16α-Iodo-E2

16α-Iodo-E2
Identifiers
	IUPAC name (8R,9S,13S,14S,16R,17R)-16-iodo-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthrene-3,17-diol;
CAS Number	7450-34-2;
PubChem CID	67087;
ChemSpider	60437;
ChEMBL	ChEMBL342892;
CompTox Dashboard (EPA)	DTXSID00275695 ;
Chemical and physical data
Formula	C18H23IO2
Molar mass	398.284 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES C[C@]12CC[C@H]3[C@H]([C@@H]1C[C@H]([C@@H]2O)I)CCC4=C3C=CC(=C4)O;
	InChI InChI=1S/C18H23IO2/c1-18-7-6-13-12-5-3-11(20)8-10(12)2-4-14(13)15(18)9-16(19)17(18)21/h3,5,8,13-17,20-21H,2,4,6-7,9H2,1H3/t13-,14-,15+,16-,17+,18+/m1/s1; Key:SSYGGPAGDDGXAF-ZXXIGWHRSA-N;

16α-Iodo-E2, or 16α-iodoestradiol, is a synthetic, steroidal, potent estrogen with slight preference for the ERα over the ERβ that is used in scientific research.^[1]^[2] The K_D of 16α-iodo-E2 for the ERα is 0.6 nM and for the ERβ is 0.24 nM, a 4-fold difference in affinity, whereas estradiol is considered to have similar affinity for the two receptor subtypes.^[2] Unlike the case of the much weaker estriol (16α-hydroxyestradiol), 16α-iodo-E2 is considered to be equipotent with estradiol in terms of estrogenic activity.^[3] Radiolabeled [16α-¹²⁵I]iodo-E2 has been employed in imaging to study the estrogen receptor.^[4]

References

[1]

[2]

[3]

[4]

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16α-Iodo-E2

See also

References

Identifiers

IUPAC name (8R,9S,13S,14S,16R,17R)-16-iodo-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthrene-3,17-diol
CAS Number	7450-34-2
PubChem CID	67087
ChemSpider	60437
ChEMBL	ChEMBL342892
CompTox Dashboard (EPA)	DTXSID00275695
Chemical and physical data
Formula	C₁₈H₂₃IO₂
Molar mass	398.284 g·mol⁻¹
3D model (JSmol)	Interactive image
SMILES C[C@]12CC[C@H]3[C@H]([C@@H]1C[C@H]([C@@H]2O)I)CCC4=C3C=CC(=C4)O
InChI InChI=1S/C18H23IO2/c1-18-7-6-13-12-5-3-11(20)8-10(12)2-4-14(13)15(18)9-16(19)17(18)21/h3,5,8,13-17,20-21H,2,4,6-7,9H2,1H3/t13-,14-,15+,16-,17+,18+/m1/s1 Key:SSYGGPAGDDGXAF-ZXXIGWHRSA-N