Iridodial

Iridodial
Names
	Preferred IUPAC name (1S,2S,5R)-2-Methyl-5-[(2S)-1-oxopropan-2-yl]cyclopentane-1-carbaldehyde
Identifiers
CAS Number	550-45-8;
3D model (JSmol)	Interactive image;
PubChem CID	53297343;
UNII	KZ2T7V54AZ ;
CompTox Dashboard (EPA)	DTXSID10970361 ;
	InChI InChI=1S/C10H16O2/c1-7-3-4-9(8(2)5-11)10(7)6-12/h5-10H,3-4H2,1-2H3/t7-,8+,9+,10-/m0/s1 Key: HMCYXRFNNOPPPR-JLIMGVALSA-N;
	SMILES C[C@H]1CC[C@@H]([C@H]1C=O)[C@H](C)C=O;
Properties
Chemical formula	C10H16O2
Molar mass	168.236 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

Iridodial is an iridoid. It is produced from 8-oxogeranial by the enzyme (IS).^[1] Iridodial is one of the substrates for the enzyme (IO) which produces 7-deoxyloganetic acid.

References[]

^ Geu-Flores, Fernando; Sherden, Nathaniel H.; Courdavault, Vincent; Burlat, Vincent; Glenn, Weslee S.; Wu, Cen; Nims, Ezekiel; Cui, Yuehua; o’Connor, Sarah E. (2012). "An alternative route to cyclic terpenes by reductive cyclization in iridoid biosynthesis". Nature. 492 (7427): 138–42. Bibcode:2012Natur.492..138G. doi:10.1038/nature11692. PMID 23172143.

[1] Geu-Flores, Fernando; Sherden, Nathaniel H.; Courdavault, Vincent; Burlat, Vincent; Glenn, Weslee S.; Wu, Cen; Nims, Ezekiel; Cui, Yuehua; o’Connor, Sarah E. (2012). "An alternative route to cyclic terpenes by reductive cyclization in iridoid biosynthesis". Nature. 492 (7427): 138–42. Bibcode:2012Natur.492..138G. doi:10.1038/nature11692. PMID 23172143.

[1]