Compounds > homochelidonine
Page last updated: 2024-11-08

homochelidonine

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

Description

homochelidonine: structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID164609
CHEBI ID31025
SCHEMBL ID13998253
MeSH IDM0507403

Synonyms (24)

Synonym
(+/-)-homochelidonine
homochelidonine
476-33-5
(4br,5s,11bs)-1,2-dimethoxy-12-methyl-5,6,11b,13-tetrahydro-4bh-[1,3]benzodioxolo[5,6-c]phenanthridin-5-ol
unii-zp901rx893
zp901rx893 ,
(4br-(4balpha,5beta,11balpha))-4b,5,6,11b,12,13-hexahydro-1,2-dimethoxy-12-methyl(1,3)benzodioxolo(5,6-c)phenanthridin-5-ol
einecs 207-505-7
norchelidonine
.alpha.-homochelidonine
(1,3)benzodioxolo(5,6-c)phenanthridin-5-ol, 4b,5,6,11b,12,13-hexahydro-1,2-dimethoxy-12-methyl-, (4br,5s,11bs)-
homochelidonine [mi]
(+)-homochelidonine
(1,3)benzodioxolo(5,6-c)phenanthridin-5-ol, 4b,5,6,11b,12,13-hexahydro-1,2-dimethoxy-12-methyl-, (4br-(4b.alpha.,5.beta.,11b.alpha.))-
homochelidonine, (+)-
(4br-(4b.alpha.,5.beta.,11b.alpha.))-4b,5,6,11b,12,13-hexahydro-1,2-dimethoxy-12-methyl(1,3)benzodioxolo(5,6-c)phenanthridin-5-ol
alpha-homochelidonine
CHEBI:31025
SCHEMBL13998253
a-allocryptopine
DTXSID20197209 ,
Q27114075
dtxcid80119700
(1,3)benzodioxolo(5,6-c)phenanthridin-5-ol, 4b,5,6,11b,12,13-hexahydro-1,2-dimethoxy-12-methyl-, (4br-(4balpha,5beta,11balpha))-
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
benzophenanthridine alkaloidA specific group of isoquinoline alkaloids that occur only in higher plants and are constituents mainly of the Papaveraceae family.
[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-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (33.33)29.6817
2010's3 (50.00)24.3611
2020's1 (16.67)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.79

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 Index12.79 (24.57)
Research Supply Index1.95 (2.92)
Research Growth Index4.73 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.79)

All Compounds (24.57)

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%
Other6 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
SubstanceRelationship StrengthStudiesTrialsClassesRoles
indole
[no description available]		2.2510indole;
polycyclic heteroarene		Escherichia coli metabolite
naphthalene
[no description available]		2.0310naphthalenes;
ortho-fused bicyclic arene		apoptosis inhibitor;
carcinogenic agent;
environmental contaminant;
mouse metabolite;
plant metabolite;
volatile oil component
(+-)stylopine
[no description available]		2.0810
iridium
Iridium: A metallic element with the atomic symbol Ir, atomic number 77, and atomic weight 192.22.		2.2510cobalt group element atom;
platinum group metal atom
palladium
Palladium: A chemical element having an atomic weight of 106.4, atomic number of 46, and the symbol Pd. It is a white, ductile metal resembling platinum, and following it in abundance and importance of applications. It is used in dentistry in the form of gold, silver, and copper alloys.. palladium : Chemical element (nickel group element atom) with atomic number 46.		2.7630metal allergen;
nickel group element atom;
platinum group metal atom
alkenes
[no description available]		2.0310
benzyne
benzyne: structure in first source. benzyne : 1,2-didehydrobenzene and its derivatives formed by substitution.		2.0710aryne;
benzyne
dihydrosanguinarine
[no description available]		2.0810benzophenanthridine alkaloidantifungal agent;
metabolite
chelidonine
chelidonine: benzophenanthridine derived from scoulerine from Chelidonium majus; RN given refers to parent cpd (chelidonine, (5bR-(5balpha,6beta,12alpha))-isomer)		3.1950alkaloid antibiotic;
alkaloid fundamental parent;
benzophenanthridine alkaloid
strychnine
Strychnine: An alkaloid found in the seeds of STRYCHNOS NUX-VOMICA. It is a competitive antagonist at glycine receptors and thus a convulsant. It has been used as an analeptic, in the treatment of nonketotic hyperglycinemia and sleep apnea, and as a rat poison.. strychnine : A monoterpenoid indole alkaloid that is strychnidine bearing a keto substituent at the 10-position.		2.2510monoterpenoid indole alkaloid;
organic heteroheptacyclic compound		avicide;
cholinergic antagonist;
glycine receptor antagonist;
neurotransmitter agent;
rodenticide
thiourea
Thiourea: A photographic fixative used also in the manufacture of resins. According to the Fourth Annual Report on Carcinogens (NTP 85-002, 1985), this substance may reasonably be anticipated to be a carcinogen (Merck Index, 9th ed). Many of its derivatives are ANTITHYROID AGENTS and/or FREE RADICAL SCAVENGERS.. thiourea : The simplest member of the thiourea class, consisting of urea with the oxygen atom substituted by sulfur.		2.2510one-carbon compound;
thioureas;
ureas		antioxidant;
chromophore
akuammicine
akuammicine: from Strychnos sp;; structure in first source. akuammicine : A monoterpenoid indole alkaloid with formula C20H22N2O2, isolated from several plant species including Alstonia spatulata, Catharanthus roseus and Vinca major.		2.2510methyl ester;
monoterpenoid indole alkaloid;
organic heteropentacyclic compound;
tertiary amino compound		plant metabolite
ConditionIndicatedRelationship StrengthStudiesTrials