Page last updated: 2024-11-08

bietaserpine

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

Description

bietaserpine: hypotensive agent; structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID20054848
CHEMBL ID3989595
CHEBI ID125518
SCHEMBL ID309277
MeSH IDM0045635

Synonyms (44)

Synonym
D07167
bietaserpine (prop.inn)
nsc-369865
53-18-9
bietaserpina [inn-spanish]
bietaserpine
methyl 13-(2-(diethylamino)ethyl)-1,2,3,4,4aalpha,5,7,8,13,13bbeta,14,14aalpha-dodecahydro-2alpha,11-dimethoxy-3beta-((3,4,5-trimethoxybenzoyl)oxy)benz(g)indolo(2,3-a)quinolizine-1beta-carboxylate
1-(2-(diethylamino)ethyl)reserpine
s 1210
methyl 1-(2-(diethylamino)ethyl)-18beta-hydroxy-11,17alpha-dimethoxy-3beta,20alpha-yohimban-16beta-carboxylate, 3,4,5-trimethoxybenzoate (ester)
methyl 13-(2-diethylaminoethyl)-2,11-dimethoxy-3-(3,4,5-trimethoxybenzoyloxy)yohimban-1-carboxylic acid
3-beta,20-alpha-yohimban-16-beta-carboxylic acid, 1-(2-(diethylamino)ethyl)-18-beta-hydroxy-11,17-alpha-dimethoxy-, methyl ester, 3,4,5-trimethoxybenzoate (ester)
einecs 200-165-0
bietaserpinum [inn-latin]
methyl 1alpha,2beta,3alpha,4,4aalpha,5,7,8,13,13bbeta,14,14aalpha-dodecahydro-1-(2-diethylaminoethyl)-2,11-dimethoxy-3beta-(3,4,5-trimethoxybenzoyloxy)-benz(g)indole-(2,3-a)quinolizine-1beta-carboxylate
n-diaethylaminoaethyl-reserpin [german]
l 652
reserpine, 1-(2-(diethylamino)ethyl)-
dl 152
nsc 369865
bietaserpine [inn:dcf]
(1r,15s,17r,18r,19s,20s)-3-[2-(diethylamino)ethyl]-6,18-dimethoxy-17-[oxo-(3,4,5-trimethoxyphenyl)methoxy]-11,12,14,15,16,17,18,19,20,21-decahydro-1h-yohimban-19-carboxylic acid methyl ester
CHEBI:125518
0p5b94fvd5 ,
n-diaethylaminoaethyl-reserpin
unii-0p5b94fvd5
bietaserpina
s-1210 ,
bietaserpinum
BRD-K25210139-001-01-3
SCHEMBL309277
bietaserpine [mi]
methyl 13-(2-(diethylamino)ethyl)-1,2,3,4,4a.alpha.,5,7,8,13,13b.beta.,14,14a.alpha.-dodecahydro-2.alpha.,11-dimethoxy-3.beta.-((3,4,5-trimethoxybenzoyl)oxy)benz(g)indolo(2,3-a)quinolizine-1.beta.-carboxylate
bietaserpine [who-dd]
bietaserpine [mart.]
bietaserpine [inn]
methyl 1-[2-(diethylamino)ethyl]-18beta-hydroxy-11,17alpha-dimethoxy-3beta,20alpha-yohimban-16beta-carboxylate, 3,4,5-trimethoxybenzoate (ester)
dl-152 free base
Q4904688
DB13575
CHEMBL3989595
DTXSID301018918
methyl (1r,15s,17r,18r,19s,20s)-3-[2-(diethylamino)ethyl]-6,18-dimethoxy-17-(3,4,5-trimethoxybenzoyl)oxy-11,12,14,15,16,17,18,19,20,21-decahydro-1h-yohimban-19-carboxylate
AKOS040750798

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" DL-152 was found to be toxic to cells of all the tumor models tested (KHT fibrosarcoma, RIF-1 fibrosarcoma, EMT-6 adenocarcinoma and Lewis lung carcinoma) when the drug was given by intraperitoneal injection to the tumor-bearing mouse and cell survival was measured by excision assay."( Factors influencing the toxicity of diethylaminoethylreserpine to tumor cells: studies with four transplantable tumors.
Lehnert, S, 1987
)
0.27
" Hypoxic cells were detectable in 10-day-old lung tumors, a time at which the tumors were still resistant to the toxic effects of DL-152."( Toxicity of diethylaminoreserpine to a transplantable tumor: the significance of the presence of hypoxic cells.
Lehnert, S, 1982
)
0.26
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
yohimban alkaloid
[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]

Research

Studies (6)

TimeframeStudies, This Drug (%)All Drugs %
pre-19906 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other8 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]