16-Hydroxycorticosterone 20-Hydroxy-21-Acid (Mixture of Diastereomers)

Ref. TR-H918430

Informations sur le produit

• Nom: 16-Hydroxycorticosterone 20-Hydroxy-21-Acid (Mixture of Diastereomers)
• Synonymes: 2-[(8S,9S,10R,11S,13S,14S,16R,17R)-11,16-dihydroxy-10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl]-2-hydroxy-acetic acid

Description

Applications 16-Hydroxycorticosterone 20-Hydroxy-21-Acid is an oxidized derivative of corticosterone (C695700), an intermediate in the biosynthesis of aldosterone (A514700), isolated from the adrenal cortex. It is also a pheramone that triggers natural behaviour in the vomeronasal system of mice.
References Schmidt, M., et al.: Endocrinol., 150, 2709 (2009), Bailey, M., et al.: J. Immunol., 182, 7888 (2009), Brunton, P., et al.: J. Neurosci., 29, 6449 (2009), Pruett, S., et al.: Toxicol. Sci., 109, 265 (2009); Fu, X., et al.: Cell, 163, 313 (2015)

• Marque: TRC

Propriétés chimiques

• Masse moléculaire: 378.46
• Formule: C₂₁H₃₀O₆
• Couleur/Forme: Neat
• InChI: InChI=1S/C21H30O6/c1-20-6-5-11(22)7-10(20)3-4-12-13-8-14(23)17(18(25)19(26)27)21(13,2)9-15(24)16(12)20/h7,12-18,23-25H,3-6,8-9H2,1-2H3,(H,26,27)/t12-,13-,14+,15-,16+,17+,18?,20-,21-/m0/s1
• Code InChI: InChIKey=JGPFNVVNPOMHOU-LSTZXZFBSA-N
• SMILES: C[C@]12C[C@H](O)[C@H]3[C@@H](CCC4=CC(=O)CC[C@@]43C)[C@@H]1C[C@@H](O)[C@@H]2[C@H](O)C(=O)O