Page last updated: 2024-12-08

purpurin 18

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

Description

purpurin 18: isolated from chlorophyll; structure given in first source; RN from Chemical Abstracts Index Guide [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID161493
CHEMBL ID499696
SCHEMBL ID272202
MeSH IDM0164417

Synonyms (20)

Synonym
purpurin 18
CHEMBL499696
puppurin 18
pp-18
21h,23h-porphine-2,20-dicarboxylic acid, 18-(2-carboxyethyl)-12-ethenyl-7-ethyl-17,18-dihydro-3,8,13,17-tetramethyl-, cyclic 2,20-anhydride, (17s-trans)-
purpurin-18
SCHEMBL272202
purpurin18
(17s-trans)-18-(2-carboxyethyl)-12-ethenyl-7-ethyl-17,18-dihydro-3,8,13,17-tetramethyl-21h,23h-porphine-2,20-dicarboxylic acid cyclic 2,20-anhydride
J-016002
RNKGDBZSPISIRN-JXFKEZNVSA-N
pyrpurin-18
HY-128972
3-[(22s,23s)-17-ethenyl-12-ethyl-13,18,22,27-tetramethyl-3,5-dioxo-4-oxa-8,24,25,26-tetrazahexacyclo[19.2.1.16,9.111,14.116,19.02,7]heptacosa-1,6,9(27),10,12,14(26),15,17,19(25),20-decaen-23-yl]propanoic acid
BCP10887
CS-0102953
A936488
(17s,18s)-18-(2-carboxyethyl)-12-vinyl-7-ethyl-17,18-dihydro-3,8,13,17-tetramethyl-21h,23h-porphyrin-2,20-dicarboxylic acid 2,20-anhydride
AT38721
AKOS040744352

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" In addition, as was shown previously, a conjugation of polyamines with several toxic agents led to an increased toxicity to cancer cells."( Conjugation of chlorins with spermine enhances phototoxicity to cancer cells in vitro.
Darmostuk, M; Drašar, P; Jurášek, M; Lengyel, K; Ruml, T; Rumlová, M; Zelenka, J, 2017
)
0.46

Compound-Compound Interactions

ExcerptReferenceRelevance
" We report here that Purpurin-18 (Pu18) in combination with light induces rapid apoptotic cell death in the human leukemia cell line (HL60) at low doses and necrosis at higher concentrations."( Purpurin-18 in combination with light leads to apoptosis or necrosis in HL60 leukemia cells.
Di Stefano, A; Ettorre, A; Giovani, C; Neri, P; Sbrana, S, 2001
)
0.31
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (23)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (4.35)18.7374
1990's0 (0.00)18.2507
2000's11 (47.83)29.6817
2010's10 (43.48)24.3611
2020's1 (4.35)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 23.88

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 moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index23.88 (24.57)
Research Supply Index3.26 (2.92)
Research Growth Index5.50 (4.65)
Search Engine Demand Index23.28 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (23.88)

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%
Other25 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]