Page last updated: 2024-12-08

prostaglandins b

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

Description

Prostaglandins B: Physiologically active prostaglandins found in many tissues and organs. They are potent pressor substances and have many other physiological activities. [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID161177
CHEMBL ID503644
SCHEMBL ID2825043
MeSH IDM0017808

Synonyms (22)

Synonym
pgb
prostaglandins b
podophyllotoxin beta-d-glucoside
furo(3',4':6,7)naphtho(2,3-d)-1,3-dioxol-6(5ah)-one, 9-(beta-d-glucopyranosyloxy)-5,8,8a,9-tetrahydro-5-(3,4,5-trimethoxyphenyl)-, (5r-(5alpha,5abeta,8aalpha,9alpha))-
podophyllotoxin 4-o-glucoside
podophyllotoxin, beta-d-glucopyranoside
sp-g iia
9-(beta-d-glucopyranosyloxy)-5,8,8a,9-tetrahydro-5-(3,4,5-trimethoxyphenyl)furo(3',4':6,7)naphtho(2,3-d)-1,3-dioxol-6(5ah)-one (5r-(5alpha,5abeta,8aalpha,9alpha))-
podophyllotoxin, 3-beta-d-glucopyranoside
podophyllotoxin-beta-d-glucoside
4,6-o-benzylide-beta-d-glucopyranosidepodophyllotoxin
nsc 163024
podophyllotoxin-beta-d-benzylidene glucoside
16481-54-2
podophyllotoxin glucoside
CHEMBL503644
(5r,5ar,8ar,9r)-5-[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-9-(3,4,5-trimethoxyphenyl)-5a,6,8a,9-tetrahydro-5h-[2]benzofuro[6,5-f][1,3]benzodioxol-8-one
SCHEMBL2825043
podophyllotoxin-4-o-glucoside
HY-N1977
CS-0018297
AKOS040762211

Research Excerpts

Dosage Studied

ExcerptRelevanceReference
" Experiments were divided into three groups: in group A, a 5000 ng dose of OC-5186 was administered via the peripheral vein, 1000 ng via the portal vein, and 200 ng/ml in University of Wisconsin (UW) solution; in group B, the OC-5186 dosage was ten times greater than that in group A; in group C (control group), liver procurement and storage were performed without OC-5186."( Protective effect of a prostaglandin oligomer on liver mitochondria in situ: time-shared measurements of fluorescence and reflectance in the cold-preserved rat liver.
Fujita, T; Hayashi, M; Kitai, T; Ohnishi, ST; Ozawa, K; Tanaka, A; Tokuka, A; Yamaoka, Y, 1992
)
0.28
" However, comparison of the dose-response curves for the actions of prostaglandins on pepsinogen secretion and cAMP revealed that detectable increases in cAMP occurred with concentrations of these agents that were about ten-fold greater than those needed to stimulate pepsinogen secretion."( Relation of prostaglandin-induced increases in cellular cAMP to stimulation of pepsinogen secretion from dispersed chief cells.
Cosowsky, L; Raufman, JP, 1987
)
0.27
" Kinetic and dose-response studies showed that PGBX mimicked te action of ionophore A23187 in PMN."( PGBX, a prostagandin derivative, mimics the action of the calcium ionophore A23187 on human neutrophils.
Korchak, HM; Serhan, CN; Weissmann, G, 1980
)
0.26
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (6)

Assay IDTitleYearJournalArticle
AID73177Cytotoxic effect against GLC4 (human small cell lung carcinoma cell line) using the microculture tetrazolium (MTT) assay based on 2 hr incubation1995Journal of medicinal chemistry, Jun-09, Volume: 38, Issue:12
Synthesis and cytotoxicity of novel lignans.
AID598807Cytotoxicity against human HeLa cells after 72 hrs by MTT assay2011Bioorganic & medicinal chemistry letters, Jun-15, Volume: 21, Issue:12
Three new cytotoxic aryltetralin lignans from Sinopodophyllum emodi.
AID338805Cytotoxicity against human HeLa cells after 4 days by trypan blue assay1992Journal of natural products, Jan, Volume: 55, Issue:1
Isolation, purification, and cytotoxicity of 5-methoxypodophyllotoxin, a lignan from a root culture of Linum flavum.
AID338804Cytotoxicity against mouse EAT cells after 4 days by trypan blue assay1992Journal of natural products, Jan, Volume: 55, Issue:1
Isolation, purification, and cytotoxicity of 5-methoxypodophyllotoxin, a lignan from a root culture of Linum flavum.
AID598808Cytotoxicity against human KB cells after 72 hrs by MTT assay2011Bioorganic & medicinal chemistry letters, Jun-15, Volume: 21, Issue:12
Three new cytotoxic aryltetralin lignans from Sinopodophyllum emodi.
AID73178Cytotoxic effect against GLC4 (human small cell lung carcinoma cell line) using the microculture tetrazolium (MTT) assay based on continuous incubation1995Journal of medicinal chemistry, Jun-09, Volume: 38, Issue:12
Synthesis and cytotoxicity of novel lignans.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (166)

TimeframeStudies, This Drug (%)All Drugs %
pre-1990113 (68.07)18.7374
1990's42 (25.30)18.2507
2000's7 (4.22)29.6817
2010's3 (1.81)24.3611
2020's1 (0.60)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 9.08

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 Index9.08 (24.57)
Research Supply Index5.16 (2.92)
Research Growth Index4.24 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (9.08)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews7 (4.05%)6.00%
Case Studies1 (0.58%)4.05%
Observational0 (0.00%)0.25%
Other165 (95.38%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]