Page last updated: 2024-11-11

peplomycin

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Description

Peplomycin: An antineoplastic agent derived from BLEOMYCIN. [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID6852373
CHEMBL ID3990196
CHEBI ID135909
MeSH IDM0026717

Synonyms (32)

Synonym
pepleomycin
peplomycin
ccris 2756
bleomycin pep
n(sup 1)-(3-((1-phenylethyl)amino)propyl)bleomycinamide
bleomycinamide, n(sup 1)-(3-((1-phenylethyl)amino)propyl)-
peplomycine [inn-french]
einecs 269-484-0
peplomycin [inn]
bleomycinamide, n1-(3-((1-phenylethyl)amino)propyl)-, (s)-
peplomycina [inn-spanish]
peplomycinum [inn-latin]
brn 0782891
CHEBI:135909
D08336
68247-85-8
peplomycin (inn)
56h9l80niz ,
peplomycinum
unii-56h9l80niz
peplomycina
peplomycine
peplomycin [jan]
peplomycin [who-dd]
n(sup 1)-(3-(((1s)-1-phenylethyl)amino)propyl)bleomycinamide
n(sup 1)-(3-(((s)-.alpha.-methylbenzyl)amino)propyl)bleomycinamide
peplomycin [mi]
CHEMBL3990196
Q27261405
DTXSID701024414
CS-0025659
HY-106364

Research Excerpts

Toxicity

In 1 carcinoma of the gall bladder peplomycin was more toxic than bleomycin.

ExcerptReferenceRelevance
"Combination of the two drugs bleomycin (BLM) and peplomycin (PEP) may enhance their antineoplastic effects; however, it is not known as to whether this enhancement is accompanied by a concomitant increase in toxicity, especially toxic lung damage."( Pulmonary toxicity of the combination of bleomycin and peplomycin--an experimental study in rats.
Burkhardt, A; Mall, G, 1991
)
0.78
" In 1 carcinoma of the gall bladder peplomycin was more toxic than bleomycin."( Comparison of bleomycin and peplomycin toxicity on clonogenic tumor cells from various human tumors.
Engelhardt, R; Fiebig, HH; Löhr, GW; Neumann, HA; Runge, HM, 1986
)
0.84
" Combination therapy of anti-platelet aggregating agents such as phthalazinol, dipyridamole, ticlopidine and indomethacin suppressed these toxic changes."( [Effects of anti-platelet aggregating agents on peplomycin induced pulmonary toxicity in mice].
Ekimoto, H; Ito, J; Okada, M; Takahashi, K, 1989
)
0.53
"The relative therapeutic and toxic effects of two new analogs were compared with bleomycin over a range of doses."( Relative pulmonary toxicity and antitumor effects of two new bleomycin analogs, pepleomycin and tallysomycin A.
Gram, TE; Siddik, ZH; Sikic, BI,
)
0.13
" Blm-BAPP was significantly more pulmonary toxic than bleomycin and had no greater activity against B16 melanoma than either bleomycin or pepleomycin."( A comparison of the pulmonary toxicity and chemotherapeutic activity of bleomycin-BAPP to bleomycin and pepleomycin.
Ginsburg, E; Gram, TE; Trush, MA, 1984
)
0.27
"The anti-tumour effects and adverse events were evaluated in 163 MIBC patients who received systemic chemotherapy (SC, n = 34), intra-arterial chemotherapy (IAC, n = 50), or combined IAC and radiotherapy (IAC + R, n = 79)."( Efficacy and safety of systemic chemotherapy and intra-arterial chemotherapy with/without radiotherapy for bladder preservation or as neo-adjuvant therapy in patients with muscle-invasive bladder cancer: a single-centre study of 163 patients.
Hayashi, N; Matsuo, T; Miyata, Y; Nomata, K; Ohba, K; Sakai, H; Sakamoto, I; Uetani, M, 2015
)
0.42
" The incidence of severe adverse events was higher in the IAC + R group (36."( Efficacy and safety of systemic chemotherapy and intra-arterial chemotherapy with/without radiotherapy for bladder preservation or as neo-adjuvant therapy in patients with muscle-invasive bladder cancer: a single-centre study of 163 patients.
Hayashi, N; Matsuo, T; Miyata, Y; Nomata, K; Ohba, K; Sakai, H; Sakamoto, I; Uetani, M, 2015
)
0.42

