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(1-S,3-S,4-R,7-S,8-S,11-S,12-S,13-S,15-R,20-R)-7,20-DIFORMAMIDOISOCYCLOAMPHILECTANE

Compound with spectra: 2 NMR, and 1 MS (GC)

(1-S,3-S,4-R,7-S,8-S,11-S,12-S,13-S,15-R,20-R)-7,20-DIFORMAMIDOISOCYCLOAMPHILECTANE
SpectraBase Compound ID KMIQl3ifp3u
InChI InChI=1S/C22H36N2O2/c1-13-9-15-10-14(2)22(4,24-12-26)18-6-5-17-20(19(15)18)16(13)7-8-21(17,3)23-11-25/h11-20H,5-10H2,1-4H3,(H,23,25)(H,24,26)/t13-,14+,15-,16+,17-,18-,19+,20+,21-,22+/m0/s1
InChIKey SJUBXKFUQQKUEC-OXEUSEQRSA-N
Mol Weight 360.5 g/mol
Molecular Formula C22H36N2O2
Exact Mass 360.277678 g/mol
Enantiomer InChIKey SJUBXKFUQQKUEC-DQOJZDKMSA-N

View Spectrum of (1-S,3-S,4-R,7-S,8-S,11-S,12-S,13-S,15-R,20-R)-7,20-DIFORMAMIDOISOCYCLOAMPHILECTANE

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum G4-72-495-2

View Spectrum of (1-S,3-S,4-R,7-S,8-S,11-S,12-S,13-S,15-R,20-R)-7,20-DIFORMAMIDOISOCYCLOAMPHILECTANE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of (1-S,3-S,4-R,7-S,8-S,11-S,12-S,13-S,15-R,20-R)-7,20-DIFORMAMIDOISOCYCLOAMPHILECTANE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (1S,3S,4R,7S,8S,11S,12S,13S,15R,20R)-7,20-bis(Formamido)-isocycloamphilectane
DIISOCYANOADOCIANE
(1S,3S,4R,7S,8S,11S,12S,13S,15R,20R)-7,20-DIISOCYANOISOCYClOAMPHILECTANE
Amoenolide G
Androst-4-ene-6-acetic acid, 17-hydroxy-3-oxo-, methyl ester, (6.beta.,17.beta.)-
5-ENDO-METHOXY-5-PHENYL-2,3-TETRAFLUOROBENZOBICYCLO[2.2.2]OCTENE
ENT-11-ALPHA-HYDROXY-18-ACETOXYKAUR-16-ENE
PHENYL-4,6-O-BENZYLIDENE-2-DEOXY-2-PHTHALIMIDO-1-SELENO-BETA-D-GLUCOPYRANOSIDE
3-Acetyl-1,2,3,4,4a,5,6,7-Octahydropyrido[3,4-d]carbazole
Pregn-5-en-20-one, 1,3-dihydroxy-, (1.alpha.,3.beta.)-
(1-alpha,5-alpha,11-alpha,17-beta)-11,17-dihydroxy-1-methylandrostane-3-one
Title Journal or Book Year
Diterpene Formamides from the Tropical Marine Sponge Cymbastela hooperi and Their Antimalarial Activity in Vitro Journal of Natural Products 2009

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