Vincamine

• Formula: C₂₁H₂₆N₂O₃
• Molecular weight: 354.4427
• IUPAC Standard InChI: InChI=1S/C21H26N2O3/c1-3-20-10-6-11-22-12-9-15-14-7-4-5-8-16(14)23(17(15)18(20)22)21(25,13-20)19(24)26-2/h4-5,7-8,18,25H,3,6,9-13H2,1-2H3/t18?,20?,21-/m0/s1 Copy

  
• IUPAC Standard InChIKey: RXPRRQLKFXBCSJ-MNLRITNHSA-N Copy
• CAS Registry Number: 1617-90-9
• Chemical structure:
  This structure is also available as a 2d Mol file
• Stereoisomers:
  • Eburnamenine-14-carboxylic acid, 14,15-dihydro-14-hydroxy-, methyl ester, (3α,14α,16α)-
• Other names: Eburnamenine-14-carboxylic acid, 14,15-dihydro-14-hydroxy-, methyl ester, (3α,14β,16α)-; (+)-Vincamine; Decincan; Devincan; Devinkan; Minorin; Minorine; Monorin; Pervincamine; Vincamin; Anasclerol (base); Novicet; Tripervan; Vinca; Vinca-Ecobi; Vinca-Minor; Vincachron; Vincafolina; Vincagil; Vincamidol; Vincapan; Vincasaunier; Vincimax; Vinkametrin; Vinodrel retard; Anasclerol; Angiopac; Arteriovinca; 14,15-Dihydro-14-hydroxyeburnamenine-14-carboxylic acid methyl ester; Equipur; Ocu-vinc; Oxygeron; Perval; Pervone; Vincadar; Vincafor; Vincapront; Alkaloid obtained from Vinca minor; 1H-Indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine, eburnamenine-14-carboxylic acid deriv.; (+)-cis-Vincamine; Methyl vincaminate; cis-Vincamine; (3α,14β,16α)-14,15-Dihydro-14-hydroxyeburnamenine-14-carboxylic acid, methyl ester; NSC-91998; Sostenil; Vincafarm; Vincalen; Vinvasaunier; Vraap
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• Information on this page:
  • Gas phase ion energetics data
  • Gas Chromatography
  • References
  • Notes
• Other data available:
  • Mass spectrum (electron ionization)
  • UV/Visible spectrum
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Gas phase ion energetics data

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: Sharon G. Lias, John E. Bartmess, Joel F. Liebman, John L. Holmes, Rhoda D. Levin, and W. Gary Mallard

Ionization energy determinations

Appearance energy determinations

Gas Chromatography

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director

Kovats' RI, non-polar column, isothermal

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References

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Czira, Tamas, et al., 1984
Czira, G.; Tamas, J.; Kalaus, G., Effects of stereoisomerism on the electron impact fragmentation of some compounds with an eburnane skeleton, Org. Mass Spectrom., 1984, 19, 555. [all data]

Musumarra, Scarlata, et al., 1987
Musumarra, G.; Scarlata, G.; Romano, G.; Cappello, G.; Clementi, S.; Giulietti, G., Qualitative organic analysis. Part 2. Identification of drugs by principal components analysis of standardized TLC data in four eluent systems and of retention indices on SE 30, J. Anal. Toxicol., 1987, 11, 4, 154-163, https://doi.org/10.1093/jat/11.4.154 . [all data]

Notes

Go To: Top, Gas phase ion energetics data, Gas Chromatography, References

• Symbols used in this document:
  

  AE	Appearance energy

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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