Pharmacokinetics

ExcerptReferenceRelevance
" The pharmacokinetic parameters of MTX in plasma and CSF were estimated."( Pharmacokinetics of methotrexate in plasma and cerebrospinal fluid.
Abe, T; Ghoda, M; Hori, S; Mori, T; Morikawa, N; Takeyama, M, 1997
)
0.3
" The half-life of MTX in the CSF in the space left by tumor removal exceeded the half-lives of MTX in the plasma and in the ventricular CSF."( Pharmacokinetics of methotrexate in plasma and cerebrospinal fluid.
Abe, T; Ghoda, M; Hori, S; Mori, T; Morikawa, N; Takeyama, M, 1997
)
0.3
" THP concentration was measured by HPLC, and the pharmacokinetic parameters of this drug were estimated in plasma and CSF."( Pharmacokinetics of intra-arterially administered pirarubicin in plasma and cerebrospinal fluid of patients with glioma.
Hori, S; Mori, T; Morikawa, N; Takeyama, M, 1998
)
0.3

Compound-Compound Interactions

The effect of local anesthetics alone and combined with hyperthermia on the cytotoxic effect of the bleomycin derivative, peplomycin, was studied. The objectives of this study were to evaluate survival in 141 patients with stage II-IV oral squamous cell carcinoma.

ExcerptReferenceRelevance
"Fourty eight patients with cancer of head of pancreas have been treated by the intra-arterial infusion of 5-FU and Mitomycin C alone or in combination with regional hyperthermia, employing microwave machine operating at a frequency of 2450 MHz."( [Hyperthermia: microwave hyperthermia in combination with intra-arterial infusion chemotherapy of cancer of the pancreas].
Endo, Y; Funatomi, H; Hatta, Y; Hirose, N; Miura, T; Sassa, T; Taguchi, S; Yoshikawa, N, 1985
)
0.27
" Experiments are described here in which Chinese hamster V-79 cells in culture and a murine squamous cell carcinoma in vivo have been used to obtain survival curves for pepleomycin alone or in combination with radiation."( The in vitro and in vivo antitumor effects of pepleomycin alone or in combination with radiation.
Komatsu, K; Matsumoto, Y; Sakamoto, K, 1985
)
0.27
"The effect of local anesthetics alone and combined with hyperthermia on the cytotoxic effect of the bleomycin derivative, peplomycin, was studied in FM3A and HeLa cells."( Selective enhancement of the cytotoxicity of the bleomycin derivative, peplomycin, by local anesthetics alone and combined with hyperthermia.
Ishida, A; Mizuno, S, 1982
)
0.7
" At this time the ITC therapy is used in combination with induced-hypertension-chemotherapy (IHC therapy)."( [The clinical effect of hyperthermia combined with induced hypertension chemotherapy].
Hayashida, S; Kobayashi, T; Sugimoto, K, 1984
)
0.27
" Ten patients with inoperable advanced esophageal cancer were treated with endoscopic local injection of PEP-CH combined with radiation using 60Co."( [Local injection of peplomycin adsorbed on activated carbon particles combined with 60Co radiation against inoperable advanced esophageal cancer--two long-term survivors].
Hagiwara, A; Kojima, O; Oyama, T; Ozaki, K; Sakakibara, T; Sakakura, C; Sasaki, S; Shimotsuma, M; Takahashi, T; Tsujimoto, H, 1993
)
0.61
" The object of this study is to evaluate the efficacy of preoperative chemotherapy combined with radiation therapy for bladder cancer."( [The long-term effect and outcome of preoperative chemotherapy combined with radiation therapy for bladder cancer].
Hayashida, S; Kamata, S; Mitsui, H; Nakane, H; Nasu, T, 1996
)
0.29
"We examined the interactive effects of hyperthermia combined with cisplatin (CDDP) (0."( In vitro effects of hyperthermia combined with cisplatin or peplomycin on the human maxillary carcinoma cell line IMC-2.
Hayashi, S; Kano, E; Kitai, R; Matsumoto, H; Ohtsubo, T; Saito, H; Saito, T; Shioura, H,
)
0.37
" In conclusion, the local administration of epinephrine combined with hyperthermia significantly retarded tumor growth without an increase in skin reactions or lung metastases."( Epinephrine or peplomycin combined with hyperthermia in irradiated Lewis lung carcinoma: effects on tumor growth, skin reaction, and lung metastasis.
Mori, T; Ohizumi, Y; Tamai, Y, 1996
)
0.65
"The objectives of this study were to evaluate survival in 141 patients with stage II-IV oral squamous cell carcinoma (OSCC) treated with preoperative intra-arterial chemotherapy with docetaxel, cisplatin, and peplomycin combined with intravenous chemotherapy using 5-fluorouracil (IADCPIVF) via the superficial temporal artery, and to clarify the prognostic factors."( Preoperative intra-arterial chemotherapy with docetaxel, cisplatin, and peplomycin combined with intravenous chemotherapy using 5-fluorouracil for oral squamous cell carcinoma.
Endo, M; Hasegawa, H; Kaneko, T; Kanno, C; Kano, M; Kitabatake, T; Monma, T; Sato, E; Takeishi, E; Yamazaki, M, 2020
)
0.98

