26 O BETA DEXTRO GLUCOPYRANOSYL 5BETA FUROSTAN 3BETA,22ALPHA,26 DIOL 12 ONE 3 O BETA DEXTRO GLUCOPYRANOSIDE;
26 O BETA DEXTRO GLUCOPYRANOSYL 5BETA FUROSTAN 3BETA,22ALPHA,26 TRIOL;
26 O BETA DEXTRO GLUCOPYRANOSYL 5BETA FUROSTAN 3BETA,22ALPHA,26 TRIOL 12 ONE 3 O BETA DEXTRO GLUCOPYRANOSIDE;
26 O BETA DEXTRO GLUCOPYRANOSYL 5BETA FUROSTAN 3BETA,22ALPHA,26 TRIOL 3 O ALPHA LEVO RHAMNOPYRANOSYL (1,4) BETA DEXTRO GLUCOPYRANOSIDE;
26 O BETA DEXTRO GLUCOPYRANOSYL 5BETA FURSTAN 3BETA,22ALPHA,26 TRIOL 3 O BETA DEXTRO GLUCOPYRANOSIDE;
5BETA SPIROSTAN 3BETA OL 3 O ALPHA DEXTRO RHAMNOPYRANOSIDE;
5BETA SPIROSTAN 3BETA OL 3 O ALPHA LEVO RHAMNOPYRANOSIDE;
BUTANOL;
SAPONIN DERIVATIVE;
SILICA GEL;
STEROID;
UNCLASSIFIED DRUG;
PLANT EXTRACT;
SAPONIN;
ARTICLE;
ASPARAGUS COCHINCHINENSIS;
CHROMATOGRAPHY;
DRUG DETERMINATION;
DRUG ISOLATION;
DRUG STRUCTURE;
ELECTROSPRAY MASS SPECTROMETRY;
HETERONUCLEAR MULTIPLE BOND CORRELATION;
HETERONUCLEAR SINGLE QUANTUM COHERENCE;
NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;
PLANT ROOT;
ASPARAGUS;
CHEMICAL STRUCTURE;
CHEMISTRY;
ISOLATION AND PURIFICATION;
Studies on the isolation of antitumor active constituents of polysaccharides from Chinese herb Asparagus cochinchinensis (Lour.) Merr. [J]
Du XH, Duo YZ Studies on the isolation of antitumor active constituents of polysaccharides from Chinese herb Asparagus cochinchinensis (Lour.) Merr. [J]. J Shenyang Pharm Coll 1990, 7(4):197-201.
Studies on the constituents of Asparagi Radix I. On the structures of furostanol oligosides of Asparagus cochinchinensis (Loureio) Merrill [J]
Tenji K, Junzo S Studies on the constituents of Asparagi Radix I. On the structures of furostanol oligosides of Asparagus cochinchinensis (Loureio) Merrill [J]. Chem Pharm Bull 1979, 27(12):3086-3094.
Detection of proto-type compounds of diosgenin and other spirostanol-glycosides [J]
Shun K, Masakazu H, Tensuya K, et al. Detection of proto-type compounds of diosgenin and other spirostanol-glycosides [J]. Chem Pharm Bull 1968, 16(6):1162-1164.
Assigning stereodiversity of the 27-Me group of furostane-type steroidal saponins via NMR chemical shifts [J]
Agrawal PK Assigning stereodiversity of the 27-Me group of furostane-type steroidal saponins via NMR chemical shifts [J]. Steroids 2005, 70(10):715-724.
Furostanol saponins and quercetin from the leaves of Helleborus virids L. [J]
Braca A, Prieto JM, Tommasi NM, et al. Furostanol saponins and quercetin from the leaves of Helleborus virids L. [J]. Phytochemistry 2004, 65(21):2921-2928.
Study on synthesis of spirostanol saponin 3-glycosylation derivatives of Anemarrhena asphodeloides Bge. [J]
Di W, Wang L, Peng T, et al. Study on synthesis of spirostanol saponin 3-glycosylation derivatives of Anemarrhena asphodeloides Bge. [J]. Chin J Med Chem 2003, 13:324-328.