Compounds > perophoramidine

Page last updated: 2024-11-10

perophoramidine

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

Description

perophoramidine: from the Philippine ascidian Perophora namei; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID Source	ID
PubMed CID	3081926
MeSH ID	M0447158

Synonyms (6)

Synonym
474779-75-4
1h,8h-pyrrolo(2',3':2,3)pyrido(4,3-o)quinindoline, 6-bromo-10,12-dichloro-2,3,14,15-tetrahydro-1-methyl-, (3ar,13bs)-rel-(+)
perophoramidine
DTXSID50963853
6-bromo-10,12-dichloro-1-methyl-2,3,14,15-tetrahydro-1h,9h-benzo[c]indolo[3,2-j]pyrrolo[3,2-e][2,6]naphthyridine
(1s)-13-bromo-4,6-dichloro-20-methyl-8,10,20,22-tetrazahexacyclo[15.7.0.01,9.02,7.011,16.017,21]tetracosa-2(7),3,5,8,11(16),12,14,21-octaene

[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (19)

Timeframe	Studies, This Drug (%)	All Drugs %
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	7 (36.84)	29.6817
2010's	10 (52.63)	24.3611
2020's	2 (10.53)	2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication Type	This drug (%)	All Drugs (%)
Trials	0 (0.00%)	5.53%
Reviews	2 (10.53%)	6.00%
Case Studies	0 (0.00%)	4.05%
Observational	0 (0.00%)	0.25%
Other	17 (89.47%)	84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Substance	Relationship Strength	Studies	Trials	Classes	Roles
tryptamine [no description available]	2.03	1	0	aminoalkylindole; aralkylamino compound; indole alkaloid; tryptamines	human metabolite; mouse metabolite; plant metabolite
physostigmine Physostigmine: A cholinesterase inhibitor that is rapidly absorbed through membranes. It can be applied topically to the conjunctiva. It also can cross the blood-brain barrier and is used when central nervous system effects are desired, as in the treatment of severe anticholinergic toxicity.	2.06	1	0	carbamate ester; indole alkaloid	antidote to curare poisoning; EC 3.1.1.8 (cholinesterase) inhibitor; miotic
isatin tribulin: endogenous MONOAMINE OXIDASE inhibitory activity extractable into ethyl acetate found in brain and many mammalian tissues and fluids; ISATIN is a major component; produced in excess following alcohol withdrawal;	2.03	1	0	indoledione	EC 1.4.3.4 (monoamine oxidase) inhibitor; plant metabolite
indoline indoline: structure given in first source	7.03	1	0	indoles
molybdenum Molybdenum: A metallic element with the atomic symbol Mo, atomic number 42, and atomic weight 95.95. It is an essential trace element, being a component of the enzymes xanthine oxidase, aldehyde oxidase, and nitrate reductase.	2.06	1	0	chromium group element atom	micronutrient
phenserine phenserine: a carbamate analog of physostigmine; a long-acting inhibitor of cholinesterase	2.06	1	0
2-oxindole 2-oxindole: RN given refers to parent cpd; structure. indolin-2-one : An indolinone carrying an oxo group at position 2.	2.06	1	0	gamma-lactam; indolinone
minfiensine minfiensine: structure in first source	3.14	1	0
communesin f communesin F: structure in first source	4.08	4	0
communesin b communesin B: from ethyl acetate extract of Penicillium sp., derived from the Mediterranean sponge Axinella verrucosa; structure in first source	4.38	6	0
communesin a communesin A: structure in first source	9.35	3	0