Dosage Studied

A new dosage form (PEP-CH) of peplomycin was tested for therapeutic efficacy against lymph node metastasis in mice.

ExcerptRelevanceReference
" Total dosage was 60 Gy of Linac irradiation under 80-110 mg infusion of PEP."( [Feasibility and radicality of PEP-chemoradiation therapy in oral squamous cell carcinoma].
Abe, A; Hibi, G; Mineno, Y; Murai, T; Oka, T; Okui, K; Sugiura, N; Tsujikawa, T; Yamauchi, T, 1990
)
0.28
"A new dosage form (PEP-CH) of peplomycin was tested for therapeutic efficacy against lymph node metastasis in mice."( Enhanced anti-cancer efficacy on lymph node metastasis using peplomycin adsorbed on small activated carbon particles.
Hagiwara, A; Ito, M; Iwamoto, A; Sasabe, T; Shimotsuma, M; Takahashi, T; Yoneyama, C, 1991
)
0.81
"A new dosage form consisting of small activated carbon particles which adsorb Aclacinomycin A, Adriamycin, Mitomycin C or Pepleomycin was prepared in order to deliver larger amounts of anticancer agents to the lymph nodes through the high ability of lymphatics to adsorb particles."( Anticancer agents adsorbed by activated carbon particles, a new form of dosage enhancing efficacy on lymphnodal metastases.
Ahn, T; Hagiwara, A; Iwamoto, A; Takahashi, T; Torii, T; Ueda, T,
)
0.13
" The schedule and dosage of each chemotherapy were as follows."( [Non-cross-resistant sequential combination chemotherapy consisting of cis-diammine-dichloroplatinum (II) mainly, based on synchronization theory, in human bladder cancer xenografts in athymic nude mice].
Okada, K; Yamauchi, T; Yoshida, O, 1986
)
0.27
"Pulmonary toxicity was examined by means of Matsuda and Takahashi's procedure in peplomycin solution, and two types of a new dosage form of peplomycin (PEP-CH), which has peplomycin adsorbed on to activated carbon particles."( Reduced pulmonary toxicity of peplomycin in a new drug-delivery system.
Hagiwara, A; Takahashi, T; Torii, T; Ueda, T, 1988
)
0.79
"The effect of a new dosage form for anti-cancer agents was studied on tissue distribution and compared with the aqueous solution form."( Activated carbon particles as anti-cancer drug carrier into regional lymph nodes.
Hagiwara, A; Iwamoto, A; Takahashi, T; Torii, T; Ueda, T, 1987
)
0.27
" In samples from eight different donors, homogeneous dose-response curves were observed."( Treatment of human clonogenic tumor cells and bone marrow progenitor cells with bleomycin and peplomycin under 40.5 degrees C hyperthermia in vitro.
Engelhardt, R; Fiebig, HH; Herrmann, DB; Neumann, HA, 1989
)
0.5
" The mean dosage of peplomycin given was 79."( [Continuous subcutaneous infusion of peplomycin in oral squamous carcinoma].
Hanazawa, Y; Kanazawa, H; Kinehara, M; Muto, M; Sato, K; Takahara, M; Takahara, T; Takahashi, K; Uchiyama, S, 1989
)
0.87
" Changes in both the PEP treatment time and dosage produced a redistribution which decreases the number of cells in the G1 phase and increased the number of cells in the S and G2-M phases."( [Experimental studies on combination chemotherapy based on cell cycle analysis].
Tsuboi, T, 1985
)
0.27
" Six patients were treated at a level of 5 mg/m2, 8 patients at 10 mg/m2 and 4 patients at 15 mg/m2 of peplomycin, each dosage being given twice weekly intravenously."( Phase I evaluation of peplomycin with special reference to pulmonary toxicity.
Hansen, HH; Rørth, M; Sørensen, PG, 1983
)
0.8
" Studying the growth-inhibitory potencies of BLM (clinical mixture), BLM-A2, BLM-B2 and PEP in the L5178y mouse lymphoma cell culture system, it was elucidated that the slopes of the dose-response curves at the ED50 concentration (around 1 microgram/ml) were steeper for PEP than for BLM."( Potentiation of the cytostatic effect of bleomycin on L5178y mouse lymphoma cells by pepleomycin.
Bachmann, M; Geisert, M; Maidhof, A; Müller, WE; Umezawa, H; Zahn, RK, 1983
)
0.27
" The toxicities in the case of intra-arterial infusion were less prominent than in the case of intravenous administration of the same dosage of the oncostatics."( [Intra-arterial infusion of oncostatics in recurrent cervical carcinoma].
Iijima, S; Inaba, J; Kawagoe, K; Sasaki, J; Tsunoda, H, 1983
)
0.27
" In a dose-response study, BLM and peplomycin (PEP) were investigated in Sprague-Dawley rats of both sexes."( Carcinogenicity of bleomycin sulfate and peplomycin sulfate after repeated subcutaneous application to rats.
Habs, M; Schmähl, D, 1984
)
0.81
"The cytokinetic response of Ehrlich ascites tumor (EAT) cells in vivo upon chronic treatment at low dosage levels with cytarabine (1-beta-D-arabinofuranosylcytosine, ara-c) bleomycin (BLM) and peplomycin (PEP) was estimated."( Cytostatic and cytotoxic response of Ehrlich ascites tumor cells in vivo on chronic treatment with cytarabine, bleomycin, and peplomycin.
Engel, P; Friedel, G; Futterman, G; Goerttler, K; Stoehr, M, 1984
)
0.66
"We have developed a new dosage form, PEP-CH, consisting of peplomycin adsorbed onto small activated carbon particles."( [Local injection of peplomycin adsorbed on activated carbon particles combined with 60Co radiation against inoperable advanced esophageal cancer--two long-term survivors].
Hagiwara, A; Kojima, O; Oyama, T; Ozaki, K; Sakakibara, T; Sakakura, C; Sasaki, S; Shimotsuma, M; Takahashi, T; Tsujimoto, H, 1993
)
0.85
"A new dosage formulation consisting of an anticancer drug bound to activated carbon particles was developed for the treatment of digestive cancer in patients in whom operation is contraindicated."( Endoscopic local injection of a new drug delivery formulation, anticancer drug bound to carbon particles, for digestive cancers: pilot study.
Hagiwara, A; Imanishi, T; Kitamura, K; Ohgaki, M; Sakakura, C; Shirasu, M; Takahashi, T; Yamasaki, J, 1997
)
0.3
"The CSF AUCs of MTX in the ventricle and the space left by tumor removal increased markedly and in parallel with the MTX dosage increase during osmotic disruption of the blood-brain barrier and intraarterial combination chemotherapy."( Pharmacokinetics of methotrexate in plasma and cerebrospinal fluid.
Abe, T; Ghoda, M; Hori, S; Mori, T; Morikawa, N; Takeyama, M, 1997
)
0.3
"A new dosage formulation consisting of anticancer drugs bound to carbon particles was developed for treating cancers of the upper digestive tract, and is designed to distribute higher levels of anticancer drug to the regional lymph nodes and at the injection site, as compared to a drug in aqueous solution form."( [Endoscopic local injection of anticancer drugs bound to carbon particles for treatment of upper digestive tract cancers--clinical trials].
Hagiwara, A; Imanishi, T; Ohgaki, M; Sakakura, C; Sawai, K; Shirasu, M; Takahashi, T; Taniguchi, H; Togawa, T; Yamaguchi, T; Yamasaki, J, 1997
)
0.3
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
glycopeptideAny carbohydrate derivative that consists of glycan moieties covalently attached to the side chains of the amino acid residues that constitute the peptide.
[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 (510)

TimeframeStudies, This Drug (%)All Drugs %
pre-1990286 (56.08)18.7374
1990's162 (31.76)18.2507
2000's49 (9.61)29.6817
2010's10 (1.96)24.3611
2020's3 (0.59)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 18.29

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 Index18.29 (24.57)
Research Supply Index6.37 (2.92)
Research Growth Index4.08 (4.65)
Search Engine Demand Index21.17 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (18.29)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials51 (9.57%)5.53%
Reviews20 (3.75%)6.00%
Case Studies85 (15.95%)4.05%
Observational0 (0.00%)0.25%
Other377 (70.73%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]