(2S,3S,4S,5R,6S)-6-{[(1S,2R,10R,11S,14R,15S)-15-ethyl-14-ethynyl-5-oxotetracyclo[8.7.0.02,7.011,15]heptadec-6-en-14-yl]oxy}-3,4,5-trihydroxyoxane-2-carboxylic acid

• ChemBase ID: 175655
• Molecular Formular: C27H36O8
• Molecular Mass: 488.56994
• Monoisotopic Mass: 488.24101811
• SMILES: C1C(=O)C=C2[C@H](C1)[C@@H]1[C@@H](CC2)[C@H]2[C@](CC1)([C@@](CC2)(C#C)O[C@@H]1O[C@H]([C@H]([C@@H]([C@@H]1O)O)O)C(=O)O)CC
• Canonical SMILES: CC[C@]12CC[C@H]3[C@H]([C@@H]1CC[C@]2(C#C)O[C@@H]1O[C@@H](C(=O)O)[C@H]([C@@H]([C@@H]1O)O)O)CCC1=CC(=O)CC[C@H]31
• InChI: InChI=1S/C27H36O8/c1-3-26-11-9-17-16-8-6-15(28)13-14(16)5-7-18(17)19(26)10-12-27(26,4-2)35-25-22(31)20(29)21(30)23(34-25)24(32)33/h2,13,16-23,25,29-31H,3,5-12H2,1H3,(H,32,33)/t16-,17+,18+,19-,20-,21-,22+,23-,25-,26-,27-/m0/s1
• InChIKey: PINPOUGXNZMMFT-HBRQQDTRSA-N

NAMES AND DATABASE IDS

Names

• IUPAC name: (2S,3S,4S,5R,6S)-6-{[(1S,2R,10R,11S,14R,15S)-15-ethyl-14-ethynyl-5-oxotetracyclo[8.7.0.0^2,^7.0^1^1,^1^5]heptadec-6-en-14-yl]oxy}-3,4,5-trihydroxyoxane-2-carboxylic acid
• IUPAC Traditional name: (2S,3S,4S,5R,6S)-6-{[(1S,2R,10R,11S,14R,15S)-15-ethyl-14-ethynyl-5-oxotetracyclo[8.7.0.0^2,^7.0^1^1,^1^5]heptadec-6-en-14-yl]oxy}-3,4,5-trihydroxyoxane-2-carboxylic acid
• Synonyms: 17-Ethynyl-18-methyl-19-nortestosterone Glucuronide; Levonorgestrel Glucuronide; D-(-)-Norgestrel β-D-Glucuronide

Database IDs

• PubChem SID: 164231565
• PubChem CID: 71751214

CALCULATED PROPERTIES

• Acid pKa: 3.6087055
• H Acceptors: 8
• H Donor: 4
• LogD (pH = 5.5): 0.32427615
• LogD (pH = 7.4): -1.1287528
• Log P: 2.2112355
• Molar Refractivity: 124.3062 cm^3
• Polarizability: 49.408314 Å^3
• Polar Surface Area: 133.52 Å^2
• Rotatable Bonds: 4
• Lipinski's Rule of Five: true

PROPERTIES

Physical Property

• Solubility: Methanol
• Apperance: White to Off White Solid
• Melting Point: 146-149°C

Safety Information

• Storage Condition: -20°C Freezer, Under Inert Atmosphere

DETAILS

Toronto Research Chemicals - N689515

A glucuronide metabolite of Levonorgestrel.