Adarotene

Adarotene
Names

IUPAC name (E)-3-[4-[3-(1-Adamantyl)-4-hydroxyphenyl]phenyl]prop-2-enoic acid
Other names 3-(4'-Hydroxy-3'-adamantylbiphenyl-4-yl)acrylic acid
Identifiers
CAS Registry Number	496868-77-0
ChemSpider	25069675
InChI InChI=1S/C25H26O3/c26-23-7-6-21(20-4-1-16(2-5-20)3-8-24(27)28)12-22(23)25-13-17-9-18(14-25)11-19(10-17)15-25/h1-8,12,17-19,26H,9-11,13-15H2,(H,27,28)/b8-3+/t17-,18+,19-,25- Key: QAWBIEIZDDIEMW-SOKLTXMDSA-N InChI=1/C25H26O3/c26-23-7-6-21(20-4-1-16(2-5-20)3-8-24(27)28)12-22(23)25-13-17-9-18(14-25)11-19(10-17)15-25/h1-8,12,17-19,26H,9-11,13-15H2,(H,27,28)/b8-3+/t17-,18+,19-,25- Key: QAWBIEIZDDIEMW-SOKLTXMDBA
Jmol-3D images	Image
PubChem	9864378
SMILES c1c(ccc(c1)c2cc(c(cc2)O)[C@@]34C[C@H]5C[C@@H](C3)C[C@@H](C4)C5)/C=C/C(=O)O
Properties
Molecular formula	C₂₅H₂₆O₃
Molar mass	374.47 g·mol⁻¹
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
Infobox references

Adarotene is a bioactive retinoid.^[1]

References

↑ Giannini, G; Brunetti, T; Battistuzzi, G; Alloatti, D; Quattrociocchi, G; Cima, MG; Merlini, L; Dallavalle, S; Cincinelli, R; Nannei, R; Vesci, L; Bucci, F; Foderà, R; Guglielmi, MB; Pisano, C; Cabri, W (2012). "New retinoid derivatives as back-ups of Adarotene". Bioorganic & Medicinal Chemistry 20 (7): 2405–15. doi:10.1016/j.bmc.2012.01.042. PMID 22365912.