chemical Research. 41 (2): 116–119. doi:10.3184/174751917X14859570937631. S2CID 100466919.
↑ Yoon WJ, Heo SJ, Han SC, Lee HJ, Kang GJ, Kang HK, et al. (August 2012). "Anti-inflammatory effect of sargachromanol G isolated from Sargassum siliquastrum in RAW 264.7 cells". Archives of Pharmacal Research. 35 (8): 1421–30. doi:10.1007/s12272-012-0812-5. PMID 22941485. S2CID 39748571.

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[1] Jang KH, Lee BH, Choi BW, Lee HS, Shin J (May 2005). "Chromenes from the brown alga Sargassum siliquastrum". Journal of Natural Products. 68 (5): 716–23. doi:10.1021/np058003i. PMID 15921416.

[2] Kang HS, Kim JP (2017). "New Chromene Derivatives with Radical Scavenging Activities from the Brown Alga Sargassum Siliquastrum". Journal of Chemical Research. 41 (2): 116–119. doi:10.3184/174751917X14859570937631. S2CID 100466919.

[3] Yoon WJ, Heo SJ, Han SC, Lee HJ, Kang GJ, Kang HK, et al. (August 2012). "Anti-inflammatory effect of sargachromanol G isolated from Sargassum siliquastrum in RAW 264.7 cells". Archives of Pharmacal Research. 35 (8): 1421–30. doi:10.1007/s12272-012-0812-5. PMID 22941485. S2CID 39748571.

[1]

[2]

[3]

Identifiers
File:Sargachromanol A.svg Sargachromanol A
File:Sargachromanol B.svg Sargachromanol B
File:Sargachromanol G.svg Sargachromanol G
CAS Number	A: 856414-50-1^checkY B: 856414-51-2 G: 856414-56-7
3D model (JSmol)	A: Interactive image B: Interactive image G: Interactive image
ChemSpider	A: 9511768 B: 9591548 G: 9582569
PubChem CID	A: 11336823 B: 11416661 G: 11407674
UNII	A: 3OG14YJA8B^checkY
SMILES A: CC1=C2C(=CC(=C1)O)CCC(O2)(C)CCC=C(C)CCC=C(C)C=O B: CC1=C2C(=CC(=C1)O)CCC(O2)(C)CCC=C(C)CCC=C(C)CO G: CC1=C2C(=CC(=C1)O)CCC(O2)(C)CCC=C(C)CCC=C(C)C(=O)C(C=C(C)C)O
Properties
Chemical formula	A: C₂₂H₃₀O₃ B: C₂₂H₃₂O₃ G: C₂₇H₃₈O₄
Molar mass	A: 342.48 g/mol B: 344.49 g/mol G: 426.60 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Sargachromanol

References

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