Our system is currently under heavy load due to increased usage. We're actively working on upgrades to improve performance. Thank you for your patience.
1998
DOI: 10.1080/10575639808048277
|View full text |Cite
|
Sign up to set email alerts
|

New Antibacterial Steroidal Alkaloids fromSarcococca Brevifolia

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1

Citation Types

0
13
0

Year Published

2002
2002
2024
2024

Publication Types

Select...
7

Relationship

0
7

Authors

Journals

citations
Cited by 15 publications
(13 citation statements)
references
References 4 publications
0
13
0
Order By: Relevance
“…The spectral data of compound 3 has been presented for the first time in this paper. Compound 4 (C 22 H 37 NO, HR-EI-MS m/z 331.2806) 16) was also isolated for the first time from this genus as a yellowish crystalline solid. This compound was earlier isolated from the leaves of Holarrhena febrifuga.…”
Section: Resultsmentioning
confidence: 92%
See 3 more Smart Citations
“…The spectral data of compound 3 has been presented for the first time in this paper. Compound 4 (C 22 H 37 NO, HR-EI-MS m/z 331.2806) 16) was also isolated for the first time from this genus as a yellowish crystalline solid. This compound was earlier isolated from the leaves of Holarrhena febrifuga.…”
Section: Resultsmentioning
confidence: 92%
“…This compound was earlier isolated from the leaves of Holarrhena febrifuga. 16) The stereochemical assignments of stereogenic centers in the compounds 1-4 were made on the basis of nuclear Overhauser effect spectroscopy (NOESY) interactions, chemical shifts comparisions with reported compounds [9][10][11][12][13][14][15][16][17][18] and biogenetic considerations keeping in view of the fact that all pregnane-type steroidal alkaloids are biosynthesized from cholesterol via pregnenolone. 19) The b-orientation of the C-20 methine proton in compounds 1-3, and equatorial position of the C-3 tigloyl group in compounds 1-2 were confirmed by comparing the spectral data with reported compounds.…”
Section: Resultsmentioning
confidence: 99%
See 2 more Smart Citations
“…Antibacterial activity of epipachysamine-E-5-ene-4-on has been observed against Bacillus cereus (MIC = 0.0625 mg/mL), Klebsiella pneumoniae (MIC = 0.25 mg/mL) and Staphylococcus aureus (MIC = 0.03125 mg/mL). Similarly, iso-N-formylchonemorphin has shown antibacterial strong activity against Bacillus cereus (MIC = 0.1250 mg/mL), Pseudomonas aeruginosa (MIC = 0.1250 mg/mL) and Staphylococcus aureus (MIC = 0.0312 mg/mL) (Jayasinghe et al, 1998).…”
Section: Antibacterial Activitymentioning
confidence: 99%