Page last updated: 2024-12-11

ski 2053r

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

Description

SKI 2053R: structure in first source; RN given in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID6918271
MeSH IDM0239684

Synonyms (6)

Synonym
AC-2111
ski-2053r
nsc-644591
ski 2053r
AKOS015964850
[(4r,5r)-5-(aminomethyl)-2-propan-2-yl-1,3-dioxolan-4-yl]methanamine;platinum;propanedioic acid

Research Excerpts

Actions

ExcerptReferenceRelevance
"SKI 2053R did not cause significant neurotoxicity or mucositis."( A Phase I study of cis-malonato[(4R,5R)-4,5-bis(aminomethyl)-1,3-dioxolane] platinum(II) in patients with advanced malignancies.
Bang, YJ; Cho, YB; Heo, DS; Kim, DK; Kim, KH; Kim, NK; Kim, TY; Lee, JA; Park, YI; Shin, SG, 2001
)
1.03

Treatment

ExcerptReferenceRelevance
"In SKI 2053R-treated groups, the time required for a mean tumor weight of 1,000 mg was 33.1 days in KATO III xenografts and 35.0 days in WiDr xenografts as compared with 30.2 and 27.2 days in CDDP-treated groups, respectively."( Antitumor activity of cis-malonato[(4R,5R)-4,5-bis(aminomethyl)-2- isopropyl-1,3-dioxolane]platinum(II), a new platinum analogue, as an anticancer agent.
Ahn, JS; Cho, YB; Hong, WS; Kim, DK; Kim, HT; Kim, KH; Kim, TS; Tai, JH, 1995
)
0.81

Toxicity

ExcerptReferenceRelevance
" The results show that SKI 2053R is embryotoxic at a minimally maternally toxic dose in rats."( Embryotoxic effects of SKI 2053R, a new potential anticancer agent, in rats.
Chung, MK; Kim, JC; Roh, JK,
)
0.75
"Heptaplatin is a newly developed platinum derivative which has been reported to be less toxic than cisplatin."( Nephrotoxicity of heptaplatin: a randomized comparison with cisplatin in advanced gastric cancer.
Ahn, JH; Bahng, H; Chang, HM; Kang, WC; Kang, YK; Kim, TW; Kim, WK; Lee, JS; Park, JS, 2002
)
0.31
" Measures to more effectively prevent nephrotoxicity should be developed for the safe use of heptaplatin."( Nephrotoxicity of heptaplatin: a randomized comparison with cisplatin in advanced gastric cancer.
Ahn, JH; Bahng, H; Chang, HM; Kang, WC; Kang, YK; Kim, TW; Kim, WK; Lee, JS; Park, JS, 2002
)
0.31
"The present study was conducted to test the possible teratogenic and toxic effects of anti-cancer drug heptaplatin (SKI 2053) on developing embryos and fetuses in gestating SWR/J mice."( Embryo-feto-toxicity of anticancer drug, heptaplatin in laboratory mice.
Abdel-Samad, MF; Abou-Tarboush, FM; Al-Ahmadi, BA; Al-Anazi, KM; Al-Faifi, MY; Farah, MA, 2010
)
0.36

Compound-Compound Interactions

ExcerptReferenceRelevance
" Overall, the present study supports the clinical development of HTP in combination with low-dose PTX against HNSCC."( Anti-tumor activity of heptaplatin in combination with 5-fluorouracil or paclitaxel against human head and neck cancer cells in vitro.
Cho, YB; Kim, SY; Kuh, HJ; Lee, JW; Lee, SH; Park, JK, 2006
)
0.33
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (19)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's9 (47.37)18.2507
2000's5 (26.32)29.6817
2010's5 (26.32)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 11.10

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 Index11.10 (24.57)
Research Supply Index3.26 (2.92)
Research Growth Index4.36 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (11.10)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials4 (19.05%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other17 (80.95%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]