Page last updated: 2024-11-08

furostanol i

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

furostanol I: from Dioscorea deltoidea; intermediate in in vivo diosgenin biosynthesis; structure given in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

protodioscin : A spirostanyl glycoside that consists of the trisaccharide alpha-L-Rha-(1->4)-[alpha-L-Rha-(1->2)]-beta-D-Glc attached to position 3 of 26-(beta-D-glucopyranosyloxy)-3beta,22-dihydroxyfurost-5-ene via a glycosidic linkage. Found in several plant species including yams, asparagus and funugreek. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

FloraRankFlora DefinitionFamilyFamily Definition
Asparagusgenus[no description available]AsparagaceaeA family of flowering subshrubs and shrubs in the class Magnoliopsida.[MeSH]
DioscoreagenusA plant genus best known for edible underground tubers. Yam may also refer to a moist variety of sweet potato, IPOMOEA BATATAS.[MeSH]DioscoreaceaeThe yam plant family, of the order Liliales, has thick roots or tubers and net-veined, heart-shaped leaves that sometimes are lobed.[MeSH]

Cross-References

ID SourceID
PubMed CID441891
CHEMBL ID4782480
CHEBI ID8588
SCHEMBL ID786390
MeSH IDM0123845

Synonyms (37)

Synonym
protodioscin
C08907
55056-80-9
90288-44-1
furostanol i
furost-5-ene-3,22,26-triol 3-chacotrioside-26-glucopyranoside
beta-d-glucopyranoside, (3beta,22alpha)-26-(beta-d-glucopyranosyloxy)-22-hydroxyfurost-5-en-3-yl o-6-deoxy-alpha-l-mannopyranosyl-(1-2)-o-(6-deoxy-alpha-l-mannopyranosyl-(1-4))-, (r-(z))-
S3830
CHEBI:8588 ,
(3beta,22r,25r)-26-(beta-d-glucopyranosyloxy)-22-hydroxyfurost-5-en-3-yl alpha-l-rhamnopyranosyl-(1->2)-[alpha-l-rhamnopyranosyl-(1->4)]-beta-d-glucopyranoside
AKOS025311548
SCHEMBL786390
Q-100623
.beta.-d-glucopyranoside, (3.beta.,22.alpha.,25r)-26-(.beta.-d-glucopyranosyloxy)-22-hydroxyfurost-5-en-3-yl o-6-deoxy-.alpha.-l-mannopyranosyl-(1->2)-o-(6-deoxy-.alpha.-l-mannopyranosyl-(1->4))-
3.beta.,22.alpha.,26-trihydroxyfurost-5-ene 3-o-.beta.-chacotrioside 26-o-.beta.-d-glucopyranoside
protodioscin [who-dd]
26-o-.beta.-d-glucopyranosyl-(25r)-furost-5-ene-3.beta.,22.alpha.,26-triol 3-o-.alpha.-l-rhamnopyranosyl-(1-2)-(.alpha.-l-rhamnopyranosyl-(1-4))-.beta.-d-glucopyranoside
D0LC3PH24P ,
protodioscin [inci]
protodioscine
unii-d0lc3ph24p
saponin c
beta-d-glucopyranoside, (3beta,22alpha,25r)-26-(beta-d-glucopyranosyloxy)-22-hydroxyfurost-5-en-3-yl o-6-deoxy-alpha-l-mannopyranosyl-(1->2)-o-(6-deoxy-alpha-l-mannopyranosyl-(1->4))-
(3beta,22r,25r)-26-(beta-d-glucopyranosyloxy)-22-hydroxyfurost-5-en-3-yl alpha-l-rhamnopyranosyl-(1->2)-(alpha-l-rhamnopyranosyl-(1->4))-beta-d-glucopyranoside
26-o-beta-d-glucopyranosyl-(25r)-furost-5-ene-3beta,22alpha,26-triol 3-o-alpha-l-rhamnopyranosyl-(1-2)-(alpha-l-rhamnopyranosyl-(1-4))-beta-d-glucopyranoside
beta-d-glucopyranoside, (3beta,22beta,25r)-26-(beta-d-glucopyranosyloxy)-22-hydroxyfurost-5-en-3-yl o-6-deoxy-alpha-l-mannopyranosyl-(1->2)-o-(6-deoxy-alpha-l-mannopyranosyl-(1->4))-
HY-N0799
CS-6050
mfcd03427682
EX-A3793
AS-75278
Q7251968
CCG-270619
26-o-beta-d-glycopyranosyl-22-hydroxyfurost-5-ene-3beta,26-diol-3-o-beta-diglucorhamnoside; protodioson; shengmating; protodioscin snap-n-shoot 0.1mg/ml(p); protodioscin(p)
A870289
furostane base-2h + o-hex, o-hex-dhex-dhex
CHEMBL4782480

Research Excerpts

Pharmacokinetics

ExcerptReferenceRelevance
" This method was applied to the pharmacokinetic studies on PG level in the rat plasma and its pharmacokinetic effect."( A new quantitation method of protodioscin by HPLC-ESI-MS/MS in rat plasma and its application to the pharmacokinetic study.
Guo, Z; Ito, Y; Li, J; Sun, W; Zhang, X, 2016
)
0.43
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
metaboliteAny intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (5)

ClassDescription
steroid saponinAny saponin derived from a hydroxysteroid.
trisaccharide derivativeAn oligosaccharide derivative that is formally obtained from a trisaccharide.
beta-D-glucosideAny D-glucoside in which the anomeric centre has beta-configuration.
pentacyclic triterpenoid
cyclic hemiketalA hemiacetal having the structure R2C(OH)OR (R =/= H), derived from a ketone by formal addition of an alcohol to the carbonyl group. The term 'cyclic hemiketals', once abandoned by IUPAC, has been reinstated as a subclass of hemiacetals.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Bioassays (4)

Assay IDTitleYearJournalArticle
AID1729698Cytotoxicity against human 293T cells assessed as reduction in cell viability after 72 hrs by MTS assay2021European journal of medicinal chemistry, Jan-15, Volume: 210Structures/cytotoxicity/selectivity relationship of natural steroidal saponins against GSCs and primary mechanism of tribulosaponin A.
AID1729697Cytotoxicity against human GSC18 cells assessed as reduction in cell viability after 72 hrs by MTS assay2021European journal of medicinal chemistry, Jan-15, Volume: 210Structures/cytotoxicity/selectivity relationship of natural steroidal saponins against GSCs and primary mechanism of tribulosaponin A.
AID1729696Cytotoxicity against human GSC3 cells assessed as reduction in cell viability after 72 hrs by MTS assay2021European journal of medicinal chemistry, Jan-15, Volume: 210Structures/cytotoxicity/selectivity relationship of natural steroidal saponins against GSCs and primary mechanism of tribulosaponin A.
AID1729699Cytotoxicity against HUVEC assessed as reduction in cell viability after 72 hrs by MTS assay2021European journal of medicinal chemistry, Jan-15, Volume: 210Structures/cytotoxicity/selectivity relationship of natural steroidal saponins against GSCs and primary mechanism of tribulosaponin A.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (54)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (1.85)18.7374
1990's0 (0.00)18.2507
2000's13 (24.07)29.6817
2010's32 (59.26)24.3611
2020's8 (14.81)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 10.62

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index10.62 (24.57)
Research Supply Index4.09 (2.92)
Research Growth Index4.72 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (10.62)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials1 (1.72%)5.53%
Reviews2 (3.45%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other55 (94.83%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]