TY - JOUR
T1 - Fast and easy GC/MS identification of myrrh resins
AU - Hanuš, L. O.
AU - Rosenthal, D.
AU - Řezanka, T.
AU - Dembitsky, V. M.
AU - Moussaief, A.
PY - 2008/12
Y1 - 2008/12
N2 - Extracts prepared from Commiphora molmol resins were analyzed by GC-MS. Twenty-two terpenoid compounds were identified in the hexane extract of the resin. Among them, 2-acetoxyfuranodiene (9.80%), furanoeudesma-1,3-diene (8.97%), isofuranogermacrene (6.71%), epicurzerenone (3.64%), 2-methoxyfuranodiene (2.97%), and lindestrene (2.74%) were the main compounds from the first myrrh resin (Tamar Ltd.), and furanoeudesma-1,3-diene (20.59%), isofuranogermacrene (17.94%), 2-acetoxyfuranodiene (8.80%), 2-methoxyfuranodiene (7.33%), and lindestrene (6.24%) from the second myrrh resin (Pamir Ltd.).
AB - Extracts prepared from Commiphora molmol resins were analyzed by GC-MS. Twenty-two terpenoid compounds were identified in the hexane extract of the resin. Among them, 2-acetoxyfuranodiene (9.80%), furanoeudesma-1,3-diene (8.97%), isofuranogermacrene (6.71%), epicurzerenone (3.64%), 2-methoxyfuranodiene (2.97%), and lindestrene (2.74%) were the main compounds from the first myrrh resin (Tamar Ltd.), and furanoeudesma-1,3-diene (20.59%), isofuranogermacrene (17.94%), 2-acetoxyfuranodiene (8.80%), 2-methoxyfuranodiene (7.33%), and lindestrene (6.24%) from the second myrrh resin (Pamir Ltd.).
UR - http://www.scopus.com/inward/record.url?scp=67349112902&partnerID=8YFLogxK
U2 - 10.1007/s11094-009-0209-z
DO - 10.1007/s11094-009-0209-z
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AN - SCOPUS:67349112902
SN - 0091-150X
VL - 42
SP - 719
EP - 720
JO - Pharmaceutical Chemistry Journal
JF - Pharmaceutical Chemistry Journal
IS - 12
ER -