// Workers AI · dad joke modeWhat did Pregomisin say to its date? "You're prego-mine.

Pregomisin
Names
	IUPAC name (8R,8′S)-4,4′,5,5′-Tetramethoxylignane-3,3′-diol
	Systematic IUPAC name 3,3′-[(2R,3S)-2,3-Dimethylbutane-1,4-diyl]bis(5,6-dimethoxyphenol)
Identifiers
CAS Number	66280-26-0 ;
3D model (JSmol)	Interactive image;
ChemSpider	158122;
PubChem CID	181796;
UNII	5AYW92EXLG ;
	InChI InChI=1S/C22H30O6/c1-13(7-15-9-17(23)21(27-5)19(11-15)25-3)14(2)8-16-10-18(24)22(28-6)20(12-16)26-4/h9-14,23-24H,7-8H2,1-6H3/t13-,14+ Key: RLRKIWSBYUZHIJ-OKILXGFUSA-N; InChI=1/C22H30O6/c1-13(7-15-9-17(23)21(27-5)19(11-15)25-3)14(2)8-16-10-18(24)22(28-6)20(12-16)26-4/h9-14,23-24H,7-8H2,1-6H3/t13-,14+ Key: RLRKIWSBYUZHIJ-OKILXGFUBC;
	SMILES C[C@H](Cc1cc(c(c(c1)OC)OC)O)[C@@H](C)Cc2cc(c(c(c2)OC)OC)O;
Properties
Chemical formula	C22H30O6
Molar mass	390.476 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Pregomisin is a chemical compound isolated from Schisandra chinensis.^[1]

References

↑ Lee, Im Seon; Jung, Keun Young; Oh, Sel Ryang; Kim, Dong Seon; Kim, Jung Hee; Lee, Jung Joon; Lee, Hyeong-Kyu; Lee, Seung-Ho; Kim, Eun-Hee; Cheong, Chaejoon (1997). "Platelet-activating factor antagonistic activity and ¹³C NMR assignment of pregomisin and chamigrenal from Schisandra chinensis". Archives of Pharmacal Research. 20 (6): 633–636. doi:10.1007/BF02975223. PMID 18982271. S2CID 36393901.

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