maculine: isolated from Esenbeckia grandiflora; structure in first source
Flora | Rank | Flora Definition | Family | Family Definition |
---|---|---|---|---|
Esenbeckia | genus | [no description available] | Rutaceae | A plant family in the order Sapindales that grows in warmer regions and has conspicuous flowers.[MeSH] |
ID Source | ID |
---|---|
PubMed CID | 68232 |
CHEMBL ID | 503675 |
CHEBI ID | 6629 |
MeSH ID | M0492396 |
Synonym |
---|
9-methoxy[1,3]dioxolo[4,5-g]furo[2,3-b]quinoline |
9-methoxy-1,3-dioxolo(4,5-g)furo(2,3-b)quinoline |
brn 0255599 |
ccris 3577 |
makulin |
nsc-94658 |
maculin |
1,5-g]furo[2,3-b]quinoline, 9-methoxy- |
nsc94658 |
9-methoxy-2h-1,3-dioxolano[4,5-g]furano[2,3-b]quinoline |
maculine |
1,3-dioxolo(4,5-g)furo(2,3-b)quinoline, 9-methoxy- |
524-89-0 |
chebi:6629 , |
CHEMBL503675 |
67w5vpj6ax , |
unii-67w5vpj6ax |
nsc 94658 |
4-27-00-06795 (beilstein handbook reference) |
1,3-dioxolo[4,5-g]furo[2,3-b]quinoline, 9-methoxy- |
9-methoxy[1,3]dioxolo[4,5-g]furo[2,3-b]quinoline # |
VPNYHHBCMOYPCJ-UHFFFAOYSA-N |
DTXSID90200416 |
AKOS030617079 |
Q27107282 |
8-methoxy-4,12,14-trioxa-2-azatetracyclo[7.7.0.03,7.011,15]hexadeca-1(16),2,5,7,9,11(15)-hexaene |
9-methoxy-[1,3]dioxolo[4,5-g]furo[2,3-b]quinoline |
XM161788 |
9-methoxy-1,3-dioxolo[4,5-g]furo[2,3-b]quinoline |
Class | Description |
---|---|
oxacycle | Any organic heterocyclic compound containing at least one ring oxygen atom. |
organonitrogen heterocyclic compound | Any organonitrogen compound containing a cyclic component with nitrogen and at least one other element as ring member atoms. |
organic heterotricyclic compound | An organic tricyclic compound in which at least one of the rings of the tricyclic skeleton contains one or more heteroatoms. |
[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] |
Assay ID | Title | Year | Journal | Article |
---|---|---|---|---|
AID436156 | Cytotoxicity against human A549 cells by SRB assay | 2008 | Journal of natural products, Nov, Volume: 71, Issue:11 | Oxidative burst inhibitory and cytotoxic indoloquinazoline and furoquinoline alkaloids from Oricia suaveolens. |
AID1755695 | Inhibition of GST-tagged recombinant RANKL/M-CSF-induced osteoclastogenesis in C57BL/6 mouse bone marrow derived macrophages assessed as TRAcP enzymatic activity incubated for 5 days with subsequent replenishment of media for 2 days and measured by leucoc | 2021 | European journal of medicinal chemistry, Jan-15, Volume: 210 | Deep learning enables discovery of highly potent anti-osteoporosis natural products. |
AID355720 | Cytotoxicity against human A2780 cells | 2003 | Journal of natural products, Apr, Volume: 66, Issue:4 | New cytotoxic alkaloids from the wood of Vepris punctata from the Madagascar rainforest. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 1 (14.29) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 3 (42.86) | 29.6817 |
2010's | 2 (28.57) | 24.3611 |
2020's | 1 (14.29) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
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 very strong demand-to-supply ratio for research on this compound.
| This Compound (101.86) All Compounds (24.57) |
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 0 (0.00%) | 5.53% |
Reviews | 0 (0.00%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 7 (100.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |