Antitumor activity and pharmacokinetics in mice of 8-carbamoyl-3-methyl-imidazo[5,1-d]-1,2,3,5-tetrazin-4(3H)-one (CCRG 81045; M & B 39831), a novel drug with potential as an alternative to dacarbazine.
about
Phase I trial of temozolomide (CCRG 81045: M&B; 39831: NSC 362856)Contemporary murine models in preclinical astrocytoma drug developmentFasting enhances the response of glioma to chemo- and radiotherapyPharmacodynamic and therapeutic investigation of focused ultrasound-induced blood-brain barrier opening for enhanced temozolomide delivery in glioma treatment.Chemotherapeutic Drugs Interfere with Gene Delivery Mediated by Chitosan-Graft-Poly(ethylenimine)Phase I dose-escalation and pharmacokinetic study of temozolomide (SCH 52365) for refractory or relapsing malignanciesTemozolomide followed by combined immunotherapy with GM-CSF, low-dose IL2 and IFN alpha in patients with metastatic melanoma.Marked inactivation of O6-alkylguanine-DNA alkyltransferase activity with protracted temozolomide schedulesPhase I study of temozolamide (TMZ) combined with procarbazine (PCB) in patients with gliomasA phase I (tumour site-specific) study of carboplatin and temozolomide in patients with advanced melanoma.Temozolomide in paediatric high-grade glioma: a key for combination therapy?Phase I study of temozolomide and irinotecan for recurrent malignant gliomas in patients receiving enzyme-inducing antiepileptic drugs: a north american brain tumor consortium studyA phase I trial of temozolomide and lomustine in newly diagnosed high-grade gliomas of childhood.Temozolomide is an active agent in children with recurrent medulloblastoma/primitive neuroectodermal tumor: an Italian multi-institutional phase II trial.Brain Radiotherapy plus Concurrent Temozolomide versus Radiotherapy Alone for Patients with Brain Metastases: A Meta-Analysis.Phase I study of temozolomide in paediatric patients with advanced cancer. United Kingdom Children's Cancer Study GroupEvaluation of the exposure equivalence of oral versus intravenous temozolomide.A peptide & peptide nucleic acid synthesis technology for transporter molecules and theranostics--the SPPS.Progress in the treatment of neuroendocrine tumors.Outcomes of patients treated with capecitabine and temozolamide for advanced pancreatic neuroendocrine tumors (PNETs) and non-PNETsThe medicinal chemistry of imidazotetrazine prodrugsAbsence of the MGMT protein as well as methylation of the MGMT promoter predict the sensitivity for temozolomideQuantitative relationship between guanine O(6)-alkyl lesions produced by Onrigin™ and tumor resistance by O(6)-alkylguanine-DNA alkyltransferase.Activity of irinotecan and temozolomide in the presence of O6-methylguanine-DNA methyltransferase inhibition in neuroblastoma pre-clinical models.Synthesis and quantitative structure-activity relationship of imidazotetrazine prodrugs with activity independent of O6-methylguanine-DNA-methyltransferase, DNA mismatch repair, and p53.Initial testing (stage 1) of temozolomide by the pediatric preclinical testing programO6-methylguanine DNA methyltransferase deficiency and response to temozolomide-based therapy in patients with neuroendocrine tumors.A prospective, phase 1/2 study of everolimus and temozolomide in patients with advanced pancreatic neuroendocrine tumor.Inhibitors of Glioma Growth that Reveal the Tumour to the Immune System.α-Carboline derivative TJY-16 inhibits tumor growth by inducing G2/M cell cycle arrest in glioma cells.Inactivation of O6-alkylguanine-DNA alkyltransferase in human peripheral blood mononuclear cells by temozolomide.Phase II trial of temozolomide in low-grade non-Hodgkin's lymphoma.Low nicotinamide mononucleotide adenylyltransferase activity in a tiazofurin-resistant cell line: effects on NAD metabolism and DNA repairA phase II study of O6-benzylguanine and temozolomide in pediatric patients with recurrent or progressive high-grade gliomas and brainstem gliomas: a Pediatric Brain Tumor Consortium study.A phase II study of temozolomide vs. procarbazine in patients with glioblastoma multiforme at first relapseEfficacy of protracted temozolomide dosing is limited in MGMT unmethylated GBM xenograft models.Silence of bFGF enhances chemosensitivity of glioma cells to temozolomide through the MAPK signal pathway.The p38 mitogen-activated protein kinase pathway links the DNA mismatch repair system to the G2 checkpoint and to resistance to chemotherapeutic DNA-methylating agentsDirect detection and quantification of abasic sites for in vivo studies of DNA damage and repair.Temozolomide and cisplatin in relapsed/refractory acute leukemia.
P2860
Q24683819-99B83C61-819F-418E-AD25-199DB62F7D29Q27026937-EC9C822A-FD07-458D-99F1-FA70ABDC14A4Q27320014-8BB67AFC-3832-4808-A59E-A69181D794E6Q27322329-DFC393A7-B73E-4C74-91A1-E00E33C84B1AQ28547144-E3395036-CCF4-4756-A853-BCE8C8B28553Q33330748-72498CB6-17FF-4852-8C14-86EEC43F2C22Q33346715-F2F25790-07FC-4B4E-A4E7-C142822F8B21Q33347264-65844C5A-9266-4A38-B277-D2EFCCA90E4CQ33349020-7A8A2785-9418-4672-AA9B-93865A3BAA10Q33357549-74185622-00C2-479A-B3F5-F1E6004AF900Q33361765-8FB3C59F-9A94-496B-B913-D4E3D0CB1BA7Q33377664-661673BB-058B-460B-B305-79EC37D923DFQ33379701-99B6C305-73A5-4D50-80E2-6D677FABCB36Q33413067-779F73F5-EDAF-42FB-827B-D76244A6A22FQ33430404-9C6E319D-404A-4319-A6B9-4E50F55B1DC5Q33503725-E0BEB183-D3ED-4F56-8365-EFE9F495E6C0Q33599155-274EEEB0-2868-4BC4-88CB-92E3E8EE553BQ33628437-009172C8-878B-4B94-BAD1-602C796DABCBQ33643643-BCB3ABFD-6234-4FC2-9089-4D0E82C55204Q33948026-9F15FEDD-3C97-416B-B28E-8B0F7D348320Q33963114-0E99A462-CB0D-4143-81D5-4CB015C440DEQ34000287-CB7884FE-8C59-412F-8FDF-FEED08E2C025Q34178990-9F550DA0-A9DE-4C6E-80BC-213DF3772F80Q34344177-2120B75D-2ECE-4681-A553-237684CB111AQ34447471-F6A4F0C9-58BA-441A-A36B-8771ADDAAD05Q34571940-070EA43F-AF63-4085-984E-36FC09E8F1EBQ35001754-375DCDBA-0BF0-4939-90FD-2767DD24CFB9Q35020652-BA34CB55-A5B9-4AEF-8779-B4EEF341BAD2Q35440540-12A1D6B4-659B-48E3-BDE3-B3FCF9242FE5Q35898306-1870AD12-C35C-42E5-B535-D3C4ED5E8578Q35978302-60D1E82F-4415-47EA-BFC8-B9D5804A423AQ36081960-564EE8BB-4CD7-4244-BC03-E265666BEDEAQ36431155-CFCE3FE0-74BD-443E-B028-EAB0C6FA8FFCQ36455403-220F2946-2007-4D63-9539-BAECF087C5BEQ36621800-B8CD03B5-F0B8-424C-AF0A-AD4EC7E49214Q36866006-672EA373-DA3B-45E8-AC4E-EA008D5B81E9Q37020085-C4C48DD6-1438-44DE-8DFD-0F46BF566B25Q37056618-2213901A-1830-4682-8B51-C61C7D99BCB3Q37188627-2A89595E-F742-465A-974A-6A32BBD092E6Q37223615-6ECFBFB6-8323-4A65-924D-3A8C24CC4DA8
P2860
Antitumor activity and pharmacokinetics in mice of 8-carbamoyl-3-methyl-imidazo[5,1-d]-1,2,3,5-tetrazin-4(3H)-one (CCRG 81045; M & B 39831), a novel drug with potential as an alternative to dacarbazine.
description
1987 nî lūn-bûn
@nan
1987 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1987 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1987年の論文
@ja
1987年論文
@yue
1987年論文
@zh-hant
1987年論文
@zh-hk
1987年論文
@zh-mo
1987年論文
@zh-tw
1987年论文
@wuu
name
Antitumor activity and pharmac ...... an alternative to dacarbazine.
@ast
Antitumor activity and pharmac ...... an alternative to dacarbazine.
@en
Antitumor activity and pharmac ...... an alternative to dacarbazine.
@nl
type
label
Antitumor activity and pharmac ...... an alternative to dacarbazine.
@ast
Antitumor activity and pharmac ...... an alternative to dacarbazine.
@en
Antitumor activity and pharmac ...... an alternative to dacarbazine.
@nl
prefLabel
Antitumor activity and pharmac ...... an alternative to dacarbazine.
@ast
Antitumor activity and pharmac ...... an alternative to dacarbazine.
@en
Antitumor activity and pharmac ...... an alternative to dacarbazine.
@nl
P2093
P1433
P1476
Antitumor activity and pharmac ...... an alternative to dacarbazine.
@en
P2093
J A Hickman
M F Stevens
N W Gibson
S P Langdon
P304
P407
P577
1987-11-01T00:00:00Z